PLANT MESSENGER PACKS ENCAPSULATING POLYPEPTIDES AND USES THEREOF

Abstract

Disclosed herein are plant messenger packs (PMPs) encapsulating one or more exogenous polypeptides. Also disclosed are methods of producing a PMP comprising an exogenous polypeptide.

Description

BACKGROUND

Polypeptides (e.g., proteins or peptides) are used in therapies (e.g., for the treatment of a disease or condition), for diagnostic purposes, and as pathogen control agents. However, current methods of delivering polypeptides to cells may be limited by the mechanism of delivery, e.g., the efficiency of delivery of the polypeptide to a cell. Therefore, there is a need in the art for methods and compositions for the delivery of polypeptides to cells.

SUMMARY OF THE INVENTION

In one aspect, the invention features a plant messenger pack (PMP) comprising one or more exogenous polypeptides, wherein the one or more exogenous polypeptides are mammalian therapeutic agents and are encapsulated by the PMP, and wherein the exogenous polypeptides are not pathogen control agents.

In some aspects, the mammalian therapeutic agent is an enzyme. In some aspects, the enzyme is a recombination enzyme or an editing enzyme.

In some aspects, the mammalian therapeutic agent is an antibody or an antibody fragment.

In some aspects, the mammalian therapeutic agent is an Fc fusion protein.

In some aspects, the mammalian therapeutic agent is a hormone. In some aspects, the mammalian therapeutic agent is insulin.

In some aspects, the mammalian therapeutic agent is a peptide.

In some aspects, the mammalian therapeutic agent is a receptor agonist or a receptor antagonist.

In some aspects, the mammalian therapeutic agent is an antibody of Table 1, a peptide of Table 2, an enzyme of Table 3, or a protein of Table 4.

In some aspects, the mammalian therapeutic agent has a size of less than 100 kD.

In some aspects, the mammalian therapeutic agent has a size of less than 50 kD.

In some aspects, the mammalian therapeutic agent has an overall charge that is neutral. In some aspects, the mammalian therapeutic agent has been modified to have a charge that is neutral. In some aspects, the mammalian therapeutic agent has an overall charge that is positive. In some aspects, the mammalian therapeutic agent has an overall charge that is negative.

In some aspects, the exogenous polypeptide is released from the PMP in a target cell with which the PMP is contacted. In some aspects, the exogenous polypeptide exerts activity in the cytoplasm of the target cell. In some aspects, the exogenous polypeptide is translocated to the nucleus of the target cell.

In some aspects, the exogenous polypeptide exerts activity in the nucleus of the target cell.

In some aspects, uptake by a cell of the exogenous polypeptide encapsulated by the PMP is increased relative to uptake of the exogenous polypeptide not encapsulated by a PMP.

In some aspects, the effectiveness of the exogenous polypeptide encapsulated by the PMP is increased relative to the effectiveness of the exogenous polypeptide not encapsulated by a PMP.

In some aspects, the exogenous polypeptide comprises at least 50 amino acid residues.

In some aspects, the exogenous polypeptide is at least 5 kD in size.

In some aspects, the PMP comprises a purified plant extracellular vesicle (EV), or a segment or extract thereof. In some aspects, the EV or segment or extract thereof is obtained from a citrus fruit, e.g., a grapefruit or a lemon.

In another aspect, the invention features a composition comprising a plurality of the PMPs of any of the above aspects.

In some aspects, the PMPs in the composition are at a concentration effective to increase the fitness of a mammal.

In some aspects, the exogenous polypeptide is at a concentration of at least 0.01, 0.1, 0.2, 0.3, 0.4, 0.5, or 1 μg polypeptide/mL.

In some aspects, at least 15% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide. In some aspects, at least 50% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide. In some aspects, at least 95% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide.

In some aspects, the composition is formulated for administration to a mammal. In some aspects, the composition is formulated for administration to a mammalian cell.

In some aspects, the composition further comprises a pharmaceutically acceptable vehicle, carrier, or excipient.

In some aspects, the composition is stable for at least one day at room temperature, and/or stable for at least one week at 4° C. In some aspects, the PMPs are stable for at least 24 hours, 48 hours, seven days, or 30 days at 4° C. In some aspects, the PMPs are further stable at a temperature of at least 20° C., 24° C., or 37° C.

In another aspect, the disclosure features a composition comprising a plurality of PMPs, wherein each of the PMPs is a plant EV, or a segment or extract thereof, wherein each of the plurality of PMPs encapsulate an exogenous polypeptide, wherein the exogenous polypeptide is a mammalian therapeutic agent, the exogenous polypeptide is not a pathogen control agent, and the composition is formulated for delivery to an animal.

In another aspect, the disclosure features a pharmaceutical composition comprising a composition according to any one of the above aspects and a pharmaceutically acceptable vehicle, carrier, or excipient.

In another aspect, the disclosure features a method of producing a PMP comprising an exogenous polypeptide, wherein the exogenous polypeptide is a mammalian therapeutic agent, and wherein the exogenous polypeptide is not a pathogen control agent, the method comprising (a) providing a solution comprising the exogenous polypeptide; and (b) loading the PMP with the exogenous polypeptide, wherein the loading causes the exogenous polypeptide to be encapsulated by the PMP.

In some aspects, the exogenous polypeptide is soluble in the solution.

In some aspects, the loading comprises one or more of sonication, electroporation, and lipid extrusion. In some aspects, the loading comprises sonication and lipid extrusion. In some aspects, the loading comprises lipid extrusion. In some aspects, PMP lipids are isolated prior to lipid extrusion. In some aspects, the isolated PMP lipids comprise glycosylinositol phosphorylceramides (GIPCs).

In another aspect, the disclosure features a method for delivering a polypeptide to a mammalian cell, the method comprising (a) providing a PMP comprising one or more exogenous polypeptides, wherein the one or more exogenous polypeptides are mammalian therapeutic agents and are encapsulated by the PMP, and wherein the exogenous polypeptides are not pathogen control agents; and (b) contacting the cell with the PMP, wherein the contacting is performed with an amount and for a time sufficient to allow uptake of the PMP by the cell. In some aspects, the cell is a cell in a subject.

In another aspect, the disclosure features a PMP, composition, pharmaceutical composition, or method of any of the above aspects, wherein the mammal is a human.

In another aspect, the disclosure features a method for treating diabetes, the method comprising administering to a subject in need thereof an effective amount of a composition comprising a plurality of PMPs, wherein one or more exogenous polypeptides are encapsulated by the PMP. In some aspects, the administration of the plurality of PMPs lowers the blood sugar of the subject. In some aspects, the exogenous polypeptide is insulin.

In another aspect, the disclosure features a PMP, composition, pharmaceutical composition, or method of any of the above aspects, wherein the PMP is not significantly degraded by gastric fluids, e.g., is not significantly degraded by fasted gastric fluids.

In a further aspect, the disclosure features a plant messenger pack (PMP) comprising one or more exogenous polypeptides, wherein the one or more exogenous polypeptides are encapsulated by the PMP.

In some aspects, the exogenous polypeptide is a therapeutic agent. In some aspects, the therapeutic agent is insulin.

In some aspects, the exogenous polypeptide is an enzyme. In some aspects, the enzyme is a recombination enzyme or an editing enzyme.

In some aspects, the exogenous peptide is a pathogen control agent.

In some aspects, the exogenous polypeptide is released from the PMP in a target cell with which the PMP is contacted. In some aspects, the exogenous polypeptide exerts activity in the cytoplasm of the target cell. In some aspects, the exogenous polypeptide is translocated to the nucleus of the target cell.

In some aspects, the exogenous polypeptide exerts activity in the nucleus of the target cell.

In some aspects, uptake by a cell of the exogenous polypeptide encapsulated by the PMP is increased relative to uptake of the exogenous polypeptide not encapsulated by a PMP.

In some aspects, the effectiveness of the exogenous polypeptide encapsulated by the PMP is increased relative to the effectiveness of the exogenous polypeptide not encapsulated by a PMP.

In some aspects, the exogenous polypeptide comprises at least 50 amino acid residues. In some aspects, the exogenous polypeptide is at least 5 kD in size.

In some aspects, the exogenous polypeptide comprises fewer than 50 amino acid residues.

In some aspects, the PMP comprises a purified plant extracellular vesicle (EV), or a segment or extract thereof. In some aspects, the EV or segment or extract thereof is obtained from a citrus fruit. In some aspects, the citrus fruit is a grapefruit or a lemon.

In another aspect, the disclosure features a composition comprising a plurality of the PMPs of any of the above aspects.

In some aspects, the PMPs in the composition are at a concentration effective to increase the fitness of an organism. In some aspects, the PMPs in the composition are at a concentration effective to decrease the fitness of an organism.

In some aspects, the exogenous polypeptide is at a concentration of at least 0.01, 0.1, 0.2, 0.3, 0.4, 0.5, or 1 μg polypeptide/mL.

In some aspects, at least 15% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide. In some aspects, at least 50% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide. In some aspects, at least 95% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide.

In some aspects, the composition is formulated for administration to an animal. In some aspects, the composition is formulated for administration to an animal cell. In some aspects, the composition further comprises a pharmaceutically acceptable vehicle, carrier, or excipient.

In some aspects, the composition is formulated for administration to a plant. In some aspects, the composition is formulated for administration to a bacterium. In some aspects, the composition is formulated for administration to a fungus.

In some aspects, the composition is stable for at least one day at room temperature, and/or stable for at least one week at 4° C. In some aspects, the PMPs are stable for at least 24 hours, 48 hours, seven days, or 30 days at 4° C. In some aspects, the PMPs are further stable at a temperature of at least 20° C., 24° C., or 37° C.

In another aspect, the disclosure features a composition comprising a plurality of PMPs, wherein each of the PMPs is a plant EV, or a segment or extract thereof, wherein each of the plurality of PMPs encapsulate an exogenous polypeptide, and wherein the composition is formulated for delivery to an animal.

In another aspect, the disclosure features a pharmaceutical composition comprising a composition according to claim 1 and a pharmaceutically acceptable vehicle, carrier, or excipient.

In another aspect, the disclosure features a method of producing a PMP comprising an exogenous polypeptide, the method comprising (a) providing a solution comprising the exogenous polypeptide; and (b) loading the PMP with the exogenous polypeptide, wherein the loading causes the exogenous polypeptide to be encapsulated by the PMP.

In some aspects, the exogenous polypeptide is soluble in the solution.

In some aspects, the loading comprises one or more of sonication, electroporation, and lipid extrusion. In some aspects, the loading comprises sonication and lipid extrusion.

In some aspects, loading comprises lipid extrusion. In some aspects, PMP lipids are isolated prior to lipid extrusion. In some aspects, the isolated PMP lipids comprise glycosylinositol phosphorylceramides (GIPCs).

In another aspect, the disclosure features a method for delivering a polypeptide to a cell, the method comprising (a) providing a PMP comprising one or more exogenous polypeptides, wherein the one or more exogenous polypeptides are encapsulated by the PMP; and (b) contacting the cell with the PMP, wherein the contacting is performed with an amount and for a time sufficient to allow uptake of the PMP by the cell.

In some aspects, the cell is an animal cell. In some aspects, the cell is a cell in a subject.

In another aspect, the disclosure features a method for treating diabetes, the method comprising administering to a subject in need thereof an effective amount of a composition comprising a plurality of PMPs, wherein one or more exogenous polypeptides are encapsulated by the PMP. In some aspects, the administration of the plurality of PMPs lowers the blood sugar of the subject. In some aspects, the exogenous polypeptide is insulin.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A is a scatter plot and a bar graph showing PMP final concentration (PMPs/mL) and PMP size (in nm) in combined PMP-containing size exclusion chromatography (SEC) fractions following filter sterilization.

FIG. 1B is a graph showing PMP protein concentration (in μg/mL) in individual eluted fractions from SEC, as measured using a bicinchoninic acid assay (BCA assay). PMPs are eluted in fractions 4-6.

FIG. 2A is a schematic diagram showing the use of the Cre reporter system with plant messenger packs (PMPs) loaded with Cre recombinase. Human embryonic kidney 293 cells (HEK293 cells) comprising a Cre reporter transgene express GFP in the absence of the Cre protein (Unrecombined reporter⁺ cell), and express RFP in the presence of the Cre protein (Recombined reporter⁺ cell). The Cre protein is delivered to the cell in a PMP (+Cre-PMP).

FIG. 2B is a set of micrographs showing expression of fluorescent proteins in HEK293 cells that have been treated with Cre recombinase (Cre) and grapefruit (GF) PMPs that have not been electroporated; GFP PMPs only; CRE only; or Cre-loaded grapefruit PMPs. The top row shows fluorescence of GFP. The middle row shows fluorescence of RFP. RFP is expressed only in cells that have received Cre-loaded GF PMPs. The bottom row shows an overlay of the GFP and RFP fluorescent signals and a brightfield channel.

FIG. 3 is a schematic diagram showing an assay for the stability of loaded PMPs provided by oral delivery. (i) shows a PMP loaded with a human insulin polypeptide and comprising the covalent membrane dye DL800 IR or Alexa488. (ii) shows an in vitro assay for stability of PMPs and insulin exposed to mimetics of gastrointestinal (GI) juice. (iii) shows an in vivo assay for stability of PMPs and insulin provided by oral delivery (PMP gavage) to a streptzotocin-induced diabetes model mouse. Blood glucose levels, blood human insulin levels, immune profile, and biodistribution of DL800-labeled PMPs are measured.

FIG. 4 is a schematic diagram showing an assay for in vivo delivery by PMPs of Cre recombinase to a mouse having a luciferase Cre reporter construct (Lox-STOP-Lox-LUC). When Cre recombinase is delivered to a cell or tissue, recombination occurs and luciferase is expressed. Biodistribution of Cre recombinase by PMPs is measured by assessing luciferase expression in mouse tissues.

FIG. 5A is a schematic diagram showing a protocol for grapefruit PMP production using a destructive juicing step involving the use of a blender, followed by ultracentrifugation and sucrose gradient purification. Images are included of the grapefruit juice after centrifugation at 1000×g for 10 min and the sucrose gradient band pattern after ultracentrifugation at 150,000×g for 2 hours.

FIG. 5B is a plot of the PMP particle distribution measured by the Spectradyne NCS1.

FIG. 6 is a schematic diagram showing a protocol for grapefruit PMP production using a mild juicing step involving use of a mesh filter, followed by ultracentrifugation and sucrose gradient purification. Images are included of the grapefruit juice after centrifugation at 1000×g for 10 min and the sucrose gradient band pattern after ultracentrifugation at 150,000×g for 2 hours.

FIG. 7A is a schematic diagram showing a protocol for grapefruit PMP production using ultracentrifugation, followed by size exclusion chromatography (SEC) to isolate the PMP-containing fractions. The eluted SEC fractions are analyzed for particle concentration (NanoFCM), median particle size (NanoFCM), and protein concentration (BCA).

FIG. 7B is a graph showing particle concentration per mL in eluted size exclusion chromatography (SEC) fractions (NanoFCM). The fractions containing the majority of PMPs (“PMP fraction”) are indicated with an arrow. PMPs are eluted in fractions 2-4.

FIG. 7C is a set of graphs and a table showing particle size in nm for selected SEC fractions, as measured using NanoFCM. The graphs show PMP size distribution in fractions 1, 3, 5, and 8.

FIG. 7D is a graph showing protein concentration in μg/mL in SEC fractions, as measured using a BCA assay. The fraction containing the majority of PMPs (“PMP fraction”) is labeled, and an arrow indicates a fraction containing contaminants.

FIG. 8A is a schematic diagram showing a protocol for scaled PMP production from 1 liter of grapefruit juice (˜7 grapefruits) using a juice press, followed by differential centrifugation to remove large debris, 100× concentration of the juice using TFF, and size exclusion chromatography (SEC) to isolate the PMP containing fractions. The SEC elution fractions are analyzed for particle concentration (NanoFCM), median particle size (NanoFCM) and protein concentration (BCA).

FIG. 8B is a pair of graphs showing protein concentration (BCA assay, top panel) and particle concentration (NanoFCM, bottom panel) of SEC eluate volume (ml) from a scaled starting material of 1000 ml of grapefruit juice, showing a high amount of contaminants in the late SEC elution volumes.

FIG. 8C is a graph showing that incubation of the crude grapefruit PMP fraction with a final concentration of 50 mM EDTA, pH 7.15 followed by overnight dialysis using a 300 kDa membrane, successfully removed contaminants present in the late SEC elution fractions, as shown by absorbance at 280 nm. There was no difference in the dialysis buffers used (PBS without calcium/magnesium pH 7.4, MES pH 6, Tris pH 8.6).

FIG. 8D is a graph showing that incubation of the crude grapefruit PMP fraction with a final concentration of 50 mM EDTA, pH 7.15, followed by overnight dialysis using a 300 kDa membrane, successfully removed contaminants present in the late elution fractions after SEC, as shown by BCA protein analysis, which, besides detecting protein, is sensitive to the presence of sugars and pectins. There was no difference in the dialysis buffers used (PBS without calcium/magnesium pH 7.4, MES pH 6, Tris pH 8.6).

FIG. 9A is a graph showing particle concentration (particles/ml) in eluted BMS plant cell culture SEC fractions, as measured by nano-flow cytometry (NanoFCM). PMPs were eluted in SEC fractions 4-6.

FIG. 9B is a graph showing absorbance at 280 nm (A.U.) in eluted BMS SEC fractions, measured on a SpectraMax® spectrophotometer. PMPs were eluted in fractions 4-6; fractions 9-13 contained contaminants.

FIG. 9C is a graph showing protein concentration (μg/ml) in eluted BMS SEC fractions, as determined by BCA analysis. PMPs were eluted in fractions 4-6; fractions 9-13 contained contaminants.

FIG. 9D is a scatter plot showing particles in the combined BMS PMP-containing SEC fractions as measured by nano-flow cytometry (NanoFCM). PMP concentration (particles/ml) was determined using a bead standard according to NanoFCM's instructions.

FIG. 9E is a graph showing the size distribution of BMS PMPs (nm) for the gated particles (background subtracted) of FIG. 6D. Median PMP size (nm) was determined using Exo bead standards according to NanoFCM's instructions.

FIG. 10 is a graph showing the luminescence (R.L.U., relative luminescence unit) of Pseudomonas aeruginosa bacteria that were treated with Ultrapure water (negative control), 3 ng free luciferase protein (protein only control) or with an effective luciferase protein dose of 3 ng by luciferase protein-loaded PMPs (PMP-Luc) in duplicate samples for 2 hrs at RT. Luciferase protein in the supernatant and pelleted bacteria was measured by luminescence using the ONE-Glo™ luciferase assay kit (Promega) and measured on a SpectraMax® spectrophotometer.

FIG. 11A is a Western blot showing insulin protein from insulin-loaded reconstructed PMPs recPMPs) that have been treated with a 1% Triton™ X-100 solution (Triton; Tx), a Proteinase K (ProtK) solution, a Tx solution followed by a ProtK solution, or a ProtK solution followed by a Tx solution. An untreated control is also shown.

FIG. 11B is a Western blot showing insulin protein from insulin-loaded recPMPs from lemon PMP lipids after incubation in simulated gastrointestinal fluids or a phosphate buffered saline (PBS) control at 37° C. PBS, pH 7.4, Fasted gastric fluid (Gastric Fasted), pH 1.6, 1 hour incubation; fasted intestinal fluid (Intestine Fasted), pH 6.4, 4 hour incubation; fed intestinal fluid (Intestine Fed), pH 5.8, 4 hour incubation.

DETAILED DESCRIPTION OF THE INVENTION

I. Definitions

As used herein, the term “encapsulate” or “encapsulated” refers to an enclosure of a moiety (e.g., an exogenous polypeptide as defined herein) within an enclosed lipid membrane structure, e.g., a lipid bilayer. The lipid membrane structure may be, e.g., a plant messenger pack (PMP) or a plant extracellular vesicle (EV), or may be obtained from or derived from a plant EV. An encapsulated moiety (e.g., an encapsulated exogenous polypeptide) is enclosed by the lipid membrane structure, e.g., such an encapsulated moiety is located in the lumen of the enclosed lipid membrane structure (e.g., the lumen of a PMP). The encapsulated moiety (e.g., the encapsulated polypeptide) may, in some instances, interact or associate with the inner face of the lipid membrane structure. The exogenous polypeptide may, in some instances, be intercalated with the lipid membrane structure. In some instances, the exogenous polypeptide has an extraluminal portion.

As used herein, the term “exogenous polypeptide” refers to a polypeptide (as is defined herein) that is encapsulated by a PMP (e.g., a PMP derived from a plant extracellular vesicle) that does not naturally occur in a plant lipid vesicle (e.g., does not naturally occur in a plant extracellular vesicle) or that is encapsulated in a PMP in an amount not found in a naturally occurring plant extracellular vesicle. The exogenous polypeptide may, in some instances, naturally occur in the plant from which the PMP is derived. In other instances, the exogenous polypeptide does not naturally occur in the plant from which the PMP is derived. The exogenous polypeptide may be artificially expressed in the plant from which the PMP is derived, e.g., may be a heterologous polypeptide. The exogenous polypeptide may be derived from another organism. In some aspects, the exogenous polypeptide is loaded into the PMP, e.g., using one or more of sonication, electroporation, lipid extraction, and lipid extrusion. The exogenous polypeptide may be, e.g., a therapeutic agent, an enzyme (e.g., a recombination enzyme or an editing enzyme), or a pathogen control agent.

As used herein, “delivering” or “contacting” refers to providing or applying a PMP composition (e.g., a PMP composition comprising an exogenous protein or peptide) to an organism, e.g., an animal, a plant, a fungus, or a bacterium. Delivery to an animal may be, e.g., oral delivery (e.g., delivery by feeding or by gavage) or systemic delivery (e.g., delivery by injection). The PMP composition may be delivered to the digestive tract, e.g., the stomach, the small intestine, or the large intestine. The PMP composition may be stable in the digestive tract.

As used herein, the term “animal” refers to humans, livestock, farm animals, invertebrates (e.g., insects), or mammalian veterinary animals (e.g., including for example, dogs, cats, horses, rabbits, zoo animals, cows, pigs, sheep, chickens, and non-human primates).

As used herein “decreasing the fitness of a pathogen” refers to any disruption to pathogen physiology as a consequence of administration of a PMP composition described herein, including, but not limited to, any one or more of the following desired effects: (1) decreasing a population of a pathogen by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (2) decreasing the reproductive rate of a pathogen by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (3) decreasing the mobility of a pathogen by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (4) decreasing the body weight or mass of a pathogen by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (5) decreasing the metabolic rate or activity of a pathogen by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; or (6) decreasing pathogen transmission (e.g., vertical or horizontal transmission of a pathogen from one insect to another) by a pathogen by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more. A decrease in pathogen fitness can be determined, e.g., in comparison to an untreated pathogen.

As used herein “decreasing the fitness of a vector” refers to any disruption to vector physiology, or any activity carried out by said vector, as a consequence of administration of a vector control composition described herein, including, but not limited to, any one or more of the following desired effects: (1) decreasing a population of a vector by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (2) decreasing the reproductive rate of a vector (e.g., insect, e.g., mosquito, tick, mite, louse) by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (3) decreasing the mobility of a vector (e.g., insect, e.g., mosquito, tick, mite, louse) by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (4) decreasing the body weight of a vector (e.g., insect, e.g., mosquito, tick, mite, louse) by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (5) increasing the metabolic rate or activity of a vector (e.g., insect, e.g., mosquito, tick, mite, louse) by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (6) decreasing vector-vector pathogen transmission (e.g., vertical or horizontal transmission of a vector from one insect to another) by a vector (e.g., insect, e.g., mosquito, tick, mite, louse) by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (7) decreasing vector-animal pathogen transmission by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (8) decreasing vector (e.g., insect, e.g., mosquito, tick, mite, louse) lifespan by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; (9) increasing vector (e.g., insect, e.g., mosquito, tick, mite, louse) susceptibility to pesticides (e.g., insecticides) by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more; or (10) decreasing vector competence by a vector (e.g., insect, e.g., mosquito, tick, mite, louse) by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, 100% or more. A decrease in vector fitness can be determined, e.g., in comparison to an untreated vector.

As used herein, the term “formulated for delivery to an animal” refers to a PMP composition that includes a pharmaceutically acceptable carrier.

As used herein, the term “formulated for delivery to a pathogen” refers to a PMP composition that includes a pharmaceutically acceptable or agriculturally acceptable carrier.

As used herein, the term “formulated for delivery to a vector” refers to a PMP composition that includes an agriculturally acceptable carrier.

As used herein, the term “infection” refers to the presence or colonization of a pathogen in an animal (e.g., in one or more parts of the animal), on an animal (e.g., on one or more parts of the animal), or in the habitat surrounding an animal, particularly where the infection decreases the fitness of the animal, e.g., by causing a disease, disease symptoms, or an immune (e.g., inflammatory) response.

As used herein the term “pathogen” refers to an organism, such as a microorganism or an invertebrate, which causes disease or disease symptoms in an animal by, e.g., (i) directly infecting the animal, (ii) by producing agents that causes disease or disease symptoms in an animal (e.g., bacteria that produce pathogenic toxins and the like), and/or (iii) that elicit an immune (e.g., inflammatory response) in animals (e.g., biting insects, e.g., bedbugs). As used herein, pathogens include, but are not limited to bacteria, protozoa, parasites, fungi, nematodes, insects, viroids and viruses, or any combination thereof, wherein each pathogen is capable, either by itself or in concert with another pathogen, of eliciting disease or symptoms in humans.

As used herein, the term polypeptide,” “peptide,” or “protein” encompasses any chain of naturally or non-naturally occurring amino acids (either D- or L-amino acids), regardless of length (e.g., at least 2, 3, 4, 5, 6, 7, 10, 12, 14, 16, 18, 20, 25, 30, 40, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, or more than 1000 amino acids), the presence or absence of post-translational modifications (e.g., glycosylation or phosphorylation), or the presence of, e.g., one or more non-amino acyl groups (for example, sugar, lipid, etc.) covalently linked to the polypeptide, and includes, for example, natural polypeptides, synthetic or recombinant polypeptides, hybrid molecules, peptoids, or peptidomimetics. The polypeptide may be, e.g. at least 0.1, at least 1, at least 5, at least 10, at least 15, at least 20, at least 30, at least 40, at least 50, or more than 50 kD in size. The polypeptide may be a full-length protein. Alternatively, the polypeptide may comprise one or more domains of a protein.

As used herein, the term “antibody” encompasses an immunoglobulin, whether natural or partly or wholly synthetically produced, and fragments thereof, capable of specifically binding to an antigen. The term also covers any protein having a binding domain which is homologous to an immunoglobulin binding domain. These proteins can be derived iron natural sources, or partly or wholly synthetically produced. “Antibody” further includes a polypeptide comprising a framework region from an immunoglobulin gene or fragments thereof that specifically binds and recognizes an antigen. Use of the term “antibody” is meant to include whole antibodies, polyclonal, monoclonal and recombinant antibodies, fragments thereof, and further includes single-chain antibodies (nanobodies); humanized antibodies; murine antibodies; chimeric, mouse-human, mouse-primate, primate-human monoclonal antibodies, anti-idiotype antibodies, antibody fragments, such as, e.g., scFv, (scFv)2, Fab, Fab′; and F(ab′)2, F(ab1)2, Fv, dAb, and Fd fragments, diabodies, and antibody-related polypeptides. “Antibody” further includes bispecific antibodies and multispecific antibodies.

The term “antigen binding fragment”, as used herein, refers to fragments of an intact immunoglobulin, and any part of a polypeptide including antigen binding regions having the ability to specifically bind to the antigen. For example, the antigen binding fragment may be a F(ab′)2 fragment, a Fab′ fragment, a Fab fragment, a Fv fragment, or a scFv fragment, but is not limited thereto. A Fab fragment has one antigen binding site and contains the variable regions of a light chain and a heavy chain, the constant region of the light chain, and the first constant region CH₁ of the heavy chain. A Fab′ fragment differs from a Fab fragment in that the Fab′ fragment additionally includes the hinge region of the heavy chain, including at least one cysteine residue at the C-terminal of the heavy chain CH₁ region.

The F(ab′)2 fragment is produced whereby cysteine residues of the Fab′ fragment are joined by a disulfide bond at the hinge region. A Fv fragment is the minimal antibody fragment having only heavy chain variable regions and light chain variable regions, and a recombinant technique for producing the Fv fragment is well known in the art, Two-chain Fv fragments may have a structure in which heavy chain variable regions are linked to light chain variable regions by a non-covalent bond. Single-chain Fv (scFv) fragments generally may have a dimer structure as in the two-chain Fv fragments in which heavy chain variable regions are covalently bound to light chain variable regions via a peptide linker or heavy and light chain variable regions are directly linked to each other at the C-terminal thereof. The antigen binding fragment may be obtained using a protease (for example, a whole antibody is digested with papain to obtain Fab fragments, and is digested with pepsin to obtain F(ab′)2 fragments), and may be prepared by a genetic recombinant technique. A dAb fragment consists of a VH domain.

Single-chain antibody molecules may comprise a polymer with a number of individual molecules, for example, dimer, trimer or other polymers.

As used herein, the term “heterologous” refers to an agent (e.g., a polypeptide) that is either (1) exogenous to the plant (e.g., originating from a source that is not the plant or plant part from which the PMP is produced) (e.g., an agent which is added to the PMP using loading approaches described herein) or (2) endogenous to the plant cell or tissue from which the PMP is produced, but present in the PMP (e.g., added to the PMP using loading approaches described herein, genetic engineering, as well as in vitro or in vivo approaches) at a concentration that is higher than that found in nature (e.g., higher than a concentration found in a naturally-occurring plant extracellular vesicle).

As used herein, “percent identity” between two sequences is determined by the BLAST 2.0 algorithm, which is described in Altschul et al., (1990) J. Mol. Biol. 215:403-410. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information.

As used herein, the term “plant” refers to whole plants, plant organs, plant tissues, seeds, plant cells, seeds, and progeny of the same. Plant cells include, without limitation, cells from seeds, suspension cultures, embryos, meristematic regions, callus tissue, leaves, roots, shoots, gametophytes, sporophytes, pollen, and microspores. Plant parts include differentiated and undifferentiated tissues including, but not limited to the following: roots, stems, shoots, leaves, pollen, seeds, fruit, harvested produce, tumor tissue, and various forms of cells and culture (e.g., single cells, protoplasts, embryos, and callus tissue). The plant tissue may be in a plant or in a plant organ, tissue, or cell culture. In addition, a plant may be genetically engineered to produce a heterologous protein or RNA.

As used herein, the term “plant extracellular vesicle”, “plant EV”, or “EV” refers to an enclosed lipid-bilayer structure naturally occurring in a plant. Optionally, the plant EV includes one or more plant EV markers. As used herein, the term “plant EV marker” refers to a component that is naturally associated with a plant, such as a plant protein, a plant nucleic acid, a plant small molecule, a plant lipid, or a combination thereof, including but not limited to any of the plant EV markers listed in the Appendix. In some instances, the plant EV marker is an identifying marker of a plant EV but is not a pesticidal agent. In some instances, the plant EV marker is an identifying marker of a plant EV and also a pesticidal agent (e.g., either associated with or encapsulated by the plurality of PMPs, or not directly associated with or encapsulated by the plurality of PMPs).

As used herein, the term “plant messenger pack” or “PMP” refers to a lipid structure (e.g., a lipid bilayer, unilamellar, multilamellar structure; e.g., a vesicular lipid structure), that is about 5-2000 nm (e.g., at least 5-1000 nm, at least 5-500 nm, at least 400-500 nm, at least 25-250 nm, at least 50-150 nm, or at least 70-120 nm) in diameter that is derived from (e.g., enriched, isolated or purified from) a plant source or segment, portion, or extract thereof, including lipid or non-lipid components (e.g., peptides, nucleic acids, or small molecules) associated therewith and that has been enriched, isolated or purified from a plant, a plant part, or a plant cell, the enrichment or isolation removing one or more contaminants or undesired components from the source plant. PMPs may be highly purified preparations of naturally occurring EVs. Preferably, at least 1% of contaminants or undesired components from the source plant are removed (e.g., at least 2%, 5%, 10%, 15%, 20%, 25%, 30%, 40%, 45%, 50%, 55%, 60%, 70%, 80%, 90%, 95%, 96%, 98%, 99%, or 100%) of one or more contaminants or undesired components from the source plant, e.g., plant cell wall components; pectin; plant organelles (e.g., mitochondria; plastids such as chloroplasts, leucoplasts or amyloplasts; and nuclei); plant chromatin (e.g., a plant chromosome); or plant molecular aggregates (e.g., protein aggregates, protein-nucleic acid aggregates, lipoprotein aggregates, or lipido-proteic structures). Preferably, a PMP is at least 30% pure (e.g., at least 40% pure, at least 50% pure, at least 60% pure, at least 70% pure, at least 80% pure, at least 90% pure, at least 99% pure, or 100% pure) relative to the one or more contaminants or undesired components from the source plant as measured by weight (w/w), spectral imaging (% transmittance), or conductivity (S/m).

In some instances, the PMP is a lipid extracted PMP (LPMP). As used herein, the terms “lipid extracted PMP” and “LPMP” refer to a PMP that has been derived from a lipid structure (e.g., a lipid bilayer, unilamellar, multilamellar structure; e.g., a vesicular lipid structure) derived from (e.g., enriched, isolated or purified from) a plant source, wherein the lipid structure is disrupted (e.g., disrupted by lipid extraction) and reassembled or reconstituted in a liquid phase (e.g., a liquid phase containing a cargo) using standard methods, e.g., reconstituted by a method comprising lipid film hydration and/or solvent injection, to produce the LPMP, as is described herein. The method may, if desired, further comprise sonication, freeze/thaw treatment, and/or lipid extrusion, e.g., to reduce the size of the reconstituted PMPs. A PMP (e.g., a LPMP) may comprise between 10% and 100% lipids derived from the lipid structure from the plant source, e.g., may contain at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, or 100% lipids derived from the lipid structure from the plant source. A PMP (e.g., a LPMP) may comprise all or a fraction of the lipid species present in the lipid structure from the plant source, e.g., it may contain at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or 100% of the lipid species present in the lipid structure from the plant source. A PMP (e.g., a LPMP) may comprise none, a fraction, or all of the protein species present in the lipid structure from the plant source, e.g., may contain 0%, less than 1%, less than 5%, less than 10%, less than 15%, less than 20%, less than 30%, less than 40%, less than 50%, less than 60%, less than 70%, less than 80%, less than 90%, less than 100%, or 100% of the protein species present in the lipid structure from the plant source. In some instances, the lipid bilayer of the PMP (e.g., LPMP) does not contain proteins. In some instances, the lipid structure of the PMP (e.g., LPMP) contains a reduced amount of proteins relative to the lipid structure from the plant source.

PMPs (e.g., LPMPs) may optionally include exogenous lipids, e.g., lipids that are either (1) exogenous to the plant (e.g., originating from a source that is not the plant or plant part from which the PMP is produced) (e.g., added the PMP using methods described herein) or (2) endogenous to the plant cell or tissue from which the PMP is produced, but present in the PMP (e.g., added to the PMP using methods described herein, genetic engineering, in vitro or in vivo approaches) at a concentration that is higher than that found in nature (e.g., higher than a concentration found in a naturally-occurring plant extracellular vesicle). The lipid composition of the PMP may include 0%, less than 1%, or at least 1%, 2%, 5%, 10%, 15%, 20%, 25%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or more than 95% exogenous lipid. Exemplary exogenous lipids include cationic lipids, ionizable lipids, zwitterionic lipids, and lipidoids.

PMPs may optionally include additional agents, such as polypeptides, therapeutic agents, polynucleotides, or small molecules. The PMPs can carry or associate with additional agents (e.g., polypeptides) in a variety of ways to enable delivery of the agent to a target plant, e.g., by encapsulating the agent, incorporation of the agent in the lipid bilayer structure, or association of the agent (e.g., by conjugation) with the surface of the lipid bilayer structure. Heterologous functional agents can be incorporated into the PMPs either in vivo (e.g., in planta) or in vitro (e.g., in tissue culture, in cell culture, or synthetically incorporated).

As used herein, the term “pure” refers to a PMP preparation in which at least a portion (e.g., at least 20%, 25%, 30%, 40%, 45%, 50%, 55%, 60%, 70%, 80%, 90%, 95%, 96%, 98%, 99%, or 100%) of plant cell wall components, plant organelles (e.g., mitochondria, chloroplasts, and nuclei), or plant molecule aggregates (protein aggregates, protein-nucleic acid aggregates, lipoprotein aggregates, or lipido-proteic structures) have been removed relative to the initial sample isolated from a plant, or part thereof.

As used herein, the term “repellent” refers to an agent, composition, or substance therein, that deters pathogen vectors (e.g., insects, e.g., mosquitos, ticks, mites, or lice) from approaching or remaining on an animal. A repellent may, for example, decrease the number of pathogen vectors on or in the vicinity of an animal, but may not necessarily kill or decreasing the fitness of the pathogen vector.

As used herein, the term “treatment” refers to administering a pharmaceutical composition to an animal or a plant for prophylactic and/or therapeutic purposes. To “prevent an infection” refers to prophylactic treatment of an animal or a plant that does not yet have a disease or condition, but which is susceptible to, or otherwise at risk of, a particular disease or condition. To “treat an infection” refers to administering treatment to an animal or a plant already suffering from a disease to improve or stabilize the animal's condition.

As used herein, the term “treat an infection” refers to administering treatment to an individual (e.g., a plant or an animal) already having a disease to improve or stabilize the individual's condition. This may involve reducing colonization of a pathogen in, on, or around an animal or a plant by one or more pathogens (e.g., by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100%) relative to a starting amount and/or allow benefit to the individual (e.g., reducing colonization in an amount sufficient to resolve symptoms). In such instances, a treated infection may manifest as a decrease in symptoms (e.g., by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100%). In some instances, a treated infection is effective to increase the likelihood of survival of an individual (e.g., an increase in likelihood of survival by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100%) or increase the overall survival of a population (e.g., an increase in likelihood of survival by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100%).

For example, the compositions and methods may be effective to “substantially eliminate” an infection, which refers to a decrease in the infection in an amount sufficient to sustainably resolve symptoms (e.g., for at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 months) in the animal or plant.

As used herein, the term “prevent an infection’ refers to preventing an increase in colonization in, on, or around an animal or plant by one or more pathogens (e.g., by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or more than 100% relative to an untreated animal or plant) in an amount sufficient to maintain an initial pathogen population (e.g., approximately the amount found in a healthy individual), prevent the onset of an infection, and/or prevent symptoms or conditions associated with infection. For example, an individual (e.g., an animal, e.g., a human) may receive prophylaxis treatment to prevent a fungal infection while being prepared for an invasive medical procedure (e.g., preparing for surgery, such as receiving a transplant, stem cell therapy, a graft, a prosthesis, receiving long-term or frequent intravenous catheterization, or receiving treatment in an intensive care unit), in immunocompromised individuals (e.g., individuals with cancer, with HIV/AIDS, or taking immunosuppressive agents), or in individuals undergoing long term antibiotic therapy.

As used herein, the term “stable PMP composition” (e.g., a composition including loaded or non-loaded PMPs) refers to a PMP composition that over a period of time (e.g., at least 24 hours, at least 48 hours, at least 1 week, at least 2 weeks, at least 3 weeks, at least 4 weeks, at least 30 days, at least 60 days, or at least 90 days) retains at least 5% (e.g., at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or 100%) of the initial number of PMPs (e.g., PMPs per mL of solution) relative to the number of PMPs in the PMP composition (e.g., at the time of production or formulation) optionally at a defined temperature range (e.g., a temperature of at least 24° C. (e.g., at least 24° C., 25° C., 26° C., 27° C., 28° C., 29° C., or 30° C.), at least 20° C. (e.g., at least 20° C., 21° C., 22° C., or 23° C.), at least 4° C. (e.g., at least 5° C., 10° C., or 15° C.), at least −20° C. (e.g., at least −20° C., −15° C., −10° C., −5° C., or 0° C.), or −80° C. (e.g., at least −80° C., −70° C., −60° C., −50° C., −40° C., or −30° C.)); or retains at least 5% (e.g., at least 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or 100%) of its activity relative to the initial activity of the PMP (e.g., at the time of production or formulation) optionally at a defined temperature range (e.g., a temperature of at least 24° C. (e.g., at least 24° C., 25° C., 26° C., 27° C., 28° C., 29° C., or 30° C.), at least 20° C. (e.g., at least 20° C., 21° C., 22° C., or 23° C.), at least 4° C. (e.g., at least 5° C., 10° C., or 15° C.), at least −20° C. (e.g., at least −20° C., −15° C., −10° C., −5° C., or 0° C.), or −80° C. (e.g., at least −80° C., −70° C., −60° C., −50° C., −40° C., or −30° C.)).

In some aspects, the stable PMP continues to encapsulate or remains associated with an exogenous polypeptide with which the PMP has been loaded, e.g., continues to encapsulate or remains associated with an exogenous polypeptide for at least 24 hours, at least 48 hours, at least 1 week, at least 2 weeks, at least 3 weeks, at least 4 weeks, at least 30 days, at least 60 days, at least 90 days, or 90 or more days.

As used herein, the term “vector” refers to an insect that can carry or transmit an animal pathogen from a reservoir to an animal. Exemplary vectors include insects, such as those with piercing-sucking mouthparts, as found in Hemiptera and some Hymenoptera and Diptera such as mosquitoes, bees, wasps, midges, lice, tsetse fly, fleas and ants, as well as members of the Arachnidae such as ticks and mites.

As used herein, the term “juice sac” or “juice vesicle” refers to a juice-containing membrane-bound component of the endocarp (carpel) of a hesperidium, e.g., a citrus fruit. In some aspects, the juice sacs are separated from other portions of the fruit, e.g., the rind (exocarp or flavedo), the inner rind (mesocarp, albedo, or pith), the central column (placenta), the segment walls, or the seeds. In some aspects, the juice sacs are juice sacs of a grapefruit, a lemon, a lime, or an orange.

II. PMPs Comprising an Encapsulated Polypeptide and Compositions Thereof

The present invention includes plant messenger packs (PMPs) and compositions including a plurality of plant messenger packs (PMP). A PMP is a lipid (e.g., lipid bilayer, unilamellar, or multilamellar structure) structure that includes a plant EV, or segment, portion, or extract (e.g., lipid extract) thereof. Plant EVs refer to an enclosed lipid-bilayer structure that naturally occurs in a plant and that is about 5-2000 nm in diameter. Plant EVs can originate from a variety of plant biogenesis pathways. In nature, plant EVs can be found in the intracellular and extracellular compartments of plants, such as the plant apoplast, the compartment located outside the plasma membrane and formed by a continuum of cell walls and the extracellular space. Alternatively, PMPs can be enriched plant EVs found in cell culture media upon secretion from plant cells. Plant EVs can be isolated from plants (e.g., from the apoplastic fluid or from extracellular media), thereby producing PMPs, by a variety of methods, further described herein.

The PMPs and PMP compositions described herein include PMPs comprising an exogenous polypeptide, e.g., an exogenous polypeptide described in Section III herein. The exogenous polypeptide may be, e.g., a therapeutic agent, a pathogen control agent (e.g., an agent having antipathogen activity (e.g., antibacterial, antifungal, antinematicidal, antiparasitic, or antiviral activity)), or an enzyme (e.g., a recombination enzyme or an editing enzyme.

The plurality of PMPs in a PMP composition may be loaded with the exogenous polypeptide such that at least 5%, at least 10%, at least 15%, at least 25%, at least 50%, at least 75%, at least 90%, or at least 95% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide.

PMPs can include plant EVs, or segments, portions, or extracts, thereof, in which the plant EVs are about 5-2000 nm in diameter. For example, the PMP can include a plant EV, or segment, portion, or extract thereof, that has a mean diameter of about 5-50 nm, about 50-100 nm, about 100-150 nm, about 150-200 nm, about 200-250 nm, about 250-300 nm, about 300-350 nm, about 350-400 nm, about 400-450 nm, about 450-500 nm, about 500-550 nm, about 550-600 nm, about 600-650 nm, about 650-700 nm, about 700-750 nm, about 750-800 nm, about 800-850 nm, about 850-900 nm, about 900-950 nm, about 950-1000 nm, about 1000-1250 nm, about 1250-1500 nm, about 1500-1750 nm, or about 1750-2000 nm. In some instances, the PMP includes a plant EV, or segment, portion, or extract thereof, that has a mean diameter of about 5-950 nm, about 5-900 nm, about 5-850 nm, about 5-800 nm, about 5-750 nm, about 5-700 nm, about 5-650 nm, about 5-600 nm, about 5-550 nm, about 5-500 nm, about 5-450 nm, about 5-400 nm, about 5-350 nm, about 5-300 nm, about 5-250 nm, about 5-200 nm, about 5-150 nm, about 5-100 nm, about 5-50 nm, or about 5-25 nm. In certain instances, the plant EV, or segment, portion, or extract thereof, has a mean diameter of about 50-200 nm. In certain instances, the plant EV, or segment, portion, or extract thereof, has a mean diameter of about 50-300 nm. In certain instances, the plant EV, or segment, portion, or extract thereof, has a mean diameter of about 200-500 nm. In certain instances, the plant EV, or segment, portion, or extract thereof, has a mean diameter of about 30-150 nm.

In some instances, the PMP may include a plant EV, or segment, portion, or extract thereof, that has a mean diameter of at least 5 nm, at least 50 nm, at least 100 nm, at least 150 nm, at least 200 nm, at least 250 nm, at least 300 nm, at least 350 nm, at least 400 nm, at least 450 nm, at least 500 nm, at least 550 nm, at least 600 nm, at least 650 nm, at least 700 nm, at least 750 nm, at least 800 nm, at least 850 nm, at least 900 nm, at least 950 nm, or at least 1000 nm. In some instances, the PMP includes a plant EV, or segment, portion, or extract thereof, that has a mean diameter less than 1000 nm, less than 950 nm, less than 900 nm, less than 850 nm, less than 800 nm, less than 750 nm, less than 700 nm, less than 650 nm, less than 600 nm, less than 550 nm, less than 500 nm, less than 450 nm, less than 400 nm, less than 350 nm, less than 300 nm, less than 250 nm, less than 200 nm, less than 150 nm, less than 100 nm, or less than 50 nm. A variety of methods (e.g., a dynamic light scattering method) standard in the art can be used to measure the particle diameter of the plant EVs, or segment, portion, or extract thereof.

In some instances, the PMP may include a plant EV, or segment, portion, or extract thereof, that has a mean surface area of 77 nm² to 3.2×10⁶ nm² (e.g., 77-100 nm², 100-1000 nm², 1000-1×10⁴ nm², 1×10⁴-1×10⁵ nm², 1×10⁵-1×10⁶ nm², or 1×10⁶-3.2×10⁶ nm²). In some instances, the PMP may include a plant EV, or segment, portion, or extract thereof, that has a mean volume of 65 nm³ to 5.3×10⁸ nm³ (e.g., 65-100 nm³, 100-1000 nm³, 1000-1×10⁴ nm³, 1×10⁴-1×10⁵ nm³, 1×10⁵-1×10⁶ nm³, 1×10⁶-1×10⁷ nm³, 1×10⁷-1×10⁸ nm³, 1×10⁸-5.3×10⁸ nm³). In some instances, the PMP may include a plant EV, or segment, portion, or extract thereof, that has a mean surface area of at least 77 nm², (e.g., at least 77 nm², at least 100 nm², at least 1000 nm², at least 1×10⁴ nm², at least 1×10⁵ nm², at least 1×10⁶ nm², or at least 2×10⁶ nm²). In some instances, the PMP may include a plant EV, or segment, portion, or extract thereof, that has a mean volume of at least 65 nm³ (e.g., at least 65 nm³, at least 100 nm³, at least 1000 nm³, at least 1×10⁴ nm³, at least 1×10⁵ nm³, at least 1×10⁶ nm³, at least 1×10⁷ nm³, at least 1×10⁸ nm³, at least 2×10⁸ nm³, at least 3×10⁸ nm³, at least 4×10⁸ nm³, or at least 5×10⁸ nm³.

In some instances, the PMP can have the same size as the plant EV or segment, extract, or portion thereof. Alternatively, the PMP may have a different size than the initial plant EV from which the PMP is produced. For example, the PMP may have a diameter of about 5-2000 nm in diameter. For example, the PMP can have a mean diameter of about 5-50 nm, about 50-100 nm, about 100-150 nm, about 150-200 nm, about 200-250 nm, about 250-300 nm, about 300-350 nm, about 350-400 nm, about 400-450 nm, about 450-500 nm, about 500-550 nm, about 550-600 nm, about 600-650 nm, about 650-700 nm, about 700-750 nm, about 750-800 nm, about 800-850 nm, about 850-900 nm, about 900-950 nm, about 950-1000 nm, about 1000-1200 nm, about 1200-1400 nm, about 1400-1600 nm, about 1600-1800 nm, or about 1800-2000 nm. In some instances, the PMP may have a mean diameter of at least 5 nm, at least 50 nm, at least 100 nm, at least 150 nm, at least 200 nm, at least 250 nm, at least 300 nm, at least 350 nm, at least 400 nm, at least 450 nm, at least 500 nm, at least 550 nm, at least 600 nm, at least 650 nm, at least 700 nm, at least 750 nm, at least 800 nm, at least 850 nm, at least 900 nm, at least 950 nm, at least 1000 nm, at least 1200 nm, at least 1400 nm, at least 1600 nm, at least 1800 nm, or about 2000 nm. A variety of methods (e.g., a dynamic light scattering method) standard in the art can be used to measure the particle diameter of the PMPs. In some instances, the size of the PMP is determined following loading of heterologous functional agents, or following other modifications to the PMPs.

In some instances, the PMP may have a mean surface area of 77 nm² to 1.3×10⁷ nm² (e.g., 77-100 nm², 100-1000 nm², 1000-1×10⁴ nm², 1×10⁴-1×10⁵ nm², 1×10⁵-1×10⁶ nm², or 1×10⁶-1.3×10⁷ nm²). In some instances, the PMP may have a mean volume of 65 nm³ to 4.2×10⁹ nm³ (e.g., 65-100 nm³, 100-1000 nm³, 1000-1×10⁴ nm³, 1×10⁴-1×10⁵ nm³, 1×10⁵-1×10⁶ nm³, 1×10⁶-1×10⁷ nm³, 1×10⁷-1×10⁸ nm³, 1×10⁸-1×10⁹ nm³, or 1×10⁹-4.2×10⁹ nm³). In some instances, the PMP has a mean surface area of at least 77 nm², (e.g., at least 77 nm², at least 100 nm², at least 1000 nm², at least 1×10⁴ nm², at least 1×10⁵ nm², at least 1×10⁶ nm², or at least 1×10⁷ nm²). In some instances, the PMP has a mean volume of at least 65 nm³ (e.g., at least 65 nm³, at least 100 nm³, at least 1000 nm³, at least 1×10⁴ nm³, at least 1×10⁵ nm³, at least 1×10⁶ nm³, at least 1×10⁷ nm³, at least 1×10⁸ nm³, at least 1×10⁹ nm³, at least 2×10⁹ nm³, at least 3×10⁹ nm³, or at least 4×10⁹ nm³).

In some instances, the PMP may include an intact plant EV. Alternatively, the PMP may include a segment, portion, or extract of the full surface area of the vesicle (e.g., a segment, portion, or extract including less than 100% (e.g., less than 90%, less than 80%, less than 70%, less than 60%, less than 50%, less than 40%, less than 30%, less than 20%, less than 10%, less than 10%, less than 5%, or less than 1%) of the full surface area of the vesicle) of a plant EV. The segment, portion, or extract may be any shape, such as a circumferential segment, spherical segment (e.g., hemisphere), curvilinear segment, linear segment, or flat segment. In instances where the segment is a spherical segment of the vesicle, the spherical segment may represent one that arises from the splitting of a spherical vesicle along a pair of parallel lines, or one that arises from the splitting of a spherical vesicle along a pair of non-parallel lines. Accordingly, the plurality of PMPs can include a plurality of intact plant EVs, a plurality of plant EV segments, portions, or extracts, or a mixture of intact and segments of plant EVs. One skilled in the art will appreciate that the ratio of intact to segmented plant EVs will depend on the particular isolation method used. For example, grinding or blending a plant, or part thereof, may produce PMPs that contain a higher percentage of plant EV segments, portions, or extracts than a non-destructive extraction method, such as vacuum-infiltration.

In instances where, the PMP includes a segment, portion, or extract of a plant EV, the EV segment, portion, or extract may have a mean surface area less than that of an intact vesicle, e.g., a mean surface area less than 77 nm², 100 nm², 1000 nm², 1×10⁴ nm², 1×10⁵ nm², 1×10⁶ nm², or 3.2×10⁶ nm²). In some instances, the EV segment, portion, or extract has a surface area of less than 70 nm², 60 nm², 50 nm², 40 nm², 30 nm², 20 nm², or 10 nm²). In some instances, the PMP may include a plant EV, or segment, portion, or extract thereof, that has a mean volume less than that of an intact vesicle, e.g., a mean volume of less than 65 nm³, 100 nm³, 1000 nm³, 1×10⁴ nm³, 1×10⁵ nm³, 1×10⁶ nm³, 1×10⁷ nm³, 1×10⁸ nm³, or 5.3×10⁸ nm³).

In instances where the PMP includes an extract of a plant EV, e.g., in instances where the PMP includes lipids extracted (e.g., with chloroform) from a plant EV, the PMP may include at least 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, or more than 99% of lipids extracted (e.g., with chloroform) from a plant EV. The PMPs in the plurality may include plant EV segments and/or plant EV-extracted lipids or a mixture thereof.

Further outlined herein are details regarding methods of producing PMPs, plant EV markers that can be associated with PMPs, and formulations for compositions including PMPs.

A. Production Methods

PMPs may be produced from plant EVs, or a segment, portion or extract (e.g., lipid extract) thereof, that occur naturally in plants, or parts thereof, including plant tissues or plant cells. An exemplary method for producing PMPs includes (a) providing an initial sample from a plant, or a part thereof, wherein the plant or part thereof comprises EVs; and (b) isolating a crude PMP fraction from the initial sample, wherein the crude PMP fraction has a decreased level of at least one contaminant or undesired component from the plant or part thereof relative to the level in the initial sample. The method can further include an additional step (c) comprising purifying the crude PMP fraction, thereby producing a plurality of pure PMPs, wherein the plurality of pure PMPs have a decreased level of at least one contaminant or undesired component from the plant or part thereof relative to the level in the crude EV fraction. Each production step is discussed in further detail, below. Exemplary methods regarding the isolation and purification of PMPs is found, for example, in Rutter and Innes, Plant Physiol. 173(1): 728-741, 2017; Rutter et al, Bio. Protoc. 7(17): e2533, 2017; Regente et al, J of Exp. Biol. 68(20): 5485-5496, 2017; Mu et al, Mol. Nutr. Food Res., 58, 1561-1573, 2014, and Regente et al, FEBS Letters. 583: 3363-3366, 2009, each of which is herein incorporated by reference.

For example, a plurality of PMPs may be isolated from a plant by a process which includes the steps of: (a) providing an initial sample from a plant, or a part thereof, wherein the plant or part thereof comprises EVs; (b) isolating a crude PMP fraction from the initial sample, wherein the crude PMP fraction has a decreased level of at least one contaminant or undesired component from the plant or part thereof relative to the level in the initial sample (e.g., a level that is decreased by at least 1%, 2%, 5%, 10%, 15%, 20%, 25%, 30%, 40%, 45%, 50%, 55%, 60%, 70%, 80%, 90%, 95%, 96%, 98%, 99%, or 100%); and (c) purifying the crude PMP fraction, thereby producing a plurality of pure PMPs, wherein the plurality of pure PMPs have a decreased level of at least one contaminant or undesired component from the plant or part thereof relative to the level in the crude EV fraction (e.g., a level that is decreased by at least 1%, 2%, 5%, 10%, 15%, 20%, 25%, 30%, 40%, 45%, 50%, 55%, 60%, 70%, 80%, 90%, 95%, 96%, 98%, 99%, or 100%).

The PMPs provided herein can include a plant EV, or segment, portion, or extract thereof, isolated from a variety of plants. PMPs may be isolated from any genera of plants (vascular or nonvascular), including but not limited to angiosperms (monocotyledonous and dicotyledonous plants), gymnosperms, ferns, selaginellas, horsetails, psilophytes, lycophytes, algae (e.g., unicellular or multicellular, e.g., archaeplastida), or bryophytes. In certain instances, PMPs can be produced from a vascular plant, for example monocotyledons or dicotyledons or gymnosperms. For example, PMPs can be produced from alfalfa, apple, Arabidopsis, banana, barley, canola, castor bean, chicory, chrysanthemum, clover, cocoa, coffee, cotton, cottonseed, corn, crambe, cranberry, cucumber, dendrobium, dioscorea, eucalyptus, fescue, flax, gladiolus, liliacea, linseed, millet, muskmelon, mustard, oat, oil palm, oilseed rape, papaya, peanut, pineapple, ornamental plants, Phaseolus, potato, rapeseed, rice, rye, ryegrass, safflower, sesame, sorghum, soybean, sugarbeet, sugarcane, sunflower, strawberry, tobacco, tomato, turfgrass, wheat or vegetable crops such as lettuce, celery, broccoli, cauliflower, cucurbits; fruit and nut trees, such as apple, pear, peach, orange, grapefruit, lemon, lime, almond, pecan, walnut, hazel; vines, such as grapes, kiwi, hops; fruit shrubs and brambles, such as raspberry, blackberry, gooseberry; forest trees, such as ash, pine, fir, maple, oak, chestnut, popular; with alfalfa, canola, castor bean, corn, cotton, crambe, flax, linseed, mustard, oil palm, oilseed rape, peanut, potato, rice, safflower, sesame, soybean, sugarbeet, sunflower, tobacco, tomato, or wheat.

PMPs may be produced from a whole plant (e.g., a whole rosettes or seedlings) or alternatively from one or more plant parts (e.g., leaf, seed, root, fruit, vegetable, pollen, phloem sap, or xylem sap). For example, PMPs can be produced from shoot vegetative organs/structures (e.g., leaves, stems, or tubers), roots, flowers and floral organs/structures (e.g., pollen, bracts, sepals, petals, stamens, carpels, anthers, or ovules), seed (including embryo, endosperm, or seed coat), fruit (the mature ovary), sap (e.g., phloem or xylem sap), plant tissue (e.g., vascular tissue, ground tissue, tumor tissue, or the like), and cells (e.g., single cells, protoplasts, embryos, callus tissue, guard cells, egg cells, or the like), or progeny of same. For instance, the isolation step may involve (a) providing a plant, or a part thereof, wherein the plant part is an Arabidopsis leaf. The plant may be at any stage of development. For example, the PMP can be produced from seedlings, e.g., 1 week, 2 week, 3 week, 4 week, 5 week, 6 week, 7 week, or 8 week old seedlings (e.g., Arabidopsis seedlings). Other exemplary PMPs can include PMPs produced from roots (e.g., ginger roots), fruit juice (e.g., grapefruit juice), vegetables (e.g., broccoli), pollen (e.g., olive pollen), phloem sap (e.g., Arabidopsis phloem sap), or xylem sap (e.g., tomato plant xylem sap). In some aspects, the PMP is produced from a citrus fruit, e.g., a grapefruit or a lemon.

PMPs can be produced from a plant, or part thereof, by a variety of methods. Any method that allows release of the EV-containing apoplastic fraction of a plant, or an otherwise extracellular fraction that contains PMPs comprising secreted EVs (e.g., cell culture media) is suitable in the present methods. EVs can be separated from the plant or plant part by either destructive (e.g., grinding or blending of a plant, or any plant part) or non-destructive (washing or vacuum infiltration of a plant or any plant part) methods. For instance, the plant, or part thereof, can be vacuum-infiltrated, ground, blended, or a combination thereof to isolate EVs from the plant or plant part, thereby producing PMPs. For instance, the isolating step may involve (b) isolating a crude PMP fraction from the initial sample (e.g., a plant, a plant part, or a sample derived from a plant or a plant part), wherein the crude PMP fraction has a decreased level of at least one contaminant or undesired component from the plant or part thereof relative to the level in the initial sample; wherein the isolating step involves vacuum infiltrating the plant (e.g., with a vesicle isolation buffer) to release and collect the apoplastic fraction. Alternatively, the isolating step may involve (b) grinding or blending the plant to release the EVs, thereby producing PMPs.

Upon isolating the plant EVs, thereby producing PMPs, the PMPs can be separated or collected into a crude PMP fraction (e.g., an apoplastic fraction). For instance, the separating step may involve separating the plurality of PMPs into a crude PMP fraction using centrifugation (e.g., differential centrifugation or ultracentrifugation) and/or filtration to separate the PMP-containing fraction from large contaminants, including plant tissue debris, plant cells, or plant cell organelles (e.g., nuclei or chloroplast). As such, the crude PMP fraction will have a decreased number of large contaminants, including, for example, plant tissue debris, plant cells, or plant cell organelles (e.g., nuclei, mitochondria or chloroplast), as compared to the initial sample from the source plant or plant part.

The crude PMP fraction can be further purified by additional purification methods to produce a plurality of pure PMPs. For example, the crude PMP fraction can be separated from other plant components by ultracentrifugation, e.g., using a density gradient (iodixanol or sucrose), size-exclusion, and/or use of other approaches to remove aggregated components (e.g., precipitation or size-exclusion chromatography). The resulting pure PMPs may have a decreased level of contaminants or undesired components from the source plant (e.g., one or more non-PMP components, such as protein aggregates, nucleic acid aggregates, protein-nucleic acid aggregates, free lipoproteins, lipido-proteic structures), nuclei, cell wall components, cell organelles, or a combination thereof) relative to one or more fractions generated during the earlier separation steps, or relative to a pre-established threshold level, e.g., a commercial release specification. For example, the pure PMPs may have a decreased level (e.g., by about 5%, 10%, 15%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or more than 100%; or by about 2× fold, 4× fold, 5× fold, 10× fold, 20× fold, 25× fold, 50× fold, 75× fold, 100× fold, or more than 100× fold) of plant organelles or cell wall components relative to the level in the initial sample. In some instances, the pure PMPs are substantially free (e.g., have undetectable levels) of one or more non-PMP components, such as protein aggregates, nucleic acid aggregates, protein-nucleic acid aggregates, free lipoproteins, lipido-proteic structures), nuclei, cell wall components, cell organelles, or a combination thereof. Further examples of the releasing and separation steps can be found in Example 1. The PMPs may be at a concentration of, e.g., 1×10⁹, 5×10⁹, 1×10¹⁰, 5×10¹⁰, 5×10¹⁰, 1×10¹¹, 2×10¹¹, 3×10¹¹, 4×10¹¹, 5×10¹¹, 6×10¹¹, 7×10¹¹, 8×10¹¹, 9×10¹¹, 1×10¹², 2×10¹², 3×10¹², 4×10¹², 5×10¹², 6×10¹², 7×10¹², 8×10¹², 9×10¹², 1×10¹³, or more than 1×10¹³ PMPs/mL.

For example, protein aggregates may be removed from isolated PMPs. For example, the isolated PMP solution can be taken through a range of pHs (e.g., as measured using a pH probe) to precipitate out protein aggregates in solution. The pH can be adjusted to, e.g., pH 3, pH 5, pH 7, pH 9, or pH 11 with the addition of, e.g., sodium hydroxide or hydrochloric acid. Once the solution is at the specified pH, it can be filtered to remove particulates. Alternatively, the isolated PMP solution can be flocculated using the addition of charged polymers, such as Polymin-P or Praestol 2640. Briefly, Polymin-P or Praestol 2640 is added to the solution and mixed with an impeller. The solution can then be filtered to remove particulates. Alternatively, aggregates can be solubilized by increasing salt concentration. For example NaCl can be added to the isolated PMP solution until it is at, e.g., 1 mol/L. The solution can then be filtered to isolate the PMPs. Alternatively, aggregates are solubilized by increasing the temperature. For example, the isolated PMPs can be heated under mixing until the solution has reached a uniform temperature of, e.g., 50° C. for 5 minutes. The PMP mixture can then be filtered to isolate the PMPs. Alternatively, soluble contaminants from PMP solutions can be separated by size-exclusion chromatography column according to standard procedures, where PMPs elute in the first fractions, whereas proteins and ribonucleoproteins and some lipoproteins are eluted later. The efficiency of protein aggregate removal can be determined by measuring and comparing the protein concentration before and after removal of protein aggregates via BCA/Bradford protein quantification. In some aspects, protein aggregates are removed before the exogenous polypeptide is encapsulated by the PMP. In other aspects, protein aggregates are removed after the exogenous polypeptide is encapsulated by the PMP.

Any of the production methods described herein can be supplemented with any quantitative or qualitative methods known in the art to characterize or identify the PMPs at any step of the production process. PMPs may be characterized by a variety of analysis methods to estimate PMP yield, PMP concentration, PMP purity, PMP composition, or PMP sizes. PMPs can be evaluated by a number of methods known in the art that enable visualization, quantitation, or qualitative characterization (e.g., identification of the composition) of the PMPs, such as microscopy (e.g., transmission electron microscopy), dynamic light scattering, nanoparticle tracking, spectroscopy (e.g., Fourier transform infrared analysis), or mass spectrometry (protein and lipid analysis). In certain instances, methods (e.g., mass spectroscopy) may be used to identify plant EV markers present on the PMP, such as markers disclosed in the Appendix. To aid in analysis and characterization, of the PMP fraction, the PMPs can additionally be labelled or stained. For example, the PMPs can be stained with 3,3′-dihexyloxacarbocyanine iodide (DIOC₆), a fluorescent lipophilic dye, PKH67 (Sigma Aldrich); Alexa Fluor® 488 (Thermo Fisher Scientific), or DyLight™ 800 (Thermo Fisher). In the absence of sophisticated forms of nanoparticle tracking, this relatively simple approach quantifies the total membrane content and can be used to indirectly measure the concentration of PMPs (Rutter and Innes, Plant Physiol. 173(1): 728-741, 2017; Rutter et al, Bio. Protoc. 7(17): e2533, 2017). For more precise measurements, and to assess the size distributions of PMPs, nanoparticle tracking, nano flow cytometry, or Tunable Resistive Pulse Sensing can be used.

During the production process, the PMPs can optionally be prepared such that the PMPs are at an increased concentration (e.g., by about 5%, 10%, 15%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or more than 100%; or by about 2× fold, 4× fold, 5× fold, 10× fold, 20× fold, 25× fold, 50× fold, 75× fold, 100× fold, or more than 100× fold) relative to the EV level in a control or initial sample. The isolated PMPs may make up about 0.1% to about 100% of the PMP composition, such as any one of about 0.01% to about 100%, about 1% to about 99.9%, about 0.1% to about 10%, about 1% to about 25%, about 10% to about 50%, about 50% to about 99%, about. In some instances, the composition includes at least any of 0.1%, 0.5%, 1%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or more PMPs, e.g., as measured by wt/vol, percent PMP protein composition, and/or percent lipid composition (e.g., by measuring fluorescently labelled lipids); See, e.g., Example 3). In some instances, the concentrated agents are used as commercial products, e.g., the final user may use diluted agents, which have a substantially lower concentration of active ingredient. In some embodiments, the composition is formulated as a PMP concentrate formulation, e.g., an ultra-low-volume concentrate formulation. In some aspects, the PMPs in the composition are at a concentration effective to increase the fitness of an organism, e.g., a plant, an animal, an insect, a bacterium, or a fungus. In other aspects, the PMPs in the composition are at a concentration effective to decrease the fitness of an organism, e.g., a plant, an animal, an insect, a bacterium, or a fungus.

As illustrated by Example 1, PMPs can be produced from a variety of plants, or parts thereof (e.g., the leaf apoplast, seed apoplast, root, fruit, vegetable, pollen, phloem, or xylem sap). For example, PMPs can be released from the apoplastic fraction of a plant, such as the apoplast of a leaf (e.g., apoplast Arabidopsis thaliana leaves) or the apoplast of seeds (e.g., apoplast of sunflower seeds). Other exemplary PMPs are produced from roots (e.g., ginger roots), fruit juice (e.g., grapefruit juice), vegetables (e.g., broccoli), pollen (e.g., olive pollen), phloem sap (e.g., Arabidopsis phloem sap), xylem sap (e.g., tomato plant xylem sap), or cell culture supernatant (e.g. BY2 tobacco cell culture supernatant). This example further demonstrates the production of PMPs from these various plant sources.

As illustrated by Example 2, PMPs can be produced and purified by a variety of methods, for example, by using a density gradient (iodixanol or sucrose) in conjunction with ultracentrifugation and/or methods to remove aggregated contaminants, e.g., precipitation or size-exclusion chromatography. For instance, Example 2 illustrates purification of PMPs that have been obtained via the separation steps outlined in Example 1. Further, PMPs can be characterized in accordance with the methods illustrated in Example 3.

In some instances, the PMPs of the present compositions and methods can be isolated from a plant, or part thereof, and used without further modification to the PMP. In other instances, the PMP can be modified prior to use, as outlined further herein.

B. Plant EV-Markers

The PMPs of the present compositions and methods may have a range of markers that identify the PMP as being produced from a plant EV, and/or including a segment, portion, or extract thereof. As used herein, the term “plant EV-marker” refers to a component that is naturally associated with a plant and incorporated into or onto the plant EV in planta, such as a plant protein, a plant nucleic acid, a plant small molecule, a plant lipid, or a combination thereof. Examples of plant EV-markers can be found, for example, in Rutter and Innes, Plant Physiol. 173(1): 728-741, 2017; Raimondo et al., Oncotarget. 6(23): 19514, 2015; Ju et al., Mol. Therapy. 21(7):1345-1357, 2013; Wang et al., Molecular Therapy. 22(3): 522-534, 2014; and Regente et al, J of Exp. Biol. 68(20): 5485-5496, 2017; each of which is incorporated herein by reference. Additional examples of plant EV-markers are listed in the Appendix, and are further outlined herein.

The plant EV marker can include a plant lipid. Examples of plant lipid markers that may be found in the PMP include phytosterol, campesterol, β-sitosterol, stigmasterol, avenasterol, glycosyl inositol phosphoryl ceramides (GIPCs), glycolipids (e.g., monogalactosyldiacylglycerol (MGDG) or digalactosyldiacylglycerol (DGDG)), or a combination thereof. For instance, the PMP may include GIPCs, which represent the main sphingolipid class in plants and are one of the most abundant membrane lipids in plants. Other plant EV markers may include lipids that accumulate in plants in response to abiotic or biotic stressors (e.g., bacterial or fungal infection), such as phosphatidic acid (PA) or phosphatidylinositol-4-phosphate (PI4P).

Alternatively, the plant EV marker may include a plant protein. In some instances, the protein plant EV marker may be an antimicrobial protein naturally produced by plants, including defense proteins that plants secrete in response to abiotic or biotic stressors (e.g., bacterial or fungal infection). Plant pathogen defense proteins include soluble N-ethylmalemide-sensitive factor association protein receptor protein (SNARE) proteins (e.g., Syntaxin-121 (SYP121; GenBank Accession No.: NP_187788.1 or NP_974288.1), Penetration1 (PEN1; GenBank Accession No: NP_567462.1)) or ABC transporter Penetration3 (PEN3; GenBank Accession No: NP_191283.2). Other examples of plant EV markers includes proteins that facilitate the long-distance transport of RNA in plants, including phloem proteins (e.g., Phloem protein2-A1 (PP2-A1), GenBank Accession No: NP_193719.1), calcium-dependent lipid-binding proteins, or lectins (e.g., Jacalin-related lectins, e.g., Helianthus annuus jacalin (Helja; GenBank: AHZ86978.1). For example, the RNA binding protein may be Glycine-Rich RNA Binding Protein-7 (GRP7; GenBank Accession Number: NP_179760.1). Additionally, proteins that regulate plasmodesmata function can in some instances be found in plant EVs, including proteins such as Synap-Totgamin A A (GenBank Accession No: NP_565495.1). In some instances, the plant EV marker can include a protein involved in lipid metabolism, such as phospholipase C or phospholipase D. In some instances, the plant protein EV marker is a cellular trafficking protein in plants. In certain instances where the plant EV marker is a protein, the protein marker may lack a signal peptide that is typically associated with secreted proteins. Unconventional secretory proteins seem to share several common features like (i) lack of a leader sequence, (ii) absence of PTMs specific for ER or Golgi apparatus, and/or (iii) secretion not affected by brefeldin A which blocks the classical ER/Golgi-dependent secretion pathway. One skilled in the art can use a variety of tools freely accessible to the public (e.g., SecretomeP Database; SUBA3 (SUBcellular localization database for Arabidopsis proteins)) to evaluate a protein for a signal sequence, or lack thereof.

In instances where the plant EV marker is a protein, the protein may have an amino acid sequence having at least 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99%, or 100% sequence identity to a plant EV marker, such as any of the plant EV markers listed in the Appendix. For example, the protein may have an amino acid sequence having at least 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99%, or 100% sequence identity to PEN1 from Arabidopsis thaliana (GenBank Accession Number: NP_567462.1).

In some instances, the plant EV marker includes a nucleic acid encoded in plants, e.g., a plant RNA, a plant DNA, or a plant PNA. For example, the PMP may include dsRNA, mRNA, a viral RNA, a microRNA (miRNA), or a small interfering RNA (siRNA) encoded by a plant. In some instances, the nucleic acid may be one that is associated with a protein that facilitates the long-distance transport of RNA in plants, as discussed herein. In some instances, the nucleic acid plant EV marker may be one involved in host-induced gene silencing (HIGS), which is the process by which plants silence foreign transcripts of plant pests (e.g., pathogens such as fungi). For example, the nucleic acid may be one that silences bacterial or fungal genes. In some instances, the nucleic acid may be a microRNA, such as miR159 or miR166, which target genes in a fungal pathogen (e.g., Verticillium dahliae). In some instances, the protein may be one involved in carrying plant defense compounds, such as proteins involved in glucosinolate (GSL) transport and metabolism, including Glucosinolate Transporter-1-1 (GTR1; GenBank Accession No: NP_566896.2), Glucosinolate Transporter-2 (GTR2; NP_201074.1), orEpithiospecific Modifier 1 (ESM1; NP_188037.1).

In instances where the plant EV marker is a nucleic acid, the nucleic acid may have a nucleotide sequence having at least 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99%, or 100% sequence identity to a plant EV marker, e.g., such as those encoding the plant EV markers listed in the Appendix. For example, the nucleic acid may have a polynucleotide sequence having at least 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99%, or 100% sequence identity to miR159 or miR166.

In some instances, the plant EV marker includes a compound produced by plants. For example, the compound may be a defense compound produced in response to abiotic or biotic stressors, such as secondary metabolites. One such secondary metabolite that be found in PMPs are glucosinolates (GSLs), which are nitrogen and sulfur-containing secondary metabolites found mainly in Brassicaceae plants. Other secondary metabolites may include allelochemicals.

In some instances, the PMP may also be identified as being produced from a plant EV based on the lack of certain markers (e.g., lipids, polypeptides, or polynucleotides) that are not typically produced by plants, but are generally associated with other organisms (e.g., markers of animal EVs, bacterial EVs, or fungal EVs). For example, in some instances, the PMP lacks lipids typically found in animal EVs, bacterial EVs, or fungal EVs. In some instances, the PMP lacks lipids typical of animal EVs (e.g., sphingomyelin). In some instances, the PMP does not contain lipids typical of bacterial EVs or bacterial membranes (e.g., LPS). In some instances, the PMP lacks lipids typical of fungal membranes (e.g., ergosterol).

Plant EV markers can be identified using any approaches known in the art that enable identification of small molecules (e.g., mass spectroscopy, mass spectrometry), lipds (e.g., mass spectroscopy, mass spectrometry), proteins (e.g., mass spectroscopy, immunoblotting), or nucleic acids (e.g., PCR analysis). In some instances, a PMP composition described herein includes a detectable amount, e.g., a pre-determined threshold amount, of a plant EV marker described herein.

C. Pharmaceutical Formulations

Included herein are PMP compositions that can be formulated into pharmaceutical compositions, e.g., for administration to an animal, such as a human. The pharmaceutical composition may be administered to an animal with a pharmaceutically acceptable diluent, carrier, and/or excipient. Depending on the mode of administration and the dosage, the pharmaceutical composition of the methods described herein will be formulated into suitable pharmaceutical compositions to permit facile delivery. The single dose may be in a unit dose form as needed.

A PMP composition may be formulated for e.g., oral administration, intravenous administration (e.g., injection or infusion), or subcutaneous administration to an animal (e.g., a human). For injectable formulations, various effective pharmaceutical carriers are known in the art (See, e.g., Remington: The Science and Practice of Pharmacy, 22^nd ed., (2012) and ASHP Handbook on Injectable Drugs, 18^th ed., (2014)).

Pharmaceutically acceptable carriers and excipients in the present compositions are nontoxic to recipients at the dosages and concentrations employed. Acceptable carriers and excipients may include buffers such as phosphate, citrate, HEPES, and TAE, antioxidants such as ascorbic acid and methionine, preservatives such as hexamethonium chloride, octadecyldimethylbenzyl ammonium chloride, resorcinol, and benzalkonium chloride, proteins such as human serum albumin, gelatin, dextran, and immunoglobulins, hydrophilic polymers such as polyvinylpyrrolidone, amino acids such as glycine, glutamine, histidine, and lysine, and carbohydrates such as glucose, mannose, sucrose, and sorbitol. The compositions may be formulated according to conventional pharmaceutical practice. The concentration of the compound in the formulation will vary depending upon a number of factors, including the dosage of the active agent (e.g., the exogenous polypeptide encapsulated by the PMP) to be administered, and the route of administration.

For oral administration to an animal, the PMP composition can be prepared in the form of an oral formulation. Formulations for oral use can include tablets, caplets, capsules, syrups, or oral liquid dosage forms containing the active ingredient(s) in a mixture with non-toxic pharmaceutically acceptable excipients. These excipients may be, for example, inert diluents or fillers (e.g., sucrose, sorbitol, sugar, mannitol, microcrystalline cellulose, starches including potato starch, calcium carbonate, sodium chloride, lactose, calcium phosphate, calcium sulfate, or sodium phosphate); granulating and disintegrating agents (e.g., cellulose derivatives including microcrystalline cellulose, starches including potato starch, croscarmellose sodium, alginates, or alginic acid); binding agents (e.g., sucrose, glucose, sorbitol, acacia, alginic acid, sodium alginate, gelatin, starch, pregelatinized starch, microcrystalline cellulose, magnesium aluminum silicate, carboxymethylcellulose sodium, methylcellulose, hydroxypropyl methylcellulose, ethylcellulose, polyvinylpyrrolidone, or polyethylene glycol); and lubricating agents, glidants, and antiadhesives (e.g., magnesium stearate, zinc stearate, stearic acid, silicas, hydrogenated vegetable oils, or talc). Other pharmaceutically acceptable excipients can be colorants, flavoring agents, plasticizers, humectants, buffering agents, and the like. Formulations for oral use may also be provided in unit dosage form as chewable tablets, non-chewable tablets, caplets, capsules (e.g., as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium). The compositions disclosed herein may also further include an immediate-release, extended release or delayed-release formulation.

For parenteral administration to an animal, the PMP compositions may be formulated in the form of liquid solutions or suspensions and administered by a parenteral route (e.g., topical, subcutaneous, intravenous, or intramuscular). The pharmaceutical composition can be formulated for injection or infusion. Pharmaceutical compositions for parenteral administration can be formulated using a sterile solution or any pharmaceutically acceptable liquid as a vehicle. Pharmaceutically acceptable vehicles include, but are not limited to, sterile water, physiological saline, or cell culture media (e.g., Dulbecco's Modified Eagle Medium (DMEM), α-Modified Eagles Medium (α-MEM), F-12 medium). Formulation methods are known in the art, see e.g., Gibson (ed.) Pharmaceutical Preformulation and Formulation (2nd ed.) Taylor & Francis Group, CRC Press (2009).

D. Agricultural Formulations

Included herein are PMP compositions that can be formulated into agricultural compositions, e.g., for administration to pathogen or pathogen vector (e.g., an insect). The agricultural composition may be administered to a pathogen or pathogen vector (e.g., an insect) with an agriculturally acceptable diluent, carrier, and/or excipient. Further examples of agricultural formulations useful in the present compositions and methods are further outlined herein.

To allow ease of application, handling, transportation, storage, and activity, the active agent, here PMPs, can be formulated with other substances. PMPs can be formulated into, for example, baits, concentrated emulsions, dusts, emulsifiable concentrates, fumigants, gels, granules, microencapsulations, seed treatments, suspension concentrates, suspoemulsions, tablets, water soluble liquids, water dispersible granules or dry flowables, wettable powders, and ultra-low volume solutions. For further information on formulation types see “Catalogue of Pesticide Formulation Types and International Coding System” Technical Monograph n° 2, 5th Edition by CropLife International (2002).

Active agents (e.g., PMPs comprising an exogenous polypeptide) can be applied most often as aqueous suspensions or emulsions prepared from concentrated formulations of such agents. Such water-soluble, water-suspendable, or emulsifiable formulations are either solids, usually known as wettable powders, or water dispersible granules, or liquids usually known as emulsifiable concentrates, or aqueous suspensions. Wettable powders, which may be compacted to form water dispersible granules, comprise an intimate mixture of the pesticide, a carrier, and surfactants. The carrier is usually selected from among the attapulgite clays, the montmorillonite clays, the diatomaceous earths, or the purified silicates. Effective surfactants, including from about 0.5% to about 10% of the wettable powder, are found among sulfonated lignins, condensed naphthalenesulfonates, naphthalenesulfonates, alkylbenzenesulfonates, alkyl sulfates, and non-ionic surfactants such as ethylene oxide adducts of alkyl phenols.

Emulsifiable concentrates can comprise a suitable concentration of PMPs, such as from about 50 to about 500 grams per liter of liquid dissolved in a carrier that is either a water miscible solvent or a mixture of water-immiscible organic solvent and emulsifiers. Useful organic solvents include aromatics, especially xylenes and petroleum fractions, especially the high-boiling naphthalenic and olefinic portions of petroleum such as heavy aromatic naphtha. Other organic solvents may also be used, such as the terpenic solvents including rosin derivatives, aliphatic ketones such as cyclohexanone, and complex alcohols such as 2-ethoxyethanol. Suitable emulsifiers for emulsifiable concentrates are selected from conventional anionic and non-ionic surfactants.

Aqueous suspensions comprise suspensions of water-insoluble pesticides dispersed in an aqueous carrier at a concentration in the range from about 5% to about 50% by weight. Suspensions are prepared by finely grinding the pesticide and vigorously mixing it into a carrier comprised of water and surfactants. Ingredients, such as inorganic salts and synthetic or natural gums may also be added, to increase the density and viscosity of the aqueous carrier.

PMPs may also be applied as granular compositions that are particularly useful for applications to the soil. Granular compositions usually contain from about 0.5% to about 10% by weight of the pesticide, dispersed in a carrier that includes clay or a similar substance. Such compositions are usually prepared by dissolving the formulation in a suitable solvent and applying it to a granular carrier which has been pre-formed to the appropriate particle size, in the range of from about 0.5 to about 3 mm. Such compositions may also be formulated by making a dough or paste of the carrier and compound and crushing and drying to obtain the desired granular particle size.

Dusts containing the present PMP formulation are prepared by intimately mixing PMPs in powdered form with a suitable dusty agricultural carrier, such as kaolin clay, ground volcanic rock, and the like. Dusts can suitably contain from about 1% to about 10% of the packets. They can be applied as a seed dressing or as a foliage application with a dust blower machine.

It is equally practical to apply the present formulation in the form of a solution in an appropriate organic solvent, usually petroleum oil, such as the spray oils, which are widely used in agricultural chemistry.

PMPs can also be applied in the form of an aerosol composition. In such compositions the packets are dissolved or dispersed in a carrier, which is a pressure-generating propellant mixture. The aerosol composition is packaged in a container from which the mixture is dispensed through an atomizing valve.

Another embodiment is an oil-in-water emulsion, wherein the emulsion includes oily globules which are each provided with a lamellar liquid crystal coating and are dispersed in an aqueous phase, wherein each oily globule includes at least one compound which is agriculturally active, and is individually coated with a monolamellar or oligolamellar layer including: (1) at least one non-ionic lipophilic surface-active agent, (2) at least one non-ionic hydrophilic surface-active agent and (3) at least one ionic surface-active agent, wherein the globules having a mean particle diameter of less than 800 nanometers. Further information on the embodiment is disclosed in U.S. patent publication 20070027034 published Feb. 1, 2007. For ease of use, this embodiment will be referred to as “OIWE.”

Additionally, generally, when the molecules disclosed above are used in a formulation, such formulation can also contain other components. These components include, but are not limited to, (this is a non-exhaustive and non-mutually exclusive list) wetters, spreaders, stickers, penetrants, buffers, sequestering agents, drift reduction agents, compatibility agents, anti-foam agents, cleaning agents, and emulsifiers. A few components are described forthwith.

A wetting agent is a substance that when added to a liquid increases the spreading or penetration power of the liquid by reducing the interfacial tension between the liquid and the surface on which it is spreading. Wetting agents are used for two main functions in agrochemical formulations: during processing and manufacture to increase the rate of wetting of powders in water to make concentrates for soluble liquids or suspension concentrates; and during mixing of a product with water in a spray tank to reduce the wetting time of wettable powders and to improve the penetration of water into water-dispersible granules. Examples of wetting agents used in wettable powder, suspension concentrate, and water-dispersible granule formulations are: sodium lauryl sulfate; sodium dioctyl sulfosuccinate; alkyl phenol ethoxylates; and aliphatic alcohol ethoxylates.

A dispersing agent is a substance which adsorbs onto the surface of particles and helps to preserve the state of dispersion of the particles and prevents them from reaggregating. Dispersing agents are added to agrochemical formulations to facilitate dispersion and suspension during manufacture, and to ensure the particles redisperse into water in a spray tank. They are widely used in wettable powders, suspension concentrates and water-dispersible granules. Surfactants that are used as dispersing agents have the ability to adsorb strongly onto a particle surface and provide a charged or steric barrier to reaggregation of particles. The most commonly used surfactants are anionic, non-ionic, or mixtures of the two types. For wettable powder formulations, the most common dispersing agents are sodium lignosulfonates. For suspension concentrates, very good adsorption and stabilization are obtained using polyelectrolytes, such as sodium naphthalene sulfonate formaldehyde condensates. Tristyrylphenol ethoxylate phosphate esters are also used. Non-ionics such as alkylarylethylene oxide condensates and EO-PO block copolymers are sometimes combined with anionics as dispersing agents for suspension concentrates. In recent years, new types of very high molecular weight polymeric surfactants have been developed as dispersing agents. These have very long hydrophobic ‘backbones’ and a large number of ethylene oxide chains forming the ‘teeth’ of a ‘comb’ surfactant. These high molecular weight polymers can give very good long-term stability to suspension concentrates because the hydrophobic backbones have many anchoring points onto the particle surfaces. Examples of dispersing agents used in agrochemical formulations are: sodium lignosulfonates; sodium naphthalene sulfonate formaldehyde condensates; tristyrylphenol ethoxylate phosphate esters; aliphatic alcohol ethoxylates; alkyl ethoxylates; EO-PO (ethylene oxide-propylene oxide) block copolymers; and graft copolymers.

An emulsifying agent is a substance which stabilizes a suspension of droplets of one liquid phase in another liquid phase. Without the emulsifying agent the two liquids would separate into two immiscible liquid phases. The most commonly used emulsifier blends contain alkylphenol or aliphatic alcohol with twelve or more ethylene oxide units and the oil-soluble calcium salt of dodecylbenzenesulfonic acid. A range of hydrophile-lipophile balance (“HLB”) values from 8 to 18 will normally provide good stable emulsions. Emulsion stability can sometimes be improved by the addition of a small amount of an EO-PO block copolymer surfactant.

A solubilizing agent is a surfactant which will form micelles in water at concentrations above the critical micelle concentration. The micelles are then able to dissolve or solubilize water-insoluble materials inside the hydrophobic part of the micelle. The types of surfactants usually used for solubilization are non-ionics, sorbitan monooleates, sorbitan monooleate ethoxylates, and methyl oleate esters.

Surfactants are sometimes used, either alone or with other additives such as mineral or vegetable oils as adjuvants to spray-tank mixes to improve the biological performance of the pesticide on the target. The types of surfactants used for bioenhancement depend generally on the nature and mode of action of the pesticide. However, they are often non-ionics such as: alkyl ethoxylates; linear aliphatic alcohol ethoxylates; aliphatic amine ethoxylates.

A carrier or diluent in an agricultural formulation is a material added to the pesticide to give a product of the required strength. Carriers are usually materials with high absorptive capacities, while diluents are usually materials with low absorptive capacities. Carriers and diluents are used in the formulation of dusts, wettable powders, granules, and water-dispersible granules.

Organic solvents are used mainly in the formulation of emulsifiable concentrates, oil-in-water emulsions, suspoemulsions, and ultra low volume formulations, and to a lesser extent, granular formulations. Sometimes mixtures of solvents are used. The first main groups of solvents are aliphatic paraffinic oils such as kerosene or refined paraffins. The second main group (and the most common) includes the aromatic solvents such as xylene and higher molecular weight fractions of C9 and C10 aromatic solvents. Chlorinated hydrocarbons are useful as cosolvents to prevent crystallization of pesticides when the formulation is emulsified into water. Alcohols are sometimes used as cosolvents to increase solvent power. Other solvents may include vegetable oils, seed oils, and esters of vegetable and seed oils.

Thickeners or gelling agents are used mainly in the formulation of suspension concentrates, emulsions, and suspoemulsions to modify the rheology or flow properties of the liquid and to prevent separation and settling of the dispersed particles or droplets. Thickening, gelling, and anti-settling agents generally fall into two categories, namely water-insoluble particulates and water-soluble polymers. It is possible to produce suspension concentrate formulations using clays and silicas. Examples of these types of materials, include, but are not limited to, montmorillonite, bentonite, magnesium aluminum silicate, and attapulgite. Water-soluble polysaccharides have been used as thickening-gelling agents for many years. The types of polysaccharides most commonly used are natural extracts of seeds and seaweeds or are synthetic derivatives of cellulose. Examples of these types of materials include, but are not limited to, guar gum; locust bean gum; carrageenam; alginates; methyl cellulose; sodium carboxymethyl cellulose (SCMC); hydroxyethyl cellulose (HEC). Other types of anti-settling agents are based on modified starches, polyacrylates, polyvinyl alcohol, and polyethylene oxide. Another good anti-settling agent is xanthan gum.

Microorganisms can cause spoilage of formulated products. Therefore preservation agents are used to eliminate or reduce their effect. Examples of such agents include, but are not limited to: propionic acid and its sodium salt; sorbic acid and its sodium or potassium salts; benzoic acid and its sodium salt; p-hydroxybenzoic acid sodium salt; methyl p-hydroxybenzoate; and 1,2-benzisothiazolin-3-one (BIT).

The presence of surfactants often causes water-based formulations to foam during mixing operations in production and in application through a spray tank. In order to reduce the tendency to foam, anti-foam agents are often added either during the production stage or before filling into bottles. Generally, there are two types of anti-foam agents, namely silicones and non-silicones. Silicones are usually aqueous emulsions of dimethyl polysiloxane, while the non-silicone anti-foam agents are water-insoluble oils, such as octanol and nonanol, or silica. In both cases, the function of the anti-foam agent is to displace the surfactant from the air-water interface.

“Green” agents (e.g., adjuvants, surfactants, solvents) can reduce the overall environmental footprint of crop protection formulations. Green agents are biodegradable and generally derived from natural and/or sustainable sources, e.g., plant and animal sources. Specific examples are: vegetable oils, seed oils, and esters thereof, also alkoxylated alkyl polyglucosides.

In some instances, PMPs can be freeze-dried or lyophilized. See U.S. Pat. No. 4,311,712. The PMPs can later be reconstituted on contact with water or another liquid. Other components can be added to the lyophilized or reconstituted liposomes, for example, other antipathogen agents, pesticidal agents, repellent agents, agriculturally acceptable carriers, or other materials in accordance with the formulations described herein.

Other optional features of the composition include carriers or delivery vehicles that protect the PMP composition against UV and/or acidic conditions. In some instances, the delivery vehicle contains a pH buffer. In some instances, the composition is formulated to have a pH in the range of about 4.5 to about 9.0, including for example pH ranges of about any one of 5.0 to about 8.0, about 6.5 to about 7.5, or about 6.5 to about 7.0.

The composition may additionally be formulated with an attractant (e.g., a chemoattractant) that attracts a pest, such as a pathogen vector (e.g., an insect), to the vicinity of the composition. Attractants include pheromones, a chemical that is secreted by an animal, especially a pest, or chemoattractants which influences the behavior or development of others of the same species. Other attractants include sugar and protein hydrolysate syrups, yeasts, and rotting meat. Attractants also can be combined with an active ingredient and sprayed onto foliage or other items in the treatment area. Various attractants are known which influence a pest's behavior as a pest's search for food, oviposition, or mating sites, or mates. Attractants useful in the methods and compositions described herein include, for example, eugenol, phenethyl propionate, ethyl dimethylisobutyl-cyclopropane carboxylate, propyl benszodioxancarboxylate, cis-7,8-epoxy-2-methyloctadecane, trans-8,trans-0-dodecadienol, cis-9-tetradecenal (with cis-11-hexadecenal), trans-11-tetradecenal, cis-11-hexadecenal, (Z)-11,12-hexadecadienal, cis-7-dodecenyl acetate, cis-8-dodecenyul acetate, cis-9-dodecenyl acetate, cis-9-tetradecenyl acetate, cis-11-tetradecenyl acetate, trans-11-tetradecenyl acetate (with cis-11), cis-9,trans-11-tetradecadienyl acetate (with cis-9,trans-12), cis-9,trans-12-tetradecadienyl acetate, cis-7,cis-11-hexadecadienyl acetate (with cis-7,trans-11), cis-3,cis-13-octadecadienyl acetate, trans-3,cis-13-octadecadienyl acetate, anethole and isoamyl salicylate.

For further information on agricultural formulations, see “Chemistry and Technology of Agrochemical Formulations” edited by D. A. Knowles, copyright 1998 by Kluwer Academic Publishers. Also see “Insecticides in Agriculture and Environment—Retrospects and Prospects” by A. S. Perry, I. Yamamoto, I. Ishaaya, and R. Perry, copyright 1998 by Springer-Verlag.

III. Exogenous Polypeptides

The present invention includes plant messenger packs (PMPs) and PMP compositions wherein the PMP encapsulates an exogenous polypeptide. The exogenous polypeptide may be enclosed within the PMP, e.g., located inside the lipid membrane structure, e.g., separated from the surrounding material or solution by both leaflets of a lipid bilayer. In some aspects, the encapsulated exogenous polypeptide may interact or associate with the inner lipid membrane of the PMP. In some aspects, the encapsulated exogenous polypeptide may interact or associate with the outer lipid membrane of the PMP. The exogenous polypeptide may, in some instances, be intercalated with the lipid membrane structure. In some instances, the exogenous polypeptide has an extraluminal portion. In some instances, the exogenous polypeptide is conjugated to the outer surface of the lipid membrane structure, e.g., using click chemistry.

The exogenous polypeptide may be a polypeptide that does not naturally occur in a plant EV. Alternatively, the exogenous polypeptide may be a polypeptide that naturally occurs in a plant EV, but that is encapsulated in a PMP in an amount not found in a naturally occurring plant extracellular vesicle. The exogenous polypeptide may, in some instances, naturally occur in the plant from which the PMP is derived. In other instances, the exogenous polypeptide does not naturally occur in the plant from which the PMP is derived. The exogenous polypeptide may be artificially expressed in the plant from which the PMP is derived, e.g., may be a heterologous polypeptide. The exogenous polypeptide may be derived from another organism. In some aspects, the exogenous polypeptide is loaded into the PMP, e.g., using one or more of sonication, electroporation, lipid extraction, and lipid extrusion.

Polypeptides included herein may include naturally occurring polypeptides or recombinantly produced variants. In some instances, the polypeptide may be a functional fragments or variants thereof (e.g., an enzymatically active fragment or variant thereof). For example, the polypeptide may be a functionally active variant of any of the polypeptides described herein with at least 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity, e.g., over a specified region or over the entire sequence, to a sequence of a polypeptide described herein or a naturally occurring polypeptide. In some instances, the polypeptide may have at least 50% (e.g., at least 50%, 60%, 70%, 80%, 90%, 95%, 97%, 99%, or greater) identity to a polypeptide of interest.

The polypeptides described herein may be formulated in a composition for any of the uses described herein. The compositions disclosed herein may include any number or type (e.g., classes) of polypeptides, such as at least about any one of 1 polypeptide, 2, 3, 4, 5, 10, 15, 20, or more polypeptides. A suitable concentration of each polypeptide in the composition depends on factors such as efficacy, stability of the polypeptide, number of distinct polypeptides in the composition, the formulation, and methods of application of the composition. In some instances, each polypeptide in a liquid composition is from about 0.1 ng/mL to about 100 mg/mL. In some instances, each polypeptide in a solid composition is from about 0.1 ng/g to about 100 mg/g.

Methods of making a polypeptide are routine in the art. See, in general, Smales & James (Eds.), Therapeutic Proteins: Methods and Protocols (Methods in Molecular Biology), Humana Press (2005); and Crommelin, Sindelar & Meibohm (Eds.), Pharmaceutical Biotechnology: Fundamentals and Applications, Springer (2013).

Methods for producing a polypeptide involve expression in plant cells, although recombinant proteins can also be produced using insect cells, yeast, bacteria, mammalian cells, or other cells under the control of appropriate promoters. Mammalian expression vectors may comprise nontranscribed elements such as an origin of replication, a suitable promoter and enhancer, and other 5′ or 3′ flanking nontranscribed sequences, and 5′ or 3′ nontranslated sequences such as necessary ribosome binding sites, a polyadenylation site, splice donor and acceptor sites, and termination sequences. DNA sequences derived from the SV40 viral genome, for example, SV40 origin, early promoter, enhancer, splice, and polyadenylation sites may be used to provide the other genetic elements required for expression of a heterologous DNA sequence. Appropriate cloning and expression vectors for use with bacterial, fungal, yeast, and mammalian cellular hosts are described in Green & Sambrook, Molecular Cloning: A Laboratory Manual (Fourth Edition), Cold Spring Harbor Laboratory Press (2012).

Various mammalian cell culture systems can be employed to express and manufacture a recombinant polypeptide agent. Examples of mammalian expression systems include CHO cells, COS cells, HeLA and BHK cell lines. Processes of host cell culture for production of protein therapeutics are described in, e.g., Zhou and Kantardjieff (Eds.), Mammalian Cell Cultures for Biologics Manufacturing (Advances in Biochemical Engineering/Biotechnology), Springer (2014). Purification of proteins is described in Franks, Protein Biotechnology: Isolation, Characterization, and Stabilization, Humana Press (2013); and in Cutler, Protein Purification Protocols (Methods in Molecular Biology), Humana Press (2010). Formulation of protein therapeutics is described in Meyer (Ed.), Therapeutic Protein Drug Products: Practical Approaches to formulation in the Laboratory, Manufacturing, and the Clinic, Woodhead Publishing Series (2012). Alternatively, the polypeptide may be a chemically synthesized polypeptide.

In some instances, the PMP includes an antibody or antigen binding fragment thereof. For example, an agent described herein may be an antibody that blocks or potentiates activity and/or function of a component of the pathogen. The antibody may act as an antagonist or agonist of a polypeptide (e.g., enzyme or cell receptor) in the pathogen. The making and use of antibodies against a target antigen in a pathogen is known in the art. See, for example, Zhiqiang An (Ed.), Therapeutic Monoclonal Antibodies: From Bench to Clinic, 1st Edition, Wiley, 2009 and also Greenfield (Ed.), Antibodies: A Laboratory Manual, 2nd Edition, Cold Spring Harbor Laboratory Press, 2013, for methods of making recombinant antibodies, including antibody engineering, use of degenerate oligonucleotides, 5′-RACE, phage display, and mutagenesis; antibody testing and characterization; antibody pharmacokinetics and pharmacodynamics; antibody purification and storage; and screening and labeling techniques.

The exogenous polypeptide may be released from the PMP in the target cell. In some aspects, the exogenous polypeptide exerts activity in the cytoplasm of the target cell or in the nucleus of the target cell. The exogenous polypeptide may be translocated to the nucleus of the target cell.

In some aspects, uptake by a cell of the exogenous polypeptide encapsulated by the PMP is increased relative to uptake of the exogenous polypeptide not encapsulated by a PMP.

In some aspects, the effectiveness of the exogenous polypeptide encapsulated by the PMP is increased relative to the effectiveness of the exogenous polypeptide not encapsulated by a PMP.

A. Therapeutic Agents

The exogenous polypeptide may be a therapeutic agent, e.g., an agent used for the prevention or treatment of a condition or a disease. In some aspects, the disease is a cancer, an autoimmine condition, or a metabolic disorder.

In some examples, the therapeutic agent is a peptide (e.g., a naturally occurring peptide, a recombinant peptide, or a synthetic peptide) or a protein (e.g., a naturally occurring protein, a recombinant protein, or a synthetic protein). In some examples, the protein is a fusion protein.

In some examples, the polypeptide is endogenous to the organism (e.g., mammal) to which the PMP is delivered. In other examples, the polypeptide is not endogenous to the organism.

In some examples, the therapeutic agent is an antibody (e.g., a monoclonal antibody, e.g., a monospecific, bispecific, or multispecific monoclonal antibody) or an antigen-binding fragment thereof (e.g., an scFv, (scFv)2, Fab, Fab′, and F(ab′)2, F(ab1)2, Fv, dAb, and Fd fragment, or a diabody), a nanobody, a conjugated antibody, or an antibody-related polypeptide.

In some examples, the therapeutic agent is an antimicrobial, antibacterial, antifungal, antinematicidal, antiparasitic, or antiviral polypeptide.

In some examples, the therapeutic agent is an allergenic, an allergen, or an antigen.

In some examples, the therapeutic agent is a vaccine (e.g., a conjugate vaccine, an inactivated vaccine, or a live attenuated vaccine),

In some examples, the therapeutic agent is an enzyme, e.g., a metabolic recombinase, a helicase, an integrase, a RNAse, a DNAse, an ubiquitination protein. In some examples, the enzyme is a recombinant enzyme.

In some examples, the therapeutic agent is a gene editing protein, e.g., a component of a CRISPR-Cas system, TALEN, or zinc finger.

In some examples, the therapeutic agent is any one of a cytokine, a hormone, a signaling ligand, a transcription factor, a receptor, a receptor antagonist, a receptor agonist, a blocking or neutralizing polypeptide, a riboprotein, or a chaperone.

In some examples, the therapeutic agent is a pore-forming protein, a cell-penetrating peptide, a cell-penetrating peptide inhibitor, or a proteolysis targeting chimera (PROTAC).

In some examples, the therapeutic agent is any one of an aptamer, a blood derivative, a cell therapy, or an immunotherapy (e.g., a cellular immunotherapy.

In some aspects, the therapeutic agent is a protein or peptide therapeutic with enzymatic activity, regulatory activity, or targeting activity, e.g., a protein or peptide with activity that affects one or more of endocrine and growth regulation, metabolic enzyme deficiencies, hematopoiesis, hemostasis and thrombosis; gastrointestinal-tract disorders; pulmonary disorders; immunodeficiencies and/or immunoregulation; fertility; aging (e.g., anti-aging activity); autophagy regulation; epigenetic regulation; oncology; or infectious diseases (e.g., anti-microbial peptides, anti-fungals, or anti-virals).

In some aspects, the therapeutic agent is a protein vaccine, e.g., a vaccine for use in protecting against a deleterious foreign agent, treating an autoimmune disease, or treating cancer (e.g., a neoantigen).

In some examples, the polypeptide is globular, fibrous, or disordered.

In some examples, the polypeptide has a size of less than 1, less than 2, less than 5, less than 10, less than 15, less than 20, less than 30, less than 40, less than 50, less than 60, less than 70, less than 80, less than 90, or less than 100 kD, e.g., has a size of 1-50 kD (e.g., 1-10, 10-20, 20-30, 30-40, or 40-50 kD) or 50-100 kD (e.g., 50-60, 60-70, 70-80, 80-90, or 90-100 kD).

In some examples, the polypeptide has an overall charge that is positive, negative, or neutral.

The polypeptide may be modified such that the overall charge is altered, e.g., modified by adding one or more charged amino acids, for example, one or more (for example, 1-10 or 5-10) positively or negatively charged amino acids, such as an arginine tail (e.g., 5-10 arginine residues) to the N-terminus or C-terminus of the polypeptide.

In some aspects, the disease is diabetes, e.g., diabetes mellitus, e.g., Type 1 diabetes mellitus.

In some aspects, diabetes is treated by administering to a patient an effective amount of a composition comprising a plurality of PMPs, wherein one or more exogenous polypeptides are encapsulated by the PMP. In some aspects, the administration of the plurality of PMPs lowers the blood sugar of the subject.

In some aspects, the therapeutic agent is insulin.

In some examples, the therapeutic agent is an antibody shown in Table 1, a peptide shown in Table 2, an enzyme shown in Table 3, or a protein shown in Table 4.

TABLE 1
Antibodies
Broad class	Molecule Type	Drug Name
Antibody	Monoclonal Antibody	1D-09C3
Antibody	Monoclonal Antibody Conjugated	212 Pb-TCMC-Trastuzumab
Antibody	Monoclonal Antibody	2141 V-11
Antibody	Monoclonal Antibody	3BNC-117
Antibody	Monoclonal Antibody	3BNC-117LS
Antibody	Monoclonal Antibody	8H-9
Antibody	Monoclonal Antibody Conjugated	A-166
Antibody	Bispecific Monoclonal Antibody	A-337
Antibody	Monoclonal Antibody	AB-011
Antibody	Monoclonal Antibody	AB-022
Antibody	Monoclonal Antibody	AB-023
Antibody	Monoclonal Antibody	AB-154
Antibody	Monoclonal Antibody	abagovomab
Antibody	Monoclonal Antibody Conjugated	ABBV-011
Antibody	Monoclonal Antibody	ABBV-0805
Antibody	Monoclonal Antibody Conjugated	ABBV-085
Antibody	Monoclonal Antibody	ABBV-151
Antibody	Monoclonal Antibody Conjugated	ABBV-155
Antibody	Bispecific Monoclonal Antibody	ABBV-184
Antibody	Monoclonal Antibody Conjugated	ABBV-321
Antibody	Monoclonal Antibody Conjugated	ABBV-3373
Antibody	Monoclonal Antibody	ABBV-368
Antibody	Monoclonal Antibody	ABBV-927
Antibody	Monoclonal Antibody	abciximab
Antibody	Monoclonal Antibody	abelacimab [INN]
Antibody	Monoclonal Antibody Conjugated	AbGn-107
Antibody	Monoclonal Antibody	AbGn-168H
Antibody	Monoclonal Antibody	abituzumab
Antibody	Monoclonal Antibody	ACT-017
Antibody	Monoclonal Antibody Conjugated	Actimab-A
Antibody	Monoclonal Antibody Conjugated	Actimab-M
Antibody	Cellular Immunotherapy; Gene Therapy;	ACTR-087 + SEA-BCMA
	Monoclonal Antibody
Antibody	Cellular Immunotherapy; Gene Therapy;	ACTR-707
	Monoclonal Antibody
Antibody	Monoclonal Antibody	adalimumab
Antibody	Monoclonal Antibody	adalimumab biosimilar
Antibody	Monoclonal Antibody; Small Molecule	adavosertib + durvalumab
Antibody	Monoclonal Antibody Conjugated	ADCT-602
Antibody	Antibody	adder [Vipera bents] antivenom
Antibody	Monoclonal Antibody	ADG-106
Antibody	Monoclonal Antibody	ADG-116
Antibody	Monoclonal Antibody	adrecizumab
Antibody	Monoclonal Antibody	aducanumab
Antibody	Monoclonal Antibody	Aerucin
Antibody	Bispecific Monoclonal Antibody	AFM-13
Antibody	Monoclonal Antibody	AGEN-1181
Antibody	Monoclonal Antibody	AGEN-2373
Antibody	Monoclonal Antibody Conjugated	AGS-16C3F
Antibody	Monoclonal Antibody	AGS-1C4D4
Antibody	Monoclonal Antibody Conjugated	AGS-62P1
Antibody	Monoclonal Antibody	AHM
Antibody	Monoclonal Antibody	AIMab-7195
Antibody	Monoclonal Antibody	AK-002
Antibody	Monoclonal Antibody	AK-101
Antibody	Bispecific Monoclonal Antibody	AK-104
Antibody	Monoclonal Antibody	AK-111
Antibody	Bispecific Monoclonal Antibody	AK-112
Antibody	Monoclonal Antibody	AL-001
Antibody	Monoclonal Antibody	AL-002
Antibody	Monoclonal Antibody	AL-003
Antibody	Monoclonal Antibody	AL-101
Antibody	Monoclonal Antibody	alemtuzumab
Antibody	Monoclonal Antibody	alirocumab
Antibody	Monoclonal Antibody Conjugated	ALTP-7
Antibody	Bispecific Monoclonal Antibody	ALXN-1720
Antibody	Antibody	AMAG-423
Antibody	Monoclonal Antibody	amatuximab
Antibody	Bispecific Monoclonal Antibody	AMG-160
Antibody	Bispecific Monoclonal Antibody	AMG-211
Antibody	Monoclonal Antibody Conjugated	AMG-224
Antibody	Monoclonal Antibody	AMG-301
Antibody	Bispecific Monoclonal Antibody	AMG-330
Antibody	Monoclonal Antibody	AMG-404
Antibody	Bispecific Monoclonal Antibody	AMG-420
Antibody	Bispecific Monoclonal Antibody	AMG-424
Antibody	Bispecific Monoclonal Antibody	AMG-427
Antibody	Bispecific Monoclonal Antibody	AMG-509
Antibody	Monoclonal Antibody	AMG-529
Antibody	Bispecific Monoclonal Antibody	AMG-673
Antibody	Bispecific Monoclonal Antibody	AMG-701
Antibody	Monoclonal Antibody	AMG-714
Antibody	Bispecific Monoclonal Antibody	AMG-757
Antibody	Monoclonal Antibody	AMG-820
Antibody	Bispecific Monoclonal Antibody	AMV-564
Antibody	Monoclonal Antibody	ANB-019
Antibody	Monoclonal Antibody	andecaliximab
Antibody	Monoclonal Antibody Conjugated	anetumab ravtansine
Antibody	Monoclonal Antibody	anifrolumab
Antibody	Antibody	anthrax immune globulin (human)
Antibody	Antibody	anti-thymocyte globulin (equine)
Antibody	Antibody	anti-thymocyte globulin (rabbit)
Antibody	Antibody	antivenin latrodectus equine
		immune F(ab)2
Antibody	Monoclonal Antibody	ANX-005
Antibody	Monoclonal Antibody	ANX-007
Antibody	Monoclonal Antibody	AP-101
Antibody	Monoclonal Antibody	apitegromab
Antibody	Monoclonal Antibody	APL-501
Antibody	Monoclonal Antibody	APL-502
Antibody	Bispecific Monoclonal Antibody	APVO-436
Antibody	Monoclonal Antibody	APX-003
Antibody	Monoclonal Antibody	APX-005M
Antibody	Monoclonal Antibody	ARGX-109
Antibody	Monoclonal Antibody	ARP-1536
Antibody	Monoclonal Antibody Conjugated	ARX-788
Antibody	Monoclonal Antibody	ascrinvacumab
Antibody	Monoclonal Antibody	ASLAN-004
Antibody	Monoclonal Antibody	ASP-1650
Antibody	Monoclonal Antibody	ASP-6294
Antibody	Monoclonal Antibody	ASP-8374
Antibody	Monoclonal Antibody	AT-1501
Antibody	Monoclonal Antibody	atezolizumab
Antibody	Monoclonal Antibody	ATI-355
Antibody	Monoclonal Antibody Conjugated	ATL-101
Antibody	Bispecific Monoclonal Antibody	ATOR-1015
Antibody	Monoclonal Antibody	ATOR-1017
Antibody	Monoclonal Antibody	ATRC-101
Antibody	Monoclonal Antibody	Atrosab
Antibody	Monoclonal Antibody Conjugated	Aurixim
Antibody	Monoclonal Antibody	AV-1
Antibody	Monoclonal Antibody	avelumab
Antibody	Monoclonal Antibody Conjugated	AVID-100
Antibody	Monoclonal Antibody Conjugated	AVID-200
Antibody	Monoclonal Antibody	axatilimab
Antibody	Monoclonal Antibody	B-001
Antibody	Monoclonal Antibody	balstilimab
Antibody	Monoclonal Antibody	basiliximab
Antibody	Monoclonal Antibody	BAT-4406
Antibody	Monoclonal Antibody	batoclimab
Antibody	Monoclonal Antibody	bavituximab
Antibody	Monoclonal Antibody	BAY-1093884
Antibody	Monoclonal Antibody	BAY-1834942
Antibody	Monoclonal Antibody	BAY-1905254
Antibody	Monoclonal Antibody Conjugated	BAY-2287411
Antibody	Monoclonal Antibody Conjugated	BAY-2315497
Antibody	Monoclonal Antibody Conjugated	BB-1701
Antibody	Monoclonal Antibody Conjugated	BC-8SA
Antibody	Monoclonal Antibody Conjugated	BC-8Y90
Antibody	Monoclonal Antibody	BCBA-445
Antibody	Monoclonal Antibody	BCD-089
Antibody	Monoclonal Antibody	BCD-096
Antibody	Bispecific Monoclonal Antibody	BCD-121
Antibody	Monoclonal Antibody	BCD-132
Antibody	Monoclonal Antibody	BCD-145
Antibody	Monoclonal Antibody	BCD-217
Antibody	Monoclonal Antibody	begelomab
Antibody	Monoclonal Antibody Conjugated	belantamab mafodotin
Antibody	Monoclonal Antibody	belimumab
Antibody	Monoclonal Antibody	bemarituzumab
Antibody	Monoclonal Antibody	benralizumab
Antibody	Monoclonal Antibody	bentracimab
Antibody	Monoclonal Antibody	bermekimab
Antibody	Monoclonal Antibody	bertilimumab
Antibody	Monoclonal Antibody Conjugated	Betalutin
Antibody	Monoclonal Antibody	bevacizumab
Antibody	Monoclonal Antibody	bevacizumab biosimilar
Antibody	Monoclonal Antibody	bezlotoxumab
Antibody	Monoclonal Antibody	BG-00011
Antibody	Monoclonal Antibody	BGB-149
Antibody	Monoclonal Antibody	BHQ-880
Antibody	Monoclonal Antibody	BI-1206
Antibody	Monoclonal Antibody	BI-201
Antibody	Monoclonal Antibody	BI-505
Antibody	Monoclonal Antibody	BI-655064
Antibody	Monoclonal Antibody	BI-655088
Antibody	Monoclonal Antibody	BI-754091
Antibody	Monoclonal Antibody	BI-754111
Antibody	Monoclonal Antibody	BI-836826
Antibody	Monoclonal Antibody	BI-836858
Antibody	Bispecific Monoclonal Antibody	BI-836880
Antibody	Monoclonal Antibody Conjugated	BIIB-015
Antibody	Monoclonal Antibody	BIIB-059
Antibody	Monoclonal Antibody	BIIB-076
Antibody	Monoclonal Antibody	bimagrumab
Antibody	Monoclonal Antibody	bimekizumab
Antibody	Monoclonal Antibody	birtamimab
Antibody	Bispecific Monoclonal Antibody	Bispecific Monoclonal Antibody to
		Agonize CD3 for Acute Myelocytic
		Leukemia
Antibody	Bispecific Monoclonal Antibody	Bispecific Monoclonal Antibody to
		Inhibit HIV 1 Env for HIV Infections
Antibody	Bispecific Monoclonal Antibody	Bispecific Monoclonal Antibody to
		Target CD3 and FLT3 for Acute
		Myelocytic Leukemia, Acute
		Lymphocytic Leukemia and
		Myelodysplastic Syndrome
Antibody	Bispecific Monoclonal Antibody	Bispecific Monoclonal Antibody to
		Target GD2 and CD3 for Oncology
Antibody	Bispecific Monoclonal Antibody	Bispecific Monoclonal Antibody to
		Target PD-L1 and CTLA4 for
		Pancreatic Ductal Adenocarcinoma
Antibody	Monoclonal Antibody	BIVV-020
Antibody	Monoclonal Antibody	BIW-8962
Antibody	Antibody	black widow spider [Latrodectus
		mactans] antivenom [equine]
Antibody	Monoclonal Antibody	bleselumab
Antibody	Bispecific Monoclonal Antibody	blinatumomab
Antibody	Monoclonal Antibody Conjugated	BMS-936561
Antibody	Monoclonal Antibody	BMS-986012
Antibody	Monoclonal Antibody Conjugated	BMS-986148
Antibody	Monoclonal Antibody	BMS-986156
Antibody	Monoclonal Antibody	BMS-986178
Antibody	Monoclonal Antibody	BMS-986179
Antibody	Monoclonal Antibody	BMS-986207
Antibody	Monoclonal Antibody	BMS-986218
Antibody	Monoclonal Antibody	BMS-986226
Antibody	Monoclonal Antibody	BMS-986253
Antibody	Monoclonal Antibody	BMS-986258
Antibody	Monoclonal Antibody	BNC-101
Antibody	Monoclonal Antibody	BOS-161721
Antibody	Antibody	botulism immune globulin
Antibody	Monoclonal Antibody	brazikumab
Antibody	Monoclonal Antibody Conjugated	brentuximab vedotin
Antibody	Monoclonal Antibody	BrevaRex MAb-AR20.5
Antibody	Monoclonal Antibody	briakinumab
Antibody	Monoclonal Antibody	brodalumab
Antibody	Monoclonal Antibody	brolucizumab
Antibody	Monoclonal Antibody	BT-063
Antibody	Antibody	BT-084
Antibody	Antibody	BT-086
Antibody	Antibody	BT-595
Antibody	Monoclonal Antibody	BTI-322
Antibody	Bispecific Monoclonal Antibody	BTRC-4017A
Antibody	Monoclonal Antibody	budigalimab
Antibody	Monoclonal Antibody	burosumab
Antibody	Monoclonal Antibody	BVX-20
Antibody	Monoclonal Antibody	cabiralizumab
Antibody	Monoclonal Antibody	CAEL-101
Antibody	Monoclonal Antibody	CAL
Antibody	Monoclonal Antibody Conjugated	camidanlumab tesirine
Antibody	Monoclonal Antibody	camrelizumab
Antibody	Monoclonal Antibody	canakinumab
Antibody	Monoclonal Antibody Conjugated	cantuzumab mertansine
Antibody	Monoclonal Antibody	caplacizumab
Antibody	Monoclonal Antibody	carotuximab
Antibody	Bispecific Monoclonal Antibody	catumaxomab
Antibody	Monoclonal Antibody	CBP-201
Antibody	Bispecific Monoclonal Antibody	CC-1
Antibody	Monoclonal Antibody	CC-90002
Antibody	Monoclonal Antibody	CC-90006
Antibody	Bispecific Monoclonal Antibody	CC-93269
Antibody	Monoclonal Antibody Conjugated	CC-99712
Antibody	Monoclonal Antibody Conjugated	CCW-702
Antibody	Monoclonal Antibody	CDX-3379
Antibody	Cellular Immunotherapy; Recombinant Protein	Cellular Immunotherapy + edodekin
		alfa
Antibody	Monoclonal Antibody	cemiplimab
Antibody	Monoclonal Antibody	cendakimab
Antibody	Monoclonal Antibody	CERC-002
Antibody	Monoclonal Antibody	CERC-007
Antibody	Monoclonal Antibody	certolizumab pegol
Antibody	Monoclonal Antibody	certolizumab pegol biosimilar
Antibody	Monoclonal Antibody	cetrelimab
Antibody	Monoclonal Antibody	cetuximab
Antibody	Monoclonal Antibody	cetuximab biosimilar
Antibody	Monoclonal Antibody Conjugated	cetuximab sarotalocan
Antibody	Monoclonal Antibody	CHOH-01
Antibody	Bispecific Monoclonal Antibody	cibisatamab
Antibody	Monoclonal Antibody	cinpanemab
Antibody	Monoclonal Antibody	CIS-43
Antibody	Monoclonal Antibody	CJM-112
Antibody	Monoclonal Antibody	clazakizumab
Antibody	Monoclonal Antibody Conjugated	clivatuzumab tetraxetan
Antibody	Monoclonal Antibody	CM-101
Antibody	Monoclonal Antibody	CNTO-6785
Antibody	Monoclonal Antibody	codrituzumab
Antibody	Monoclonal Antibody Conjugated	cofetuzumab pelidotin
Antibody	Monoclonal Antibody	COM-701
Antibody	Monoclonal Antibody	concizumab
Antibody	Monoclonal Antibody	COR-001
Antibody	Antibody	coral snake [Micrurus] (polyvalent)
		immunoglobulin F (ab) 2 + Fab
		immunoglobulin G antivenom
Antibody	Monoclonal Antibody	cosibelimab
Antibody	Monoclonal Antibody	CPI-006
Antibody	Monoclonal Antibody	crenezumab
Antibody	Monoclonal Antibody	crizanlizumab
Antibody	Monoclonal Antibody	crovalimab
Antibody	Monoclonal Antibody	CS-1001
Antibody	Monoclonal Antibody	CS-1003
Antibody	Monoclonal Antibody	CSL-311
Antibody	Monoclonal Antibody	CSL-324
Antibody	Monoclonal Antibody	CSL-346
Antibody	Monoclonal Antibody	CSL-360
Antibody	Monoclonal Antibody	CTX-471
Antibody	Monoclonal Antibody	cusatuzumab
Antibody	Antibody	Cutaquig
Antibody	Antibody	Cuvitru
Antibody	Monoclonal Antibody	CX-072
Antibody	Monoclonal Antibody Conjugated	CX-2009
Antibody	Monoclonal Antibody Conjugated	CX-2029
Antibody	Monoclonal Antibody	Cyto-111
Antibody	Antibody	cytomegalovirus immune globulin
		(human)
Antibody	Monoclonal Antibody; Small Molecule	dabrafenib mesylate +
		panitumumab + trametinib dimethyl
		sulfoxide
Antibody	Monoclonal Antibody	daclizumab
Antibody	Monoclonal Antibody	dalotuzumab
Antibody	Antisense Oligonucleotide; Monoclonal Antibody	danvatirsen + durvalumab
Antibody	Monoclonal Antibody	dapirolizumab pegol
Antibody	Monoclonal Antibody	daratumumab
Antibody	Monoclonal Antibody	daxdilimab
Antibody	Monoclonal Antibody	DE-098
Antibody	Antibody	death adder [Acanthophis
		antarcticus] antivenom [equine]
Antibody	Monoclonal Antibody	demcizumab
Antibody	Monoclonal Antibody	denosumab
Antibody	Monoclonal Antibody	denosumab biosimilar
Antibody	Monoclonal Antibody	depatuxizumab
Antibody	Monoclonal Antibody Conjugated	depatuxizumab mafodotin
Antibody	Monoclonal Antibody	dezamizumab
Antibody	Antibody	digoxin immune Fab (ovine)
Antibody	Monoclonal Antibody	dilpacimab
Antibody	Monoclonal Antibody	dinutuximab
Antibody	Monoclonal Antibody	dinutuximab beta
Antibody	Monoclonal Antibody	diridavumab
Antibody	Monoclonal Antibody	DKN-01
Antibody	Monoclonal Antibody Conjugated	DNP-001
Antibody	Monoclonal Antibody	DNP-002
Antibody	Monoclonal Antibody	domagrozumab
Antibody	Monoclonal Antibody	donanemab
Antibody	Monoclonal Antibody	dostarlimab
Antibody	Monoclonal Antibody Conjugated	DP-303C
Antibody	Monoclonal Antibody Conjugated	DS-1062
Antibody	Monoclonal Antibody Conjugated	DS-7300
Antibody	Monoclonal Antibody	DS-8273
Antibody	Monoclonal Antibody	dupilumab
Antibody	Monoclonal Antibody	durvalumab
Antibody	Monoclonal Antibody	durvalumab + monalizumab
Antibody	Monoclonal Antibody	durvalumab + oleclumab
Antibody	Monoclonal Antibody; Small Molecule	durvalumab + selumetinib sulfate
Antibody	Monoclonal Antibody	durvalumab + tremelimumab
Antibody	Monoclonal Antibody	EBI-031
Antibody	Monoclonal Antibody	eculizumab
Antibody	Monoclonal Antibody	eculizumab biosimilar
Antibody	Monoclonal Antibody	edrecolomab
Antibody	Monoclonal Antibody	efalizumab
Antibody	Monoclonal Antibody	efgartigimod alfa
Antibody	Monoclonal Antibody	efungumab
Antibody	Monoclonal Antibody	elezanumab
Antibody	Monoclonal Antibody	elgemtumab
Antibody	Monoclonal Antibody	elipovimab
Antibody	Monoclonal Antibody	elotuzumab
Antibody	Monoclonal Antibody	emactuzumab
Antibody	Monoclonal Antibody	emapalumab
Antibody	Bispecific Monoclonal Antibody	emicizumab
Antibody	Monoclonal Antibody	enamptcumab
Antibody	Monoclonal Antibody Conjugated	enapotamab vedotin
Antibody	Monoclonal Antibody Conjugated	enfortumab vedotin
Antibody	Monoclonal Antibody	enoblituzumab
Antibody	Monoclonal Antibody	ensituximab
Antibody	Bispecific Monoclonal Antibody	epcoritamab
Antibody	Monoclonal Antibody	epratuzumab
Antibody	Monoclonal Antibody	eptinezumab
Antibody	Monoclonal Antibody	erenumab
Antibody	Bispecific Monoclonal Antibody	ertumaxomab
Antibody	Bispecific Monoclonal Antibody	ERY-974
Antibody	Monoclonal Antibody	etaracizumab
Antibody	Monoclonal Antibody	etigilimab
Antibody	Monoclonal Antibody	etokimab
Antibody	Monoclonal Antibody	etrolizumab
Antibody	Monoclonal Antibody	evinacumab
Antibody	Monoclonal Antibody	evolocumab
Antibody	Monoclonal Antibody; Synthetic Peptide	exenatide + ND-017
Antibody	Monoclonal Antibody	F-598
Antibody	Bispecific Monoclonal Antibody	faricimab
Antibody	Monoclonal Antibody	farletuzumab
Antibody	Monoclonal Antibody	fasinumab
Antibody	Monoclonal Antibody	FAZ-053
Antibody	Monoclonal Antibody	FB-704A
Antibody	Monoclonal Antibody	FB-825
Antibody	Antibody	FBF-001
Antibody	Antibody	Ferritarg
Antibody	Monoclonal Antibody Conjugated	FF-21101
Antibody	Monoclonal Antibody	ficlatuzumab
Antibody	Bispecific Monoclonal Antibody	flotetuzumab
Antibody	Monoclonal Antibody	FLYSYN
Antibody	Monoclonal Antibody	FM-101
Antibody	Monoclonal Antibody Conjugated	FOR-46
Antibody	Monoclonal Antibody	foralumab
Antibody	Monoclonal Antibody	FR-104
Antibody	Monoclonal Antibody	fremanezumab
Antibody	Monoclonal Antibody	fresolimumab
Antibody	Monoclonal Antibody	FS-102
Antibody	Bispecific Monoclonal Antibody	FS-118
Antibody	Monoclonal Antibody	fulranumab
Antibody	Monoclonal Antibody	galcanezumab
Antibody	Monoclonal Antibody	ganitumab
Antibody	Monoclonal Antibody	gantenerumab
Antibody	Monoclonal Antibody	garadacimab
Antibody	Monoclonal Antibody	garetosmab
Antibody	Monoclonal Antibody	gatipotuzumab
Antibody	Monoclonal Antibody	GC-1118A
Antibody	Monoclonal Antibody	GEM-103
Antibody	Bispecific Monoclonal Antibody	GEM-333
Antibody	Bispecific Monoclonal Antibody	GEM-3PSCA
Antibody	Monoclonal Antibody Conjugated	gemtuzumab ozogamicin
Antibody	Bispecific Monoclonal Antibody	GEN-1046
Antibody	Monoclonal Antibody	gevokizumab
Antibody	Monoclonal Antibody	gimsilumab
Antibody	Monoclonal Antibody	girentuximab
Antibody	Monoclonal Antibody Conjugated	glembatumumab vedotin
Antibody	Monoclonal Antibody	GLS-010
Antibody	Monoclonal Antibody	GMA-102
Antibody	Monoclonal Antibody	GMA-161
Antibody	Monoclonal Antibody	GMA-301
Antibody	Monoclonal Antibody	golimumab
Antibody	Monoclonal Antibody	gosuranemab
Antibody	Monoclonal Antibody	GR-1501
Antibody	Bispecific Monoclonal Antibody	gremubamab
Antibody	Bispecific Monoclonal Antibody	GS-1423
Antibody	Monoclonal Antibody	GSK-1070806
Antibody	Monoclonal Antibody	GSK-2330811
Antibody	Monoclonal Antibody	GSK-2831781
Antibody	Monoclonal Antibody	GSK-3050002
Antibody	Monoclonal Antibody	GSK-3174998
Antibody	Monoclonal Antibody	GSK-3359609
Antibody	Monoclonal Antibody	GSK-3511294
Antibody	Monoclonal Antibody	GT-103
Antibody	Monoclonal Antibody	guselkumab
Antibody	Monoclonal Antibody	GWN-323
Antibody	Monoclonal Antibody	H-11
Antibody	Monoclonal Antibody	HAB-21
Antibody	Monoclonal Antibody	HBM-4003
Antibody	Monoclonal Antibody	HDIT-101
Antibody	Antibody	hepatitis B immune globulin
		(human)
Antibody	Antibody	hepatitis C virus immune globulin
		(human)
Antibody	Monoclonal Antibody	HLX-06
Antibody	Monoclonal Antibody	HLX-07
Antibody	Monoclonal Antibody	HLX-10
Antibody	Monoclonal Antibody	HLX-20
Antibody	Monoclonal Antibody	HPN-217
Antibody	Monoclonal Antibody	HPN-424
Antibody	Monoclonal Antibody	HPN-536
Antibody	Monoclonal Antibody	HS-006
Antibody	Monoclonal Antibody Conjugated	HTI-1066
Antibody	Monoclonal Antibody	Hu8F4
Antibody	Antibody	human immunoglobulin
		antistaphylococcal
Antibody	Monoclonal Antibody	ianalumab
Antibody	Monoclonal Antibody	ibalizumab
Antibody	Monoclonal Antibody	IBI-101
Antibody	Monoclonal Antibody	IBI-188
Antibody	Monoclonal Antibody	IBI-306
Antibody	Bispecific Monoclonal Antibody	IBI-322
Antibody	Monoclonal Antibody Conjugated	ibritumomab tiuxetan
Antibody	Monoclonal Antibody	IC-14
Antibody	Monoclonal Antibody	ICT-01
Antibody	Monoclonal Antibody	idarucizumab
Antibody	Monoclonal Antibody	ieramilimab
Antibody	Monoclonal Antibody	ifabotuzumab
Antibody	Monoclonal Antibody	IFX-1
Antibody	Monoclonal Antibody	IGEM-F
Antibody	Bispecific Monoclonal Antibody	IGM-2323
Antibody	Antibody	immune globulin (human)
Antibody	Antibody	immune globulin (human) 2
Antibody	Bispecific Monoclonal Antibody	INBRX-105
Antibody	Monoclonal Antibody	INCAGN-1876
Antibody	Monoclonal Antibody	INCAGN-1949
Antibody	Monoclonal Antibody	INCAGN-2385
Antibody	Monoclonal Antibody	inclacumab
Antibody	Monoclonal Antibody Conjugated	indatuximab ravtansine
Antibody	Monoclonal Antibody Conjugated	indusatumab vedotin
Antibody	Monoclonal Antibody	inebilizumab
Antibody	Monoclonal Antibody	infliximab
Antibody	Monoclonal Antibody	infliximab biobetter
Antibody	Monoclonal Antibody	infliximab biosimilar
Antibody	Monoclonal Antibody	INM-004
Antibody	Monoclonal Antibody	inolimomab
Antibody	Monoclonal Antibody Conjugated	inotuzumab ozogamicin
Antibody	Monoclonal Antibody Conjugated	Iodine-131-Kab201
Antibody	Monoclonal Antibody Conjugated	Iomab-B
Antibody	Monoclonal Antibody	IPH-5401
Antibody	Monoclonal Antibody	ipilimumab
Antibody	Monoclonal Antibody	ipilimumab + nivolumab
Antibody	Monoclonal Antibody	isatuximab
Antibody	Bispecific Monoclonal Antibody	ISB-1302
Antibody	Bispecific Monoclonal Antibody	ISB-1342
Antibody	Monoclonal Antibody	ISB-830
Antibody	Monoclonal Antibody	iscalimab
Antibody	Monoclonal Antibody	ISU-104
Antibody	Monoclonal Antibody	itolizumab
Antibody	Monoclonal Antibody	ixekizumab
Antibody	Monoclonal Antibody	IXTM-200
Antibody	Monoclonal Antibody	JMT-103
Antibody	Monoclonal Antibody	JNJ-0839
Antibody	Monoclonal Antibody	JNJ-3657
Antibody	Monoclonal Antibody	JNJ-4500
Antibody	Bispecific Monoclonal Antibody	JNJ-6372
Antibody	Bispecific Monoclonal Antibody	JNJ-67571244
Antibody	Bispecific Monoclonal Antibody	JNJ-7564
Antibody	Bispecific Monoclonal Antibody	JNJ-7957
Antibody	Bispecific Monoclonal Antibody	JNJ-9178
Antibody	Monoclonal Antibody	JS-004
Antibody	Monoclonal Antibody	JTX-4014
Antibody	Monoclonal Antibody	JY-025
Antibody	Monoclonal Antibody	K-170
Antibody	Monoclonal Antibody	KHK-2823
Antibody	Monoclonal Antibody	KHK-4083
Antibody	Monoclonal Antibody	KHK-6640
Antibody	Monoclonal Antibody Conjugated	Kid EDV
Antibody	Monoclonal Antibody	KLA-167
Antibody	Bispecific Monoclonal Antibody	KN-026
Antibody	Bispecific Monoclonal Antibody	KN-046
Antibody	Monoclonal Antibody	KSI-301
Antibody	Monoclonal Antibody	KY-1005
Antibody	Monoclonal Antibody Conjugated	labetuzumab govitecan
Antibody	Monoclonal Antibody	lacnotuzumab
Antibody	Monoclonal Antibody	lacutamab
Antibody	Monoclonal Antibody Conjugated	ladiratuzumab vedotin
Antibody	Monoclonal Antibody	lanadelumab
Antibody	Monoclonal Antibody	LBL-007
Antibody	Monoclonal Antibody Conjugated	LDOS-47
Antibody	Monoclonal Antibody	lebrikizumab
Antibody	Monoclonal Antibody	lecanemab
Antibody	Monoclonal Antibody	Lemtrada
Antibody	Monoclonal Antibody	lenvervimab
Antibody	Monoclonal Antibody	lenzilumab
Antibody	Monoclonal Antibody	leronlimab
Antibody	Monoclonal Antibody	letolizumab
Antibody	Monoclonal Antibody	ligelizumab
Antibody	Monoclonal Antibody	lintuzumab
Antibody	Monoclonal Antibody; Recombinant Peptide	liraglutide + NN-8828
Antibody	Monoclonal Antibody	lirilumab
Antibody	Monoclonal Antibody	LKA-651
Antibody	Monoclonal Antibody	LLG-783
Antibody	Monoclonal Antibody	lodapolimab
Antibody	Monoclonal Antibody Conjugated	loncastuximab tesirine
Antibody	Monoclonal Antibody Conjugated	lorvotuzumab mertansine
Antibody	Monoclonal Antibody	LuAF-82422
Antibody	Monoclonal Antibody	LuAF-87908
Antibody	Monoclonal Antibody	lulizumab pegol
Antibody	Monoclonal Antibody	lumiliximab
Antibody	Monoclonal Antibody	LVGN-6051
Antibody	Monoclonal Antibody	LY-3022855
Antibody	Monoclonal Antibody	LY-3041658
Antibody	Monoclonal Antibody	LY-3127804
Antibody	Bispecific Monoclonal Antibody	LY-3434172
Antibody	Antibody	LY-3435151
Antibody	Antibody	LY-3454738
Antibody	Monoclonal Antibody	LZM-009
Antibody	Bispecific Monoclonal Antibody	M-1095
Antibody	Antibody	M-254
Antibody	Monoclonal Antibody	M-6495
Antibody	Bispecific Monoclonal Antibody	M-802
Antibody	Monoclonal Antibody	mAb-114
Antibody	Monoclonal Antibody	magrolimab
Antibody	Monoclonal Antibody	margetuximab
Antibody	Monoclonal Antibody	marstacimab
Antibody	Monoclonal Antibody	MAU-868
Antibody	Monoclonal Antibody	mavrilimumab
Antibody	Bispecific Monoclonal Antibody	MCLA-117
Antibody	Bispecific Monoclonal Antibody	MCLA-145
Antibody	Bispecific Monoclonal Antibody	MCLA-158
Antibody	Monoclonal Antibody	MDX-1097
Antibody	Monoclonal Antibody	MEDI-0618
Antibody	Monoclonal Antibody	MEDI-1341
Antibody	Monoclonal Antibody	MEDI-1814
Antibody	Monoclonal Antibody	MEDI-3506
Antibody	Monoclonal Antibody	MEDI-3617 + tremelimumab
Antibody	Monoclonal Antibody	MEDI-5117
Antibody	Monoclonal Antibody Conjugated	MEDI-547
Antibody	Monoclonal Antibody	MEDI-570
Antibody	Bispecific Monoclonal Antibody	MEDI-5752
Antibody	Bispecific Monoclonal Antibody	MEDI-7352
Antibody	Monoclonal Antibody	melrilimab
Antibody	Monoclonal Antibody	MEN-1112
Antibody	Monoclonal Antibody	mepolizumab
Antibody	Monoclonal Antibody	metelimumab
Antibody	Monoclonal Antibody	MG-1113A
Antibody	Monoclonal Antibody	MGA-012
Antibody	Monoclonal Antibody	MGB-453
Antibody	Monoclonal Antibody Conjugated	MGC-018
Antibody	Bispecific Monoclonal Antibody	MGD-013
Antibody	Monoclonal Antibody	MIL-62
Antibody	Monoclonal Antibody	milatuzumab
Antibody	Monoclonal Antibody	mirikizumab
Antibody	Monoclonal Antibody Conjugated	mirvetuximab soravtansine
Antibody	Monoclonal Antibody	mitazalimab
Antibody	Monoclonal Antibody	MK-1308
Antibody	Monoclonal Antibody	MK-1654
Antibody	Monoclonal Antibody	MK-3655
Antibody	Monoclonal Antibody	MK-4166
Antibody	Monoclonal Antibody	MK-4280
Antibody	Monoclonal Antibody	MK-5890
Antibody	Monoclonal Antibody	mogamulizumab
Antibody	Monoclonal Antibody	monalizumab
Antibody	Monoclonal Antibody Conjugated	Monoclonal Antibody Conjugate to
		Target CD20 for Leukemia and
		Burkitt Lymphoma
Antibody	Monoclonal Antibody Conjugated	Monoclonal Antibody Conjugate to
		Target CD45 for Oncology
Antibody	Monoclonal Antibody Conjugated	Monoclonal Antibody Conjugate to
		Target CEA for Metastatic Liver,
		Colorectal Cancer and Solid Tumor
Antibody	Monoclonal Antibody Conjugated	Monoclonal Antibody Conjugate to
		Target CEACAM5 for Non Small
		Cell Lung Cancer and Metastatic
		Colorectal Cancer
Antibody	Monoclonal Antibody Conjugated	Monoclonal Antibody Conjugated to
		Target EPCAM for Colorectal
		Cancer
Antibody	Monoclonal Antibody Conjugated	Monoclonal Antibody Conjugated to
		Target PSMA for Prostate Cancer
Antibody	Monoclonal Antibody	Monoclonal Antibody for
		Coronavirus Disease 2019 (COVID-
		19)
Antibody	Monoclonal Antibody	Monoclonal Antibody for Dengue
Antibody	Monoclonal Antibody	Monoclonal Antibody to Antagonize
		IL-2R Beta for Celiac Disease,
		Oncology and Tropical Spastic
		Paraparesis
Antibody	Monoclonal Antibody	Monoclonal Antibody to Inhibit
		ANXA3 for Hepatocellular
		Carcinoma
Antibody	Monoclonal Antibody	Monoclonal Antibody to Inhibit CD4
		for HIV-1
Antibody	Monoclonal Antibody	Monoclonal Antibody to Inhibit GD2
		for Oncology
Antibody	Monoclonal Antibody	Monoclonal Antibody to Inhibit
		Glycoprotein 120 for HIV-1
		infections
Antibody	Monoclonal Antibody	Monoclonal Antibody to Inhibit IL-
		17A and IL-17F for Unspecified
		Indication
Antibody	Monoclonal Antibody	Monoclonal Antibody to Inhibit PD-
		L1 for Solid Tumor
Antibody	Monoclonal Antibody	Monoclonal Antibody to Inhibit PD1
		for Solid Tumors
Antibody	Monoclonal Antibody	Monoclonal Antibody to Inhibit TNF-
		Alpha for Dupuytren's contracture
Antibody	Monoclonal Antibody Conjugated	Monoclonal Antibody to Target
		CD66b for Blood Cancer and
		Metabolic Disorders
Antibody	Monoclonal Antibody	Monoclonal Antibody to Target
		GP41 for HIV Infections
Antibody	Monoclonal Antibody	MOR-106
Antibody	Monoclonal Antibody	MOR-202
Antibody	Monoclonal Antibody Conjugated	MORAb-202
Antibody	Bispecific Monoclonal Antibody	mosunetuzumab
Antibody	Monoclonal Antibody Conjugated	moxetumomab pasudotox
Antibody	Monoclonal Antibody	MSB-2311
Antibody	Monoclonal Antibody	MSC-1
Antibody	Monoclonal Antibody	MT-2990
Antibody	Monoclonal Antibody	MT-3921
Antibody	Monoclonal Antibody	murlentamab
Antibody	Monoclonal Antibody	muromonab-CD3
Antibody	Monoclonal Antibody	MVT-5873
Antibody	Monoclonal Antibody	namilumab
Antibody	Monoclonal Antibody Conjugated	naratuximab emtansine
Antibody	Monoclonal Antibody	narsoplimab
Antibody	Monoclonal Antibody	natalizumab
Antibody	Monoclonal Antibody	natalizumab biosimilar
Antibody	Bispecific Monoclonal Antibody	navicixizumab
Antibody	Monoclonal Antibody	naxitamab
Antibody	Monoclonal Antibody	NC-318
Antibody	Monoclonal Antibody	nebacumab
Antibody	Monoclonal Antibody	necitumumab
Antibody	Monoclonal Antibody	nemolizumab
Antibody	Monoclonal Antibody	netakimab
Antibody	Monoclonal Antibody	NGM-120
Antibody	Monoclonal Antibody	NI-006
Antibody	Monoclonal Antibody	NI-0101
Antibody	Monoclonal Antibody	nidanilimab
Antibody	Monoclonal Antibody	nimacimab
Antibody	Monoclonal Antibody	nimotuzumab
Antibody	Monoclonal Antibody	nimotuzumab biosimilar
Antibody	Monoclonal Antibody	nipocalimab
Antibody	Monoclonal Antibody	nirsevimab
Antibody	Monoclonal Antibody	NIS-793
Antibody	Monoclonal Antibody	nivolumab
Antibody	Monoclonal Antibody Conjugated	NJH-395
Antibody	Bispecific Monoclonal Antibody	NNC-03653769A
Antibody	Antibody	NP-024
Antibody	Antibody	NP-025
Antibody	Monoclonal Antibody	NP-137
Antibody	Monoclonal Antibody	NPC-21
Antibody	Bispecific Monoclonal Antibody	NXT-007
Antibody	Monoclonal Antibody	NZV-930
Antibody	Monoclonal Antibody	obexelimab
Antibody	Monoclonal Antibody	OBI-888
Antibody	Monoclonal Antibody Conjugated	OBI-999
Antibody	Monoclonal Antibody	obiltoxaximab
Antibody	Monoclonal Antibody	obinutuzumab
Antibody	Monoclonal Antibody Conjugated	OBT-076
Antibody	Monoclonal Antibody	ocaratuzumab
Antibody	Monoclonal Antibody	ocrelizumab
Antibody	Bispecific Monoclonal Antibody	odronextamab
Antibody	Monoclonal Antibody	ofatumumab
Antibody	Monoclonal Antibody	olaratumab
Antibody	Monoclonal Antibody	oleclumab
Antibody	Monoclonal Antibody	olendalizumab
Antibody	Monoclonal Antibody	olinvacimab
Antibody	Monoclonal Antibody	olokizumab
Antibody	Monoclonal Antibody	omalizumab
Antibody	Monoclonal Antibody	omalizumab biosimilar
Antibody	Monoclonal Antibody Conjugated	omburtamab
Antibody	Monoclonal Antibody	omodenbamab
Antibody	Monoclonal Antibody	ONC-392
Antibody	Monoclonal Antibody	ontamalimab
Antibody	Monoclonal Antibody	ontuxizumab
Antibody	Monoclonal Antibody	opicinumab
Antibody	Monoclonal Antibody	oregovomab
Antibody	Monoclonal Antibody	orilanolimab
Antibody	Monoclonal Antibody	orticumab
Antibody	Monoclonal Antibody	OS-2966
Antibody	Monoclonal Antibody	OSE-127
Antibody	Monoclonal Antibody	osocimab
Antibody	Monoclonal Antibody	otelixizumab
Antibody	Monoclonal Antibody	otilimab
Antibody	Monoclonal Antibody	otlertuzumab
Antibody	Monoclonal Antibody Conjugated	OTSA-101
Antibody	Monoclonal Antibody Conjugated	OXS-1750
Antibody	Monoclonal Antibody Conjugated	OXS-2050
Antibody	Monoclonal Antibody	ozoralizumab
Antibody	Monoclonal Antibody	P-2G12
Antibody	Monoclonal Antibody	pagibaximab
Antibody	Monoclonal Antibody	palivizumab
Antibody	Monoclonal Antibody	pamrevlumab
Antibody	Monoclonal Antibody	panitumumab
Antibody	Monoclonal Antibody	panobacumab
Antibody	Bispecific Monoclonal Antibody	pasotuxizumab
Antibody	Monoclonal Antibody	PAT-SC1
Antibody	Monoclonal Antibody	patritumab
Antibody	Monoclonal Antibody	PC-mAb
Antibody	Monoclonal Antibody	PD-0360324
Antibody	Monoclonal Antibody	pembrolizumab
Antibody	Monoclonal Antibody	pepinemab
Antibody	Monoclonal Antibody	pertuzumab
Antibody	Monoclonal Antibody	pertuzumab + trastuzumab
Antibody	Monoclonal Antibody	PF-04518600
Antibody	Monoclonal Antibody	PF-06480605
Antibody	Antibody	PF-06730512
Antibody	Monoclonal Antibody	PF-06823859
Antibody	Bispecific Monoclonal Antibody	PF-06863135
Antibody	Monoclonal Antibody	pidilizumab
Antibody	Antibody	pit viper snake [Crotalidae]
		(polyvalent) immunoglobulin F(ab′)2
		antivenom [equine]
Antibody	Bispecific Monoclonal Antibody	plamotamab
Antibody	Monoclonal Antibody	PNT-001
Antibody	Monoclonal Antibody Conjugated	polatuzumab vedotin
Antibody	Antibody	PolyCAb
Antibody	Monoclonal Antibody	pozelimab
Antibody	Monoclonal Antibody	prasinezumab
Antibody	Monoclonal Antibody	pritumumab
Antibody	Monoclonal Antibody	PRL3-ZUMAB
Antibody	Monoclonal Antibody	prolgolimab
Antibody	Monoclonal Antibody	PRV-300
Antibody	Bispecific Monoclonal Antibody	PRV-3279
Antibody	Monoclonal Antibody	PRX-004
Antibody	Bispecific Monoclonal Antibody	PSB-205
Antibody	Monoclonal Antibody	PTX-35
Antibody	Monoclonal Antibody	PTZ-329
Antibody	Monoclonal Antibody	PTZ-522
Antibody	Monoclonal Antibody	quetmolimab
Antibody	Monoclonal Antibody	QX-002N
Antibody	Monoclonal Antibody	R-1549
Antibody	Monoclonal Antibody	rabies immune globulin (human)
Antibody	Monoclonal Antibody	racotumomab
Antibody	Monoclonal Antibody Conjugated	Radspherin
Antibody	Monoclonal Antibody	ramucirumab
Antibody	Monoclonal Antibody	ranibizumab
Antibody	Monoclonal Antibody	ranibizumab biosimilar
Antibody	Monoclonal Antibody	ranibizumab SR
Antibody	Monoclonal Antibody	ravagalimab
Antibody	Monoclonal Antibody	ravulizumab
Antibody	Monoclonal Antibody	ravulizumab next generation
Antibody	Monoclonal Antibody	raxibacumab
Antibody	Monoclonal Antibody Conjugated	RC-48
Antibody	Monoclonal Antibody
Antibody	Monoclonal Antibody	REGN-3048
Antibody	Monoclonal Antibody	REGN-3051
Antibody	Monoclonal Antibody	REGN-3500
Antibody	Bispecific Monoclonal Antibody	REGN-4018
Antibody	Monoclonal Antibody	REGN-4461
Antibody	Antibody	REGN-5069
Antibody	Bispecific Monoclonal Antibody	REGN-5458
Antibody	Bispecific Monoclonal Antibody	REGN-5459
Antibody	Bispecific Monoclonal Antibody	REGN-5678
Antibody	Monoclonal Antibody	REGN-5713
Antibody	Monoclonal Antibody	REGN-5714
Antibody	Monoclonal Antibody	REGN-5715
Antibody	Monoclonal Antibody	relatlimab
Antibody	Monoclonal Antibody	reslizumab
Antibody	Antibody	respiratory syncytial virus immune
		globulin (human)
Antibody	Monoclonal Antibody	RG-6125
Antibody	Bispecific Monoclonal Antibody	RG-6139
Antibody	Monoclonal Antibody	RG-6149
Antibody	Bispecific Monoclonal Antibody; Monoclonal	RG-6160
	Antibody
Antibody	Monoclonal Antibody	RG-6292
Antibody	Antibody	RG-70240
Antibody	Monoclonal Antibody Conjugated	RG-7861
Antibody	Bispecific Monoclonal Antibody	RG-7992
Antibody	Antibody	rho(D) immune globulin (human)
Antibody	Monoclonal Antibody	rilotumumab
Antibody	Monoclonal Antibody	risankizumab
Antibody	Monoclonal Antibody	rituximab
Antibody	Monoclonal Antibody	rituximab biosimilar
Antibody	Bispecific Monoclonal Antibody	RO-7082859
Antibody	Bispecific Monoclonal Antibody	RO-7121661
Antibody	Monoclonal Antibody	roledumab
Antibody	Bispecific Monoclonal Antibody	romilkimab
Antibody	Monoclonal Antibody	romosozumab
Antibody	Monoclonal Antibody Conjugated	rovalpituzumab tesirine
Antibody	Monoclonal Antibody	rozanolixizumab
Antibody	Monoclonal Antibody Conjugated	rozibafusp alfa
Antibody	Monoclonal Antibody	RZ-358
Antibody	Antibody	SAB-301
Antibody	Monoclonal Antibody Conjugated	sacituzumab govitecan
Antibody	Monoclonal Antibody	SAIT-301
Antibody	Monoclonal Antibody Conjugated	SAR-408701
Antibody	Monoclonal Antibody	SAR-439459
Antibody	Bispecific Monoclonal Antibody	SAR-440234
Antibody	Monoclonal Antibody	SAR-441236
Antibody	Monoclonal Antibody	sarilumab
Antibody	Monoclonal Antibody	sasanlimab
Antibody	Monoclonal Antibody	satralizumab
Antibody	Monoclonal Antibody Conjugated	SC-003
Antibody	Antibody	scorpion (polyvalent)
		immunoglobulin F(ab′)2 antivenom
Antibody	Antibody	scorpion [centruroides] (polyvalent)
		immunoglobulin F(ab′) 2 antivenom
		[equine]
Antibody	Monoclonal Antibody	SCT-200
Antibody	Monoclonal Antibody	SCT-630
Antibody	Monoclonal Antibody	SEA-BCMA
Antibody	Monoclonal Antibody	SEA-CD40
Antibody	Monoclonal Antibody	secukinumab
Antibody	Monoclonal Antibody	selicrelumab
Antibody	Monoclonal Antibody	semorinemab
Antibody	Monoclonal Antibody	setrusumab
Antibody	Monoclonal Antibody Conjugated	SGNCD-228A
Antibody	Monoclonal Antibody Conjugated	SGNCD-47M
Antibody	Antibody	SHR-1209
Antibody	Monoclonal Antibody	SHR-1316
Antibody	Monoclonal Antibody	siltuximab
Antibody	Monoclonal Antibody	Simponi Aria
Antibody	Monoclonal Antibody	sintilimab
Antibody	Monoclonal Antibody	siplizumab
Antibody	Monoclonal Antibody	sirukumab
Antibody	Monoclonal Antibody Conjugated	SKB-264
Antibody	Monoclonal Antibody	solanezumab
Antibody	Monoclonal Antibody	spartalizumab
Antibody	Monoclonal Antibody	spesolimab
Antibody	Monoclonal Antibody	SRF-617
Antibody	Monoclonal Antibody	SSS-07
Antibody	Monoclonal Antibody	STIA-1014
Antibody	Monoclonal Antibody Conjugated	STRO-001
Antibody	Monoclonal Antibody Conjugated	STRO-002
Antibody	Monoclonal Antibody	Sulituzumab
Antibody	Monoclonal Antibody	sutimlimab
Antibody	Monoclonal Antibody	suvratoxumab
Antibody	Monoclonal Antibody Conjugated	SYD-1875
Antibody	Monoclonal Antibody	Sym-015
Antibody	Monoclonal Antibody	Sym-021
Antibody	Monoclonal Antibody	Sym-022
Antibody	Monoclonal Antibody	Sym-023
Antibody	Monoclonal Antibody	SYN-004
Antibody	Monoclonal Antibody	SYN-023
Antibody	Monoclonal Antibody	TAB-014
Antibody	Monoclonal Antibody	TAB-08
Antibody	Monoclonal Antibody	tafasitamab
Antibody	Antibody	taipan [Oxyuranus scutellatus]
		antivenom [equine]
Antibody	Monoclonal Antibody	TAK-079
Antibody	Monoclonal Antibody Conjugated	TAK-164
Antibody	Monoclonal Antibody	talacotuzumab
Antibody	Monoclonal Antibody	tanezumab
Antibody	Monoclonal Antibody Conjugated	telisotuzumab vedotin
Antibody	Monoclonal Antibody	temelimab
Antibody	Monoclonal Antibody	teplizumab
Antibody	Monoclonal Antibody	teprotumumab
Antibody	Monoclonal Antibody	tesidolumab
Antibody	Antibody	tetanus immune globulin
Antibody	Monoclonal Antibody	tezepelumab
Antibody	Monoclonal Antibody Conjugated	TF-2
Antibody	Bispecific Monoclonal Antibody	TG-1801
Antibody	Monoclonal Antibody	THR-317
Antibody	Bispecific Monoclonal Antibody	tibulizumab
Antibody	Monoclonal Antibody	tilavonemab
Antibody	Monoclonal Antibody	tildrakizumab
Antibody	Monoclonal Antibody	timigutuzumab
Antibody	Monoclonal Antibody	timolumab
Antibody	Monoclonal Antibody	tiragolumab
Antibody	Monoclonal Antibody	tislelizumab
Antibody	Monoclonal Antibody Conjugated	tisotumab vedotin
Antibody	Monoclonal Antibody	TJC-4
Antibody	Monoclonal Antibody	TJD-5
Antibody	Monoclonal Antibody	TJM-2
Antibody	Monoclonal Antibody	TM-123
Antibody	Bispecific Monoclonal Antibody	TMB-365
Antibody	Bispecific Monoclonal Antibody	TNB-383B
Antibody	Monoclonal Antibody	tocilizumab
Antibody	Monoclonal Antibody	tocilizumab biosimilar
Antibody	Monoclonal Antibody	tomaralimab
Antibody	Monoclonal Antibody	tomuzotuximab
Antibody	Monoclonal Antibody	toripalimab
Antibody	Monoclonal Antibody	tosatoxumab
Antibody	Monoclonal Antibody Conjugated	tositumomab + Iodine I 131
		tositumomab
Antibody	Monoclonal Antibody	tralokinumab
Antibody	Monoclonal Antibody	trastuzumab
Antibody	Monoclonal Antibody	trastuzumab biosimilar
Antibody	Monoclonal Antibody Conjugated	trastuzumab deruxtecan
Antibody	Monoclonal Antibody Conjugated	trastuzumab duocarmazine
Antibody	Monoclonal Antibody Conjugated	trastuzumab emtansine
Antibody	Monoclonal Antibody	tremelimumab
Antibody	Monoclonal Antibody	trevogrumab
Antibody	Monoclonal Antibody	TRK-950
Antibody	Monoclonal Antibody Conjugated	TRPH-222
Antibody	Monoclonal Antibody	TTX-030
Antibody	Monoclonal Antibody Conjugated	TX-250
Antibody	Monoclonal Antibody Conjugated	U-31402
Antibody	Monoclonal Antibody	U-31784
Antibody	Monoclonal Antibody	UB-221
Antibody	Monoclonal Antibody	UB-421
Antibody	Monoclonal Antibody	UB-621
Antibody	Monoclonal Antibody	ublituximab
Antibody	Monoclonal Antibody; Small Molecule	ublituximab + umbralisib tosylate
Antibody	Monoclonal Antibody	UBP-1213
Antibody	Monoclonal Antibody	UC-961
Antibody	Monoclonal Antibody	UCB-0107
Antibody	Monoclonal Antibody	UCB-6114
Antibody	Monoclonal Antibody	UCB-7858
Antibody	Monoclonal Antibody	ulocuplumab
Antibody	Monoclonal Antibody	urelumab
Antibody	Monoclonal Antibody	ustekinumab
Antibody	Monoclonal Antibody	ustekinumab biosimilar
Antibody	Monoclonal Antibody	utomilumab
Antibody	Monoclonal Antibody Conjugated	vadastuximab talirine
Antibody	Bispecific Monoclonal Antibody	vanucizumab
Antibody	Antibody
Antibody	Monoclonal Antibody	varisacumab
Antibody	Monoclonal Antibody	varlilumab
Antibody	Monoclonal Antibody	vedolizumab
Antibody	Monoclonal Antibody	veltuzumab
Antibody	Monoclonal Antibody	VIR-2482
Antibody	Monoclonal Antibody	VIS-410
Antibody	Monoclonal Antibody	VIS-649
Antibody	Monoclonal Antibody	vixarelimab
Antibody	Monoclonal Antibody Conjugated	VLS-101
Antibody	Monoclonal Antibody	vobarilizumab
Antibody	Monoclonal Antibody	vofatamab
Antibody	Monoclonal Antibody	volagidemab
Antibody	Monoclonal Antibody	vopratelimab
Antibody	Monoclonal Antibody	VRC-01
Antibody	Monoclonal Antibody	VRC-07523LS
Antibody	Monoclonal Antibody	vunakizumab
Antibody	Monoclonal Antibody Conjugated	W-0101
Antibody	Monoclonal Antibody	WBP-297
Antibody	Antibody
Antibody	Antibody	Xembify
Antibody	Monoclonal Antibody	xentuzumab
Antibody	Monoclonal Antibody	Xgeva
Antibody	Bispecific Monoclonal Antibody	XmAb-14045
Antibody	Bispecific Monoclonal Antibody	XmAb-22841
Antibody	Bispecific Monoclonal Antibody	XmAb-23104
Antibody	Monoclonal Antibody Conjugated	XMT-1536
Antibody	Monoclonal Antibody	XOMA-213
Antibody	Monoclonal Antibody	YS-110
Antibody	Monoclonal Antibody	YYB-101
Antibody	Monoclonal Antibody	zagotenemab
Antibody	Monoclonal Antibody	zalifrelimab
Antibody	Monoclonal Antibody	zanolimumab
Antibody	Bispecific Monoclonal Antibody	zenocutuzumab
Antibody	Monoclonal Antibody	zolbetuximab
Antibody	Bispecific Monoclonal Antibody	ZW-25
Antibody/Enzyme	Antibody; Recombinant Enzyme	hyaluronidase (recombinant,
		human) + immune globulin (human)
Antibody/protein	Fusion Protein; Monoclonal Antibody	durvalumab + oportuzumab
		monatox

TABLE 2
Peptides
Broad
class	Molecule Type	Drug Name
Peptide	Synthetic Peptide	A-10 + AS-21
Peptide	Synthetic Peptide	A-6
Peptide	Recombinant Peptide	AB-101
Peptide	Recombinant Peptide	AB-102
Peptide	Recombinant Peptide	AB-301
Peptide	Synthetic Peptide	abaloparatide
Peptide	Synthetic Peptide	abarelix
Peptide	Synthetic Peptide	ABT-510
Peptide	Recombinant Peptide	AC-2592
Peptide	Synthetic Peptide	ACP-003
Peptide	Synthetic Peptide	ACP-004
Peptide	Synthetic Peptide	ACP-015
Peptide	Synthetic Peptide	AcPepA
Peptide	Synthetic Peptide	ACX-107
Peptide	Synthetic Peptide	Adipotide
Peptide	Recombinant Peptide	ADV-P2
Peptide	Synthetic Peptide	AE-3763
Peptide	Synthetic Peptide	AEM-28
Peptide	Synthetic Peptide	afamelanotide acetate
Peptide	Synthetic Peptide	AFPep
Peptide	Synthetic Peptide	AGM-310
Peptide	Recombinant Peptide	AI-401
Peptide	Synthetic Peptide	AIM-102
Peptide	Recombinant Peptide	AIM-DX
Peptide	Synthetic Peptide	AKL-0707
Peptide	Recombinant Peptide	AKS-178
Peptide	Synthetic Peptide	AL-242A1
Peptide	Synthetic Peptide	AL-41A1
Peptide	Synthetic Peptide	AL-78898A
Peptide	Synthetic Peptide	albenatide
Peptide	Synthetic Peptide	albuvirtide LAR
Peptide	Synthetic Peptide	alisporivir
Peptide	Synthetic Peptide	ALM-201
Peptide	Synthetic Peptide	Alpha-1H
Peptide	Synthetic Peptide	Alpha-HGA
Peptide	Synthetic Peptide	ALRev-1
Peptide	Synthetic Peptide	ALRN-5281
Peptide	Synthetic Peptide	ALRN-6924
Peptide	Synthetic Peptide	ALY-688
Peptide	Synthetic Peptide	AMC-303
Peptide	Synthetic Peptide	Ampion
Peptide	Synthetic Peptide	AMY-106
Peptide	Synthetic Peptide	anaritide acetate
Peptide	Synthetic Peptide	angiotensin II acetate
Peptide	Recombinant Peptide	ANX-042
Peptide	Synthetic Peptide	AP-138
Peptide	Recombinant Peptide	APH-0907
Peptide	Synthetic Peptide	APL-180
Peptide	Synthetic Peptide	APL-9
Peptide	Synthetic Peptide	APP-018
Peptide	Synthetic Peptide	apraglutide
Peptide	Synthetic Peptide	ARG-301
Peptide	Synthetic Peptide	argipressin
Peptide	Synthetic Peptide	ARI-1778
Peptide	Synthetic Peptide	Artpep-2
Peptide	Synthetic Peptide	ASP-5006
Peptide	Recombinant Peptide	AT-247
Peptide	Recombinant Peptide	AT-270
Peptide	Synthetic Peptide	ATN-161
Peptide	Synthetic Peptide	atosiban
Peptide	Synthetic Peptide	atosiban acetate
Peptide	Synthetic Peptide	Atrigel-GHRP-1
Peptide	Recombinant Peptide	ATX-101
Peptide	Synthetic Peptide	AVE-3247
Peptide	Synthetic Peptide	avexitide acetate
Peptide	Synthetic Peptide	B27-PD
Peptide	Synthetic Peptide	bacitracin
Peptide	Synthetic Peptide	barusiban
Peptide	Synthetic Peptide	BBI-11008
Peptide	Synthetic Peptide	BBI-21007
Peptide	Synthetic Peptide	BDM-E
Peptide	Synthetic Peptide	BI-456906
Peptide	Synthetic Peptide	BI-473494
Peptide	Synthetic Peptide	bicalutamide + leuprolide acetate
Peptide	Recombinant Peptide	BIOD-105
Peptide	Recombinant Peptide	BIOD-107
Peptide	Recombinant Peptide	BIOD-123
Peptide	Recombinant Peptide	BIOD-125
Peptide	Recombinant Peptide	BIOD-238
Peptide	Recombinant Peptide	BIOD-250
Peptide	Recombinant Peptide	BIOD-531
Peptide	Recombinant Peptide	BIOD-Adjustable Basal
Peptide	Synthetic Peptide	bivalirudin
Peptide	Synthetic Peptide	bivalirudin trifluoroacetate
Peptide	Peptide; Synthetic Peptide	BL-3020
Peptide	Synthetic Peptide	BMS-686117
Peptide	Synthetic Peptide	BMTP-11
Peptide	Synthetic Peptide	BN-005
Peptide	Synthetic Peptide	BN-006
Peptide	Synthetic Peptide	BN-008
Peptide	Synthetic Peptide	BN-054
Peptide	Synthetic Peptide	BNZ-1
Peptide	Recombinant Peptide	BNZ-2
Peptide	Synthetic Peptide	BPI-3016
Peptide	Synthetic Peptide	BQ-123
Peptide	Synthetic Peptide	bremelanotide acetate
Peptide	Synthetic Peptide	brimapitide
Peptide	Synthetic Peptide	BRM-521
Peptide	Synthetic Peptide	BT-5528
Peptide	Synthetic Peptide	BTI-410
Peptide	Synthetic Peptide	bulevirtide
Peptide	Synthetic Peptide	buserelin acetate
Peptide	Synthetic Peptide	buserelin acetate ER
Peptide	Synthetic Peptide	Bynfezia
Peptide	Synthetic Peptide	C-16G2
Peptide	Synthetic Peptide	calcitonin
Peptide	Recombinant Peptide	calcitonin DR
Peptide	Recombinant Peptide	Capsulin IR
Peptide	Recombinant Peptide	Capsulin OAD
Peptide	Recombinant Peptide	CAR Peptide
Peptide	Synthetic Peptide	carbetocin
Peptide	Recombinant Peptide	Cardeva
Peptide	Recombinant Peptide	carperitide
Peptide	Synthetic Peptide	CBLB-612
Peptide	Synthetic Peptide	CBP-501
Peptide	Synthetic Peptide	CBX-129801
Peptide	Recombinant Peptide	celmoleukin
Peptide	Recombinant Peptide	cenderitide
Peptide	Synthetic Peptide	cetrorelix
Peptide	Synthetic Peptide	cetrorelix acetate
Peptide	Synthetic Peptide	CGX-1007
Peptide	Synthetic Peptide	CGX-1160
Peptide	Synthetic Peptide	cibinetide
Peptide	Synthetic Peptide	CIGB-300
Peptide	Recombinant Peptide	CIGB-370
Peptide	Synthetic Peptide	CIGB-500
Peptide	Synthetic Peptide	CIGB-552
Peptide	Synthetic Peptide	CIGB-814
Peptide	Synthetic Peptide	cilengitide
Peptide	Recombinant Peptide	CJC-1525
Peptide	Synthetic Peptide	CMS-024
Peptide	Synthetic Peptide	CN-105
Peptide	Recombinant Peptide	CobOral Insulin
Peptide	Synthetic Peptide	COG-1410
Peptide	Recombinant Peptide	Combulin
Peptide	Synthetic Peptide	corticorelin acetate
Peptide	Synthetic Peptide	corticotropin
Peptide	Synthetic Peptide	cosyntropin
Peptide	Synthetic Peptide	cosyntropin SR
Peptide	Synthetic Peptide	CPT-31
Peptide	Synthetic Peptide	CTCE-9908
Peptide	Recombinant Peptide	DACRA-042
Peptide	Recombinant Peptide	DACRA-089
Peptide	Synthetic Peptide	dalazatide
Peptide	Synthetic Peptide	danegaptide
Peptide	Synthetic Peptide	dasiglucagon
Peptide	Synthetic Peptide	DasKloster-0274-01
Peptide	Synthetic Peptide	davunetide
Peptide	Synthetic Peptide	DD-04107
Peptide	Synthetic Peptide	degarelix acetate
Peptide	Synthetic Peptide	delcasertib acetate
Peptide	Synthetic Peptide	delmitide acetate
Peptide	Synthetic Peptide	Dennexin
Peptide	Synthetic Peptide	Des-Asp Angiotensin 1
Peptide	Recombinant Peptide	desirudin
Peptide	Synthetic Peptide	desmopressin
Peptide	Synthetic Peptide	desmopressin acetate
Peptide	Synthetic Peptide	desmopressin acetate ODT
Peptide	Synthetic Peptide	DiaPep-277
Peptide	Synthetic Peptide	difelikefalin
Peptide	Synthetic Peptide	Dipep
Peptide	Synthetic Peptide	disitertide
Peptide	Synthetic Peptide	DMI-4983
Peptide	Synthetic Peptide	dolcanatide
Peptide	Synthetic Peptide	DP-2018
Peptide	Synthetic Peptide	DPC-016
Peptide	Synthetic Peptide	DT-109
Peptide	Synthetic Peptide	DT-110
Peptide	Synthetic Peptide	DTI-100
Peptide	Synthetic Peptide	DTI-117
Peptide	Synthetic Peptide	dusquetide
Peptide	Synthetic Peptide	Dyofins
Peptide	Synthetic Peptide	E-21R
Peptide	Synthetic Peptide	EA-230
Peptide	Recombinant Peptide	EB-613
Peptide	Synthetic Peptide	Edotreotide Labeled Yttrium 90
Peptide	Synthetic Peptide	edotreotide lutetium Lu-177
Peptide	Synthetic Peptide	edratide
Peptide	Recombinant Peptide	efpeglenatide
Peptide	Recombinant Peptide; Synthetic Peptide	efpeglenatide + HM-12470
Peptide	Synthetic Peptide	elamipretide hydrochloride
Peptide	Synthetic Peptide	elcatonin
Peptide	Synthetic Peptide	ELIGO-3233
Peptide	Synthetic Peptide	elsiglutide
Peptide	Recombinant Peptide	endostatin
Peptide	Synthetic Peptide	enfuvirtide
Peptide	Peptide; Synthetic Peptide	Engedi-1000
Peptide	Synthetic Peptide	ENKASTIM-iv
Peptide	Synthetic Peptide	EP-100
Peptide	Synthetic Peptide	EP-302
Peptide	Synthetic Peptide	EP-342
Peptide	Synthetic Peptide	EP-94
Peptide	Synthetic Peptide	EPO-018B
Peptide	Synthetic Peptide	eptifibatide
Peptide	Recombinant Peptide	ES-135
Peptide	Synthetic Peptide	etelcalcetide hydrochloride
Peptide	Synthetic Peptide	ETX-112
Peptide	Synthetic Peptide	Evitar
Peptide	Synthetic Peptide	exenatide
Peptide	Synthetic Peptide	exenatide + Synthetic Peptide 1
Peptide	Synthetic Peptide	exenatide + Synthetic Peptide 2
Peptide	Synthetic Peptide	exenatide biobetter
Peptide	Synthetic Peptide	exenatide biosimilar
Peptide	Synthetic Peptide	exenatide CR
Peptide	Synthetic Peptide	exenatide ER
Peptide	Synthetic Peptide	exenatide Once Monthly
Peptide	Synthetic Peptide	exenatide SR
Peptide	Synthetic Peptide	exendin-(9-39)
Peptide	Synthetic Peptide	EXT-307
Peptide	Synthetic Peptide	EXT-405
Peptide	Synthetic Peptide	EXT-418
Peptide	Synthetic Peptide	EXT-600
Peptide	Synthetic Peptide	EXT-607
Peptide	Synthetic Peptide	EXT-705
Peptide	Recombinant Peptide	Extendin-Fc
Peptide	Synthetic Peptide	FE-204205
Peptide	Synthetic Peptide	FF-3
Peptide	Recombinant Peptide	Fiasp
Peptide	Synthetic Peptide	FM-19
Peptide	Synthetic Peptide	FNS-007
Peptide	Synthetic Peptide	forigerimod acetate
Peptide	Synthetic Peptide	Foxy-5
Peptide	Synthetic Peptide	FP-001
Peptide	Synthetic Peptide	FP-002
Peptide	Synthetic Peptide	FP-005
Peptide	Synthetic Peptide	FPP-003
Peptide	Recombinant Peptide	FT-105
Peptide	Synthetic Peptide	FX-06
Peptide	Synthetic Peptide	G-3215
Peptide	Synthetic Peptide	ganirelix acetate
Peptide	Synthetic Peptide	glatiramer acetate
Peptide	Synthetic Peptide	glatiramer acetate ER
Peptide	Synthetic Peptide	glatiramer biosimilar
Peptide	Synthetic Peptide	glepaglutide
Peptide	Recombinant Peptide	GLP-1
Peptide	Recombinant Peptide	glucagon
Peptide	Recombinant Peptide	glucagon biosimilar
Peptide	Recombinant Peptide	Glucagon-Like Peptide-1 + insulin human
Peptide	Synthetic Peptide	glucosaminylmuramyl dipeptide
Peptide	Synthetic Peptide	GM-6
Peptide	Synthetic Peptide	GO-2032C
Peptide	Synthetic Peptide	golotimod
Peptide	Synthetic Peptide	gonadorelin
Peptide	Synthetic Peptide	gonadorelin acetate
Peptide	Synthetic Peptide	goserelin
Peptide	Synthetic Peptide	goserelin acetate
Peptide	Synthetic Peptide	goserelin ER
Peptide	Synthetic Peptide	goserelin LA
Peptide	Synthetic Peptide	goserelin SR
Peptide	Recombinant Peptide	GP-40031
Peptide	Synthetic Peptide	GSAO
Peptide	Synthetic Peptide	HaemoPlax
Peptide	Synthetic Peptide	hbEGF
Peptide	Recombinant Peptide	HDV-I
Peptide	Synthetic Peptide	hepcidin acetate
Peptide	Synthetic Peptide	histrelin
Peptide	Recombinant Peptide	HM-12460A
Peptide	Recombinant Peptide	HM-12470
Peptide	Recombinant Peptide	HM-12480
Peptide	Recombinant Peptide	HM-15136
Peptide	Synthetic Peptide	HM-15211
Peptide	Synthetic Peptide	Homspera
Peptide	Synthetic Peptide	HPI-1201
Peptide	Synthetic Peptide	HPI-201
Peptide	Synthetic Peptide	HPI-363
Peptide	Synthetic Peptide	hPTH-137
Peptide	Synthetic Peptide	HTD-4010
Peptide	Synthetic Peptide	HTL-001
Peptide	Recombinant Peptide	Humalog
Peptide	Synthetic Peptide	HXTC-901
Peptide	Synthetic Peptide	Hydrogel Exenatide
Peptide	Synthetic Peptide	icatibant acetate
Peptide	Synthetic Peptide	IIIM-1
Peptide	Synthetic Peptide	IMB-1007
Peptide	Synthetic Peptide	ImmTher
Peptide	Recombinant Peptide	insulin
Peptide	Recombinant Peptide	insulin (bovine)
Peptide	Recombinant Peptide	insulin aspart
Peptide	Recombinant Peptide	insulin aspart 1
Peptide	Recombinant Peptide	insulin aspart biosimilar
Peptide	Recombinant Peptide	insulin aspart injection
Peptide	Recombinant Peptide	insulin degludec
Peptide	Recombinant Peptide	insulin degludec LAR
Peptide	Recombinant Peptide	insulin detemir
Peptide	Recombinant Peptide	insulin glargine
Peptide	Recombinant Peptide	insulin glargine 1
Peptide	Recombinant Peptide	insulin glargine biosimilar
Peptide	Recombinant Peptide	insulin glargine biosimilar 2
Peptide	Recombinant Peptide	insulin glargine ER
Peptide	Recombinant Peptide	insulin glargine LA
Peptide	Recombinant Peptide	insulin glulisine
Peptide	Recombinant Peptide	insulin human
Peptide	Recombinant Peptide	insulin human (recombinant)
Peptide	Recombinant Peptide	insulin human 1
Peptide	Recombinant Peptide	Insulin Human 30/70 Mix Marvel
Peptide	Recombinant Peptide	Insulin Human Long Marvel
Peptide	Recombinant Peptide	Insulin Human Rapid Marvel
Peptide	Recombinant Peptide	insulin human U100
Peptide	Recombinant Peptide	insulin human zinc
Peptide	Recombinant Peptide	insulin I 131
Peptide	Recombinant Peptide	insulin isophane
Peptide	Recombinant Peptide	insulin isophane human
Peptide	Recombinant Peptide	insulin lispro
Peptide	Recombinant Peptide	insulin lispro 2
Peptide	Recombinant Peptide	insulin lispro U100
Peptide	Recombinant Peptide	insulin lispro U200
Peptide	Recombinant Peptide	insulin lispro U300
Peptide	Recombinant Peptide	insulin neutral
Peptide	Recombinant Peptide	insulin peglispro
Peptide	Recombinant Peptide	insulin tregopil
Peptide	Recombinant Peptide	Insulin-PH20
Peptide	Recombinant Peptide	Insulin-B12 Conjugate
Peptide	Recombinant Peptide	insulin, neutral
Peptide	Recombinant Peptide	Insuman
Peptide	Synthetic Peptide	IP-1510
Peptide	Synthetic Peptide	IP-151OD
Peptide	Synthetic Peptide	ipamorelin
Peptide	Synthetic Peptide	IPL-344
Peptide	Synthetic Peptide	IPP-102199
Peptide	Synthetic Peptide	IPP-204106
Peptide	Recombinant Peptide	Ir-CPI
Peptide	Synthetic Peptide	ISF-402
Peptide	Recombinant Peptide	isophane protamine recombinant human
		insulin
Peptide	Synthetic Peptide	ITCA-650
Peptide	Synthetic Peptide	ITF-1697
Peptide	Recombinant Peptide	ITF-2984
Peptide	Recombinant Peptide	JDSCR-103
Peptide	Synthetic Peptide	JMR-132
Peptide	Synthetic Peptide	JNJ-26366821
Peptide	Synthetic Peptide	JNJ-38488502
Peptide	Synthetic Peptide	K-13
Peptide	Synthetic Peptide	kahalalide F
Peptide	Synthetic Peptide	KAI-1678
Peptide	Recombinant Peptide	KBP-088
Peptide	Synthetic Peptide	KES-0001
Peptide	Synthetic Peptide	Kisspeptin-10
Peptide	Synthetic Peptide	KRX-0402
Peptide	Synthetic Peptide	KSL-W
Peptide	Recombinant Peptide	KUR-112
Peptide	Recombinant Peptide	KUR-113
Peptide	Synthetic Peptide	L-1AD3
Peptide	Recombinant Peptide	LAI-287
Peptide	Recombinant Peptide	LAI-338
Peptide	Synthetic Peptide	lanreotide acetate PR
Peptide	Synthetic Peptide	lanreotide SR
Peptide	Synthetic Peptide	larazotide acetate
Peptide	Synthetic Peptide	LAT-8881
Peptide	Synthetic Peptide	LBT-1000
Peptide	Synthetic Peptide	LBT-3627
Peptide	Synthetic Peptide	LBT-5001
Peptide	Synthetic Peptide	LBT-6030
Peptide	Synthetic Peptide	LC-002
Peptide	Synthetic Peptide	leconotide
Peptide	Synthetic Peptide	leuprolide
Peptide	Synthetic Peptide	leuprolide acetate
Peptide	Small Molecule; Synthetic Peptide	leuprolide acetate + norethindrone
Peptide	Synthetic Peptide	leuprolide acetate ER
Peptide	Synthetic Peptide	leuprolide acetate PR
Peptide	Synthetic Peptide	leuprolide acetate SR
Peptide	Synthetic Peptide	leuprorelin acetate PR
Peptide	Synthetic Peptide	leuprorelin ER
Peptide	Synthetic Peptide	LH-021
Peptide	Synthetic Peptide	LH-024
Peptide	Synthetic Peptide	linaclotide
Peptide	Synthetic Peptide	linaclotide DR2
Peptide	Recombinant Peptide	Linjeta
Peptide	Recombinant Peptide	liraglutide
Peptide	Synthetic Peptide	liraglutide biobetter
Peptide	Recombinant Peptide	liraglutide biosimilar
Peptide	Synthetic Peptide	livoletide
Peptide	Synthetic Peptide	lixisenatide
Peptide	Synthetic Peptide	lobradimil
Peptide	Synthetic Peptide	LP-003
Peptide	Synthetic Peptide	LTX-315
Peptide	Synthetic Peptide; Vaccine	LTX-315 + tertomotide
Peptide	Synthetic Peptide	LTX-401
Peptide	Synthetic Peptide	lutetium Lu 177 dotatate
Peptide	Synthetic Peptide	LY-2510924
Peptide	Synthetic Peptide	LY-3143753
Peptide	Synthetic Peptide	LY-3185643
Peptide	Recombinant Peptide	LY-3209590
Peptide	Synthetic Peptide	LY-3305677
Peptide	Synthetic Peptide	LY-355703
Peptide	Recombinant Peptide	LY-900027
Peptide	Recombinant Peptide	Lyumjev
Peptide	Synthetic Peptide	M-012
Peptide	Recombinant Peptide	Macrulin
Peptide	Synthetic Peptide	MALP-2S
Peptide	Synthetic Peptide	mannatide
Peptide	Synthetic Peptide	metenkefalin
Peptide	Synthetic Peptide	mibenratide
Peptide	Synthetic Peptide	mifamurtide
Peptide	Synthetic Peptide	mitolactol
Peptide	Recombinant Peptide	MOD-1001
Peptide	Recombinant Peptide	MOD-1002
Peptide	Recombinant Peptide	MOD-6030
Peptide	Recombinant Peptide	MOD-6031
Peptide	Synthetic Peptide	motixafortide
Peptide	Synthetic Peptide	Motrem
Peptide	Synthetic Peptide	MP-3167
Peptide	Synthetic Peptide	MPE-002
Peptide	Recombinant Peptide	MSTMB-103
Peptide	Synthetic Peptide	MT-1002
Peptide	Synthetic Peptide	MTX-1604
Peptide	Synthetic Peptide	MVT-602
Peptide	Synthetic Peptide	NAX-8102
Peptide	Synthetic Peptide	NBI-6024
Peptide	Synthetic Peptide	NBI-69734
Peptide	Synthetic Peptide	NBP-14
Peptide	Synthetic Peptide	nemifitide ditriflutate
Peptide	Synthetic Peptide	nepadutant
Peptide	Synthetic Peptide	Nephrilin
Peptide	Recombinant Peptide	nerinetide
Peptide	Synthetic Peptide	Nerofe
Peptide	Recombinant Peptide	nesiritide
Peptide	Recombinant Peptide	Neucardin
Peptide	Recombinant Peptide	NL-005
Peptide	Synthetic Peptide	NLY-001
Peptide	Recombinant Peptide	NN-1952
Peptide	Recombinant Peptide	NN-1954
Peptide	Recombinant Peptide	NN-1955
Peptide	Recombinant Peptide	NN-1956
Peptide	Recombinant Peptide	NN-1965
Peptide	Synthetic Peptide	NN-9277
Peptide	Synthetic Peptide	NN-9423
Peptide	Recombinant Peptide	NN-9513
Peptide	Synthetic Peptide	NN-9536
Peptide	Synthetic Peptide	NN-9747
Peptide	Synthetic Peptide	NN-9775
Peptide	Synthetic Peptide	NN-9838
Peptide	Synthetic Peptide	NN-9931
Peptide	Synthetic Peptide	NNZ-2591
Peptide	Synthetic Peptide	NOV-004
Peptide	Synthetic Peptide	NRP-2945
Peptide	Synthetic Peptide	NRX-1051
Peptide	Recombinant Peptide	NsG-0501
Peptide	Recombinant Peptide	NTRA-2112
Peptide	Recombinant Peptide	NTRA-9620
Peptide	Synthetic Peptide	NX-210
Peptide	Recombinant Peptide	OA-150
Peptide	Synthetic Peptide	OB-3
Peptide	Synthetic Peptide	obinepitide
Peptide	Synthetic Peptide	octreotide
Peptide	Synthetic Peptide	octreotide acetate
Peptide	Synthetic Peptide	octreotide acetate CR
Peptide	Synthetic Peptide	octreotide acetate LA
Peptide	Synthetic Peptide	octreotide acetate LAR
Peptide	Synthetic Peptide	octreotide acetate MAR
Peptide	Synthetic Peptide	octreotide acetate microspheres
Peptide	Synthetic Peptide	octreotide acetate PR
Peptide	Synthetic Peptide	octreotide acetate SR
Peptide	Synthetic Peptide	octreotide LA
Peptide	Synthetic Peptide	OHR/AVR-118
Peptide	Recombinant Peptide	OI-320GT
Peptide	Recombinant Peptide	OI-338GT
Peptide	Synthetic Peptide	OK-201
Peptide	Synthetic Peptide	OKI-179
Peptide	Synthetic Peptide	OKI-422
Peptide	Recombinant Peptide	OMO-103
Peptide	Recombinant Peptide	ONCase-PEG
Peptide	Synthetic Peptide	ONK-102
Peptide	Synthetic Peptide	ONL-1204
Peptide	Synthetic Peptide	Oratonin
Peptide	Synthetic Peptide	orilotimod potassium
Peptide	Synthetic Peptide	ornipressin
Peptide	Synthetic Peptide	ORTD-1
Peptide	Synthetic Peptide	OXE-103
Peptide	Recombinant Peptide	Oxymera
Peptide	Synthetic Peptide	oxyntomodulin
Peptide	Synthetic Peptide	oxytocin
Peptide	Synthetic Peptide	ozarelix
Peptide	Recombinant Peptide	Ozempic
Peptide	Synthetic Peptide	P-17
Peptide	Synthetic Peptide	P-28
Peptide	Synthetic Peptide	P-28R
Peptide	Synthetic Peptide	P-8
Peptide	Recombinant Peptide	parathyroid hormone
Peptide	Synthetic Peptide	pasireotide
Peptide	Synthetic Peptide	pasireotide LAR
Peptide	Recombinant Peptide	PB-1023
Peptide	Synthetic Peptide	PB-119
Peptide	Synthetic Peptide	PCO-01
Peptide	Synthetic Peptide	PCO-02
Peptide	Synthetic Peptide	PDC-31
Peptide	Recombinant Peptide	PE-0139
Peptide	Synthetic Peptide	PEG Exenatide
Peptide	Synthetic Peptide	pegapamodutide
Peptide	Synthetic Peptide	pegcetacoplan
Peptide	Synthetic Peptide	peginesatide
Peptide	Synthetic Peptide	Pegylated Thymalfasin
Peptide	Recombinant Peptide	PEN-221
Peptide	Peptide
Peptide	Synthetic Peptide	Peptide T
Peptide	Peptide	Peptide to Inhibit Amyloid Beta Peptide for
		Alzheimer's Disease
Peptide	Peptide	Peptide to Inhibit GRP-78 for Melanoma
Peptide	Synthetic Peptide	PHIN-1138
Peptide	Synthetic Peptide	PHIN-837
Peptide	Synthetic Peptide	PI-0824
Peptide	Recombinant Peptide	PI-406
Peptide	Synthetic Peptide	pidotimod
Peptide	Synthetic Peptide	PIN-201104
Peptide	Synthetic Peptide	PL-3994
Peptide	Synthetic Peptide	PL-8177
Peptide	Synthetic Peptide	Plannexin
Peptide	Synthetic Peptide	plecanatide
Peptide	Synthetic Peptide	PLG-0206
Peptide	Synthetic Peptide	plitidepsin
Peptide	Synthetic Peptide	PMZ-2123
Peptide	Synthetic Peptide	PN-943
Peptide	Synthetic Peptide	PNT-2002
Peptide	Synthetic Peptide	polyethylene glycol loxenatide LAR
Peptide	Synthetic Peptide	PP-1420
Peptide	Synthetic Peptide	pramlintide
Peptide	Synthetic Peptide	Preimplantation Factor
Peptide	Synthetic Peptide	PRI-002
Peptide	Synthetic Peptide	PRI-003
Peptide	Synthetic Peptide	PRI-004
Peptide	Synthetic Peptide	protamine sulfate
Peptide	Recombinant Peptide	protamine zinc insulin
Peptide	Recombinant Peptide	Protaphane
Peptide	Synthetic Peptide	PT-302
Peptide	Synthetic Peptide	PT-320
Peptide	Synthetic Peptide	PT-330
Peptide	Synthetic Peptide	PTG-200
Peptide	Synthetic Peptide	PZ-128
Peptide	Peptide	QUB-3164
Peptide	Recombinant Peptide	rE-4
Peptide	Synthetic Peptide	REC-0438
Peptide	Recombinant Peptide	Recombinant Human Intestinal Trefoil
		Factor
Peptide	Recombinant Peptide	Recombinant Peptide 1 to Agonize Insulin
		Receptor for Type 1 and Type 2 Diabetes
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize
		Calcitonin Gene Related Peptide Receptor
		for Osteoporosis and Hypertension
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize GHRH
		for Cardiovascular, Central Nervous
		System, Musculoskeletal and Metabolic
		Disorders
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize GLP1R
		for Type 2 Diabetes
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize Insulin
		receptor for Diabetes
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize Insulin
		Receptor for Type 1 and Type 2 Diabetes
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize Insulin
		Receptor for Type 1 Diabetes
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize Insulin
		Receptor for Type 2 Diabetes
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize PTH-R
		for Post Menopausal Osteoporosis
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize PTH1R
		for Bone Fracture
Peptide	Recombinant Peptide	Recombinant Peptide to Agonize PTH1R
		for Hypoparathyroidism
Peptide	Recombinant Peptide	Recombinant Peptide to Inhibit TNF Alpha
		for Crohn's Disease, Asthma And
		Metabolic Syndrome
Peptide	Recombinant Peptide	Recombinant Peptide-1 to Activate GLP-1
		for Type 2 Diabetes
Peptide	Recombinant Peptide	Recombinant Peptides 6 to Agonize
		Insulin Receptor for Type 1 and Type 2
		Diabetes
Peptide	Recombinant Peptide	Recombinant Peptides to Activate GLP-1
		for Type-2 Diabetes
Peptide	Recombinant Peptide	Recombinant Peptides to Agonize Insulin
		Receptor for Type 1 and Type 2 Diabetes
Peptide	Recombinant Peptide	Recombinant Peptides to Agonize MFN2
		for Charcot Marie Tooth Disease Type IIA
		and Hypertrophic Cardiomyopathy
Peptide	Synthetic Peptide	Reg-O3
Peptide	Synthetic Peptide	relamorelin
Peptide	Synthetic Peptide	reltecimod sodium
Peptide	Recombinant Peptide	Rescue-G
Peptide	Synthetic Peptide	RGN-352
Peptide	Recombinant Peptide	Rh-RGD-Hirudin
Peptide	Synthetic Peptide	risuteganib
Peptide	Synthetic Peptide	romidepsin
Peptide	Synthetic Peptide	RPI-78M
Peptide	Synthetic Peptide	RPI-MN
Peptide	Recombinant Peptide	RTP-025
Peptide	Synthetic Peptide	rusalatide acetate
Peptide	Synthetic Peptide	Rybelsus
Peptide	Recombinant Peptide	SAR-161271
Peptide	Synthetic Peptide	SAR-425899
Peptide	Recombinant Peptide	Saxenda
Peptide	Synthetic Peptide	SBI-1301
Peptide	Synthetic Peptide	SBT-20
Peptide	Synthetic Peptide	SBT-272
Peptide	Synthetic Peptide	SCO-094
Peptide	Synthetic Peptide	SER-130
Peptide	Synthetic Peptide	setmelanotide
Peptide	Synthetic Peptide	setmelanotide ER
Peptide	Synthetic Peptide	SGX-943
Peptide	Recombinant Peptide	somatostatin
Peptide	Recombinant Peptide	somatrem
Peptide	Recombinant Peptide	somatrogon
Peptide	Synthetic Peptide	SORC-13
Peptide	Synthetic Peptide	sovateltide
Peptide	Synthetic Peptide	SRI-31277
Peptide	Synthetic Peptide	STR-324
Peptide	Synthetic Peptide	Synthetic Peptide 1 to Inhibit PD-L1 for
		Oncology
Peptide	Synthetic Peptide	Synthetic Peptide for Dengue
Peptide	Synthetic Peptide	Synthetic Peptide for Huntington Disease
Peptide	Synthetic Peptide	Synthetic Peptide for Oncology
Peptide	Synthetic Peptide	Synthetic Peptide for Zika Virus Infection
Peptide	Synthetic Peptide	Synthetic Peptide to Agonize GLP1R for
		Type 2 Diabetes
Peptide	Synthetic Peptide	Synthetic Peptide to Agonize Insulin
		Receptor for Type 2 Diabetes
Peptide	Synthetic Peptide	Synthetic Peptide to Inhibit Alpha
		Synuclein for Parkinson's Disease
Peptide	Synthetic Peptide	Synthetic Peptide to Inhibit Connexin 43
		for Optic Neuropathy
Peptide	Synthetic Peptide	Synthetic Peptide to Inhibit ELK1 for
		Central Nervous System Disorders
Peptide	Synthetic Peptide	Synthetic Peptide to Inhibit PCSK9 for
		Hypercholesterolemia
Peptide	Synthetic Peptide	Synthetic Peptide to Inhibit SOD1 for
		Amyotrophic Lateral Sclerosis
Peptide	Synthetic Peptide	Synthetic Peptide to Inhibit Tau for
		Tauopathies
Peptide	Synthetic Peptide	Synthetic Peptide to Inhibit TNF-Alpha for
		Rheumatoid Arthritis
Peptide	Synthetic Peptide	Synthetic Peptide to Inhibit VEGFD for
		Oncology
Peptide	Synthetic Peptide	Synthetic Peptide to Modulate GHSR for
		Chronic Kidney Disease
Peptide	Synthetic Peptide	Synthetic Peptide to Target CCKBR for
		Medullary Thyroid Cancer
Peptide	Synthetic Peptide	Synthetic Peptide to Target Somatostatin
		Receptor for Neuroendocrine
		Gastroenteropancreatic Tumors
Peptide	Synthetic Peptide	Synthetic Peptide to Target Somatostatin
		Receptor for Neuroendocrine Tumors
Peptide	Synthetic Peptide	Synthetic Peptides to Activate TMEM173
		for Oncology
Peptide	Synthetic Peptide	Synthetic Peptides to Agonize DOR1 and
		MOR1 for Irritable Bowel Syndome with
		Diarrhea
Peptide	Synthetic Peptide	Synthetic Peptides to Agonize GLP1R for
		Type 2 Diabetes
Peptide	Synthetic Peptide	Synthetic Peptides to Agonize TLR for
		Oncology
Peptide	Synthetic Peptide	Synthetic Peptides to Antagonize CXCR7
		for Oncology
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit Beta Catenin
		for Oncology
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit Complement
		C3 for Unspecified Indication
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit Cyclin E for
		Oncology
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit
		CyclinA/CDK2 for Oncology
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit DRB1 for
		Multiple Sclerosis
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit E1 and E2
		Glycoprotein for HCV
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit Factor D for
		Geographic Atrophy, Paroxysmal
		Nocturnal Hemoglobinuria and Renal
		Disease
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit Glycoprotein
		VI for Thrombosis
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit MCL1 for
		Oncology
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit SMURF2 for
		Fibrosis and Oncology
Peptide	Synthetic Peptide	Synthetic Peptides to Inhibit TREM-1 for
		Oncology, Sepsis, Rheumatoid Arthritis,
		Retinopathy Of Prematurity and
		Hemorrhagic Shock
Peptide	Recombinant Peptide	T-0005
Peptide	Synthetic Peptide	T-20K
Peptide	Recombinant Peptide	TAC-201
Peptide	Synthetic Peptide	Tatbeclin-1
Peptide	Recombinant Peptide	TBR-760
Peptide	Synthetic Peptide	TCANG-05
Peptide	Synthetic Peptide	TCMCB-07
Peptide	Recombinant Peptide	teduglutide
Peptide	Synthetic Peptide	teicoplanin
Peptide	Recombinant Peptide	teriparatide
Peptide	Recombinant Peptide	teriparatide acetate
Peptide	Recombinant Peptide	teriparatide biosimilar
Peptide	Synthetic Peptide	terlipressin
Peptide	Synthetic Peptide	tesamorelin acetate
Peptide	Synthetic Peptide	THR-149
Peptide	Synthetic Peptide	thymalfasin
Peptide	Synthetic Peptide
Peptide	Recombinant Peptide	tifacogin
Peptide	Synthetic Peptide	tirzepatide
Peptide	Synthetic Peptide	TPX-100
Peptide	Synthetic Peptide	triptorelin
Peptide	Synthetic Peptide	triptorelin acetate
Peptide	Synthetic Peptide	triptorelin acetate ER
Peptide	Synthetic Peptide	triptorelin acetate SR
Peptide	Synthetic Peptide	triptorelin pamoate
Peptide	Synthetic Peptide	triptorelin pamoate ER
Peptide	Synthetic Peptide	triptorelin SR
Peptide	Synthetic Peptide	TXA-127
Peptide	Synthetic Peptide	TXA-302
Peptide	Recombinant Peptide	UGP-281
Peptide	Recombinant Peptide	UGP-302
Peptide	Recombinant Peptide	Ultratard
Peptide	Recombinant Peptide	Uni-E4
Peptide	Synthetic Peptide	Upelior
Peptide	Synthetic Peptide	V-10
Peptide	Synthetic Peptide	VAL-201
Peptide	Synthetic Peptide	vapreotide acetate
Peptide	Synthetic Peptide	vasopressin
Peptide	Synthetic Peptide	veldoreotide ER
Peptide	Synthetic Peptide	veldoreotide IR
Peptide	Synthetic Peptide	VG-1177
Peptide	Recombinant Peptide	VIAcal
Peptide	Recombinant Peptide	vosoritide
Peptide	Recombinant Peptide	VTCG-15
Peptide	Peptide	XG-402
Peptide	Peptide	XG-404
Peptide	Synthetic Peptide	Y-14
Peptide	Synthetic Peptide	YH-14618
Peptide	Synthetic Peptide	ziconotide
Peptide	Synthetic Peptide	zilucoplan
Peptide	Recombinant Peptide	Znsulin
Peptide	Synthetic Peptide	ZP-10000
Peptide	Synthetic Peptide	ZP-7570
Peptide	Synthetic Peptide	ZT-01
Peptide	Recombinant Peptide	ZT-031
Peptide	Synthetic Peptide	ZYKR-1

TABLE 3
Enzymes
Broad class	Molecule Type	Drug Name
Enzyme	Recombinant Enzyme	AB-002
Enzyme	Recombinant Enzyme	ACN-00177
Enzyme	Recombinant Enzyme	agalsidase alfa
Enzyme	Recombinant Enzyme	agalsidase beta
Enzyme	Recombinant Enzyme	albutrepenonacog alfa ER
Enzyme	Recombinant Enzyme	alglucerase
Enzyme	Recombinant Enzyme	alglucosidase alfa
Enzyme	Recombinant Enzyme	alteplase
Enzyme	Recombinant Enzyme	alteplase biosimilar
Enzyme	Enzyme	ancrod
Enzyme	Enzyme	anistreplase
Enzyme	Recombinant Enzyme	apadamtase alfa
Enzyme	Recombinant Enzyme	APN-01
Enzyme	Recombinant Enzyme	asfotase alfa
Enzyme	Enzyme	asparaginase
Enzyme	Recombinant Enzyme	avalglucosidase alfa
Enzyme	Recombinant Enzyme	BCT-100
Enzyme	Recombinant Enzyme	bRESCAP
Enzyme	Enzyme	bromelains
Enzyme	Recombinant Enzyme	calaspargase pegol
Enzyme	Recombinant Enzyme	cerliponase alfa
Enzyme	Enzyme	chymopapain
Enzyme	Enzyme	chymotrypsin
Enzyme	Recombinant Enzyme	coagulation factor IX (recombinant)
Enzyme	Recombinant Enzyme	coagulation factor IX (recombinant) biosimilar
Enzyme	Recombinant Enzyme	coagulation factor VIIa (recombinant) biosimilar
Enzyme	Recombinant Enzyme	coagulation factor XIII A-subunit (recombinant)
Enzyme	Enzyme	collagenase clostridium histolyticum
Enzyme	Recombinant Enzyme	condoliase
Enzyme	Recombinant Enzyme	CP-205
Enzyme	Recombinant Enzyme	CUSA-081
Enzyme	Recombinant Enzyme	dalcinonacog alfa
Enzyme	Recombinant Enzyme	elapegademase
Enzyme	Recombinant Enzyme	elosulfase alfa
Enzyme	Recombinant Enzyme	ERYGEN
Enzyme	Recombinant Enzyme	exebacase
Enzyme	Recombinant Enzyme	galsulfase
Enzyme	Recombinant Enzyme	glucarpidase
Enzyme	Enzyme	hemocoagulase
Enzyme	Recombinant Enzyme	HGT-1111
Enzyme	Recombinant Enzyme	hRESCAP
Enzyme	Recombinant Enzyme	idursulfase
Enzyme	Recombinant Enzyme	idursulfase beta
Enzyme	Recombinant Enzyme	imiglucerase
Enzyme	Recombinant Enzyme	imiglucerase biosimilar
Enzyme	Recombinant Enzyme	imlifidase
Enzyme	Recombinant Enzyme	JR-141
Enzyme	Recombinant Enzyme	JZP-458
Enzyme	Recombinant Enzyme	KTP-001
Enzyme	Recombinant Enzyme	laronidase
Enzyme	Recombinant Enzyme	lesinidase alfa
Enzyme	Recombinant Enzyme	Lumizyme
Enzyme	Recombinant Enzyme	marzeptacog alfa (activated)
Enzyme	Recombinant Enzyme	MEDI-6012
Enzyme	Recombinant Enzyme	MOSS-AGAL
Enzyme	Recombinant Enzyme	ocriplasmin
Enzyme	Recombinant Enzyme	olipudase alfa
Enzyme	Recombinant Enzyme	OT-58
Enzyme	Enzyme	pegademase bovine
Enzyme	Recombinant Enzyme	pegadricase
Enzyme	Recombinant Enzyme	pegargiminase
Enzyme	Recombinant Enzyme	pegaspargase
Enzyme	Recombinant Enzyme	pegaspargase biosimilar
Enzyme	Recombinant Enzyme	pegcrisantaspase
Enzyme	Recombinant Enzyme	pegloticase
Enzyme	Recombinant Enzyme	pegunigalsidase alfa
Enzyme	Recombinant Enzyme	pegvaliase
Enzyme	Recombinant Enzyme	pegvorhyaluronidase alfa
Enzyme	Recombinant Enzyme	pegzilarginase
Enzyme	Recombinant Enzyme	PF-05230907
Enzyme	Enzyme	PRP
Enzyme	Recombinant Enzyme	PT-01
Enzyme	Recombinant Enzyme	ranpirnase
Enzyme	Recombinant Enzyme	rasburicase
Enzyme	Recombinant Enzyme
Enzyme	Recombinant Enzyme	Recombinant Glucosylceramidase Replacement for
		Type I and Type III Gaucher's Disease
Enzyme	Recombinant Enzyme	Recombinant Human Alkaline Phosphatase
		Replacement for Acute Renal Failure,
		Hypophosphatasia, Sepsis and Ulcerative Colitis
Enzyme	Recombinant Enzyme	Recombinant Urate Oxidase Replacement for Acute
		Hyperuricemia
Enzyme	Recombinant Enzyme	reteplase
Enzyme	Recombinant Enzyme	sebelipase alfa
Enzyme	Recombinant Enzyme	SHP-610
Enzyme	Enzyme	SOBI-003
Enzyme	Recombinant Enzyme	Spectrila
Enzyme	Recombinant Enzyme	staphylokinase
Enzyme	Enzyme	streptokinase
Enzyme	Recombinant Enzyme	TAK-611
Enzyme	Recombinant Enzyme	taliglucerase alfa
Enzyme	Recombinant Enzyme	tenecteplase
Enzyme	Recombinant Enzyme	TNX-1300
Enzyme	Recombinant Enzyme	tonabacase
Enzyme	Recombinant Enzyme	tralesinidase alfa
Enzyme	Enzyme	urokinase
Enzyme	Recombinant Enzyme	velaglucerase alfa
Enzyme	Recombinant Enzyme	velmanase alfa
Enzyme	Recombinant Enzyme	vestronidase alfa
Enzyme	Recombinant Enzyme	vonapanitase
Enzyme	Recombinant Enzyme	VX-210

TABLE 4
Proteins
Broad Class	Molecule Type	Drug Name
Protein	Recombinant Protein	3K3A-APC
Protein	Fusion Protein	abatacept
Protein	Recombinant Protein	abicipar pegol
Protein	Protein	abobotulinumtoxin A next generation
Protein	Protein	abobotulinumtoxinA
Protein	Recombinant Protein	ABY-035
Protein	Recombinant Protein	ABY-039
Protein	Protein	ACP-014
Protein	Recombinant Protein	ACT-101
Protein	Fusion Protein	AD-214
Protein	Fusion Protein	aflibercept
Protein	Fusion Protein	aflibercept biosimilar
Protein	Fusion Protein	AGT-181
Protein	Fusion Protein	AGT-182
Protein	Fusion Protein	AKR-001
Protein	Protein	Albicin
Protein	Recombinant Protein	albiglutide
Protein	Fusion Protein	albinterferon alfa-2b
Protein	Recombinant Protein	aldafermin
Protein	Recombinant Protein	aldesleukin
Protein	Fusion Protein	alefacept
Protein	Fusion Protein	ALKS-4230
Protein	Fusion Protein	ALPN-101
Protein	Fusion Protein	ALT-801
Protein	Fusion Protein	ALTP-1
Protein	Fusion Protein	ALX-148
Protein	Recombinant Protein	AMRS-001
Protein	Recombinant Protein	anakinra
Protein	Recombinant Protein	ancestim
Protein	Recombinant Protein	andexanet alfa
Protein	Recombinant Protein	antihemophilic factor (recombinant)
Protein	Recombinant Protein	antihemophilic factor (human)
Protein	Recombinant Protein	antihemophilic factor (recombinant) biosimilar
Protein	Fusion Protein	antihemophilic factor (recombinant), FcFusion
		protein
Protein	Recombinant Protein	antihemophilic factor (recombinant), PEGylated
Protein	Recombinant Protein	antihemophilic factor (recombinant),
		plasma/albumin free
Protein	Recombinant Protein	antihemophilic factor (recombinant),
		plasma/albumin free method
Protein	Recombinant Protein	antihemophilic factor (recombinant), porcine
		sequence
Protein	Recombinant Protein	antihemophilic factor (recombinant), single chain
Protein	Recombinant Protein	antithrombin (recombinant)
Protein	Fusion Protein	APN-301
Protein	Fusion Protein	APO-010
Protein	Fusion Protein	Aravive-S6
Protein	Fusion Protein	asunercept
Protein	Fusion Protein	atacicept
Protein	Fusion Protein	ATYR-1923
Protein	Recombinant Protein	ATYR-1940
Protein	Recombinant Protein	AU-011
Protein	Recombinant Protein	aviscumine
Protein	Recombinant Protein	avotermin
Protein	Fusion Protein	balugrastim
Protein	Recombinant Protein	batroxobin
Protein	Recombinant Protein	BBT-015
Protein	Recombinant Protein	BCD-131
Protein	Protein	bee venom
Protein	Fusion Protein	belatacept
Protein	Recombinant Protein	bempegaldesleukin
Protein	Protein	beractant
Protein	Recombinant Protein	BG-8962
Protein	Fusion Protein	bintrafusp alfa
Protein	Recombinant Protein	BIO89-100
Protein	Fusion Protein	BIVV-001
Protein	Fusion Protein	blisibimod
Protein	Recombinant Protein; Small	boceprevir + peginterferon alfa-2b + ribavirin
	Molecule
Protein	Protein	botulinum toxin type A
Protein	Protein	BXQ-350
Protein	Protein	C1 esterase inhibitor (human)
Protein	Recombinant Protein	C1-esterase inhibitor
Protein	Protein	Cadisurf
Protein	Recombinant Protein	Cardiotrophin-1
Protein	Protein	CB-24
Protein	Fusion Protein	CD-24Fc
Protein	Recombinant Protein	CDX-301
Protein	Recombinant Protein	cepeginterferon alfa-2b
Protein	Recombinant Protein	CER-001
Protein	Recombinant Protein	CG-100
Protein	Recombinant Protein	CG-367
Protein	Recombinant Protein	choriogonadotropin alfa
Protein	Recombinant Protein	chorionic gonadotropin
Protein	Recombinant Protein	CIGB-128
Protein	Protein	CIGB-845
Protein	Recombinant Protein	cimaglermin alfa
Protein	Recombinant Protein	cintredekin besudotox
Protein	Fusion Protein	coagulation factor IX (recombinant), Fc fusion
		protein
Protein	Recombinant Protein	coagulation factor IX (recombinant), glycopegylated
Protein	Recombinant Protein	coagulation Factor VIIa (Recombinant)
Protein	Recombinant Protein	coagulation factor VIII (recombinant) biosimilar
Protein	Fusion Protein	conbercept
Protein	Recombinant Protein	conestat alfa
Protein	Recombinant Protein	corifollitropin alfa
Protein	Fusion Protein	CSL-689
Protein	Recombinant Protein	CSL-730
Protein	Fusion Protein	CTI-1601
Protein	Fusion Protein	CUE-101
Protein	Recombinant Protein	CVBT-141A
Protein	Recombinant Protein	CVBT-141C
Protein	Recombinant Protein	CYT-6091
Protein	Recombinant Protein	CYT-99007
Protein	Recombinant Protein	Cyto-012
Protein	Recombinant Protein	dapiclermin
Protein	Recombinant Protein	darbepoetin alfa
Protein	Recombinant Protein	darbepoetin alfa biosimilar LA
Protein	Recombinant Protein	darbepoetin alfa LA
Protein	Fusion Protein	darleukin
Protein	Fusion Protein	daromun
Protein	Fusion Protein	dazodalibep
Protein	Fusion Protein	Dekavil
Protein	Recombinant Protein	denenicokin
Protein	Fusion Protein	denileukin diftitox
Protein	Protein	Dextran-Hemoglobin
Protein	Fusion Protein	DI-Leu16-IL2
Protein	Recombinant Protein	dianexin
Protein	Recombinant Protein	dibotermin alfa
Protein	Recombinant Protein	DM-199
Protein	Fusion Protein	DMX-101
Protein	Fusion Protein	DNL-310
Protein	Recombinant Protein	drotrecogin alfa (activated)
Protein	Fusion Protein	DSP-107
Protein	Fusion Protein	dulaglutide
Protein	Recombinant Protein	ecallantide
Protein	Recombinant Protein	ECI-301
Protein	Recombinant Protein	edodekin alfa
Protein	Fusion Protein	efavaleukin alfa
Protein	Fusion Protein	efineptakin alfa
Protein	Recombinant Protein	efinopegdutide
Protein	Recombinant Protein	eflapegrastim
Protein	Recombinant Protein	efpegsomatropin
Protein	Fusion Protein	eftansomatropin alfa
Protein	Fusion Protein	eftilagimod alfa
Protein	Fusion Protein	eftozanermin alfa
Protein	Recombinant Protein	empegfilgrastim
Protein	Recombinant Protein	entolimod
Protein	Fusion Protein	envafolimab
Protein	Recombinant Protein	epidermal growth factor
Protein	Recombinant Protein	epoetin alfa
Protein	Recombinant Protein	epoetin alfa Long Acting
Protein	Recombinant Protein	epoetin beta
Protein	Recombinant Protein	epoetin delta
Protein	Recombinant Protein	epoetin theta
Protein	Recombinant Protein	epoetin zeta
Protein	Recombinant Protein	ErepoXen
Protein	Fusion Protein	etanercept
Protein	Fusion Protein	etanercept biosimilar
Protein	Protein	EYS-611
Protein	Fusion Protein	F-627
Protein	Fusion Protein	F-652
Protein	Fusion Protein	F-899
Protein	Recombinant Protein	Fertavid
Protein	Fusion Protein	fexapotide triflutate
Protein	Fusion Protein	fibromun
Protein	Recombinant Protein	filgrastim
Protein	Recombinant Protein	follicle stimulating hormone
Protein	Recombinant Protein	follitropin alfa
Protein	Recombinant Protein
Protein	Recombinant Protein	follitropin beta
Protein	Recombinant Protein	follitropin delta
Protein	Recombinant Protein	FOV-2501
Protein	Recombinant Protein	FSH-GEX
Protein	Fusion Protein
Protein	Fusion Protein	Fusion Protein to Antagonize EGFR for
		Glioblastoma Multiforme and Malignant Glioma
Protein	Fusion Protein	Fusion Protein to Inhibit CD25 for Oncology
Protein	Fusion Protein	Fusion Protein to Target Mesothelin for Oncology
Protein	Recombinant Protein	GEM-ONJ
Protein	Protein	gemibotulinumtoxin A
Protein	Recombinant Protein	GR-007
Protein		GT-0486
Protein	Fusion Protein	GXG-3
Protein	Fusion Protein	GXG-6
Protein	Protein	Haegarda
Protein	Protein	haptoglobin (human)
Protein	Fusion Protein	HB-0021
Protein	Protein	hemoglobin glutamer-250 (bovine)
Protein	Protein	hemoglobin raffimer
Protein	Recombinant Protein	HER-902
Protein	Recombinant Protein	HM-15912
Protein	Fusion Protein	HX-009
Protein	Fusion Protein	IBI-302
Protein	Fusion Protein	ICON-1
Protein	Fusion Protein	IGN-002
Protein	Fusion Protein	IMCF-106C
Protein	Fusion Protein	IMM-01
Protein	Protein	INB-03
Protein	Fusion Protein	inbakicept
Protein	Fusion Protein	INBRX-101
Protein	Protein	incobotulinumtoxin A
Protein	Protein	INS-068
Protein	Protein	interferon alfa
Protein	Recombinant Protein	interferon alfa-2a
Protein	Recombinant Protein	interferon alfa-2b
Protein	Recombinant Protein; Small	interferon alfa-2b + ribavirin
	Molecule
Protein	Recombinant Protein	interferon alfa-n3
Protein	Recombinant Protein	interferon alfacon-1
Protein	Recombinant Protein	interferon alpha-n1
Protein	Recombinant Protein	interferon beta-1a
Protein	Recombinant Protein	interferon beta-1b
Protein	Recombinant Protein	interferon gamma-1b
Protein	Recombinant Protein	IRL-201805
Protein	Recombinant Protein	KAN-101
Protein	Fusion Protein	KD-033
Protein	Protein	KER-050
Protein	Fusion Protein	KH-903
Protein	Recombinant Protein	KMRC-011
Protein	Recombinant Protein	Kovaltry
Protein	Recombinant Protein	KP-100IT
Protein	Recombinant Protein	lenograstim
Protein	Recombinant Protein	lepirudin
Protein	Fusion Protein	LEVI-04
Protein	Recombinant Protein	liatermin
Protein	Fusion Protein	LIB-003
Protein	Recombinant Protein	lipegfilgrastim
Protein	Fusion Protein	LMB-100
Protein	Recombinant Protein	lonapegsomatropin
Protein	Protein	LTI-01
Protein	Fusion Protein	luspatercept
Protein	Recombinant Protein	lusupultide
Protein	Recombinant Protein	lutropin alfa
Protein	Recombinant Protein	M-9241
Protein	Fusion Protein	MDNA-55
Protein	Recombinant Protein	mecasermin
Protein	Recombinant Protein	mecasermin rinfabate
Protein	Protein	Menopur
Protein	Protein	menotropins
Protein	Recombinant Protein	methoxy polyethylene glycol-epoetin beta
Protein	Recombinant Protein	metreleptin
Protein	Recombinant Protein	MG-29
Protein	Recombinant Protein	molgramostim
Protein	Recombinant Protein	MP-0250
Protein	Recombinant Protein	MP-0274
Protein	Recombinant Protein	MP-0310
Protein	Fusion Protein	MT-3724
Protein	Recombinant Protein	Multiferon
Protein	Recombinant Protein	Multikine
Protein	Recombinant Protein	NA-704
Protein	Fusion Protein	naptumomab estafenatox
Protein	Recombinant Protein	NE-180
Protein	Recombinant Protein	nepidermina
Protein	Recombinant Protein	NGM-386
Protein	Recombinant Protein	NGM-395
Protein	Fusion Protein	NGR-hTNF
Protein	Protein	nivobotulinumtoxin A
Protein	Fusion Protein	NIZ-985
Protein	Recombinant Protein	NKTR-255
Protein	Recombinant Protein	NKTR-358
Protein	Recombinant Protein	NL-201
Protein	Recombinant Protein	NMIL-121
Protein	Recombinant Protein	NN-7128
Protein	Protein	NN-9215
Protein	Recombinant Protein	NN-9499
Protein	Recombinant Protein	novaferon
Protein	Fusion Protein	NPT-088
Protein	Fusion Protein	NPT-189
Protein	Protein	NStride APS
Protein	Fusion Protein	olamkicept
Protein	Protein	onabotulinumtoxin A
Protein	Protein	onabotulinumtoxinA biosimilar
Protein	Protein	onabotulinumtoxinA SR
Protein	Recombinant Protein	Oncolipin-IT
Protein	Recombinant Protein	OPK-88005
Protein	Fusion Protein	oportuzumab monatox
Protein	Recombinant Protein	oprelvekin
Protein	Recombinant Protein	OPT-302
Protein	Protein	OTO-413
Protein	Fusion Protein	OXS-1550
Protein	Fusion Protein	OXS-3550
Protein	Recombinant Protein	palifermin
Protein	Fusion Protein	PB-1046
Protein	Recombinant Protein	PBB-8-IN
Protein	Recombinant Protein	PD-1 Antagonist + ropeginterferon alfa-2b
Protein	Recombinant Protein	PEG-EPO
Protein	Recombinant Protein	pegbelfermin
Protein	Recombinant Protein	pegfilgrastim
Protein	Recombinant Protein	pegilodecakin
Protein	Recombinant Protein	peginterferon alfa-2a
Protein	Recombinant Protein; Small	peginterferon alfa-2a + ribavirin
	Molecule
Protein	Recombinant Protein	peginterferon alfa-2b
Protein	Recombinant Protein; Small	peginterferon alfa-2b + ribavirin
	Molecule
Protein	Recombinant Protein	peginterferon beta-1a
Protein	Recombinant Protein	peginterferon lambda-1a
Protein	Recombinant Protein	pegvisomant
Protein	Fusion Protein	PF-06755347
Protein	Recombinant Protein	PIN-2
Protein	Protein	plasminogen (human)
Protein	Protein	plasminogen (human) 1
Protein	Fusion Protein	PR-15
Protein	Protein	prabotulinumtoxin A biosimilar
Protein	Recombinant Protein	Prolanta
Protein	Recombinant Protein	PRS-080
Protein	Fusion Protein	PRS-343
Protein	Recombinant Protein	PRT-01
Protein	Protein	PRTX-100
Protein	Fusion Protein	PT-101
Protein	Recombinant Protein	PTR-01
Protein	Recombinant Protein	PTX-9908
Protein	Fusion Protein	QL-1207
Protein	Fusion Protein	RC-28
Protein	Recombinant Protein	RecD-1
Protein	Recombinant Protein	Recombinant Factor VIII Replacement for
		Hemophilia A
Protein	Recombinant Protein	Recombinant Plasma Gelsolin Replacement for
		Infectious Disease
Protein	Recombinant Protein	Recombinant Protein to Agonize BMPR1A,
		BMPR1B and BMPR2 for Colorectal Cancer and
		Glioblastoma Multiforme
Protein	Recombinant Protein	Recombinant Protein to Agonize IFNAR1 and
		IFNAR2 for Oncology
Protein	Recombinant Protein	Recombinant Protein to Inhibit CD13 for
		Lymphoma and Solid Tumor
Protein	Recombinant Protein	Recombinant Protein to Inhibit Coagulation Factor
		XIV for Hemophilia A and Hemophilia B
Protein	Recombinant Protein	Recombinant Protein to Target FLT1 for Pre-
		Eclampsia
Protein	Fusion Protein	reveglucosidase alfa
Protein	Fusion Protein	RG-6290
Protein	Fusion Protein	RG-7461
Protein	Fusion Protein	RG-7835
Protein	Recombinant Protein	RG-7880
Protein	Fusion Protein	rilonacept
Protein	Protein	rimabotulinumtoxin B
Protein	Recombinant Protein	RMC-035
Protein	Fusion Protein	RO-7227166
Protein	Fusion Protein	romiplostim
Protein	Fusion Protein	romiplostim biosimilar
Protein	Recombinant Protein	ropeginterferon alfa-2b
Protein	Recombinant Protein	RP-72
Protein	Fusion Protein	RPH-104
Protein	Fusion Protein	RPH-203
Protein	Fusion Protein	RSLV-132
Protein	Protein	RT-002
Protein	Fusion Protein	SAL-016
Protein	Recombinant Protein	Sanguinate
Protein	Fusion Protein	SAR-442085
Protein	Recombinant Protein	sargramostim
Protein	Recombinant Protein	SC-0806
Protein	Fusion Protein	SCB-313
Protein	Recombinant Protein	serelaxin
Protein	Fusion Protein	SFR-9216
Protein	Recombinant Protein	SHP-608
Protein	Fusion Protein	SHR-1501
Protein	Recombinant Protein	SIM-0710
Protein	Fusion Protein	SL-279252
Protein	Fusion Protein	SOC-101
Protein	Recombinant Protein	somapacitan
Protein	Recombinant Protein	somatropin
Protein	Recombinant Protein	somatropin pegol
Protein	Recombinant Protein	somatropin PR
Protein	Recombinant Protein	somatropin SR
Protein	Recombinant Protein	somavaratan
Protein	Fusion Protein	sotatercept
Protein	Recombinant Protein	sprifermin
Protein	Recombinant Protein	SubQ-8
Protein	Recombinant Protein	Sylatron
Protein	Fusion Protein	T-Guard
Protein	Recombinant Protein	TA-46
Protein	Recombinant Protein	tadekinig alfa
Protein	Fusion Protein	tagraxofusp
Protein	Protein	TAK-101
Protein	Fusion Protein	TAK-169
Protein	Fusion Protein	TAK-573
Protein	Fusion Protein	TAK-671
Protein	Fusion Protein	talditercept alfa
Protein	Recombinant Protein	tasonermin
Protein	Recombinant Protein	TBI-302
Protein	Recombinant Protein	tbo-filgrastim
Protein	Fusion Protein	tebentafusp
Protein	Fusion Protein	Teleukin
Protein	Fusion Protein	telitacicept
Protein	Fusion Protein	TG-103
Protein	Recombinant Protein	THOR-707
Protein	Recombinant Protein	thrombomodulin alfa
Protein	Recombinant Protein	thrombopoietin
Protein	Recombinant Protein	thyrotropin alfa
Protein	Recombinant Protein	tiprelestat
Protein	Recombinant Protein	topsalysin
Protein	Recombinant Protein	TransMID
Protein	Fusion Protein	trebananib
Protein	Fusion Protein	TTI-621
Protein	Fusion Protein	TTI-622
Protein	Fusion Protein	tucotuzumab celmoleukin
Protein	Recombinant Protein	TVN-102
Protein	Fusion Protein	UCHT-1
Protein	Fusion Protein	VAL-1221
Protein	Fusion Protein	Vas-01
Protein	Recombinant Protein	vatreptacog alfa (activated)
Protein	Fusion Protein	VB-4847
Protein	Recombinant Protein	von willebrand factor (recombinant)
Protein	Fusion Protein	YSPSL
Protein	Fusion Protein	ziv-aflibercept
Protein	Protein	ZK-001
Protein	Recombinant Protein	Zorbtive

B. Enzymes

The exogenous polypeptide may be an enzyme, e.g., an enzyme that catalyzes a biological reaction that is of use in the prevention or treatment of a condition or a disease, the prevention or treatment of a pathogen infection, the diagnosis of a disease, or the diagnosis of a disease or condition.

The enzyme may be a recombination enzyme, e.g., a Cre recombinase enzyme. In some aspects, the Cre recombinase enzyme is delivered by a PMP to a cell comprising a Cre reporter construct.

The enzyme may be an editing enzyme, e.g., a gene editing enzyme. In some aspects, the gene editing enzyme is a, e.g., a component of a CRISPR-Cas system (e.g., a Cas9 enzyme), a TALEN, or a zinc finger nuclease.

C. Pathogen Control Agents

The exogenous polypeptide may be a pathogen control agent, e.g., a polypeptide that is an antibacterial, antifungal, insecticidal, nematicidal, antiparasitic, or virucidal. In some instances, the PMP or PMP composition described herein includes a polypeptide or functional fragments or derivative thereof, that targets pathways in the pathogen. A PMP composition including a polypeptide as described herein can be administered to a pathogen, a vector thereof, in an amount and for a time sufficient to: (a) reach a target level (e.g., a predetermined or threshold level) of polypeptide concentration; and (b) decrease or eliminate the pathogen. In some instances, a PMP composition including a polypeptide as described herein can be administered to an animal having or at risk of an infection by a pathogen in an amount and for a time sufficient to: (a) reach a target level (e.g., a predetermined or threshold level) of polypeptide concentration in the animal; and (b) decrease or eliminate the pathogen. The polypeptides described herein may be formulated in a PMP composition for any of the methods described herein, and in certain instances, may be associated with the PMP thereof.

Examples of polypeptides that can be used herein can include an enzyme (e.g., a metabolic recombinase, a helicase, an integrase, a RNAse, a DNAse, or an ubiquitination protein), a pore-forming protein, a signaling ligand, a cell penetrating peptide, a transcription factor, a receptor, an antibody, a nanobody, a gene editing protein (e.g., CRISPR-Cas system, TALEN, or zinc finger), riboprotein, a protein aptamer, or a chaperone.

The PMP described herein may include a bacteriocin. In some instances, the bacteriocin is naturally produced by Gram-positive bacteria, such as Pseudomonas, Streptomyces, Bacillus, Staphylococcus, or lactic acid bacteria (LAB, such as Lactococcus lactis). In some instances, the bacteriocin is naturally produced by Gram-negative bacteria, such as Hafnia alvei, Citrobacter freundii, Klebsiella oxytoca, Klebsiella pneumonia, Enterobacter cloacae, Serratia plymithicum, Xanthomonas campestris, Erwinia carotovora, Ralstonia solanacearum, or Escherichia coli. Exemplary bacteriocins include, but are not limited to, Class I-IV LAB antibiotics (such as lantibiotics), colicins, microcins, and pyocins.

The PMP described herein may include an antimicrobial peptide (AMP). Any AMP suitable for inhibiting a microorganism may be used. AMPs are a diverse group of molecules, which are divided into subgroups on the basis of their amino acid composition and structure. The AMP may be derived or produced from any organism that naturally produces AMPs, including AMPs derived from plants (e.g., copsin), insects (e.g., mastoparan, poneratoxin, cecropin, moricin, melittin), frogs (e.g., magainin, dermaseptin, aurein), and mammals (e.g., cathelicidins, defensins and protegrins).

IV. Methods for Producing a PMP Comprising an Exogenous Polypeptide

In another aspect, the disclosure, in general, features a method of producing a PMP comprising an exogenous polypeptide. The method accordingly comprises (a) providing a solution comprising the exogenous polypeptide; and (b) loading the PMP with the exogenous polypeptide, wherein the loading causes the exogenous polypeptide to be encapsulated by the PMP.

The exogenous polypeptide may be placed in a solution, e.g., a phosphate-buffered saline (PBS) solution. The exogenous polypeptide may or may not be soluble in the solution. If the polypeptide is not soluble in the solution, the pH of the solution may be adjusted until the polypeptide is soluble in the solution. Insoluble polypeptides are also useful for loading.

Loading of the PMP with the exogenous polypeptide may comprise or consist of sonication of a solution comprising the exogenous polypeptide (e.g., a soluble or insoluble exogenous polypeptide) and a plurality of PMPs to induce poration of the PMPs and diffusion of the polypeptide into the PMPs, e.g., sonication according to the protocol described in Wang et al., Nature Comm., 4: 1867, 2013.

Alternatively, loading of the PMP with the exogenous polypeptide may comprise or consist of electroporation of a solution comprising the exogenous polypeptide (e.g., a soluble or insoluble exogenous polypeptide) and a plurality of PMPs, e.g., electroporation according to the protocol described in Wahlgren et al., Nucl. Acids. Res., 40(17), e130, 2012.

Alternatively, a small amount of a detergent (e.g., saponin) can be added to increase loading of the exogenous polypeptide into PMPs, e.g., as described in Fuhrmann et al., J Control Release., 205: 35-44, 2015.

Loading of the PMP with the exogenous polypeptide may comprise or consist of lipid extraction and lipid extrusion. Briefly, PMP lipids may be isolated by adding MeOH:CHCl₃ (e.g., 3.75 mL 2:1 (v/v) MeOH:CHCl₃) to PMPs in a PBS solution (e.g., 1 mL of PMPs in PBS) and vortexing the mixture. CHCl₃ (e.g., 1.25 mL) and ddH₂O (e.g., 1.25 mL) are then added sequentially and vortexed. The mixture is then centrifuged at 2,000 r.p.m. for 10 min at 22° C. in glass tubes to separate the mixture into two phases (aqueous phase and organic phase). The organic phase sample containing the PMP lipids is dried by heating under nitrogen (2 psi). To produce polypeptide-loaded PMPs, the isolated PMP lipids are mixed with the polypeptide solution and passed through a lipid extruder, e.g., according to the protocol from Haney et al., J Control Release, 207: 18-30, 2015.

PMP lipids may also be isolated using methods that isolate additional plant lipid classes, e.g., glycosylinositol phosphorylceramides (GIPCs), as described in Casas et al., Plant Physiology, 170: 367-384, 2016. Briefly, to extract PMP lipids including GIPCs, chloroform:methanol:HCl (e.g., 3.5 mL of chloroform:methanol:HCl (200:100:1, v/v/v)) plus butylated hydroxytoluene (e.g., 0.01% (w/v) of butylated hydroxytoluene) is added to and incubated with the PMPs. Next, NaCl (e.g., 2 mL of 0.9% (w/v) NaCl) is added and vortexed for 5 minutes. The sample is then centrifuged to induce the organic phase to aggregate at the bottom of the glass tube, and the organic phase is collected. The upper phase may undergo reextraction with chloroform (e.g., 4 mL of pure chloroform) to isolate lipids. The organic phases are combined and dried. After drying, the aqueous phase is resuspended in water (e.g., 1 mL of pure water) and GIPCs are back-extracted using butanol-1 (e.g., 1 mL of butanol-1) twice. To produce polypeptide-loaded PMPs, the isolated PMP lipid phases are mixed with the polypeptide solution and are passed through a lipid extruder according to the protocol from Haney et al., J Control Release, 207: 18-30, 2015. Alternatively, lipids may be extracted with methyl tertiary-butyl ether (MTBE):methanol:water plus butylated hydroxytoluene (BHT) or with propan-2-ol:hexane:water.

In some aspects, isolated GIPCs may be added to isolated PMP lipids.

In some aspects, loading of the PMP with the exogenous polypeptide comprises sonication and lipid extrusion, as described above.

In some aspects the exogenous polypeptide may be pre-complexed (e.g., using protamine sulfate), or a cationic lipid (e.g., DOTAP) may be added to facilitate encapsulation of negatively charged proteins.

Before use, the loaded PMPs may be purified, e.g., as described in Example 2, to remove polypeptides that are not bound to or encapsulated by the PMP. Loaded PMPs may be characterized as described in Example 3, and their stability may be tested as described in Example 4. Loading of the exogenous polypeptide may be quantified by methods known in the art for the quantification of proteins. For example, the Pierce Quantitative Colorimetric Peptide Assay may be used on a small sample of the loaded and unloaded PMPs, or a Western blot using specific antibodies may be used to detect the exogenous polypeptide. Alternatively, polypeptides may be fluorescently labeled, and fluorescence may be used to determine the labeled exogenous polypeptide concentration in loaded and unloaded PMPs.

V. Therapeutic Methods

The PMPs and PMP compositions described herein are useful in a variety of therapeutic methods, particularly for the prevention or treatment of a condition or disease or for the prevention or treatment of pathogen infections in animals. The present methods involve delivering the PMP compositions described herein to an animal.

Provided herein are methods of administering to an animal a PMP composition disclosed herein. The methods can be useful for preventing or treating a condition or disease or for preventing a pathogen infection in an animal.

For example, provided herein is a method of treating an animal having a fungal infection, wherein the method includes administering to the animal an effective amount of a PMP composition including a plurality of PMPs, wherein the plurality of PMPs comprise an exogenous polypeptide that is a pathogen control agent, e.g., an antifungal agent. In some instances, the fungal infection is caused by Candida albicans. In some instances, the method decreases or substantially eliminates the fungal infection.

In another aspect, provided herein is a method of treating an animal having a bacterial infection, wherein the method includes administering to the animal an effective amount of a PMP composition including a plurality of PMPs. In some instances, the method includes administering to the animal an effective amount of a PMP composition including a plurality of PMPs, wherein the plurality of PMPs comprise an exogenous polypeptide that is a pathogen control agent, e.g., an antibacterial agent. In some instances, the bacterium is a Streptococcus spp., Pneumococcus spp., Pseudomonas spp., Shigella spp, Salmonella spp., Campylobacter spp., or an Escherichia spp. In some instances, the method decreases or substantially eliminates the bacterial infection. In some instances, the animal is a human, a veterinary animal, or a livestock animal.

The present methods are useful to treat an infection (e.g., as caused by an animal pathogen) in an animal, which refers to administering treatment to an animal already suffering from a disease to improve or stabilize the animal's condition. This may involve reducing colonization of a pathogen in, on, or around an animal by one or more pathogens (e.g., by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100%) relative to a starting amount and/or allow benefit to the individual (e.g., reducing colonization in an amount sufficient to resolve symptoms). In such instances, a treated infection may manifest as a decrease in symptoms (e.g., by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100%). In some instances, a treated infection is effective to increase the likelihood of survival of an individual (e.g., an increase in likelihood of survival by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100%) or increase the overall survival of a population (e.g., an increase in likelihood of survival by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or 100%). For example, the compositions and methods may be effective to “substantially eliminate” an infection, which refers to a decrease in the infection in an amount sufficient to sustainably resolve symptoms (e.g., for at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 months) in the animal.

The present methods are useful to prevent an infection (e.g., as caused by an animal pathogen), which refers to preventing an increase in colonization in, on, or around an animal by one or more pathogens (e.g., by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or more than 100% relative to an untreated animal) in an amount sufficient to maintain an initial pathogen population (e.g., approximately the amount found in a healthy individual), prevent the onset of an infection, and/or prevent symptoms or conditions associated with infection. For example, individuals may receive prophylaxis treatment to prevent a fungal infection while being prepared for an invasive medical procedure (e.g., preparing for surgery, such as receiving a transplant, stem cell therapy, a graft, a prosthesis, receiving long-term or frequent intravenous catheterization, or receiving treatment in an intensive care unit), in immunocompromised individuals (e.g., individuals with cancer, with HIV/AIDS, or taking immunosuppressive agents), or in individuals undergoing long term antibiotic therapy.

The PMP composition can be formulated for administration or administered by any suitable method, including, for example, orally, intravenously, intramuscularly, subcutaneously, intradermally, percutaneously, intraarterially, intraperitoneally, intralesionally, intracranially, intraarticularly, intraprostatically, intrapleurally, intratracheally, intrathecally, intranasally, intravaginally, intrarectally, topically, intratumorally, peritoneally, subconjunctivally, intravesicularly, mucosally, intrapericardially, intraumbilically, intraocularly, intraorbitally, topically, transdermally, intravitreally (e.g., by intravitreal injection), by eye drop, by inhalation (e.g., by a nebulizer), by injection, by implantation, by infusion, by continuous infusion, by localized perfusion bathing target cells directly, by catheter, by lavage, in cremes, or in lipid compositions. The compositions utilized in the methods described herein can also be administered systemically or locally. The method of administration can vary depending on various factors (e.g., the compound or composition being administered and the severity of the condition, disease, or disorder being treated). In some instances, the PMP composition is administered intravenously, intramuscularly, subcutaneously, topically, orally, transdermally, intraperitoneally, intraorbitally, by implantation, by inhalation, intrathecally, intraventricularly, or intranasally. Dosing can be by any suitable route, e.g., orally or by injections, such as intravenous or subcutaneous injections, depending in part on whether the administration is brief or chronic. Various dosing schedules including but not limited to single or multiple administrations over various time-points, bolus administration, and pulse infusion are contemplated herein.

For the prevention or treatment of an infection described herein (when used alone or in combination with one or more other additional therapeutic agents) will depend on the type of disease to be treated, the severity and course of the disease, whether the is administered for preventive or therapeutic purposes, previous therapy, the patient's clinical history and response to the PMP composition. The PMP composition can be, e.g., administered to the patient at one time or over a series of treatments. For repeated administrations over several days or longer, depending on the condition, the treatment would generally be sustained until a desired suppression of disease symptoms occurs or the infection is no longer detectable. Such doses may be administered intermittently, e.g., every week or every two weeks (e.g., such that the patient receives, for example, from about two to about twenty, doses of the PMP composition. An initial higher loading dose, followed by one or more lower doses may be administered. However, other dosage regimens may be useful. The progress of this therapy is easily monitored by conventional techniques and assays.

In some instances, the amount of the PMP composition administered to individual (e.g., human) may be in the range of about 0.01 mg/kg to about 5 g/kg (e.g., about 0.01 mg/kg-0.1 mg/kg, about 0.1 mg/kg-1 mg/kg, about 1 mg/kg-10 mg/kg, about 10 mg/kg-100 mg/kg, about 100 mg/kg-1 g/kg, or about 1 g/kg-5 g/kg), of the individual's body weight. In some instances, the amount of the PMP composition administered to individual (e.g., human) is at least 0.01 mg/kg (e.g., at least 0.01 mg/kg, at least 0.1 mg/kg, at least 1 mg/kg, at least 10 mg/kg, at least 100 mg/kg, at least 1 g/kg, or at least 5 g/kg), of the individual's body weight. The dose may be administered as a single dose or as multiple doses (e.g., 2, 3, 4, 5, 6, 7, or more than 7 doses). In some instances, the PMP composition administered to the animal may be administered alone or in combination with an additional therapeutic agent or pathogen control agent. The dose of an antibody administered in a combination treatment may be reduced as compared to a single treatment. The progress of this therapy is easily monitored by conventional techniques.

In one aspect, the disclosure features a method for treating diabetes, the method comprising administering to a subject in need thereof an effective amount of a composition comprising a plurality of PMPs, wherein one or more exogenous polypeptides are encapsulated by the PMP. The administration of the plurality of PMPs may lower the blood sugar of the subject. In some aspects, the exogenous polypeptide is insulin.

VI. Agricultural Methods

The PMP compositions described herein are useful in a variety of agricultural methods, particularly for the prevention or treatment of pathogen infections in animals and for the control of the spread of such pathogens, e.g., by pathogen vectors. The present methods involve delivering the PMP compositions described herein to a pathogen or a pathogen vector.

The compositions and related methods can be used to prevent infestation by or reduce the numbers of pathogens or pathogen vectors in any habitats in which they reside (e.g., outside of animals, e.g., on plants, plant parts (e.g., roots, fruits and seeds), in or on soil, water, or on another pathogen or pathogen vector habitat. Accordingly, the compositions and methods can reduce the damaging effect of pathogen vectors by for example, killing, injuring, or slowing the activity of the vector, and can thereby control the spread of the pathogen to animals. Compositions disclosed herein can be used to control, kill, injure, paralyze, or reduce the activity of one or more of any pathogens or pathogen vectors in any developmental stage, e.g., their egg, nymph, instar, larvae, adult, juvenile, or desiccated forms. The details of each of these methods are described further below.

A. Delivery to a Pathogen

Provided herein are methods of delivering a PMP composition to a pathogen, such as one disclosed herein, by contacting the pathogen with a PMP composition comprising an exogenous polypeptide, e.g., a pathogen control agent. The methods can be useful for decreasing the fitness of a pathogen, e.g., to prevent or treat a pathogen infection or control the spread of a pathogen as a consequence of delivery of the PMP composition. Examples of pathogens that can be targeted in accordance with the methods described herein include bacteria (e.g., Streptococcus spp., Pneumococcus spp., Pseudomonas spp., Shigella spp, Salmonella spp., Campylobacter spp., or an Escherichia spp), fungi (Saccharomyces spp. or a Candida spp), parasitic insects (e.g., Cimex spp), parasitic nematodes (e.g., Heligmosomoides spp), or parasitic protozoa (e.g., Trichomoniasis spp).

For example, provided herein is a method of decreasing the fitness of a pathogen, the method including delivering to the pathogen any of the compositions described herein, wherein the method decreases the fitness of the pathogen relative to an untreated pathogen. In some embodiments, the method includes delivering a PMP composition comprising an exogenous polypeptide, e.g., a pathogen control agent to at least one habitat where the pathogen grows, lives, reproduces, feeds, or infests. In some instances of the methods described herein, the composition is delivered as a pathogen comestible composition for ingestion by the pathogen. In some instances of the methods described herein, the composition is delivered (e.g., to a pathogen) as a liquid, a solid, an aerosol, a paste, a gel, or a gas.

Also provided herein is a method of decreasing the fitness of a parasitic insect, wherein the method includes delivering to the parasitic insect a PMP composition including a plurality of PMPs comprising an exogenous polypeptide, e.g., a pathogen control agent. For example, the parasitic insect may be a bedbug. Other non-limiting examples of parasitic insects are provided herein. In some instances, the method decreases the fitness of the parasitic insect relative to an untreated parasitic insect

Additionally provided herein is a method of decreasing the fitness of a parasitic nematode, wherein the method includes delivering to the parasitic nematode a PMP composition including a plurality of PMPs comprising an exogenous polypeptide, e.g., a pathogen control agent. For example, the parasitic nematode is Heligmosomoides polygyrus. Other non-limiting examples of parasitic nematodes are provided herein. In some instances, the method decreases the fitness of the parasitic nematode relative to an untreated parasitic nematode.

Further provided herein is a method of decreasing the fitness of a parasitic protozoan, wherein the method includes delivering to the parasitic protozoan a PMP composition including a plurality of PMPs comprising an exogenous polypeptide, e.g., a pathogen control agent. For example, the parasitic protozoan may be T. vaginalis. Other non-limiting examples of parasitic protozoans are provided herein. In some instances, the method decreases the fitness of the parasitic protozoan relative to an untreated parasitic protozoan.

A decrease in the fitness of the pathogen as a consequence of delivery of a PMP composition can manifest in a number of ways. In some instances, the decrease in fitness of the pathogen may manifest as a deterioration or decline in the physiology of the pathogen (e.g., reduced health or survival) as a consequence of delivery of the PMP composition. In some instances, the fitness of an organism may be measured by one or more parameters, including, but not limited to, reproductive rate, fertility, lifespan, viability, mobility, fecundity, pathogen development, body weight, metabolic rate or activity, or survival in comparison to a pathogen to which the PMP composition has not been administered. For example, the methods or compositions provided herein may be effective to decrease the overall health of the pathogen or to decrease the overall survival of the pathogen. In some instances, the decreased survival of the pathogen is about 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or greater than 100% greater relative to a reference level (e.g., a level found in a pathogen that does not receive a PMP composition comprising an exogenous polypeptide, e.g., a pathogen control agent. In some instances, the methods and compositions are effective to decrease pathogen reproduction (e.g., reproductive rate, fertility) in comparison to a pathogen to which the PMP composition has not been administered. In some instances, the methods and compositions are effective to decrease other physiological parameters, such as mobility, body weight, life span, fecundity, or metabolic rate, by about 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or greater than 100% relative to a reference level (e.g., a level found in a pathogen that does not receive a PMP composition).

In some instances, the decrease in pest fitness may manifest as an increase in the pathogen's sensitivity to an antipathogen agent and/or a decrease in the pathogen's resistance to an antipathogen agent in comparison to a pathogen to which the PMP composition has not been delivered. In some instances, the methods or compositions provided herein may be effective to increase the pathogen's sensitivity to a pesticidal agent by about 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or greater than 100% relative to a reference level (e.g., a level found in a pest that does not receive a PMP composition).

In some instances, the decrease in pathogen fitness may manifest as other fitness disadvantages, such as a decreased tolerance to certain environmental factors (e.g., a high or low temperature tolerance), a decreased ability to survive in certain habitats, or a decreased ability to sustain a certain diet in comparison to a pathogen to which the pathogen control (composition has not been delivered. In some instances, the methods or compositions provided herein may be effective to decrease pathogen fitness in any plurality of ways described herein. Further, the PMP composition may decrease pathogen fitness in any number of pathogen classes, orders, families, genera, or species (e.g., 1 pathogen species, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30, 40, 50, 60, 70, 80, 90, 100, 150, 200, 200, 250, 500, or more pathogen species). In some instances, the PMP composition acts on a single pest class, order, family, genus, or species.

Pathogen fitness may be evaluated using any standard methods in the art. In some instances, pest fitness may be evaluated by assessing an individual pathogen. Alternatively, pest fitness may be evaluated by assessing a pathogen population. For example, a decrease in pathogen fitness may manifest as a decrease in successful competition against other pathogens, thereby leading to a decrease in the size of the pathogen population.

VII. Methods for Treatment of Pathogens or Vectors Thereof

The PMP compositions and related methods described herein are useful to decrease the fitness of an animal pathogen and thereby treat or prevent infections in animals. Examples of animal pathogens, or vectors thereof, that can be treated with the present compositions or related methods are further described herein.

A. Fungi

The PMP compositions and related methods can be useful for decreasing the fitness of a fungus, e.g., to prevent or treat a fungal infection in an animal. Included are methods for delivering a PMP composition to a fungus by contacting the fungus with the PMP composition. Additionally or alternatively, the methods include preventing or treating a fungal infection (e.g., caused by a fungus described herein) in an animal at risk of or in need thereof, by administering to the animal a PMP composition.

The PMP compositions and related methods are suitable for treatment or preventing of fungal infections in animals, including infections caused by fungi belonging to Ascomycota (Fusarium oxysporum, Pneumocystis jirovecii, Aspergillus spp., Coccidioides immitis/posadasii, Candida albicans), Basidiomycota (Filobasidiella neoformans, Trichosporon), Microsporidia (Encephalitozoon cuniculi, Enterocytozoon bieneusi), Mucoromycotina (Mucor circinelloides, Rhizopus oryzae, Lichtheimia corymbifera).

In some instances, the fungal infection is one caused by a belonging to the phylum Ascomycota, Basidomycota, Chytridiomycota, Microsporidia, or Zygomycota. The fungal infection or overgrowth can include one or more fungal species, e.g., Candida albicans, C. tropicalis, C. parapsilosis, C. glabrata, C. auris, C. krusei, Saccharomyces cerevisiae, Malassezia globose, M. restricta, or Debaryomyces hansenii, Gibberella moniliformis, Alternaria brassicicola, Cryptococcus neoformans, Pneumocystis carinii, P. jirovecii, P. murina, P. oryctolagi, P. wakefieldiae, and Aspergillus clavatus. The fungal species may be considered a pathogen or an opportunistic pathogen.

In some instances, the fungal infection is caused by a fungus in the genus Candida (i.e., a Candida infection). For example, a Candida infection can be caused by a fungus in the genus Candida that is selected from the group consisting of C. albicans, C. glabrata, C. dubliniensis, C. krusei, C. auris, C. parapsilosis, C. tropicalis, C. orthopsilosis, C. guilliermondii, C. rugose, and C. lusitaniae. Candida infections that can be treated by the methods disclosed herein include, but are not limited to candidemia, oropharyngeal candidiasis, esophageal candidiasis, mucosal candidiasis, genital candidiasis, vulvovaginal candidiasis, rectal candidiasis, hepatic candidiasis, renal candidiasis, pulmonary candidiasis, splenic candidiasis, otomycosis, osteomyelitis, septic arthritis, cardiovascular candidiasis (e.g., endocarditis), and invasive candidiasis.

B. Bacteria

The PMP compositions and related methods can be useful for decreasing the fitness of a bacterium, e.g., to prevent or treat a bacterial infection in an animal. Included are methods for administering a PMP composition to a bacterium by contacting the bacteria with the PMP composition. Additionally or alternatively, the methods include preventing or treating a bacterial infection (e.g., caused by a bacteria described herein) in an animal at risk of or in need thereof, by administering to the animal a PMP composition.

The PMP compositions and related methods are suitable for preventing or treating a bacterial infection in animals caused by any bacteria described further below. For example, the bacteria may be one belonging to Bacillales (B. anthracis, B. cereus, S. aureus, L. monocytogenes), Lactobacillales (S. pneumoniae, S. pyogenes), Clostridiales (C. botulinum, C. difficile, C. perfringens, C. tetani), Spirochaetales (Borrelia burgdorferi, Treponema pallidum), Chlamydiales (Chlamydia trachomatis, Chlamydophila psittaci), Actinomycetales (C. diphtheriae, Mycobacterium tuberculosis, M. avium), Rickettsiales (R. prowazekii, R. rickettsii, R. typhi, A. phagocytophilum, E. chaffeensis), Rhizobiales (Brucella melitensis), Burkholderiales (Bordetella pertussis, Burkholderia mallei, B. pseudomallei), Neisseriales (Neisseria gonorrhoeae, N. meningitidis), Campylobacterales (Campylobacter jejuni, Helicobacter pylon), Legionellales (Legionella pneumophila), Pseudomonadales (A. baumannii, Moraxella catarrhalis, P. aeruginosa), Aeromonadales (Aeromonas sp.), Vibrionales (Vibrio cholerae, V. parahaemolyticus), Thiotrichales, Pasteurellales (Haemophilus influenzae), Enterobacteriales (Klebsiella pneumoniae, Proteus mirabilis, Yersinia pestis, Y. enterocolitica, Shigella flexneri, Salmonella enterica, E. coli).

EXAMPLES

The following are examples of the various methods of the invention. It is understood that various other embodiments may be practiced, given the general description provided above.

Example 1: Crude Isolation of Plant Messenger Packs from Plants

This example describes the crude isolation of plant messenger packs (PMPs) from various plant sources, including the leaf apoplast, seed apoplast, root, fruit, vegetable, pollen, phloem, xylem sap and plant cell culture medium.

Experimental Design:

a) PMP Isolation from the Apoplast of Arabidopsis thaliana Leaves

Arabidopsis (Arabidopsis thaliana Col-0) seeds are surface sterilized with 50% bleach and plated on 0.53 Murashige and Skoog medium containing 0.8% agar. The seeds are vernalized for 2 d at 4° C. before being moved to short-day conditions (9-h days, 22° C., 150 μEm⁻²). After 1 week, the seedlings are transferred to Pro-Mix PGX. Plants are grown for 4-6 weeks before harvest.

PMPs are isolated from the apoplastic wash of 4-6-week old Arabidopsis rosettes, as described by Rutter and Innes, Plant Physiol., 173(1): 728-741, 2017. Briefly, whole rosettes are harvested at the root and vacuum infiltrated with vesicle isolation buffer (20 mM MES, 2 mM CaCl₂, and 0.1 M NaCl, pH 6).

Infiltrated plants are carefully blotted to remove excess fluid, placed inside 30-mL syringes, and centrifuged in 50 mL conical tubes at 700 g for 20 min at 2° C. to collect the apoplast extracellular fluid containing PMPs. Next, the apoplast extracellular fluid is filtered through a 0.85 μm filter to remove large particles, and PMPs are purified as described in Example 2.

b) PMP Isolation from the Apoplast of Sunflower Seeds

Intact sunflower seeds (H. annuus L.) and are imbibed in water for 2 hours, peeled to remove the pericarp, and the apoplastic extracellular fluid is extracted by a modified vacuum infiltration-centrifugation procedure, adapted from Regente et al., FEBS Letters, 583: 3363-3366, 2009. Briefly, seeds are immersed in vesicle isolation buffer (20 mM MES, 2 mM CaCl₂, and 0.1 M NaCl, pH 6) and subjected to three vacuum pulses of 10 s, separated by 30 s intervals at a pressure of 45 kPa. The infiltrated seeds are recovered, dried on filter paper, placed in fritted glass filters, and centrifuged for 20 min at 400 g at 4° C. The apoplast extracellular fluid is recovered, filtered through a 0.85 μm filter to remove large particles, and PMPs are purified as described in Example 2.

c) PMP Isolation from Ginger Roots

Fresh ginger (Zingiber officinale) rhizomes are purchased from a local supplier and washed 3× with PBS. A total of 200 grams of washed roots is ground in a mixer (Osterizer 12-speed blender) at the highest speed for 10 min (pause 1 min for every 1 min of blending), and PMPs are isolated as described in Zhuang et al., J Extracellular Vesicles, 4(1): 28713, 2015. Briefly, gingerjuice is sequentially centrifuged at 1,000 g for 10 min, 3,000 g for 20 min and 10,000 g for 40 min to remove large particles from the PMP-containing supernatant. PMPs are purified as described in Example 2.

d) PMP Isolation from Grapefruit Juice

Fresh grapefruits (Citrus x paradisi) are purchased from a local supplier, the skins are removed, and the fruit is manually pressed, or ground in a mixer (Osterizer 12-speed blender) at the highest speed for 10 min (pause 1 min for every minute of blending) to collect the juice, as described by Wang et al., Molecular Therapy, 22(3): 522-534, 2014 with minor modifications. Briefly, juice/juice pulp is sequentially centrifuged at 1,000 g for 10 min, 3,000 g for 20 min, and 10,000 g for 40 min to remove large particles from the PMP-containing supernatant. PMPs are purified as described in Example 2.

e) PMP Isolation from a Broccoli Vegetable

Broccoli (Brassica oleracea var. italica) PMPs are isolated as previously described (Deng et al., Molecular Therapy, 25(7): 1641-1654, 2017). Briefly, fresh broccoli is purchased from a local supplier, washed three times with PBS, and ground in a mixer (Osterizer 12-speed blender) at the highest speed for 10 min (pause 1 min for every minute of blending). Broccoli juice is then sequentially centrifuged at 1,000 g for 10 min, 3,000 g for 20 min, and 10,000 g for 40 min to remove large particles from the PMP-containing supernatant. PMPs are purified as described in Example 2.

f) PMP Isolation from Olive Pollen

Olive (Olea europaea) pollen PMPs are isolated as previously described in Prado et al., Molecular Plant. 7(3):573-577, 2014. Briefly, olive pollen (0.1 g) is hydrated in a humid chamber at room temperature for 30 min before transferring to petri dishes (15 cm in diameter) containing 20 ml germination medium: 10% sucrose, 0.03% Ca(NO₃)₂, 0.01% KNO₃, 0.02% MgSO₄, and 0.03% H₃BO₃. Pollen is germinated at 30° C. in the dark for 16 h. Pollen grains are considered germinated only when the tube is longer than the diameter of the pollen grain. Cultured medium containing PMPs is collected and cleared of pollen debris by two successive filtrations on 0.85 um filters by centrifugation. PMPs are purified as described in Example 2.

g) PMP Isolation from Arabidopsis Phloem Sap

Arabidopsis (Arabidopsis thaliana Col-0) seeds are surface sterilized with 50% bleach and plated on 0.53 Murashige and Skoog medium containing 0.8% agar. The seeds are vernalized for 2 d at 4° C. before being moved to short-day conditions (9-h days, 22° C., 150 μEm⁻²). After 1 week, the seedlings are transferred to Pro-Mix PGX. Plants are grown for 4-6 weeks before harvest.

Phloem sap from 4-6-week old Arabidopsis rosette leaves is collected as described by Tetyuk et al., JoVE. 80, 2013. Briefly, leaves are cut at the base of the petiole, stacked, and placed in a reaction tube containing 20 mM K2-EDTA for one hour in the dark to prevent sealing of the wound. Leaves are gently removed from the container, washed thoroughly with distilled water to remove all EDTA, put in a clean tube, and phloem sap is collected for 5-8 hours in the dark. Leaves are discarded, phloem sap is filtered through a 0.85 μm filter to remove large particles, and PMPs are purified as described in Example 2.

h) PMP Isolation from Tomato Plant Xylem Sap

Tomato (Solanum lycopersicum) seeds are planted in a single pot in an organic-rich soil, such as Sunshine Mix (Sun Gro Horticulture, Agawam, Mass.) and maintained in a greenhouse between 22° C. and 28° C. About two weeks after germination, at the two true-leaf stage, the seedlings are transplanted individually into pots (10 cm diameter and 17 cm deep) filled with sterile sandy soil containing 90% sand and 10% organic mix. Plants are maintained in a greenhouse at 22-28° C. for four weeks.

Xylem sap from 4-week old tomato plants is collected as described by Kohlen et al., Plant Physiology. 155(2):721-734, 2011. Briefly, tomato plants are decapitated above the hypocotyl, and a plastic ring is placed around the stem. The accumulating xylem sap is collected for 90 min after decapitation. Xylem sap is filtered through a 0.85 μm filter to remove large particles, and PMPs are purified as described in Example 2.

i) PMP Isolation from Tobacco BY-2 Cell Culture Medium

Tobacco BY-2 (Nicotiana tabacum L cv. Bright Yellow 2) cells are cultured in the dark at 26° C., on a shaker at 180 rpm in MS (Murashige and Skoog, 1962) BY-2 cultivation medium (pH 5.8) comprising MS salts (Duchefa, Haarlem, Netherlands, at #M0221) supplemented with 30 g/L sucrose, 2.0 mg/L potassium dihydrogen phosphate, 0.1 g/L myo-inositol, 0.2 mg/L 2,4-dichlorophenoxyacetic acid, and 1 mg/L thiamine HCl. The BY-2 cells are subcultured weekly by transferring 5% (v/v) of a 7-day-old cell culture into 100 mL fresh liquid medium. After 72-96 hours, BY-2 cultured medium is collected and centrifuged at 300 g at 4° C. for 10 minutes to remove cells. The supernatant containing PMPs is collected and cleared of debris by filtration on 0.85 um filter. PMPs are purified as described in Example 2.

Example 2: Production of Purified Plant Messenger Packs (PMPs)

This example describes the production of purified PMPs from crude PMP fractions as described in Example 1, using ultrafiltration combined with size-exclusion chromatography, a density gradient (iodixanol or sucrose), and the removal of aggregates by precipitation or size-exclusion chromatography.

Experimental Design:

a) Production of Purified Grapefruit PMPs Using Ultrafiltration Combined with Size-Exclusion Chromatography

The crude grapefruit PMP fraction from Example 1a is concentrated using 100-kDA molecular weight cut-off (MWCO) Amicon spin filter (Merck Millipore). Subsequently, the concentrated crude PMP solution is loaded onto a PURE-EV size exclusion chromatography column (HansaBioMed Life Sciences Ltd) and isolated according to the manufacturer's instructions. The purified PMP-containing fractions are pooled after elution. Optionally, PMPs can be further concentrated using a 100-kDa MWCO Amicon spin filter, or by Tangential Flow Filtration (TFF). The purified PMPs are analyzed as described in Example 3.

b) Production of Purified Arabidopsis Apoplast PMPs Using an Iodixanol Gradient

Crude Arabidopsis leaf apoplast PMPs are isolated as described in Example 1a, and PMPs are produced by using an iodixanol gradient as described in Rutter and Innes, Plant Physiol. 173(1): 728-741, 2017. To prepare discontinuous iodixanol gradients (OptiPrep; Sigma-Aldrich), solutions of 40% (v/v), 20% (v/v), 10% (v/v), and 5% (v/v) iodixanol are created by diluting an aqueous 60% OptiPrep stock solution in vesicle isolation buffer (VIB; 20 mM MES, 2 mM CaCl2, and 0.1 M NaCl, pH6). The gradient is formed by layering 3 ml of 40% solution, 3 mL of 20% solution, 3 mL of 10% solution, and 2 mL of 5% solution. The crude apoplast PMP solution from Example 1a is centrifuged at 40,000 g for 60 min at 4° C. The pellet is resuspended in 0.5 ml of VIB and layered on top of the gradient. Centrifugation is performed at 100,000 g for 17 h at 4° C. The first 4.5 ml at the top of the gradient is discarded, and subsequently 3 volumes of 0.7 ml that contain the apoplast PMPs are collected, brought up to 3.5 mL with VIB and centrifuged at 100,000 g for 60 min at 4° C. The pellets are washed with 3.5 ml of VIB and repelleted using the same centrifugation conditions. The purified PMP pellets are combined for subsequent analysis, as described in Example 3.

c) Production of Purified Grapefruit PMPs Using a Sucrose Gradient

Crude grapefruit juice PMPs are isolated as described in Example 1d, centrifuged at 150,000 g for 90 min, and the PMP-containing pellet is resuspended in 1 ml PBS as described in Mu et al., Molecular Nutrition & Food Research. 58(7):1561-1573, 2014. The resuspended pellet is transferred to a sucrose step gradient (8%/15%/30%/45%/60%) and centrifuged at 150,000 g for 120 min to produce purified PMPs. Purified grapefruit PMPs are harvested from the 30%/45% interface, and subsequently analyzed, as described in Example 3.

d) Removal of Aggregates from Grapefruit PMPs

In order to remove protein aggregates from produced grapefruit PMPs as described in Example 1d or purified PMPs from Example 2a-c, an additional purification step can be included. The produced PMP solution is taken through a range of pHs to precipitate protein aggregates in solution. The pH is adjusted to 3, 5, 7, 9, or 11 with the addition of sodium hydroxide or hydrochloric acid. pH is measured using a calibrated pH probe. Once the solution is at the specified pH, it is filtered to remove particulates. Alternatively, the isolated PMP solution can be flocculated using the addition of charged polymers, such as Polymin-P or Praestol 2640. Briefly, 2-5 g per L of Polymin-P or Praestol 2640 is added to the solution and mixed with an impeller. The solution is then filtered to remove particulates. Alternatively, aggregates are solubilized by increasing salt concentration. NaCl is added to the PMP solution until it is at 1 mol/L. The solution is then filtered to purify the PMPs. Alternatively, aggregates are solubilized by increasing the temperature. The isolated PMP mixture is heated under mixing until it has reached a uniform temperature of 50° C. for 5 minutes. The PMP mixture is then filtered to isolate the PMPs. Alternatively, soluble contaminants from PMP solutions are separated by size-exclusion chromatography column according to standard procedures, where PMPs elute in the first fractions, whereas proteins and ribonucleoproteins and some lipoproteins are eluted later. The efficiency of protein aggregate removal is determined by measuring and comparing the protein concentration before and after removal of protein aggregates via BCA/Bradford protein quantification. The produced PMPs are analyzed as described in Example 3.

Example 3: Plant Messenger Pack Characterization

This example describes the characterization of PMPs produced as described in Example 1 or Example 2.

Experimental Design:

a) Determining PMP Concentration

PMP particle concentration is determined by Nanoparticle Tracking Analysis (NTA) using a Malvern NanoSight, nano flow cytometry using a NanoFCM, or by Tunable Resistive Pulse Sensing (TRPS) using an Spectradyne CS1, following the manufacturer's instructions. The protein concentration of purified PMPs is determined by using the DC Protein assay (Bio-Rad). The lipid concentration of purified PMPs is determined using a fluorescent lipophilic dye, such as DiOC6 (ICN Biomedicals) as described by Rutter and Innes, Plant Physiol. 173(1): 728-741, 2017. Briefly, purified PMP pellets from Example 2 are resuspended in 100 ml of 10 mM DiOC6 (ICN Biomedicals) diluted with MES buffer (20 mM MES, pH 6) plus 1% plant protease inhibitor cocktail (Sigma-Aldrich) and 2 mM 2,29-dipyridyl disulfide. The resuspended PMPs are incubated at 37° C. for 10 min, washed with 3 mL of MES buffer, repelleted (40,000 g, 60 min, at 4° C.), and resuspended in fresh MES buffer. DiOC6 fluorescence intensity is measured at 485 nm excitation and 535 nm emission.

b) Biophysical and Molecular Characterization of PMPs

PMPs are characterized by electron and cryo-electron microscopy on a JEOL 1010 transmission electron microscope, following the protocol from Wu et al., Analyst. 140(2):386-406, 2015. The size and zeta potential of the PMPs are also measured using a Malvern Zetasizer or iZon qNano, following the manufacturer's instructions. Lipids are isolated from PMPs using chloroform extraction and characterized with LC-MS/MS as demonstrated in Xiao et al. Plant Cell. 22(10): 3193-3205, 2010. Glycosyl inositol phosphorylceramides (GIPCs) lipids are extracted and purified as described by Cacas et al., Plant Physiology. 170: 367-384, 2016, and analyzed by LC-MS/MS as described above. Total RNA, DNA, and protein are characterized using Quant-It kits from Thermo Fisher according to instructions. Proteins on the PMPs are characterized by LC-MS/MS following the protocol in Rutter and Innes, Plant Physiol. 173(1): 728-741, 2017. RNA and DNA are extracted using Trizol, prepared into libraries with the TruSeq Total RNA with Ribo-Zero Plant kit and the Nextera Mate Pair Library Prep Kit from Illumina, and sequenced on an Illumina MiSeq following manufacturer's instructions.

Example 4: Characterization of Plant Messenger Pack Stability

This example describes measuring the stability of PMPs under a wide variety of storage and physiological conditions.

Experimental Design:

PMPs produced as described in Examples 1 and 2 are subjected to various conditions. PMPs are suspended in water, 5% sucrose, or PBS and left for 1, 7, 30, and 180 days at −20° C., 4° C., 20° C., and 37° C. PMPs are also suspended in water and dried using a rotary evaporator system and left for 1, 7, and 30, and 180 days at 4° C., 20° C., and 37° C. PMPs are also suspended in water or 5% sucrose solution, flash-frozen in liquid nitrogen and lyophilized. After 1, 7, 30, and 180 days, dried and lyophilized PMPs are then resuspended in water. The previous three experiments with conditions at temperatures above 0° C. are also exposed to an artificial sunlight simulator in order to determine content stability in simulated outdoor UV conditions. PMPs are also subjected to temperatures of 37° C., 40° C., 45° C., 50° C., and 55° C. for 1, 6, and 24 hours in buffered solutions with a pH of 1, 3, 5, 7, and 9 with or without the addition of 1 unit of trypsin or in other simulated gastric fluids.

After each of these treatments, PMPs are bought back to 20° C., neutralized to pH 7.4, and characterized using some or all of the methods described in Example 3.

Example 5. Loading PMPs with Polypeptide Cargo

This example describes methods of loading PMPs with polypeptides.

PMPs are produced as described in Example 1 and Example 2. To load polypeptides (e.g., proteins or peptides) into PMPs, PMPs are placed in solution with the polypeptide in phosphate-buffered saline (PBS). If the polypeptide is insoluble, the pH of the solution is adjusted until the polypeptide is soluble. If the polypeptide is still insoluble, the insoluble polypeptide is used. The solution is then sonicated to induce poration and diffusion into the PMPs according to the protocol from Wang et al., Nature Comm., 4: 1867, 2013. Alternatively, PMPs are electroporated according to the protocol from Wahlgren et al., Nucl. Acids. Res., 40(17), e130, 2012.

Alternatively, PMP lipids are isolated by adding 3.75 mL 2:1 (v/v) MeOH:CHCl₃ to 1 mL of PMPs in PBS and vortexing the mixture. CHCl₃ (1.25 mL) and ddH₂O (1.25 mL) are added sequentially and vortexed. The mixture is then centrifuged at 2,000 r.p.m. for 10 min at 22° C. in glass tubes to separate the mixture into two phases (aqueous phase and organic phase). The organic phase sample containing the PMP lipids is dried by heating under nitrogen (2 psi). To produce polypeptide-loaded PMPs, the isolated PMP lipids are mixed with the polypeptide solution and passed through a lipid extruder according to the protocol from Haney et al., J Control Release, 207: 18-30, 2015.

Alternatively, PMP lipids are isolated using methods that isolate additional plant lipid classes, including glycosylinositol phosphorylceramides (GIPCs), as described in Casas et al., Plant Physiology, 170: 367-384, 2016. Briefly, to extract PMP lipids including GIPCs, 3.5 mL of chloroform:methanol:HCl (200:100:1, v/v/v) plus 0.01% (w/v) of butylated hydroxytoluene, is added to and incubated with the PMPs. Next, 2 mL of 0.9% (w/v) NaCl is added and vortexed for 5 minutes. The sample is then centrifuged to induce the organic phase to aggregate at the bottom of the glass tube, and the organic phase is collected. The upper phase undergoes reextraction with 4 mL of pure chloroform to isolate lipids. The organic phases are combined and dried. After drying, the aqueous phase is resuspended with 1 mL of pure water and GIPCs are back-extracted using 1 mL of butanol-1 twice. To produce polypeptide-loaded PMPs, the isolated PMP lipid phases are mixed with the polypeptide solution and are passed through a lipid extruder according to the protocol from Haney et al., J Control Release, 207: 18-30, 2015.

Alternatively, 3.5 mL of methyl tertiary-butyl ether (MTBE):methanol:water (100:30:25, v/v/v) plus 0.01% (w/v) butylated hydroxytoluene (BHT) is added to and incubated with the PMPs. After incubation, 2 mL of 0.9% NaCl is added, is vortexed for 5 minutes, and is centrifuged. The organic phase (upper) is collected and the aqueous phase (lower) is subjected to reextraction with 4 mL of pure MTBE. The organic phases are combined and dried. After drying, the aqueous phase is resuspend with 1 mL of pure water and GIPCs are back-extracted using 1 mL of butanol-1 twice. To produce protein-loaded PMPs, the isolated PMP lipid phases are mixed with the protein solution and passed through a lipid extruder according to the protocol from Haney et al., J Control Release, 207: 18-30, 2015.

Alternatively, 3.5 mL of propan-2-ol:hexane:water (55:20:25, v/v/v) is incubated with the sample for 15 mins at 60° C. with occasional shaking. After incubation, samples are spun down at 500× g and the supernatant is transferred, and the process is repeated with 3.5 mL of the extraction solvent. Supernatants are combined and dried, followed by resuspension in 1 mL of pure water. GIPCs are then back-extracted with 1 mL of butanol-1 twice. GIPCs can be added to PMP lipids isolated via methods described in this example. To produce protein-loaded PMPs, the isolated PMP lipids are mixed with the protein solution and passed through a lipid extruder according to the protocol from Haney et al., J Control Release, 207: 18-30, 2015.

Before use, the loaded PMPs are purified using the methods as described in Example 2 to remove polypeptides that are not bound to or encapsulated by the PMP. Loaded PMPs are characterized as described in Example 3, and their stability is tested as described in Example 4. To measure loading of the protein or peptide, the Pierce Quantitative Colorimetric Peptide Assay is used on a small sample of the loaded and unloaded PMPs, or using Western blot detection using protein-specific antibodies. Alternatively, proteins can be fluorescently labeled, and fluorescence can be used to determine the labeled protein concentration in loaded and unloaded PMPs.

Example 6: Treatment of Human Cells with Cre Recombinase Protein-Loaded PMPs

This example demonstrates loading of PMPs with a model protein with the purpose of delivering a functional protein into human cells. In this example, Cre recombinase is used as a model protein, and human embryonic kidney 293 cells (HEK293 cells) comprising a Cre reporter transgene (Hek293-LoxP-GFP-LoxP-RFP) (Puro; GenTarget, Inc.), are used as a model human cell line.

a) Production of Grapefruit PMPs Using TFF Combined with SEC

Red organic grapefruits were obtained from a local Whole Foods Market®. Two liters of grapefruit juice was collected using a juice press, and was subsequently centrifuged at 3000×g for 20 minutes, followed by 10,000×g for 40 minutes to remove large debris. PMPs were incubated in a final concentration of 50 mM EDTA (pH 7) for 30 minutes, and were subsequently passaged through a 1 μm and a 0.45 μm filter. Filtered juice was concentrated by tangential flow filtration (TFF) to 700 mL, washed with 500 mL of PBS, and concentrated to a final volume of 400 mL juice (total concentration 5×). Concentrated juice was dialyzed overnight in PBS using a 300 kDa dialysis membrane to remove contaminants. Subsequently, the dialyzed juice was further concentrated by TFF to a final concentration of 50 mL. Next, we used size exclusion chromatography to elute the PMP-containing fractions, and analyzed PMP size and concentration by nano-flow cytometry (NanoFCM) and protein concentration using a Pierce™ bicinchoninic acid (BCA) assay according to the manufacturer's instructions (FIGS. 1A and 1B). SEC fractions 8-12 contained contaminants. SEC fractions 4-6 contained purified PMPs and were pooled together, filter sterilized using 0.85 μm, 0.4 μm and 0.22 μm syringe filters, analyzed by NanoFCM (FIG. 1A) and used for loading Cre recombinase protein.

b) Loading of Cre Recombinase Protein into Grapefruit PMPs

Cre recombinase protein (ab134845) was obtained from Abcam, and was dissolved in UltraPure water to a final concentration of 0.5 mg/mL protein. Filter-sterilized PMPs were loaded with Cre recombinase protein by electroporation, using a protocol adapted from Rachael W. Sirianni and Bahareh Behkam (eds.), Targeted Drug Delivery: Methods and Protocols, Methods in Molecular Biology, vol. 1831. PMPs alone (PMP control), Cre recombinase protein alone (protein control), or PMP+Cre recombinase protein (protein-loaded PMPs) were mixed with 2× electroporation buffer (42% Optiprep™ (Sigma, D1556) in UltraPure water), see Table 5. Samples were transferred into a chilled cuvettes and electroporated at 0.400 kV, 125 μF (0.125 mF), resistance low 100Ω-high 600Ω with two pulses (4-10 ms) using a Biorad GenePulser. The reaction was put on ice for 10 minutes, and transferred to a pre-ice chilled 1.5 ml ultracentrifuge tube. All samples containing PMPs were washed 3 times by adding 1.4 ml ultrapure water, followed by ultracentrifugation (100,000 g for 1.5 h at 4° C.). The final pellet was resuspended in a minimal volume of UltraPure water (30-50 μL) and kept at 4° C. until use. After electroporation, samples containing Cre protein only were diluted in UltraPure water (as indicated in Table 5), and stored at 4° C. until use.

TABLE 5
Cre recombinase protein loading into grapefruit PMPs.
								Cre	Cre
								recombinase	recombinase
			(b)					treatment	treatment
			Loading:					dose:	dose:
		(a) PMP	Cre	(c)				Assuming	Assuming
		loading:	recombinase	Loading:				100% loading	10% loading
		PMPs	protein	Final				efficiency,	efficiency,
		added to	(0.5 mg/mL)	volume of	PMP		Treatment:	maximum Cre	maximum Cre
		electro-	added to	PMP	concen-	Treatment:	PMP	recombinase	recombinase
	Input PMP	poration	electro-	formulation	tration	Amount of	treatment	protein	protein
	concen-	reaction	poration	after	after	(c) added	concen-	concen-	concen-
	tration	mixture	mixture	washing	loading	to cells	tration	tration	tration
	(PMPs/mL)	(μL)	(μL)	(μL)	(PMPs/mL)	(μL)	(PMPs/mL)	(μg/mL)	(μg/mL)
Cre-	3.37 × 1012	40	40	50	3.28 × 1011	10	2.63 × 1010	40.00	4.00
PMP
electro-
poration
Cre-	3.37 × 1012	20	20	54	2.92 × 1011	30	3.25 × 1010	55.56	5.56
PMP not
electro-
poration
(loading
control)
PMP	3.37 × 1012	10	0	48	5.49 × 1010	24	2.74 × 109	0.00	0.00
only
electro-
poration
(PMP
only
control)
Cre	0.5 mg/mL		10	35		6		8.57
recombinase
electro-
poration
(protein
only
control)

c) Treatment of Hek293 LoxP-GFP-LoxP-RFP Cells with Cre-Recombinase-Loaded Grapefruit PMPs

The Hek293 LoxP-GFP-LoxP-RFP (Puro) human Cre-reporter cell line was purchased from GenTarget, Inc., and was maintained according to the manufacturer's instructions without antibiotic selection. Cells were seeded into a 96 well plate and were treated for 24 hrs in complete medium with Cre-recombinase-loaded PMPs (electroporated PMPs+Cre recombinase protein; 2.63×10¹⁰ PMPs/mL), electroporated PMPs (PMP only control; 2.74×10⁹ PMPs/mL), electroporated Cre recombinase protein (protein only control; 8.57 μg/mL), or non-electroporated PMPs+Cre recombinase protein (loading control; 3.25×10¹⁰ PMPs/mL), as indicated in Table 5. After 24 hrs, cells were washed twice with Dulbecco's phosphate-buffered saline (DPBS), and fresh complete cell culture medium is added. 96-100 hrs post treatment, cells were imaged using an EVOS FL 2 fluorescence imaging system (Invitrogen). When Cre recombinase protein is functionally delivered into the cells and transported to the nucleus, GFP is recombined out, inducing a color switch in the cells from green to red (FIG. 2A). The presence of red fluorescent cells therefore indicates functional delivery of Cre recombinase protein by PMPs. FIG. 2B shows that recombined red fluorescent cells are observed only when cells are exposed to Cre-recombinase-loaded PMPs, while these are absent in the control treated Hek293 LoxP-GFP-LoxP-RFP cells. Our data shows that PMPs can be loaded with protein, and can functionally deliver protein cargo into human cells.

Example 7: Treatment of Diabetic Mice with Insulin-Loaded PMPs

This example describes loading of PMPs with a protein with the purpose of delivering the protein in vivo via oral and systemic administration. In this example, insulin is used as a model protein, and streptozotocin-induced diabetic mice are used as an in vivo model (FIG. 3). This example further shows that PMPs are stable throughout the gastrointestinal (GI) tract and are able to protect protein cargo.

Therapeutic Design:

The PMP solution is formulated to an effective insulin dose of 0, 0.001, 0.01, 0.1, 0.5, 1 mg/ml in PBS.

Experimental Protocol:

a) Loading of Lemon PMPs with Insulin Protein

PMPs are produced from lemon juice and other plant sources according to Example 1-2. Human recombinant insulin (Gibco) and labeled insulin-FITC (Sigma Aldrich 13661) are solubilized at a concentration of 3 mg/ml in 10 mM HCl, pH 3. PMPs are placed in solution with the protein in PBS. If the protein is insoluble, pH is adjusted until it is soluble. If the protein is still insoluble, the insoluble protein is used. The solution is then sonicated to induce poration and diffusion into the PMP according to the protocol from Wang et al., Nature Comm., 4: 1867, 2013. Alternatively, the solution can be passed through a lipid extruder according to the protocol from Haney et al., J Control Release, 207: 18-30, 2015. Alternatively, PMPs can be electroporated according to the protocol from Wahlgren et al., Nucl. Acids. Res., 40(17), e130, 2012.

To produce protein-loaded PMPs, insulin or FITC-insulin can alternatively be loaded by mixing PMP-isolated lipids with the protein, and resealing using extrusion or sonication as described in Example 5. In brief, solubilized PMP lipids are mixed with a solution of insulin protein (pH 3, 10 mM HCl), sonicated for 20 minutes at 40° C., and extruded using polycarbonate membranes. Alternatively, insulin protein can be precomplexed prior to PMP lipid mixing with protamine sulfate (Sigma, P3369) in a 5:1 ratio, to facilitate encapsulation.

Insulin-loaded PMPs are purified by spinning down (100,000×g for 1 hour at 4° C.) and washing the pellet 2 times with acidic water (pH 4), followed by one wash with PBS (pH 7.4) to remove un-encapsulated protein in the supernatant. Alternatively, other purification methods can be used as described in Example 2. The final pellet is resuspended in a minimal volume of PBS (30-50 μL) and stored at 4° C. until use. Insulin-loaded PMPs are characterized as described in Example 3, and their stability is tested as described in Example 4.

Insulin encapsulation of PMPs is measured by HPLC, Western blot (anti-insulin antibody, Abcam ab181547) or by human insulin ELISA (Abcam, ab100578). FITC-insulin-loaded PMPs can alternatively be analyzed by fluorescence (Ex/Em 490/525). Pierce MicroBCA™ analysis (Thermo Scientific™) can be used to determine total protein concentration before and after loading. The Loading Efficacy (%) is determined by dividing the incorporated insulin (ug) by the total amount of insulin (ug) added to the reaction. PMP loading capacity is determined by dividing the amount of incorporated insulin (ug) by the number of labeled PMPs (in case of FITC-insulin) or PMPs (unlabeled insulin).

b) Gastro-Intestinal Stability of Insulin-FITC Loaded Lemon PMPs In Vitro

To determine the stability of PMPs in the GI tract, and the ability of PMPs to protect protein cargo from degradation, insulin-FITC-loaded PMPs are subjected to fasted and fed GI stomach and intestinal fluid mimetics purchased from Biorelevant (UK), which are prepared according to the manufacturer's instruction: FaSSIF (Fasted, small intestine, pH 6.5), FeSSIF (Fed, small intestine, pH 5, supplemented with pancreatin), FaSSGF (Fasted, stomach, pH 1.6), FaSSIF-V2 (Fasted, small intestine, pH 6.5), FeSSIF-V2 (Fed, small intestine, with digestive components, pH 5.8).

Twenty μl of insulin-FITC-loaded PMPs with an effective dose of 0 (PMP only control), 0.001, 0.01, 0.1, 0.5, 1 mg/ml Insulin-FITC, or free 0 (PBS control), 0.001, 0.01, 0.1, 0.5, 1 mg/ml Insulin-FITC are incubated with I mL of stomach, fed, and fasted intestinal juices (FaSSIF, F2SSIF, FaSSGF, FaSSIF-V2 and FeSSIF-V2), PMS (negative control), and PBS+0.1% SDS (PMP degradation control) for 1, 2, 3, 4, and 6 hours at 37° C. Alternatively, insulin-FITC-loaded PMPs or free protein are subsequently exposed to F2SSIF>FASSIF-V2 or F2SSIF>FESSIF-V2 for 1, 2, 3, 4, and 6 hours at 37° C. for each step. Next, Insulin-FITC-loaded PMPs are pelleted by ultracentrifugation at 100,000×g for 1 h at 4° C. Pellets are resuspended in 25-50 mM Tris pH 8.6, and analyzed for fluorescence intensity (Ex/Em 490/525), FITC⁺PMP concentration, PMP size, and insulin protein concentration. PMP supernatants after pelleting, and insulin-FITC protein only samples are analyzed by fluorescence intensity after adjusting the pH of the solutions to pH 8-9 (bicarbonate buffer), the presence of particles in the solution and their size is measured, and after precipitation, insulin protein concentration is determined by Western blot. To show that PMPs are stable throughout the GI tract and that their protein cargo is protected from degradation, total fluorescence (spectrophotometer), total insulin protein (Western), PMP size and fluorescent PMP concentration (NanoFCM) of Insulin-FITC-labeled PMPs and free Insulin-FITC protein are compared between the different GI juice mimetics and the PBS control. Insulin-FITC-labeled PMPs are stable when fluorescent PMPs and Insulin-FITC protein can be detected after GI juice exposure, compare to PBS incubation.

c) Treatment of Diabetic Mice with Insulin-Loaded PMPs Via Oral Administration

To show the ability of PMPs to deliver functional protein in vivo, PMPs are loaded with human recombinant insulin using the methods described in Example 7a. PMPs are labeled with DyLight-800 (DL800) infrared membrane dye (Invitrogen). Briefly, DyLight800 is dissolved in DMSO to a final concentration of 10 mg/mL and 200 μL of PMPs (1-3×10¹² PMPs/mL) are mixed with 5 μL dye and are incubated for 1 h at room temperature on a shaker. Labeled PMPs are washed 2-3 times by ultracentrifuge at 100,000×g for 1 hr at 4° C., and pellets are resuspended with 1.5 ml UltraPure water. The final DyLight800 labeled pellets are resuspended in a minimal amount of UltraPure PBS and are characterized using methods described herein.

Mouse experiments are performed at a contract research organization, using a well-established streptozotocin (STZ)-induced diabetic mouse model, and mice are treated and monitored according to standard procedures. In short, eight week old streptozotocin (STZ)-induced diabetic male C57BL/6J mice are orally gavaged with 300 μl insulin-loaded PMPs with an effective dose of 0 (PMP only control), 0.01, 0.1, 0.5, 1 mg/mL insulin, or free 0 (PBS control), 0.1, 0.5, 1 mg/mL insulin (5 mice per group). Blood glucose levels of the mice are monitored after 2, 4, 6, 12 and 24 hours, and at the end point, blood samples are collected for ELISA to determine human insulin levels in the mouse. PMPs can effectively deliver insulin orally when blood glucose levels are induced, when compared to free insulin, unloaded PMPs or PBS. The biodistribution of the PMPs is determined by isolating mouse organs and tissues at the experimental endpoint and measuring infrared fluorescence at 800 nm using a Licor Odyssey imager.

d) Treatment of Diabetic Mice with Insulin-Loaded PMPs Via IV Administration

To show the ability of PMPs to deliver functional protein in vivo, PMPs are loaded with human recombinant insulin using methods described in Example 7a. PMPs are labeled with DyLight-800 (DL800) infrared membrane dye (Invitrogen). Briefly, DyLight800 is dissolved in DMSO to a final concentration of 10 mg/mL and 200 μL of PMPs (1-3×10¹² PMPs/mL) are mixed with 5 μL dye and are incubated for 1 h at room temperature on a shaker. Labeled PMPs are washed 2-3 times by ultracentrifuge at 100,000×g for 1 hr at 4° C., and pellets are resuspended with 1.5 ml UltraPure water. The final DyLight800 labeled pellets are resuspended in a minimal amount of UltraPure PBS and are characterized using methods described herein.

Mouse experiments are performed at a contract research organization, using a well-established streptozotocin (STZ)-induced diabetic mouse model, and mice are treated and monitored according to standard procedures. In short, eight week old streptozotocin (STZ)-induced diabetic male C57BL/6J mice are systemically administered insulin-PMPs by tail vein injection with an effective dose of 0 (PMP only control), 0.01, 0.1, 0.5, 1 mg/ml Insulin, PBS (negative control), or 10-20 mg/kg free insulin (positive control) (5 mice per group). Blood glucose levels of the mice are monitored after 2, 4, 6, 12 and 24 hours, and at the end point, blood samples are collected for ELISA to determine human insulin levels in the mouse. PMPs can effectively deliver insulin systemically when blood glucose levels are induced, when compared unloaded PMPs and PBS. The biodistribution of the PMPs is determined by isolating mouse organs and tissues at the experimental endpoint, and measuring infrared fluorescence at 800 nm using a Licor Odyssey imager.

e) Treatment of Diabetic Mice with Insulin-Loaded PMPs Via IP Administration

To show the ability of PMPs to deliver functional protein in vivo, PMPs are loaded with human recombinant insulin using methods described in Example 7a. PMPs are labeled with DyLight-800 (DL800) infrared membrane dye (Invitrogen). Briefly, DyLight800 is dissolved in DMSO to a final concentration of 10 mg/mL and 200 μL of PMPs (1-3×10¹² PMPs/mL) are mixed with 5 μL dye and are incubated for 1 h at room temperature on a shaker. Labeled PMPs are washed 2-3 times by ultracentrifuge at 100,000×g for 1 hr at 4° C., and pellets are resuspended with 1.5 ml UltraPure water. The final DyLight800 labeled pellets are resuspended in a minimal amount of UltraPure PBS and are characterized using methods described herein.

Mouse experiments are performed at a contract research organization, using a well-established streptozotocin (STZ)-induced diabetic mouse model, and mice are treated and monitored according to standard procedures. In short, eight week old streptozotocin (STZ)-induced diabetic male C57BL/6J mice, are administered insulin-PMPs by intraperitoneal (IP) injection with an effective dose of 0 (PMP only control), 0.01, 0.1, 0.5, 1 mg/ml insulin, PBS (negative control), or 10-20 mg/kg free insulin (positive control) (5 mice per group). Blood glucose levels of the mice are monitored after 2, 4, 6, 12 and 24 hours, and at the end point, blood samples are collected for ELISA to determine human insulin levels in the mouse. PMPs can effectively deliver insulin systemically when blood glucose levels are induced, when compared unloaded PMPs and PBS. The biodistribution of the PMPs is determined by isolating mouse organs and tissues at the experimental endpoint and measuring infrared fluorescence at 800 nm, using a Licor Odyssey imager.

Example 8: Treatment of Human, Bacterial, Fungal, Plant, and Nematode Cells with Protein-Loaded Plant Messenger Packs

A. Treatment of Human Cells with Protein-Loaded PMPs

This example describes loading of PMPs with a protein for the purpose of delivering a protein cargo to enhance or reduce fitness in mammalian cells. This example describes PMPs loaded with GFP that are taken up by human cells, and it further describes that protein-loaded PMPs are stable and retain their activity over a range of processing and environmental conditions. In this example, GFP is used as a model protein or polypeptide, and A549 lung cancer cells are used as model human cell line.

Therapeutic Dose:

PMPs loaded with GFP, formulated in water to a concentration that delivers 0 (unloaded PMP control), 0.01, 0.1, 1, 5, 10, or 100 μg/ml GFP protein-loaded in PMPs.

Experimental Protocol:

a) Loading of Lemon PMPs with GFP Protein

PMPs are produced from lemon juice and other plant sources according to Example 1. Green fluorescent protein is synthesized commercially (Abcam) and solubilized in PBS. PMPs are placed in solution with the protein in PBS. If the protein is insoluble, pH is adjusted until it is soluble. If the protein is still insoluble, the insoluble protein is used. The solution is then sonicated to induce poration and diffusion into the PMP according to the protocol from Wang et al., Nature Comm., 4: 1867, 2013. Alternatively, the solution can be passed through a lipid extruder according to the protocol from Haney et al., J Control Release, 207: 18-30, 2015. Alternatively, PMPs can be electroporated according to the protocol from Wahlgren et al., Nucl. Acids. Res., 40(17), e130, 2012.

To produce protein-loaded PMPs, GFP can alternatively be loaded by mixing PMP-isolated lipids with the protein, and resealing using extrusion or sonication as described in Example 5. In brief, solubilized PMP lipids are mixed with a solution of GFP protein (pH 5-6, in PBS), sonicated for 20 minutes at 40° C., and extruded using polycarbonate membranes. Alternatively, GFP protein can be precomplexed prior to PMP lipid mixing with protamine (Sigma) in a 10:1 ratio to facilitate encapsulation.

GFP-loaded PMPs are purified by spinning down (100,000×g for 1 hour at 4° C.) and washing the pellet three times to remove un-encapsulated protein in the supernatant, or by using other methods as described in Example 2. GFP-loaded PMPs are characterized as described in Example 3, and their stability is tested as described in Example 4. GFP encapsulation of PMPs is measured by Western blot or fluorescence.

b) Treatment of Human A549 Cells with GFP-Loaded Lemon PMPs

A549 lung cancer cells were purchased from the ATCC (CCL-185) and maintained in F12K medium supplemented with 10% FBS according to the manufacturer's instructions. To determine GFP-loaded PMP uptake by human cells, A549 cells are plated in a 48 well plate at a concentration of 1E5 cells/well, and cells are allowed to adhere for at least 6 hours at 37° C. or overnight. Next, medium is aspirated and cells are incubated with 0 (unloaded PMP control), 0.01, 0.1, 1, 5, 10, or 100 μg/ml GFP-loaded lemon-derived PMPs, or unloaded 0 (negative control), 0.01, 0.1, 1, 5, 10, or 100 μg/ml GFP protein in complete medium. After incubation of 2, 6, 12 and 24 hours at 37° C., the medium is aspirated and cells are gently washed 3 times for 5 minutes with DPBS or complete medium. Optionally, if tolerated, A549 cells are incubated with 0.5% triton X100 with/without ProtK (2 mg/mL) for 10 minutes at 37° C. to burst and degrade PMPs and protein that are not taken up by the cells. Next, images are acquired on a high-resolution fluorescence microscope. Uptake of GFP-loaded PMPs or GFP protein alone by A549 is demonstrated when the cytoplasm of the cell turns green. The percentage of GFP-loaded PMP treated cells with a green cytoplasm compared to control treatments with PBS and GFP only are recorded to determine uptake. In addition, GFP uptake by cells is measured by Western blot using an anti-GFP antibody (Abcam), after total protein isolation in treated and untreated cells, using standard methods. GFP protein levels are recorded and compared between cells treated with GFP-loaded PMPs, GFP protein alone, and untreated cells to determine uptake.

B. Treatment of Bacteria with Protein-Loaded PMPs

This example describes loading of PMPs with a protein for the purpose of delivering a protein cargo to enhance or reduce fitness in bacteria. This example describes PMPs loaded with GFP that are taken up by bacteria, and it further describes that protein-loaded PMPs are stable and retain their activity over a range of processing and environmental conditions. In this example, GFP is used as a model protein or peptide, and E. coli are used as a model bacterium.

Therapeutic Dose:

PMPs loaded with GFP are formulated as described in Example 8A.

Experimental Protocol:

a) Loading of Lemon PMPs with GFP Protein

PMPs are produced as described in Example 8A.

b) Delivery of GFP-Loaded Lemon PMPs to E. coli

E. coli are acquired from ATCC (#25922) and grown on Trypticase Soy Agar/broth at 37° C. according to the manufacturer's instructions. To determine the GFP-loaded PMP uptake by E. coli, 10 uL of a 1 mL overnight bacterial suspension is incubated with 0 (unloaded PMP control), 0.01, 0.1, 1, 5, 10, 100 μg/mL GFP-loaded lemon-derived PMPs, or unloaded 0 (negative control), 0.01, 0.1, 1, 5, 10, 100 μg/mL GFP protein in liquid culture. After incubation of 5 min, 30 min and 1 h at room temperature, bacteria are washed 4 times with 0.5% triton X100, and optional ProtK treatment (2 mg/ml ProtK, 10 minutes at 37° C.; if tolerated by the bacteria) to burst and degrade PMPs and protein that are not taken up by the bacteria. Next, images are acquired on a high-resolution fluorescence microscope. Uptake of GFP-loaded PMPs or GFP protein alone by bacteria is demonstrated when the cytoplasm of the bacteria turns green. The percentage of GFP-loaded PMP treated bacteria with a green cytoplasm compared to control treatments with PBS and GFP only are recorded to determine uptake. In addition, GFP uptake by bacteria is measured by Western blot using an anti-GFP antibody (Abcam), after total protein isolation in treated and untreated bacteria, using standard methods. GFP protein levels are recorded and compared between bacteria treated with GFP-loaded PMPs, GFP protein alone, and untreated bacteria to determine uptake.

B. Treatment of Fungi with Protein-Loaded PMPs

This example describes loading of PMPs with a protein for the purpose of delivering a protein cargo to enhance or reduce fitness in fungi. This example describes PMPs loaded with GFP that are taken up by fungi (including yeast), and it further describes that protein-loaded PMPs are stable and retain their activity over a range of processing and environmental conditions. In this example, GFP is used as a model peptide and protein, and Saccharomyces cerevisiae is used as a model fungus.

Therapeutic Dose:

PMPs loaded with GFP are formulated as described in Example 8A.

Experimental Protocol:

a) Loading of Lemon PMPs with GFP Protein

PMPs are produced as described in Example 8A.

b) Delivery of GFP-Loaded Lemon PMPs to Saccharomyces cerevisiae

Saccharomyces cerevisiae is obtained from the ATCC (#9763) and maintained at 30° C. in yeast extract peptone dextrose broth (YPD) as indicated by the manufacturer. To determine the PMP uptake by S. cerevisiae, yeast cells are grown to an OD₆₀₀ of 0.4-0.6 in selection media, and incubated with 0 (unloaded PMP control), 0.01, 0.1, 1, 5, 10, 100 μg/ml GFP-loaded lemon-derived PMPs, or unloaded 0 (negative control), 0.01, 0.1, 1, 5, 10, 100 μg/ml GFP protein, in liquid culture. After incubation of 5 min, 30 min and 1 h at room temperature, yeast cells are washed 4 times with 0.5% triton X100, and optional ProtK treatment (2 mg/ml ProtK, 10 minutes at 37° C.; if tolerated by the cells) to burst and degrade PMPs and protein that are not taken up by the bacteria. Next, images are acquired on a high-resolution fluorescence microscope. Uptake of GFP-loaded PMPs or GFP protein alone by yeast is demonstrated when the cytoplasm of the yeast cell turns green. The percentage of GFP-loaded PMP treated yeast with a green cytoplasm compared to control treatments with PBS and GFP only are recorded to determine uptake. In addition, GFP uptake by yeast is measured by Western blot using an anti-GFP antibody (Abcam), after total protein isolation in treated and untreated yeast, using standard methods. GFP protein levels are recorded and compared between yeast treated with GFP-loaded PMPs, GFP protein alone, and untreated yeast to determine uptake.

C. Treatment of a Plant with Protein-Loaded PMPs

This example describes loading of PMPs with a protein for the purpose of delivering a protein cargo to enhance or reduce fitness in plants. This example describes PMPs loaded with GFP that are taken up by plants, and it further describes that protein-loaded PMPs are stable and retain their activity over a range of processing and environmental conditions. In this example, GFP is used as a model protein and peptide, and Arabidopsis thaliana seedlings are used as model plant.

Therapeutic Dose:

PMPs loaded with GFP are formulated as described in Example 8A.

Experimental Protocol:

a) Loading of Lemon PMPs with GFP Protein

PMPs are produced as described in Example 8A.

b) Delivery of GFP-Loaded PMPs to Arabidopsis thaliana Seedlings

Wild-type Columbia (Col)-1 ecotype Arabidopsis thaliana is obtained from the Arabidopsis Biological Resource Center (ABRC). Seeds are surface sterilized with a solution containing 70% (v/v) ethanol and 0.05% (v/v) Triton X-100, and are germinated on sterile plates in liquid medium containing half-strength Murashige and Skoog (MS), supplemented with 0.5% sucrose and 2.5 mM MES, pH 5.6. Three day old seedlings are treated with 0 (unloaded PMP control), 0.01, 0.1, 1, 5, 10, 100 μg/ml GFP-loaded lemon-derived PMPs, or unloaded 0 (negative control), 0.01, 0.1, 1, 5, 10, 100 μg/ml GFP protein, added to the MS medium for 6, 12, 24 and 48 hours. After treatment, seedlings are extensively washed in MS medium, optionally supplemented with 0.5% Triton X100, followed by ProtK treatment (2 mg/mL ProtK, 10 minutes at 37° C.; if tolerated by the seedlings) to burst and degrade PMPs and protein that are not taken up by the plant. Next, images are acquired on a high-resolution fluorescence microscope to detect GFP in the roots, leaves and other plant parts. GFP-loaded PMPs or GFP protein alone is taken up by seedlings when GFP protein localization can be detected in plant tissues. The number of seedlings with green fluorescence is compared between GFP-loaded PMPs and control treatments with PBS and GFP only to determine uptake. In addition, GFP uptake by seedlings can be quantified by Western blot using an anti-GFP antibody (Abcam), after total protein isolation in treated and untreated seedlings, using standard methods. GFP protein levels are recorded and compared between seedlings treated with GFP-loaded PMPs, GFP protein alone, and untreated seedlings to determine uptake.

D. Treatment of a Nematode with Protein-Loaded PMPs

This example describes loading of PMPs with a protein for the purpose of delivering a protein cargo to enhance or reduce fitness in nematodes. This example describes PMPs loaded with GFP that are taken up by nematodes, and it further describes that protein-loaded PMPs are stable and retain their activity over a range of processing and environmental conditions. In this example, GFP is used as a model peptide, and C. elegans is used as a model nematode.

Therapeutic Dose:

PMPs loaded with GFP are formulated as described in Example 8A.

Experimental Protocol:

a) Loading of Lemon PMPs with GFP Protein

PMPs are produced as described in Example 8A.

b) Delivery of GFP-Loaded PMPs to C. elegans

C. elegans wild-type N2 Bristol strain (C. elegans Genomics Center) are maintained on an Escherichia coli (strain OP50) lawn on nematode growth medium (NGM) agar plates (3 g/l NaCl, 17 g/l agar, 2.5 g/l peptone, 5 mg/l cholesterol, 25 mM KH₂PO₄ (pH 6.0), 1 mM CaCl₂), 1 mM MgSO₄) at 20° C., from L1 until the L4 stage.

One-day old C. elegans are transferred to a new plate and are fed 0 (unloaded PMP control), 0.01, 0.1, 1, 5, 10, 100 μg/ml GFP-loaded lemon-derived PMPs, or unloaded 0 (negative control), 0.01, 0.1, 1, 5, 10, 100 μg/ml GFP protein in a liquid solution following the feeding protocol in Conte et al., Curr. Protoc. Mol. Bio., 109: 26.3.1-26.330, 2015. Worms are next examined for GFP-loaded PMP uptake in the digestive tract by using a fluorescent microscope for green fluorescence, compared to unloaded PMP-treatment, or GFP protein alone and a sterile water control. In addition, GFP uptake by C. elegans can be quantified by Western blot using an anti-GFP antibody (Abcam), after total protein isolation in treated and untreated nematodes, using standard methods. GFP protein levels are recorded and compared between nematodes treated with GFP-loaded PMPs, GFP protein alone, and untreated C. elegans to determine uptake.

E. In Vivo Delivery of Cre Recombinase to a Mouse

This example describes loading of PMPs with a protein with the purpose of delivering the protein in vivo via oral and systemic administration. In this example, Cre recombinase is used as a model protein, and mice having a luciferase Cre reporter construct (Lox-STOP-Lox-LUC) are used as an in vivo model (FIG. 4).

Delivery of a Cre recombinase to a mouse, as outlined in FIG. 4, may be performed using any of the methods described herein. Expression of luciferase in a mouse tissue indicates that Cre has been delivered by PMPs to the tissue.

Example 9: PMP Production from Blended Fruit Juice Using Ultracentrifugation and Sucrose Gradient Purification

This example demonstrates that PMPs can be produced from fruit by blending the fruit and using a combination of sequential centrifugation to remove debris, ultracentrifugation to pellet crude PMPs, and using a sucrose density gradient to purify PMPs. In this example, grapefruit was used as a model fruit.

a) Production of Grapefruit PMPs by Ultracentrifugation and Sucrose Density Gradient Purification

A workflow for grapefruit PMP production using a blender, ultracentrifugation and sucrose gradient purification is shown in FIG. 5A. One red grapefruit was purchased from a local Whole Foods Market®, and the albedo, flavedo, and segment membranes were removed to collect juice sacs, which were homogenized using a blender at maximum speed for 10 minutes. One hundred mL juice was diluted 5× with PBS, followed by subsequent centrifugation at 1000×g for 10 minutes, 3000× g for 20 minutes, and 10,000× g for 40 minutes to remove large debris. 28 mL of cleared juice was ultracentrifuged on a Sorvall™ MX 120 Plus Micro-Ultracentrifuge at 150,000× g for 90 minutes at 4° C. using a S50-ST (4×7 mL) swing bucket rotor to obtain a crude PMP pellet which was resuspended in PBS pH 7.4. Next, a sucrose gradient was prepared in Tris-HCL pH7.2, crude PMPs were layered on top of the sucrose gradient (from top to bottom: 8, 15. 30. 45 and 60% sucrose), and spun down by ultracentrifugation at 150,000×g for 120 minutes at 4° C. using a S50-ST (4×7 mL) swing bucket rotor. One mL fractions were collected and PMPs were isolated at the 30-45% interface. The fractions were washed with PBS by ultracentrifugation at 150,000×g for 120 minutes at 4° C. and pellets were dissolved in a minimal amount of PBS.

PMP concentration (1×10⁹ PMPs/mL) and median PMP size (121.8 nm) were determined using a Spectradyne nCS1™ particle analyzer, using a TS-400 cartridge (FIG. 5B). The zeta potential was determined using a Malvern Zetasizer Ultra and was −11.5+/−0.357 mV.

This example demonstrates that grapefruit PMPs can be isolated using ultracentrifugation combined with sucrose gradient purification methods. However, this method induced severe gelling of the samples at all PMP production steps and in the final PMP solution.

Example 10: PMP Production from Mesh-Pressed Fruit Juice Using Ultracentrifugation and Sucrose Gradient Purification

This example demonstrates that cell wall and cell membrane contaminants can be reduced during the PMP production process by using a milder juicing process (mesh strainer). In this example, grapefruit was used as a model fruit.

a) Mild Juicing Reduces Gelling During PMP Production from Grapefruit PMPs

Juice sacs were isolated from a red grapefruit as described in Example 9. To reduce gelling during PMP production, instead of using a destructive blending method, juice sacs were gently pressed against a tea strainer mesh to collect the juice and to reduce cell wall and cell membrane contaminants. After differential centrifugation, the juice was more clear than after using a blender, and one clean PMP-containing sucrose band at the 30-45% intersection was observed after sucrose density gradient centrifugation (FIG. 6). There was overall less gelling during and after PMP production.

Our data shows that use of a mild juicing step reduces gelling caused by contaminants during PMP production when compared to a method comprising blending.

Example 11: PMP Production Using Ultracentrifugation and Size Exclusion Chromatography

This example describes the production of PMPs from fruits by using Ultracentrifugation (UC) and Size Exclusion Chromatography (SEC). In this example, grapefruit is used as a model fruit.

a) Production of Grapefruit PMPs Using UC and SEC

Juice sacs were isolated from a red grapefruit, as described in Example 9a, and were gently pressed against a tea strainer mesh to collect 28 ml juice. The workflow for grapefruit PMP production using UC and SEC is depicted in FIG. 7A. Briefly, juice was subjected to differential centrifugation at 1000×g for 10 minutes, 3000× g for 20 minutes, and 10,000× g for 40 minutes to remove large debris. 28 ml of cleared juice was ultracentrifuged on a Sorvall™ MX 120 Plus Micro-Ultracentrifuge at 100,000× g for 60 minutes at 4° C. using a S50-ST (4×7 mL) swing bucket rotor to obtain a crude PMP pellet which was resuspended in MES buffer (20 mM MES, NaCl, pH 6). After washing the pellets twice with MES buffer, the final pellet was resuspended in 1 ml PBS, pH 7.4. Next, we used size exclusion chromatography to elute the PMP-containing fractions. SEC elution fractions were analyzed by nano-flow cytometry using a NanoFCM to determine PMP size and concentration using concentration and size standards provided by the manufacturer. In addition, absorbance at 280 nm (SpectraMax®) and protein concentration (Pierce™ BCA assay, ThermoFisher) were determined on SEC fractions to identify in which fractions PMPs are eluted (FIGS. 7B-7D). SEC fractions 2-4 were identified as the PMP-containing fractions. Analysis of earlier- and later-eluting fractions indicated that SEC fraction 3 is the main PMP-containing fraction, with a concentration of 2.83×10¹¹ PMPs/mL (57.2% of all particles in the 50-120 nm size range), with a median size of 83.6 nm+/−14.2 nm (SD). While the late elution fractions 8-13 had a very low concentration of particles as shown by NanoFCM, protein contaminants were detected in these fractions by BCA analysis.

Our data shows that TFF and SEC can be used to isolate purified PMPs from late-eluting contaminants, and that a combination of the analysis methods used here can identify PMP fractions from late-eluting contaminants.

Example 12: Scaled PMP Production Using Tangential Flow Filtration and Size Exclusion Chromatography Combined with EDTA/Dialysis to Reduce Contaminants

This example describes the scaled production of PMPs from fruits by using Tangential Flow Filtration (TFF) and Size Exclusion Chromatography (SEC), combined with an EDTA incubation to reduce the formation of pectin macromolecules, and overnight dialysis to reduce contaminants. In this example, grapefruit is used as a model fruit.

a) Production of Grapefruit PMPs Using TFF and SEC

Red grapefruits were obtained from a local Whole Foods Market®, and 1000 ml juice was isolated using a juice press. The workflow for grapefruit PMP production using TFF and SEC is depicted in FIG. 8A. Juice was subjected to differential centrifugation at 1000×g for 10 minutes, 3000× g for 20 minutes, and 10,000× g for 40 minutes to remove large debris. Cleared grapefruit juice was concentrated and washed once using a TFF (5 nm pore size) to 2 mL (100×). Next, we used size exclusion chromatography to elute the PMP-containing fractions. SEC elution fractions were analyzed by nano-flow cytometry using a NanoFCM to determine PMP concentration using concentration and size standards provided by the manufacturer. In addition, protein concentration (Pierce™ BCA assay, ThermoFisher) was determined for SEC fractions to identify the fractions in which PMPs are eluted. The scaled production from 1 liter of juice (100× concentrated) also concentrated a high amount of contaminants in the late SEC fractions as can be detected by BCA assay (FIG. 8B, top panel). The overall total PMP yield (FIG. 8B, bottom panel) was lower in the scaled production when compared to single grapefruit isolations, which may indicate loss of PMPs.

b) Reducing Contaminants by EDTA Incubation and Dialysis

Red grapefruits were obtained from a local Whole Foods Market®, and 800 ml juice was isolated using a juice press. Juice was subjected to differential centrifugation at 1000×g for 10 minutes, 3000× g for 20 minutes, and 10,000× g for 40 minutes to remove large debris, and filtered through a 1 μm and 0.45 μm filter to remove large particles. Cleared grapefruit juice was split into 4 different treatment groups containing 125 ml juice each. Treatment Group 1 was processed as described in Example 4a, concentrated and washed (PBS) to a final concentration of 63×, and subjected to SEC. Prior to TFF, 475 ml juice was incubated with a final concentration of 50 mM EDTA, pH 7.15 for 1.5 hrs at RT to chelate iron and reduce the formation of pectin macromolecules. Afterwards, juice was split in three treatment groups that underwent TFF concentration with either a PBS (without calcium/magnesium) pH 7.4, MES pH 6, or Tris pH 8.6 wash to a final juice concentration of 63×. Next, samples were dialyzed in the same wash buffer overnight at 4° C. using a 300 kDa membrane and subjected to SEC. Compared to the high contaminant peak in the late elution fractions of the TFF only control, EDTA incubation followed by overnight dialysis strongly reduced contaminants, as shown by absorbance at 280 nm (FIG. 8C) and BCA protein analysis (FIG. 8D), which is sensitive to the presence of sugars and pectins. There was no difference in the dialysis buffers used (PBS without calcium/magnesium pH 7.4, MES pH 6, Tris pH 8.6).

Our data indicates that incubation with EDTA followed by dialysis reduces the amount of co-purified contaminants, facilitating scaled PMP production.

Example 13: PMP Production from Plant Cell Culture Medium

This example demonstrates that PMPs can be produced from plant cell culture. In this example, the Zea mays Black Mexican Sweet (BMS) cell line is used as a model plant cell line.

a) Production of Zea mays BMS Cell Line PMPs

The Zea mays Black Mexican sweet (BMS) cell line was purchased from the ABRC and was grown in Murashige and Skoog basal medium pH 5.8, containing 4.3 g/L Murashige and Skoog Basal Salt Mixture (Sigma M5524), 2% sucrose (S0389, Millipore Sigma), 1× MS vitamin solution (M3900, Millipore Sigma), 2 mg/L 2,4-dichlorophenoxyacetic acid (D7299, Millipore Sigma) and 250 ug/L thiamine HCL (V-014, Millipore Sigma), at 24° C. with agitation (110 rpm), and was passaged 20% volume/volume every 7 days.

Three days after passaging, 160 ml BMS cells was collected and spun down at 500× g for 5 min to remove cells, and 10,000×g for 40 min to remove large debris. Medium was passed through a 0.45 μm filter to remove large particles, and filtered medium was concentrated and washed (100 ml MES buffer, 20 mM MES, 100 mM NaCL, pH 6) by TFF (5 nm pore size) to 4 mL (40×). Next, we used size exclusion chromatography to elute the PMP-containing fractions, which were analyzed by NanoFCM for PMP concentration, by absorbance at 280 nm (SpectraMax®), and by a protein concentration assay (Pierce™ BCA assay, ThermoFisher) to verify the PMP-containing fractions and late fractions containing contaminants (FIGS. 9A-9C). SEC fractions 4-6 contained purified PMPs (fractions 9-13 contained contaminants), and were pooled together. The final PMP concentration (2.84×10¹⁰ PMPs/ml) and median PMP size (63.2 nm+/−12.3 nm SD) in the combined PMP containing fractions were determined by NanoFCM, using concentration and size standards provided by the manufacturer (FIGS. 9D-9E).

These data show that PMPs can be isolated, purified, and concentrated from plant liquid culture media.

Example 14: Treatment of a Microbe with Protein Loaded PMPs

This example demonstrates that PMPs can be exogenously loaded with a protein, PMPs can protect their cargo from degradation, and PMPs can deliver their functional cargo to an organism. In this example, grapefruit PMPs are used as model PMP, Pseudomonas aeruginosa bacteria is used as a model organism, and luciferase protein is used as a model protein.

While protein and peptide-based drugs have great potential to impact the fitness of a wide variety pathogenic bacteria and fungi that are resistant or hard to treat, their deployment has been unsuccessful due to their instability and formulation challenges.

a) Production of Grapefruit PMPs Using TFF Combined with SEC

Red organic grapefruits were obtained from a local Whole Foods Market®. Four liters of grapefruit juice were collected using a juice press, pH adjusted to pH4 with NaOH, incubated with 1 U/ml pectinase (Sigma, 17389) to remove pectin contaminants, and subsequently centrifuged at 3,000 g for 20 minutes, followed by 10,000 g for 40 minutes to remove large debris. Next, the processed juice was incubated with 500 mM EDTA pH8.6, to a final concentration of 50 mM EDTA, pH7.7 for 30 minutes to chelate calcium and prevent the formation of pectin macromolecules. Subsequently, the EDTA-treated juice was passaged through an 11 m, 1 m and 0.45 m filter to remove large particles. Filtered juice was washed and concentrated by Tangential Flow Filtration (TFF) using a 300 kDa TFF. Juice was concentrated 5×, followed by a 6 volume exchange wash with PBS, and further filtrated to a final concentration 198 mL (20×). Next, we used size exclusion chromatography to elute the PMP-containing fractions, which were analyzed by absorbance at 280 nm (SpectraMax®) and protein concentration (Pierce™ BCA assay, ThermoFisher) to verify the PMP-containing fractions and late fractions containing contaminants. SEC fractions 3-7 contained purified PMPs (fractions 9-12 contained contaminants), were pooled together, were filter sterilized by sequential filtration using 0.8 m, 0.45 m and 0.22 m syringe filters, and were concentrated further by pelleting PMPs for 1.5 hrs at 40,000× g and resuspending the pellet in 4 ml UltraPure™ DNase/RNase-Free Distilled Water (ThermoFisher, 10977023). Final PMP concentration (7.56×10¹² PMPs/ml) and average PMP size (70.3 nm+/−12.4 nm SD) were determined by NanoFCM, using concentration and size standards provided by the manufacturer.

b) Loading of Luciferase Protein into Grapefruit PMPs

Grapefruit PMPs were produced as described in Example 14a. Luciferase (Luc) protein was purchased from LSBio (cat. no. LS-G5533-150) and dissolved in PBS, pH7.4 to a final concentration of 300 μg/mL. Filter-sterilized PMPs were loaded with luciferase protein by electroporation, using a protocol adapted from Rachael W. Sirianni and Bahareh Behkam (eds.), Targeted Drug Delivery: Methods and Protocols, Methods in Molecular Biology, vol. 1831. PMPs alone (PMP control), luciferase protein alone (protein control), or PMP+luciferase protein (protein-loaded PMPs), were mixed with 4.8× electroporation buffer (100% Optiprep (Sigma, D1556) in UltraPure water) to have a final 21% Optiprep concentration in the reaction mix (see Table 6). Protein control was made by mixing luciferase protein with UltraPure water instead of Optiprep (protein control), as the final PMP-Luc pellet was diluted in water. Samples were transferred into chilled cuvettes and electroporated at 0.400 kV, 125 μF (0.125 mF), resistance low 100Ω-high 600Ω with two pulses (4-10 ms) using a Biorad GenePulser®. The reaction was put on ice for 10 minutes, and transferred to a pre-ice chilled 1.5 ml ultracentrifuge tube. All samples containing PMPs were washed 3 times by adding 1.4 ml ultrapure water, followed by ultracentrifugation (100,000×g for 1.5 h at 4° C.). The final pellet was resuspended in a minimal volume of UltraPure water (50 μL) and kept at 4° C. until use. After electroporation, samples containing luciferase protein only were not washed by centrifugation and were stored at 4° C. until use.

To determine the PMP loading capacity, one microliter of Luciferase-loaded PMPs (PMP-Luc) and one microliter of unloaded PMPs were used. To determine the amount of Luciferase protein loaded in the PMPs, a Luciferase protein (LSBio, LS-G5533-150) standard curve was made (10, 30, 100, 300, and 1000 ng). Luciferase activity in all samples and standards was assayed using the ONE-Glo™ luciferase assay kit (Promega, E6110) and measuring luminescence using a SpectraMax® spectrophotometer. The amount of luciferase protein loaded in PMPs was determined using a standard curve of Luciferase protein (LSBio, LS-G5533-150) and normalized to the luminescence in the unloaded PMP sample. The loading capacity (ng luciferase protein per 1E+9 particles) was calculated as the luciferase protein concentration (ng) divided by the number of loaded PMPs (PMP-Luc). The PMP-Luc loading capacity was 2.76 ng Luciferase protein/1×10⁹ PMPs.

Our results indicate that PMPs can be loaded with a model protein that remains active after encapsulation.

TABLE 6
Luciferase protein loading strategy using electroporation.
	Luciferase	Luciferase	PMP
	PMP (protein-	(protein	(PMP
	loaded PMPs)	control)	control)
Luciferase protein (300	25	25	0
μg/mL (μL)
Optiprep 100% (μL)	14.7	0	14.7
UltraPure water (μL)	10.3	45	35.3
PMP GF (PMP stock	20	0	20
concentration = 7.56 × 1012
PMP/mL)
Final volume	70	70	70
Note:
25 μL luciferase is equivalent to 7.5 μg luciferase protein.

c) Treatment of Pseudomonas aeruginosa with Luciferase Protein-Loaded Grapefruit PMPs

Pseudomonas aeruginosa (ATCC) was grown overnight at 30° C. in tryptic soy broth supplemented with 50 ug/ml Rifampicin, according to the supplier's instructions. Pseudomonas aeruginosa cells (total volume of 5 ml) were collected by centrifugation at 3,000×g for 5 min. Cells were washed twice with 10 ml 10 mM MgCl₂ and resuspended in 5 ml 10 mM MgCl₂. The OD600 was measured and adjusted to 0.5.

Treatments were performed in duplicate in 1.5 ml Eppendorf tubes, containing 50 μl of the resuspended Pseudomonas aeruginosa cells supplemented with either 3 ng of PMP-Luc (diluted in Ultrapure water), 3 ng free luciferase protein (protein only control; diluted in Ultrapure water), or Ultrapure water (negative control). Ultrapure water was added to 75 μl in all samples. Samples were mixed and incubated at room temperature for 2 h and covered with aluminum foil. Samples were next centrifuged at 6,000×g for 5 min, and 70 μl of the supernatant was collected and saved for luciferase detection. The bacterial pellet was subsequently washed three times with 500 μl 10 mM MgCl₂ containing 0.5% Triton X-100 to remove/burst PMPs that were not taken up. A final wash with 1 ml 10 mM MgCl₂ was performed to remove residual Triton X-100. 970 μl of the supernatant was removed (leaving the pellet in 30 ul wash buffer) and 20 μl 10 mM MgCl₂ and 25 μl Ultrapure water were added to resuspend the Pseudomonas aeruginosa pellets. Luciferase protein was measured by luminescence using the ONE-Glo™ luciferase assay kit (Promega, E6110), according to the manufacturer's instructions. Samples (bacterial pellet and supernatant samples) were incubated for 10 minutes, and luminescence was measured on a SpectraMax® spectrophotometer. Pseudomonas aeruginosa treated with Luciferase protein-loaded grapefruit PMPs had a 19.3 fold higher luciferase expression than treatment with free luciferase protein alone or the Ultrapure water control (negative control), indicating that PMPs are able to efficiently deliver their protein cargo into bacteria (FIG. 10). In addition, PMPs appear to protect luciferase protein from degradation, as free luciferase protein levels in both the supernatant and bacterial pellets are very low. Considering the treatment dose was 3 ng luciferase protein, based on the luciferase protein standard curve, free luciferase protein in supernatant or bacterial pellets after 2 hours of RT incubation in water corresponds to <0.1 ng luciferase protein, indicating protein degradation.

Our data shows that PMPs can deliver a protein cargo into organisms, and that PMPs can protect their cargo from degradation by the environment.

Example 15: Insulin-Loaded PMPs Protect their Protein Cargo from Enzymatic Degradation

This example demonstrates that human insulin protein was loaded into lemon and grapefruit PMPs and that PMP-encapsulated insulin is protected from degradation by proteinase K and simulated gastrointestinal (GI) fluids. Compositions that can withstand degradation by GI fluids may be useful for oral delivery of compounds, e.g., proteins.

a) Production of PMPs

Lemons and grapefruits were obtained from a local grocery store. Fruits were washed with 1% Liquinox® (Alconox®) detergent and rinsed under warm water. Six liters each of lemon and grapefruit juice were collected using a juice press, depulped through a 1 mm mesh pore size metal strainer, and adjusted to pH 4.5 with 10 N sodium hydroxide before the addition of pectinase enzyme at a final concentration of 0.5 U/mL (Pectinase from Aspergillus niger, Sigma). The juice was incubated with the pectinase enzyme for 2 hours at 25° C. and subsequently centrifuged at 3,000×g for 20 minutes, followed by centrifugation at 10,000×g for 40 minutes to remove large debris. Next, EDTA was added to the processed juice to a final concentration of 50 mM, and pH was adjusted to 7.5. Juice clarification was performed by vacuum filtration through 11 μm filter paper (Whatman®), followed by 1 μM syringe-filtration (glass fiber, VWR®) and 0.45 μM vacuum filtration (PES, Celltreat® Scientific Products) to remove large particles.

Filtered juice was subsequently concentrated, washed, and concentrated again by tangential flow filtration (TFF) using a 300 kDa pore size hollow fiber filter. Juice was concentrated 8×, followed by diafiltration into 10 diavolumes of 1×PBS (pH 7.4), and further concentrated to a final concentration of 50× based on the initial juice volume. Next, we used size exclusion chromatography (SEC; maxiPURE-EVs size exclusion chromatography columns, HansaBioMed Life Sciences) to elute the PMP-containing fractions, which were analyzed by absorbance at 280 nm (SpectraMax® spectrophotometer) and protein concentration was determined by BCA assay (Pierce™ BCA Protein Assay Kit, Thermo Scientific) to verify the PMP-containing fractions and late fractions containing contaminants. Lemon SEC fractions 3-8 (early fractions) contained purified PMPs; fractions 9-14 contained contaminants. Grapefruit SEC fractions 3-7 (early fractions) contained purified PMPs; fractions 8-14 contained contaminants. The early fractions were combined and filter-sterilized by sequential filtration using 1 μm glass fiber syringe filters (Acrodisc®, Pall Corporation), 0.45 μm syringe filters (Whatman® PURADISC™), and 0.22 μm (Whatman® PURADISC™) syringe filters under aseptic conditions in a tissue culture hood. Then, PMPs were concentrated by ultracentrifugation for 1.5 hours at 40,000×g at 4° C. The PMP pellet was resuspended in 5.5 mL of sterile 1×PBS (pH 7.4). Final PMP concentration (7.59×10¹³ lemon PMPs/mL; 3.54×10¹³ grapefruit PMPs/mL) and PMP median size were determined by NanoFCM, using concentration and size standards provided by the manufacturer. Protein concentration of the final PMP suspension was determined by BCA (Pierce™ BCA Protein Assay Kit, Thermo Scientific) (lemon PMPs 1.1 mg/mL; grapefruit PMPs 4.4 mg/mL). 2 mL of the produced lemon PMPs and 2 mL of the produced grapefruit PMPs were ultracentrifuged (1.5 hours, 40,000×g, 4° C.) to replace the PBS buffer with UltraPure™ water (Invitrogen), and the concentration was remeasured by NanoFCM (8.42×10¹³ lemon PMPs/mL; 3.29×10¹³ grapefruit PMPs/mL). These PMP suspensions were used for lipid extraction as described in Example 15b.

b) Loading of PMPs with Insulin Protein

Total lipids from lemon and grapefruit PMPs were extracted using the Bligh-Dyer method (Bligh and Dyer, Can J Biochem Physiol, 37: 911-917, 1959). PMP pellets were prepared by ultracentrifugation at 40,000×g for 1.5 hours at 4° C. and resuspended in UltraPure™ water (Invitrogen). In a glass tube, a mixture of chloroform:methanol (CHCl₃:MeOH) at a 1:2 v/v ratio was prepared. For each 1 mL PMP sample, 3.75 mL of CHCl₃:MeOH was added and vortexed. Then, 1.25 mL CHCl₃ was added and vortexed. Finally, 1.25 mL UltraPure™ water (Invitrogen) was added and vortexed. This preparation was centrifuged at 210×g in table-top centrifuge for 5 minutes at room temperature to give a two-phase system (aqueous on top, organic at the bottom). The organic phase was recovered using a glass Pasteur pipette, taking care to avoid both the aqueous phase and the interphase. The organic phase was aliquoted into smaller volumes containing approximately 2-3 mg of lipids (1 L of citrus juice yields approximately 3-5×10¹³ PMPs, which corresponds to approximately 10 mg of lipids). Lipid aliquots were dried under nitrogen gas and stored at −20° C. until use.

Recombinant human insulin (Gibco, cat. no. A11382II) was dissolved in 10 mM hydrochloric acid at 10 mg/mL and diluted to 1 mg/mL in water. Insulin-loaded lipid reconstructed PMPs (recPMPs) were prepared from 3 mg dried lemon PMP lipids and 0.6 mg insulin (5:1 w/w ratio), which was added to the lipid film at a volume of 600 μL. Glass beads (˜7-8) were added, and the solution was agitated at room temperature for 1-2 hours. The samples were then sonicated in a water bath sonicator (Branson) for 5 minutes at room temperature, vortexed, and agitated again at room temperature for 1-2 hours. The formulations were then extruded using an Mini Extruder (Avanti® Polar Lipids) with sequential 800 nm, 400 nm, and 200 nm polycarbonate membranes. Subsequently, the formulation was purified using a Zeba™ Spin Desalting Column (40 kDa MWCO, Thermo Fisher Scientific), followed by ultracentrifugation at 100,000×g for 45 minutes, and washed once with UltraPure™ water. The pellet was resuspended in 1×PBS (pH 7.4) to a final concentration of 7.94×10¹¹ recPMPs/mL, measured using nanoFCM.

Insulin-loaded grapefruit recPMPs were similarly formulated, except that 2 mg of dried lipids was mixed with 0.4 mg insulin (maintaining the 5:1 w/w ratio). Samples were agitated at room temperature for 3.5 hours, sonicated for 5 minutes, vortexed, and again sonicated for 5 minutes, all at room temperature. Extrusion was performed as described above. Purification was done using Amicon® Ultra centrifugation filters (100K MWCO, Millipore) at 14,000×g for 5 minutes (repeated once), followed by Zeba™ Spin Desalting Column (40 kDa MWCO, Thermo Fisher Scientific) and ultracentrifugation as described above. The pellet was resuspended in 1×PBS to a final concentration of 1.19×10¹² recPMPs/mL, measured using nanoFCM.

To assess insulin loading into recPMPs and to test whether insulin-loaded recPMPs from lemon and grapefruit PMP lipids can protect human insulin protein, a proteinase K (ProtK) treatment followed by Western blot analysis was performed. To this end, insulin-loaded recPMP samples were incubated with 20 μg/mL ProtK (New England Biolabs® Inc.) in 50 mM Tris hydrochloride (pH 7.5) and 5 mM calcium chloride at 37° C. for 1 hour with agitation.

To assess insulin protein levels, samples (10 μL) were diluted with Laemmli sample buffer with Orange G (Sigma) substituted for bromophenol blue to eliminate signal interference during imaging. Samples were boiled for 10 minutes, cooled on ice, loaded onto Tris-glycine gels (TGX™, Bio-Rad). Subsequently, gels were transferred onto nitrocellulose membranes using an iBlot™ 2 system (Invitrogen) according to the manufacturer's instructions. Nitrocellulose membranes were briefly washed with 1×PBS (pH 7.4) and blocked with Odyssey blocking buffer (Li-COR) for 1 hour at room temperature. Membranes were then incubated with 1:1000 rabbit anti-insulin primary antibody (ab181547, Abcam), followed by 1:10,000 goat anti-rabbit IRDye® 800CW secondary antibody (Li-COR) for 2 hours each. Membranes were washed three times after each antibody incubation with 1×PBS with 0.1% Tween® 20 (Sigma) and a final rinse in 1×PBS. Membranes were imaged on an iBright™ 1500 FL (Invitrogen™). Lemon and grapefruit insulin-recPMP samples showed comparable levels of insulin protein with and without ProtK treatment, indicating that the insulin is encapsulated and protected within the PMPs. Quantification of the amount of loaded insulin based on free insulin protein standards and normalized for PMP concentration revealed loading of 21 ng of insulin per 10⁹ lemon recPMPs.

To determine whether lysing the PMP lipid membrane before or after proteinase K (ProtK) treatment affected insulin stability, grapefruit insulin-loaded recPMP samples were treated with (1) 1% TRITON™ X-100 for 30 minutes (lysing the lipid membranes and exposing the protein cargo); (2) 10 μg/mL ProtK treatment for 1 hour; (3) 1% TRITON™ X-100 for 30 minutes, followed by 10 μg/mL ProtK treatment for 1 hour, and inactivating the reaction by adding 10 mM PMSF; and (4) 10 μg/ml ProtK treatment for 1 hour, inactivating ProtK by adding 10 mM PMSF, followed by 1% TRITON™ X-100 for 30 minutes. All treatments were performed at 37° C. with agitation. A Western blot for insulin was performed for each sample as described above (FIG. 11A). Encapsulated insulin cargo was degraded only when PMP membranes were lysed by TRITON™ X-100 prior to ProtK digestion, demonstrating that insulin protein is encapsulated inside the PMPs and that PMPs protect protein cargo from enzymatic digestion by ProtK.

c) Stability of Insulin-Loaded PMPs in GI Fluids

To further assess the stability of encapsulated insulin, loaded PMPs prepared from lemon lipids were exposed to simulated GI fluids that contain relevant bile acids, digestive enzymes, and pH to mimic distinct gastrointestinal environments and conditions. Digestive buffers were purchased from Biorelevant and prepared according to the manufacturer's instructions. The following buffers were used: FaSSGF (fasted stomach, pH 1.6), FaSSIF (fasted small intestines, pH 6.4), and FeSSIF (fed small intestines, pH 5.8). 1×PBS (pH 7.4) was used as negative control. For each sample, 980 μL buffer was added to 20 μL insulin-loaded recPMPs (lemon; 7.94×10¹¹ recPMPs/mL) under low vortexing. Each treatment (buffer condition) was performed in duplicate. Insulin-loaded recPMPs were incubated in FaSSGF for 1 hour and in all other buffers for 4 hours to approximate the passage times in the human digestive system. All incubations were performed at 37° C. under slow rotation. Following incubation at 37° C., samples were placed on ice and centrifuged at 100,000×g for 50 minutes to pellet the insulin-loaded recPMPs. Samples were washed once by resuspension in UltraPure™ water (Invitrogen) and centrifuged again. Pellets were then resuspended in 10 μL UltraPure™ water and used for Western blot analysis to detect insulin protein as described above. Imaging of the GI buffer-treated samples (FIG. 11B) revealed that insulin-loaded recPMPs are stable in buffers simulating both fasted stomach (FaSSGF) and fasted small intestines (FaSSIF). In simulated fed small intestine (FeSSIF) buffer, however, insulin could not be detected (FIG. 11B), indicating that under these conditions insulin-loaded recPMPs vesicles were not able to protect insulin from degradation. Free insulin protein was stable only in 1×PBS, but unstable in all three GI buffers used (data not shown). Taken together, these experiments show that reconstructed PMPs from citrus lipids protect their protein payload from degradation by low pH (FaSSGF) and digestive enzymes/GI fluids (ProtK, FaSSIF).

Other Embodiments

Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, the descriptions and examples should not be construed as limiting the scope of the invention. The disclosures of all patent and scientific literature cited herein are expressly incorporated in their entirety by reference.

Other embodiments are within the claims.

APPENDIX

TABLE 7
Plant EV-Markers
Example Species	Accession No.	Protein Name
Arabidopsis thaliana	C0LGG8	Probable LRR receptor-like serine/threonine-protein kinase
		At1g53430 (EC 2.7.11.1)
Arabidopsis thaliana	F4HQT8	Uncharacterized protein
Arabidopsis thaliana	F4HWU0	Protein kinase superfamily protein
Arabidopsis thaliana	F4I082	Bifunctional inhibitor/lipid-transfer protein/seed storage 2S
		albumin superfamily protein
Arabidopsis thaliana	F4I3M3	Kinase with tetratricopeptide repeat domain-containing
		protein
Arabidopsis thaliana	F4IB62	Leucine-rich repeat protein kinase family protein
Arabidopsis thaliana	O03042	Ribulose bisphosphate carboxylase large chain (RuBisCO
		large subunit) (EC 4.1.1.39)
Arabidopsis thaliana	O03986	Heat shock protein 90-4 (AtHSP90.4) (AtHsp90-4) (Heat
		shock protein 81-4) (Hsp81-4)
Arabidopsis thaliana	O04023	Protein SRC2 homolog (AtSRC2)
Arabidopsis thaliana	O04309	Jacalin-related lectin 35 (JA-responsive protein 1)
		(Myrosinase-binding protein-like At3g16470)
Arabidopsis thaliana	O04314	PYK10-binding protein 1 (Jacalin-related lectin 30) (Jasmonic
		acid-induced protein)
Arabidopsis thaliana	O04922	Probable glutathione peroxidase 2 (EC 1.11.1.9)
Arabidopsis thaliana	O22126	Fasciclin-like arabinogalactan protein 8 (AtAGP8)
Arabidopsis thaliana	O23179	Patatin-like protein 1 (AtPLP1 (EC 3.1.1.—) (Patatin-related
		phospholipase A IIgamma) (pPLAIIg) (Phospholipase A IVA)
		(AtPLAIVA)
Arabidopsis thaliana	O23207	Probable NAD(P)H dehydrogenase (quinone) FQR1-like 2
		(EC 1.6.5.2)
Arabidopsis thaliana	O23255	Adenosylhomocysteinase 1 (AdoHcyase 1) (EC 3.3.1.1)
		(Protein EMBRYO DEFECTIVE 1395) (Protein
		HOMOLOGY-DEPENDENT GENE SILENCING 1)
		(S-adenosyl-L-homocysteine hydrolase 1)
		(SAH hydrolase 1)
Arabidopsis thaliana	O23482	Oligopeptide transporter 3 (AtOPT3)
Arabidopsis thaliana	O23654	V-type proton ATPase catalytic subunit A (V-ATPase subunit
		A) (EC 3.6.3.14) (V-ATPase 69 kDa subunit) (Vacuolar H(+)-ATPase
		subunit A) (Vacuolar proton pump subunit alpha)
Arabidopsis thaliana	O48788	Probable inactive receptor kinase At2g26730
Arabidopsis thaliana	O48963	Phototropin-1 (EC 2.7.11.1) (Non-phototropic hypocotyl
		protein 1) (Root phototropism protein 1)
Arabidopsis thaliana	O49195	Vegetative storage protein 1
Arabidopsis thaliana	O50008	5-methyltetrahydropteroyltriglutamate--homocysteine
		methyltransferase 1 (EC 2.1.1.14) (Cobalamin-independent
		methionine synthase 1) (AtMS1) (Vitamin-B12-independent
		methionine synthase 1)
Arabidopsis thaliana	O64696	Putative uncharacterized protein At2g34510
Arabidopsis thaliana	O65572	Carotenoid 9,10(9′,10′)-cleavage dioxygenase 1 (EC
		1.14.99.n4) (AtCCD1) (Neoxanthin cleavage enzyme NC1)
		(AtNCED1)
Arabidopsis thaliana	O65660	PLAT domain-containing protein 1 (AtPLAT1) (PLAT domain
		protein 1)
Arabidopsis thaliana	O65719	Heat shock 70 kDa protein 3 (Heat shock cognate 70 kDa
		protein 3) (Heat shock cognate protein 70-3) (AtHsc70-3)
		(Heat shock protein 70-3) (AtHsp70-3)
Arabidopsis thaliana	O80517	Uclacyanin-2 (Blue copper-binding protein II) (BCB II)
		(Phytocyanin 2) (Uclacyanin-II)
Arabidopsis thaliana	O80576	At2g44060 (Late embryogenesis abundant protein, group 2)
		(Similar to late embryogenesis abundant proteins)
Arabidopsis thaliana	O80725	ABC transporter B family member 4 (ABC transporter
		ABCB.4) (AtABCB4) (Multidrug resistance protein 4)
		(P-glycoprotein 4)
Arabidopsis thaliana	O80837	Remorin (DNA-binding protein)
Arabidopsis thaliana	O80852	Glutathione S-transferase F9 (AtGSTF9) (EC 2.5.1.18)
		(AtGSTF7) (GST class-phi member 9)
Arabidopsis thaliana	O80858	Expressed protein (Putative uncharacterized protein
		At2g30930) (Putative uncharacterized protein At2g30930;
		F7F1.14)
Arabidopsis thaliana	O80939	L-type lectin-domain containing receptor kinase IV.1
		(Arabidopsis thaliana lectin-receptor kinase e) (AthlecRK-e)
		(LecRK-IV.1) (EC 2.7.11.1) (Lectin Receptor Kinase 1)
Arabidopsis thaliana	O80948	Jacalin-related lectin 23 (Myrosinase-binding protein-like
		At2g39330)
Arabidopsis thaliana	O82628	V-type proton ATPase subunit G1 (V-ATPase subunit G1)
		(Vacuolar H(+)-ATPase subunit G isoform 1) (Vacuolar
		proton pump subunit G1)
Arabidopsis thaliana	P10795	Ribulose bisphosphate carboxylase small chain 1A,
		chloroplastic (RuBisCO small subunit 1A) (EC 4.1.1.39)
Arabidopsis thaliana	P10896	Ribulose bisphosphate carboxylase/oxygenase activase,
		chloroplastic (RA) (RuBisCO activase)
Arabidopsis thaliana	P17094	60S ribosomal protein L3-1 (Protein EMBRYO DEFECTIVE
		2207)
Arabidopsis thaliana	P19456	ATPase 2, plasma membrane-type (EC 3.6.3.6) (Proton
		pump 2)
Arabidopsis thaliana	P20649	ATPase 1, plasma membrane-type (EC 3.6.3.6) (Proton
		pump 1)
Arabidopsis thaliana	P22953	Probable mediator of RNA polymerase II transcription subunit
		37e (Heat shock 70 kDa protein 1) (Heat shock cognate 70
		kDa protein 1) (Heat shock cognate protein 70-1) (AtHsc70-1)
		(Heat shock protein 70-1) (AtHsp70-1) (Protein
		EARLY-RESPONSIVE TO DEHYDRATION 2)
Arabidopsis thaliana	P23586	Sugar transport protein 1 (Glucose transporter) (Hexose
		transporter 1)
Arabidopsis thaliana	P24636	Tubulin beta-4 chain (Beta-4-tubulin)
Arabidopsis thaliana	P25696	Bifunctional enolase 2/transcriptional activator (EC 4.2.1.11)
		(2-phospho-D-glycerate hydro-lyase 2) (2-phosphoglycerate
		dehydratase 2) (LOW EXPRESSION OF OSMOTICALLY
		RESPONSIVE GENES 1)
Arabidopsis thaliana	P25856	Glyceraldehyde-3-phosphate dehydrogenase GAPA1,
		chloroplastic (EC 1.2.1.13) (NADP-dependent
		glyceraldehydephosphate dehydrogenase A subunit 1)
Arabidopsis thaliana	P28186	Ras-related protein RABE1c (AtRABE1c) (Ras-related
		protein Ara-3) (Ras-related protein Rab8A) (AtRab8A)
Arabidopsis thaliana	P30302	Aquaporin PIP2-3 (Plasma membrane intrinsic protein 2-3)
		(AtPIP2; 3) (Plasma membrane intrinsic protein 2c) (PIP2c)
		(RD28-PIP) (TMP2C) (Water stress-induced tonoplast
		intrinsic protein) (WSI-TIP) [Cleaved into: Aquaporin PIP2-3,
		N-terminally processed]
Arabidopsis thaliana	P31414	Pyrophosphate-energized vacuolar membrane proton pump
		1 (EC 3.6.1.1) (Pyrophosphate-energized inorganic
		pyrophosphatase 1) (H(+)-PPase 1) (Vacuolar proton
		pyrophosphatase 1) (Vacuolar proton pyrophosphatase 3)
Arabidopsis thaliana	P32961	Nitrilase 1 (EC 3.5.5.1)
Arabidopsis thaliana	P38666	60S ribosomal protein L24-2 (Protein SHORT VALVE 1)
Arabidopsis thaliana	P39207	Nucleoside diphosphate kinase 1 (EC 2.7.4.6) (Nucleoside
		diphosphate kinase I) (NDK I) (NDP kinase I) (NDPK I)
Arabidopsis thaliana	P42643	14-3-3-like protein GF14 chi (General regulatory factor 1)
Arabidopsis thaliana	P42737	Beta carbonic anhydrase 2, chloroplastic (AtbCA2)
		(AtbetaCA2) (EC 4.2.1.1) (Beta carbonate dehydratase 2)
Arabidopsis thaliana	P42759	Dehydrin ERD10 (Low-temperature-induced protein LTI45)
Arabidopsis thaliana	P42761	Glutathione S-transferase F10 (AtGSTF10) (EC 2.5.1.18)
		(AtGSTF4) (GST class-phi member 10) (Protein EARLY
		RESPONSE TO DEHYDRATION 13)
Arabidopsis thaliana	P42763	Dehydrin ERD14
Arabidopsis thaliana	P42791	60S ribosomal protein L18-2
Arabidopsis thaliana	P43286	Aquaporin PIP2-1 (Plasma membrane intrinsic protein 2-1)
		(AtPIP2; 1) (Plasma membrane intrinsic protein 2a) (PIP2a)
		[Cleaved into: Aquaporin PIP2-1, N-terminally processed]
Arabidopsis thaliana	P46286	60S ribosomal protein L8-1 (60S ribosomal protein L2)
		(Protein EMBRYO DEFECTIVE 2296)
Arabidopsis thaliana	P46422	Glutathione S-transferase F2 (AtGSTF2) (EC 2.5.1.18) (24
		kDa auxin-binding protein) (AtPM24) (GST class-phi member 2)
Arabidopsis thaliana	P47998	Cysteine synthase 1 (EC 2.5.1.47) (At.OAS.5-8) (Beta-substituted
		Ala synthase 1; 1) (ARAth-Bsas1; 1) (CSase A)
		(AtCS-A) (Cys-3A) (O-acetylserine (thiol)-lyase 1) (OAS-TL
		A) (O-acetylserine sulfhydrylase) (Protein ONSET OF LEAF
		DEATH 3)
Arabidopsis thaliana	P48347	14-3-3-like protein GF14 epsilon (General regulatory factor 10)
Arabidopsis thaliana	P48491	Triosephosphate isomerase, cytosolic (TIM) (Triose-phosphate
		isomerase) (EC 5.3.1.1)
Arabidopsis thaliana	P50318	Phosphoglycerate kinase 2, chloroplastic (EC 2.7.2.3)
Arabidopsis thaliana	P53492	Actin-7 (Actin-2)
Arabidopsis thaliana	P54144	Ammonium transporter 1 member 1 (AtAMT1; 1)
Arabidopsis thaliana	P92963	Ras-related protein RABB1c (AtRABB1c) (Ras-related
		protein Rab2A) (AtRab2A)
Arabidopsis thaliana	P93004	Aquaporin PIP2-7 (Plasma membrane intrinsic protein 2-7)
		(AtPIP2; 7) (Plasma membrane intrinsic protein 3) (Salt
		stress-induced major intrinsic protein) [Cleaved into:
		Aquaporin PIP2-7, N-terminally processed]
Arabidopsis thaliana	P93025	Phototropin-2 (EC 2.7.11.1) (Defective in chloroplast
		avoidance protein 1) (Non-phototropic hypocotyl 1-like
		protein 1) (AtKin7) (NPH1-like protein 1)
Arabidopsis thaliana	P93819	Malate dehydrogenase 1, cytoplasmic (EC 1.1.1.37)
		(Cytosolic NAD-dependent malate dehydrogenase 1)
		(cNAD-MDH1) (Cytosolic malate dehydrogenase 1)
		(Cytosolic MDH1)
Arabidopsis thaliana	Q03250	Glycine-rich RNA-binding protein 7 (AtGR-RBP7) (AtRBG7)
		(Glycine-rich protein 7) (AtGRP7) (Protein COLD,
		CIRCADIAN RHYTHM, AND RNA BINDING 2) (Protein CCR2)
Arabidopsis thaliana	Q05431	L-ascorbate peroxidase 1, cytosolic (AP) (AtAPx01) (EC
		1.11.1.11)
Arabidopsis thaliana	Q06611	Aquaporin PIP1-2 (AtPIP1; 2) (Plasma membrane intrinsic
		protein 1b) (PIP1b) (Transmembrane protein A) (AthH2)
		(TMP-A)
Arabidopsis thaliana	Q07488	Blue copper protein (Blue copper-binding protein) (AtBCB)
		(Phytocyanin 1) (Stellacyanin)
Arabidopsis thaliana	Q0WLB5	Clathrin heavy chain 2
Arabidopsis thaliana	Q0WNJ6	Clathrin heavy chain 1
Arabidopsis thaliana	Q1ECE0	Vesicle-associated protein 4-1 (Plant VAP homolog 4-1)
		(AtPVA41) (Protein MEMBRANE-ASSOCIATED MANNITOL-INDUCED)
		(AtMAMI) (VAMP-associated protein 4-1)
Arabidopsis thaliana	Q38882	Phospholipase D alpha 1 (AtPLDalpha1) (PLD alpha 1) (EC
		3.1.4.4) (Choline phosphatase 1) (PLDalpha)
		(Phosphatidylcholine-hydrolyzing phospholipase D 1)
Arabidopsis thaliana	Q38900	Peptidyl-prolyl cis-trans isomerase CYP19-1 (PPIase CYP19-1)
		(EC 5.2.1.8) (Cyclophilin of 19 kDa 1) (Rotamase
		cyclophilin-3)
Arabidopsis thaliana	Q39033	Phosphoinositide phospholipase C 2 (EC 3.1.4.11)
		(Phosphoinositide phospholipase PLC2) (AtPLC2) (PI-PLC2)
Arabidopsis thaliana	Q39085	Delta(24)-sterol reductase (EC 1.3.1.72) (Cell elongation
		protein DIMINUTO) (Cell elongation protein Dwarf1) (Protein
		CABBAGE1) (Protein ENHANCED VERY-LOW-FLUENCE
		RESPONSE 1)
Arabidopsis thaliana	Q39228	Sugar transport protein 4 (Hexose transporter 4)
Arabidopsis thaliana	Q39241	Thioredoxin H5 (AtTrxh5) (Protein LOCUS OF
		INSENSITIVITY TO VICTORIN 1) (Thioredoxin 5) (AtTRX5)
Arabidopsis thaliana	Q39258	V-type proton ATPase subunit E1 (V-ATPase subunit E1)
		(Protein EMBRYO DEFECTIVE 2448) (Vacuolar H(+)-
		ATPase subunit E isoform 1) (Vacuolar proton pump subunit E1)
Arabidopsis thaliana	Q42112	60S acidic ribosomal protein P0-2
Arabidopsis thaliana	Q42403	Thioredoxin H3 (AtTrxh3) (Thioredoxin 3) (AtTRX3)
Arabidopsis thaliana	Q42479	Calcium-dependent protein kinase 3 (EC 2.7.11.1)
		(Calcium-dependent protein kinase isoform CDPK6) (AtCDPK6)
Arabidopsis thaliana	Q42547	Catalase-3 (EC 1.11.1.6)
Arabidopsis thaliana	Q56WH1	Tubulin alpha-3 chain
Arabidopsis thaliana	Q56WK6	Patellin-1
Arabidopsis thaliana	Q56X75	CASP-like protein 4D2 (AtCASPL4D2)
Arabidopsis thaliana	Q56ZI2	Patellin-2
Arabidopsis thaliana	Q7Y208	Glycerophosphodiester phosphodiesterase GDPDL1 (EC
		3.1.4.46) (Glycerophosphodiester phosphodiesterase-like 1)
		(ATGDPDL1) (Glycerophosphodiesterase-like 3) (Protein
		SHV3-LIKE 2)
Arabidopsis thaliana	Q84VZ5	Uncharacterized GPI-anchored protein At5g19240
Arabidopsis thaliana	Q84WU7	Eukaryotic aspartyl protease family protein (Putative
		uncharacterized protein At3g51330)
Arabidopsis thaliana	Q8GUL8	Uncharacterized GPI-anchored protein At5g19230
Arabidopsis thaliana	Q8GYA4	Cysteine-rich receptor-like protein kinase 10 (Cysteine-rich
		RLK10) (EC 2.7.11.—) (Receptor-like protein kinase 4)
Arabidopsis thaliana	Q8GYN5	RPM1-interacting protein 4
Arabidopsis thaliana	Q8GZ99	At5g49760 (Leucine-rich repeat protein kinase family protein)
		(Leucine-rich repeat receptor-like protein kinase) (Putative
		receptor protein kinase)
Arabidopsis thaliana	Q8L636	Sodium/calcium exchanger NCL (Na(+)/Ca(2+)-exchange
		protein NCL) (Protein NCX-like) (AtNCL)
Arabidopsis thaliana	Q8L7S1	At1g45200 (At1g45200/At1g45200) (Triacylglycerol
		lipase-like 1)
Arabidopsis thaliana	Q8LAA6	Probable aquaporin PIP1-5 (AtPIP1; 5) (Plasma membrane
		intrinsic protein 1d) (PIP1d)
Arabidopsis thaliana	Q8LCP6	Endoglucanase 10 (EC 3.2.1.4) (Endo-1,4-beta glucanase 10)
Arabidopsis thaliana	Q8RWV0	Transketolase-1, chloroplastic (TK) (EC 2.2.1.1)
Arabidopsis thaliana	Q8S8Q6	Tetraspanin-8
Arabidopsis thaliana	Q8VZG8	MDIS1-interacting receptor like kinase 2 (AtMIK2) (Probable
		LRR receptor-like serine/threonine-protein kinase
		At4g08850) (EC 2.7.11.1)
Arabidopsis thaliana	Q8VZU2	Syntaxin-132 (AtSYP132)
Arabidopsis thaliana	Q8W4E2	V-type proton ATPase subunit B3 (V-ATPase subunit B3)
		(Vacuolar H(+)-ATPase subunit B isoform 3) (Vacuolar
		proton pump subunit B3)
Arabidopsis thaliana	Q8W4S4	V-type proton ATPase subunit a3 (V-ATPase subunit a3)
		(V-type proton ATPase 95 kDa subunit a isoform 3) (V-ATPase
		95 kDa isoform a3) (Vacuolar H(+)-ATPase subunit a isoform
		3) (Vacuolar proton pump subunit a3) (Vacuolar proton
		translocating ATPase 95 kDa subunit a isoform 3)
Arabidopsis thaliana	Q93VG5	40S ribosomal protein S8-1
Arabidopsis thaliana	Q93XY5	Tetraspanin-18 (TOM2A homologous protein 2)
Arabidopsis thaliana	Q93YS4	ABC transporter G family member 22 (ABC transporter
		ABCG.22) (AtABCG22) (White-brown complex homolog
		protein 23) (AtWBC23)
Arabidopsis thaliana	Q93Z08	Glucan endo-1,3-beta-glucosidase 6 (EC 3.2.1.39)
		((1 −> 3)-beta-glucan endohydrolase 6)
		((1 −> 3)-beta-glucanase 6) (Beta-1,3-endoglucanase
		6) (Beta-1,3-glucanase 6)
Arabidopsis thaliana	Q940M8	3-oxo-5-alpha-steroid 4-dehydrogenase (DUF1295)
		(At1g73650/F25P22_7)
Arabidopsis thaliana	Q944A7	Probable serine/threonine-protein kinase At4g35230 (EC
		2.7.11.1)
Arabidopsis thaliana	Q944G5	Protein NRT1/PTR FAMILY 2.10 (AtNPF2.10) (Protein
		GLUCOSINOLATE TRANSPORTER-1)
Arabidopsis thaliana	Q94AZ2	Sugar transport protein 13 (Hexose transporter 13)
		(Multicopy suppressor of snf4 deficiency protein 1)
Arabidopsis thaliana	Q94BT2	Auxin-induced in root cultures protein 12
Arabidopsis thaliana	Q94CE4	Beta carbonic anhydrase 4 (AtbCA4) (AtbetaCA4) (EC
		4.2.1.1) (Beta carbonate dehydratase 4)
Arabidopsis thaliana	Q94KI8	Two pore calcium channel protein 1 (Calcium channel protein
		1) (AtCCH1) (Fatty acid oxygenation up-regulated protein 2)
		(Voltage-dependent calcium channel protein TPC1) (AtTPC1)
Arabidopsis thaliana	Q96262	Plasma membrane-associated cation-binding protein 1
		(AtPCAP1) (Microtubule-destabilizing protein 25)
Arabidopsis thaliana	Q9C5Y0	Phospholipase D delta (AtPLDdelta) (PLD delta) (EC 3.1.4.4)
Arabidopsis thaliana	Q9C7F7	Non-specific lipid transfer protein GPI-anchored 1
		(AtLTPG-1) (Protein LTP-GPI-ANCHORED 1)
Arabidopsis thaliana	Q9C821	Proline-rich receptor-like protein kinase PERK15 (EC
		2.7.11.1) (Proline-rich extensin-like receptor kinase 15)
		(AtPERK15)
Arabidopsis thaliana	Q9C8G5	CSC1-like protein ERD4 (Protein EARLY-RESPONSIVE TO
		DEHYDRATION STRESS 4)
Arabidopsis thaliana	Q9C9C5	60S ribosomal protein L6-3
Arabidopsis thaliana	Q9CAR7	Hypersensitive-induced response protein 2 (AtHIR2)
Arabidopsis thaliana	Q9FFH6	Fasciclin-like arabinogalactan protein 13
Arabidopsis thaliana	Q9FGT8	Temperature-induced lipocalin-1 (AtTIL1)
Arabidopsis thaliana	Q9FJ62	Glycerophosphodiester phosphodiesterase GDPDL4 (EC
		3.1.4.46) (Glycerophosphodiester phosphodiesterase-like 4)
		(ATGDPDL4) (Glycerophosphodiesterase-like 1) (Protein
		SHV3-LIKE 1)
Arabidopsis thaliana	Q9FK68	Ras-related protein RABA1c (AtRABA1c)
Arabidopsis thaliana	Q9FKS8	Lysine histidine transporter 1
Arabidopsis thaliana	Q9FM65	Fasciclin-like arabinogalactan protein 1
Arabidopsis thaliana	Q9FNH6	NDR1/HIN1-like protein 3
Arabidopsis thaliana	Q9FRL3	Sugar transporter ERD6-like 6
Arabidopsis thaliana	Q9FWR4	Glutathione S-transferase DHAR1, mitochondrial (EC
		2.5.1.18) (Chloride intracellular channel homolog 1) (CLIC
		homolog 1) (Glutathione-dependent dehydroascorbate
		reductase 1) (AtDHAR1) (GSH-dependent dehydroascorbate
		reductase 1) (mtDHAR)
Arabidopsis thaliana	Q9FX54	Glyceraldehyde-3-phosphate dehydrogenase GAPC2,
		cytosolic (EC 1.2.1.12) (NAD-dependent
		glyceraldehydephosphate dehydrogenase C subunit 2)
Arabidopsis thaliana	Q9LE22	Probable calcium-binding protein CML27 (Calmodulin-like
		protein 27)
Arabidopsis thaliana	Q9LEX1	At3g61050 (CaLB protein) (Calcium-dependent lipid-binding
		(CaLB domain) family protein)
Arabidopsis thaliana	Q9LF79	Calcium-transporting ATPase 8, plasma membrane-type (EC
		3.6.3.8) (Ca(2+)-ATPase isoform 8)
Arabidopsis thaliana	Q9LJG3	GDSL esterase/lipase ESM1 (EC 3.1.1.—) (Extracellular lipase
		ESM1) (Protein EPITHIOSPECIFIER MODIFIER 1)
		(AtESM1)
Arabidopsis thaliana	Q9LJI5	V-type proton ATPase subunit d1 (V-ATPase subunit d1)
		(Vacuolar H(+)-ATPase subunit d isoform 1) (Vacuolar proton
		pump subunit d1)
Arabidopsis thaliana	Q9LME4	Probable protein phosphatase 2C 9 (AtPP2C09) (EC
		3.1.3.16) (Phytochrome-associated protein phosphatase 2C)
		(PAPP2C)
Arabidopsis thaliana	Q9LNP3	At1g17620/F11A6_23 (F1L3.32) (Late embryogenesis
		abundant (LEA) hydroxyproline-rich glycoprotein family)
		(Putative uncharacterized protein At1g17620)
Arabidopsis thaliana	Q9LNW1	Ras-related protein RABA2b (AtRABA2b)
Arabidopsis thaliana	Q9LQU2	Protein PLANT CADMIUM RESISTANCE 1 (AtPCR1)
Arabidopsis thaliana	Q9LQU4	Protein PLANT CADMIUM RESISTANCE 2 (AtPCR2)
Arabidopsis thaliana	Q9LR30	Glutamate--glyoxylate aminotransferase 1 (AtGGT2) (EC
		2.6.1.4) (Alanine aminotransferase GGT1) (EC 2.6.1.2)
		(Alanine--glyoxylate aminotransferase GGT1) (EC 2.6.1.44)
		(Alanine-2-oxoglutarate aminotransferase 1) (EC 2.6.1.—)
Arabidopsis thaliana	Q9LSI9	Inactive LRR receptor-like serine/threonine-protein kinase
		BIR2 (Protein BAK1-INTERACTING RECEPTOR-LIKE
		KINASE 2)
Arabidopsis thaliana	Q9LSQ5	NAD(P)H dehydrogenase (quinone) FQR1 (EC 1.6.5.2)
		(Flavodoxin-like quinone reductase 1)
Arabidopsis thaliana	Q9LUT0	Protein kinase superfamily protein (Putative uncharacterized
		protein At3g17410) (Serine/threonine protein kinase-like
		protein)
Arabidopsis thaliana	Q9LV48	Proline-rich receptor-like protein kinase PERK1 (EC 2.7.11.1)
		(Proline-rich extensin-like receptor kinase 1) (AtPERK1)
Arabidopsis thaliana	Q9LX65	V-type proton ATPase subunit H (V-ATPase subunit H)
		(Vacuolar H(+)-ATPase subunit H) (Vacuolar proton pump
		subunit H)
Arabidopsis thaliana	Q9LYG3	NADP-dependent malic enzyme 2 (AtNADP-ME2)
		(NADP-malic enzyme 2) (EC 1.1.1.40)
Arabidopsis thaliana	Q9M088	Glucan endo-1,3-beta-glucosidase 5 (EC 3.2.1.39)
		((1 −> 3)-beta-glucan endohydrolase 5)
		((1 −> 3)-beta-glucanase 5) (Beta-1,3-endoglucanase
		5) (Beta-1,3-glucanase 5)
Arabidopsis thaliana	Q9M2D8	Uncharacterized protein At3g61260
Arabidopsis thaliana	Q9M386	Late embryogenesis abundant (LEA) hydroxyproline-rich
		glycoprotein family (Putative uncharacterized protein
		At3g54200) (Putative uncharacterized protein F24B22.160)
Arabidopsis thaliana	Q9M390	Protein NRT1/PTR FAMILY 8.1 (AtNPF8.1) (Peptide
		transporter PTR1)
Arabidopsis thaliana	Q9M5P2	Secretory carrier-associated membrane protein 3 (AtSC3)
		(Secretory carrier membrane protein 3)
Arabidopsis thaliana	Q9M8T0	Probable inactive receptor kinase At3g02880
Arabidopsis thaliana	Q9SDS7	V-type proton ATPase subunit C (V-ATPase subunit C)
		(Vacuolar H(+)-ATPase subunit C) (Vacuolar proton pump
		subunit C)
Arabidopsis thaliana	Q9SEL6	Vesicle transport v-SNARE 11 (AtVTI11) (Protein SHOOT
		GRAVITROPISM 4) (Vesicle soluble NSF attachment protein
		receptor VTI1a) (AtVTI1a) (Vesicle transport v-SNARE
		protein VTI1a)
Arabidopsis thaliana	Q9SF29	Syntaxin-71 (AtSYP71)
Arabidopsis thaliana	Q9SF85	Adenosine kinase 1 (AK 1) (EC 2.7.1.20) (Adenosine
		5′-phosphotransferase 1)
Arabidopsis thaliana	Q9SIE7	PLAT domain-containing protein 2 (AtPLAT2) (PLAT domain
		protein 2)
Arabidopsis thaliana	Q9SIM4	60S ribosomal protein L14-1
Arabidopsis thaliana	Q9SIU8	Probable protein phosphatase 2C 20 (AtPP2C20) (EC
		3.1.3.16) (AtPPC3; 1.2)
Arabidopsis thaliana	Q9SJ81	Fasciclin-like arabinogalactan protein 7
Arabidopsis thaliana	Q9SKB2	Leucine-rich repeat receptor-like serine/threonine/tyrosine-protein
		kinase SOBIR1 (EC 2.7.10.1) (EC 2.7.11.1) (Protein
		EVERSHED) (Protein SUPPRESSOR OF BIR1-1)
Arabidopsis thaliana	Q9SKR2	Synaptotagmin-1 (NTMC2T1.1) (Synaptotagmin A)
Arabidopsis thaliana	Q9SLF7	60S acidic ribosomal protein P2-2
Arabidopsis thaliana	Q9SPE6	Alpha-soluble NSF attachment protein 2 (Alpha-SNAP2)
		(N-ethylmaleimide-sensitive factor attachment protein alpha 2)
Arabidopsis thaliana	Q9SRH6	Hypersensitive-induced response protein 3 (AtHIR3)
Arabidopsis thaliana	Q9SRY5	Glutathione S-transferase F7 (EC 2.5.1.18) (AtGSTF8) (GST
		class-phi member 7) (Glutathione S-transferase 11)
Arabidopsis thaliana	Q9SRZ6	Cytosolic isocitrate dehydrogenase [NADP] (EC 1.1.1.42)
Arabidopsis thaliana	Q9SSK5	MLP-like protein 43
Arabidopsis thaliana	Q9SU13	Fasciclin-like arabinogalactan protein 2
Arabidopsis thaliana	Q9SU40	Monocopper oxidase-like protein SKU5 (Skewed roots)
Arabidopsis thaliana	Q9SUR6	Cystine lyase CORI3 (EC 4.4.1.35) (Protein CORONATINE
		INDUCED 3) (Protein JASMONIC ACID RESPONSIVE 2)
		(Tyrosine aminotransferase CORI3)
Arabidopsis thaliana	Q9SVC2	Syntaxin-122 (AtSYP122) (Synt4)
Arabidopsis thaliana	Q9SVF0	Putative uncharacterized protein AT4g38350 (Putative
		uncharacterized protein F22I13.120)
Arabidopsis thaliana	Q9SW40	Major facilitator superfamily protein (Putative uncharacterized
		protein AT4g34950) (Putative uncharacterized protein
		T11I11.190)
Arabidopsis thaliana	Q9SYT0	Annexin D1 (AnnAt1) (Annexin A1)
Arabidopsis thaliana	Q9SZ11	Glycerophosphodiester phosphodiesterase GDPDL3 (EC
		3.1.4.46) (Glycerophosphodiester phosphodiesterase-like 3)
		(ATGDPDL3) (Glycerophosphodiesterase-like 2) (Protein
		MUTANT ROOT HAIR 5) (Protein SHAVEN 3)
Arabidopsis thaliana	Q9SZN1	V-type proton ATPase subunit B2 (V-ATPase subunit B2)
		(Vacuolar H(+)-ATPase subunit B isoform 2) (Vacuolar
		proton pump subunit B2)
Arabidopsis thaliana	Q9SZP6	AT4g38690/F20M13_250 (PLC-like phosphodiesterases
		superfamily protein) (Putative uncharacterized protein
		AT4g38690) (Putative uncharacterized protein F20M13.250)
Arabidopsis thaliana	Q9SZR1	Calcium-transporting ATPase 10, plasma membrane-type
		(EC 3.6.3.8) (Ca(2+)-ATPase isoform 10)
Arabidopsis thaliana	Q9T053	Phospholipase D gamma 1 (AtPLDgamma1) (PLD gamma 1)
		(EC 3.1.4.4) (Choline phosphatase) (Lecithinase D)
		(Lipophosphodiesterase II)
Arabidopsis thaliana	Q9T076	Early nodulin-like protein 2 (Phytocyanin-like protein)
Arabidopsis thaliana	Q9T0A0	Long chain acyl-CoA synthetase 4 (EC 6.2.1.3)
Arabidopsis thaliana	Q9T0G4	Putative uncharacterized protein AT4g10060 (Putative
		uncharacterized protein T5L19.190)
Arabidopsis thaliana	Q9XEE2	Annexin D2 (AnnAt2)
Arabidopsis thaliana	Q9XGM1	V-type proton ATPase subunit D (V-ATPase subunit D)
		(Vacuolar H(+)-ATPase subunit D) (Vacuolar proton pump
		subunit D)
Arabidopsis thaliana	Q9XI93	At1g13930/F16A14.27 (F16A14.14) (F7A19.2 protein)
		(Oleosin-B3-like protein)
Arabidopsis thaliana	Q9XIE2	ABC transporter G family member 36 (ABC transporter
		ABCG.36) (AtABCG36) (Pleiotropic drug resistance protein
		8) (Protein PENETRATION 3)
Arabidopsis thaliana	Q9ZPZ4	Putative uncharacterized protein (Putative uncharacterized
		protein At1g09310) (T31J12.3 protein)
Arabidopsis thaliana	Q9ZQX4	V-type proton ATPase subunit F (V-ATPase subunit F)
		(V-ATPase 14 kDa subunit) (Vacuolar H(+)-ATPase subunit F)
		(Vacuolar proton pump subunit F)
Arabidopsis thaliana	Q9ZSA2	Calcium-dependent protein kinase 21 (EC 2.7.11.1)
Arabidopsis thaliana	Q9ZSD4	Syntaxin-121 (AtSYP121) (Syntaxin-related protein At-Syr1)
Arabidopsis thaliana	Q9ZV07	Probable aquaporin PIP2-6 (Plasma membrane intrinsic
		protein 2-6) (AtPIP2; 6) (Plasma membrane intrinsic protein
		2e) (PIP2e) [Cleaved into: Probable aquaporin PIP2-6,
		N-terminally processed]
Arabidopsis thaliana	Q9ZVF3	MLP-like protein 328
Arabidopsis thaliana	Q9ZWA8	Fasciclin-like arabinogalactan protein 9
Arabidopsis thaliana	Q9ZSD4	SYR1, Syntaxin Related Protein 1, also known as SYP121,
		PENETRATION1/PEN1 (Protein PENETRATION 1)
Citrus lemon	A1ECK0	Putative glutaredoxin
Citrus lemon	A9YVC9	Pyrophosphate--fructose 6-phosphate 1-phosphotransferase
		subunit beta (PFP) (EC 2.7.1.90) (6-phosphofructokinase,
		pyrophosphate dependent) (PPi-PFK)
		(Pyrophosphate-dependent 6-phosphofructose-1-kinase)
Citrus lemon	B2YGY1	Glycosyltransferase (EC 2.4.1.—)
Citrus lemon	B6DZD3	Glutathione S-transferase Tau2 (Glutathione transferase
		Tau2)
Citrus lemon	C3VIC2	Translation elongation factor
Citrus lemon	C8CPS0	Importin subunit alpha
Citrus lemon	D3JWB5	Flavanone 3-hydroxylase
Citrus lemon	E0ADY2	Putative caffeic acid O-methyltransferase
Citrus lemon	E5DK62	ATP synthase subunit alpha (Fragment)
Citrus lemon	E9M5S3	Putative L-galactose-1-phosphate phosphatase
Citrus lemon	F1CGQ9	Heat shock protein 90
Citrus lemon	F8WL79	Aminopeptidase (EC 3.4.11.—)
Citrus lemon	F8WL86	Heat shock protein
Citrus lemon	K9JG59	Abscisic acid stress ripening-related protein
Citrus lemon	Q000W4	Fe(III)-chelate reductase
Citrus lemon	Q39538	Heat shock protein (Fragment)
Citrus lemon	Q5UEN6	Putative signal recognition particle protein
Citrus lemon	Q8GV08	Dehydrin
Citrus lemon	Q8L893	Cytosolic phosphoglucomutase (Fragment)
Citrus lemon	Q8S990	Polygalacturonase-inhibiting protein
Citrus lemon	Q8W3U6	Polygalacturonase-inhibitor protein
Citrus lemon	Q93XL8	Dehydrin COR15
Citrus lemon	Q941Q1	Non-symbiotic hemoglobin class 1
Citrus lemon	Q9MBF3	Glycine-rich RNA-binding protein
Citrus lemon	Q9SP55	V-type proton ATPase subunit G (V-ATPase subunit G)
		(Vacuolar proton pump subunit G)
Citrus lemon	Q9THJ8	Ribulose bisphosphate carboxylase large chain (EC 4.1.1.39)
		(Fragment)
Citrus lemon	Q9ZST2	Pyrophosphate--fructose 6-phosphate 1-phosphotransferase
		subunit alpha (PFP) (6-phosphofructokinase, pyrophosphate
		dependent) (PPi-PFK) (Pyrophosphate-dependent
		6-phosphofructose-1-kinase)
Citrus lemon	Q9ZWH6	Polygalacturonase inhibitor
Citrus lemon	S5DXI9	Nucleocapsid protein
Citrus lemon	S5NFC6	GTP cyclohydrolase
Citrus lemon	V4RG42	Uncharacterized protein
Citrus lemon	V4RGP4	Uncharacterized protein
Citrus lemon	V4RHN8	Uncharacterized protein
Citrus lemon	V4RJ07	Uncharacterized protein
Citrus lemon	V4RJK9	Adenosylhomocysteinase (EC 3.3.1.1)
Citrus lemon	V4RJM1	Uncharacterized protein
Citrus lemon	V4RJX1	40S ribosomal protein S6
Citrus lemon	V4RLB2	Uncharacterized protein
Citrus lemon	V4RMX8	Uncharacterized protein
Citrus lemon	V4RNA5	Uncharacterized protein
Citrus lemon	V4RP81	Glycosyltransferase (EC 2.4.1.—)
Citrus lemon	V4RPZ5	Adenylyl cyclase-associated protein
Citrus lemon	V4RTN9	Histone H4
Citrus lemon	V4RUZ4	Phosphoserine aminotransferase (EC 2.6.1.52)
Citrus lemon	V4RVF6	Uncharacterized protein
Citrus lemon	V4RXD4	Uncharacterized protein
Citrus lemon	V4RXG2	Uncharacterized protein
Citrus lemon	V4RYA0	Uncharacterized protein
Citrus lemon	V4RYE3	Uncharacterized protein
Citrus lemon	V4RYH3	Uncharacterized protein
Citrus lemon	V4RYX8	Uncharacterized protein
Citrus lemon	V4RZ12	Coatomer subunit beta′
Citrus lemon	V4RZ89	Uncharacterized protein
Citrus lemon	V4RZE3	Uncharacterized protein
Citrus lemon	V4RZF3	1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase (EC
		1.13.11.54) (Acireductone dioxygenase (Fe(2+)-requiring))
		(ARD) (Fe-ARD)
Citrus lemon	V4RZM7	Uncharacterized protein
Citrus lemon	V4RZX6	Uncharacterized protein
Citrus lemon	V4S1V0	Uncharacterized protein
Citrus lemon	V4S2B6	Uncharacterized protein
Citrus lemon	V4S2N1	Uncharacterized protein
Citrus lemon	V4S2S5	Uncharacterized protein (Fragment)
Citrus lemon	V4S346	Uncharacterized protein
Citrus lemon	V4S3T8	Uncharacterized protein
Citrus lemon	V4S409	Cyanate hydratase (Cyanase) (EC 4.2.1.104) (Cyanate
		hydrolase) (Cyanate lyase)
Citrus lemon	V4S4E4	Histone H2B
Citrus lemon	V4S4F6	Flavin-containing monooxygenase (EC 1.—.—.—)
Citrus lemon	V4S4J1	Uncharacterized protein
Citrus lemon	V4S4K9	Uncharacterized protein
Citrus lemon	V4S535	Proteasome subunit alpha type (EC 3.4.25.1)
Citrus lemon	V4S5A8	Isocitrate dehydrogenase [NADP] (EC 1.1.1.42)
Citrus lemon	V4S5G8	Uncharacterized protein
Citrus lemon	V4S5I6	Uncharacterized protein
Citrus lemon	V4S5N4	Uncharacterized protein (Fragment)
Citrus lemon	V4S5Q3	Uncharacterized protein
Citrus lemon	V4S5X8	Uncharacterized protein
Citrus lemon	V4S5Y1	Uncharacterized protein
Citrus lemon	V4S6P4	Calcium-transporting ATPase (EC 3.6.3.8)
Citrus lemon	V4S6W0	Uncharacterized protein
Citrus lemon	V4S6W7	Uncharacterized protein (Fragment)
Citrus lemon	V4S6Y4	Uncharacterized protein
Citrus lemon	V4S773	Ribosomal protein L19
Citrus lemon	V4S7U0	Uncharacterized protein
Citrus lemon	V4S7U5	Uncharacterized protein
Citrus lemon	V4S7W4	Pyruvate kinase (EC 2.7.1.40)
Citrus lemon	V4S885	Uncharacterized protein
Citrus lemon	V4S8T3	Peptidyl-prolyl cis-trans isomerase (PPIase) (EC 5.2.1.8)
Citrus lemon	V4S920	Uncharacterized protein
Citrus lemon	V4S999	Uncharacterized protein
Citrus lemon	V4S9G5	Phosphoglycerate kinase (EC 2.7.2.3)
Citrus lemon	V4S9Q6	Beta-amylase (EC 3.2.1.2)
Citrus lemon	V4SA44	Serine/threonine-protein phosphatase (EC 3.1.3.16)
Citrus lemon	V4SAE0	Alpha-1,4 glucan phosphorylase (EC 2.4.1.1)
Citrus lemon	V4SAF6	Uncharacterized protein
Citrus lemon	V4SAI9	Eukaryotic translation initiation factor 3 subunit M (eIF3m)
Citrus lemon	V4SAJ5	Ribosomal protein
Citrus lemon	V4SAR3	Uncharacterized protein
Citrus lemon	V4SB37	Uncharacterized protein
Citrus lemon	V4SBI0	Elongation factor 1-alpha
Citrus lemon	V4SBI8	D-3-phosphoglycerate dehydrogenase (EC 1.1.1.95)
Citrus lemon	V4SBL9	Polyadenylate-binding protein (PABP)
Citrus lemon	V4SBR1	S-formylglutathione hydrolase (EC 3.1.2.12)
Citrus lemon	V4SBR6	Uncharacterized protein
Citrus lemon	V4SCG7	Uncharacterized protein
Citrus lemon	V4SCJ2	Uncharacterized protein
Citrus lemon	V4SCQ6	Peptidyl-prolyl cis-trans isomerase (PPIase) (EC 5.2.1.8)
Citrus lemon	V4SDJ8	Uncharacterized protein
Citrus lemon	V4SE41	Protein DETOXIFICATION (Multidrug and toxic compound
		extrusion protein)
Citrus lemon	V4SE90	Uncharacterized protein
Citrus lemon	V4SED1	Succinate dehydrogenase [ubiquinone] flavoprotein subunit,
		mitochondrial (EC 1.3.5.1)
Citrus lemon	V4SEI1	Uncharacterized protein
Citrus lemon	V4SEN9	Uncharacterized protein
Citrus lemon	V4SEX8	Uncharacterized protein
Citrus lemon	V4SF31	Uncharacterized protein
Citrus lemon	V4SF69	40S ribosomal protein S24
Citrus lemon	V4SF76	Cysteine synthase (EC 2.5.1.47)
Citrus lemon	V4SFK3	Uncharacterized protein
Citrus lemon	V4SFL4	Uncharacterized protein
Citrus lemon	V4SFW2	Uncharacterized protein
Citrus lemon	V4SGC9	Uncharacterized protein
Citrus lemon	V4SGJ4	Uncharacterized protein
Citrus lemon	V4SGN4	Uncharacterized protein
Citrus lemon	V4SGV6	Uncharacterized protein
Citrus lemon	V4SGV7	Uncharacterized protein
Citrus lemon	V4SHH1	Plasma membrane ATPase (EC 3.6.3.6) (Fragment)
Citrus lemon	V4SHI2	Uncharacterized protein
Citrus lemon	V4SHJ3	Uncharacterized protein
Citrus lemon	V4SI86	Uncharacterized protein
Citrus lemon	V4SI88	Uncharacterized protein
Citrus lemon	V4SIA2	Uncharacterized protein
Citrus lemon	V4SIC1	Phospholipase D (EC 3.1.4.4)
Citrus lemon	V4SJ14	Uncharacterized protein
Citrus lemon	V4SJ48	Uncharacterized protein
Citrus lemon	V4SJ69	Uncharacterized protein
Citrus lemon	V4SJD9	Uncharacterized protein
Citrus lemon	V4SJS7	Uncharacterized protein
Citrus lemon	V4SJT5	Uncharacterized protein
Citrus lemon	V4SKA2	Uncharacterized protein
Citrus lemon	V4SKG4	Glucose-6-phosphate isomerase (EC 5.3.1.9)
Citrus lemon	V4SKJ1	Uncharacterized protein
Citrus lemon	V4SL90	Uncharacterized protein
Citrus lemon	V4SLC6	Proteasome subunit beta type (EC 3.4.25.1)
Citrus lemon	V4SLI7	Uncharacterized protein
Citrus lemon	V4SLQ6	Uncharacterized protein
Citrus lemon	V4SMD8	Uncharacterized protein
Citrus lemon	V4SMN7	Uncharacterized protein
Citrus lemon	V4SMV5	Uncharacterized protein
Citrus lemon	V4SN00	Uncharacterized protein
Citrus lemon	V4SNA9	Uncharacterized protein
Citrus lemon	V4SNC1	Uncharacterized protein
Citrus lemon	V4SNC4	Aconitate hydratase (Aconitase) (EC 4.2.1.3)
Citrus lemon	V4SNZ3	Uncharacterized protein
Citrus lemon	V4SP86	Uncharacterized protein
Citrus lemon	V4SPM1	40S ribosomal protein S12
Citrus lemon	V4SPW4	40S ribosomal protein S4
Citrus lemon	V4SQ71	Uncharacterized protein
Citrus lemon	V4SQ89	Uncharacterized protein
Citrus lemon	V4SQ92	Uncharacterized protein
Citrus lemon	V4SQC7	Peroxidase (EC 1.11.1.7)
Citrus lemon	V4SQG3	Uncharacterized protein
Citrus lemon	V4SR15	Uncharacterized protein
Citrus lemon	V4SRN3	Transmembrane 9 superfamily member
Citrus lemon	V4SS09	Uncharacterized protein
Citrus lemon	V4SS11	Uncharacterized protein
Citrus lemon	V4SS50	Uncharacterized protein
Citrus lemon	V4SSB6	Uncharacterized protein
Citrus lemon	V4SSB8	Proteasome subunit alpha type (EC 3.4.25.1)
Citrus lemon	V4SSL7	Uncharacterized protein
Citrus lemon	V4SSQ1	Uncharacterized protein
Citrus lemon	V4SST6	Uncharacterized protein
Citrus lemon	V4SSW9	Uncharacterized protein
Citrus lemon	V4SSX5	Uncharacterized protein
Citrus lemon	V4SU82	Uncharacterized protein
Citrus lemon	V4SUD3	Uncharacterized protein
Citrus lemon	V4SUL7	Uncharacterized protein
Citrus lemon	V4SUP3	Uncharacterized protein
Citrus lemon	V4SUT4	UDP-glucose 6-dehydrogenase (EC 1.1.1.22)
Citrus lemon	V4SUY5	Uncharacterized protein
Citrus lemon	V4SV60	Serine/threonine-protein phosphatase (EC 3.1.3.16)
Citrus lemon	V4SV61	Uncharacterized protein
Citrus lemon	V4SVI5	Proteasome subunit alpha type (EC 3.4.25.1)
Citrus lemon	V4SVI6	Uncharacterized protein
Citrus lemon	V4SW04	Uncharacterized protein (Fragment)
Citrus lemon	V4SWD9	Uncharacterized protein
Citrus lemon	V4SWJ0	40S ribosomal protein S3a
Citrus lemon	V4SWQ9	Uncharacterized protein
Citrus lemon	V4SWR9	Uncharacterized protein
Citrus lemon	V4SWU9	Fructose-bisphosphate aldolase (EC 4.1.2.13)
Citrus lemon	V4SX11	Uncharacterized protein
Citrus lemon	V4SX99	Uncharacterized protein
Citrus lemon	V4SXC7	Proteasome subunit alpha type (EC 3.4.25.1)
Citrus lemon	V4SXQ5	Uncharacterized protein
Citrus lemon	V4SXW1	Beta-adaptin-like protein
Citrus lemon	V4SXY9	Uncharacterized protein
Citrus lemon	V4SY74	Uncharacterized protein
Citrus lemon	V4SY90	Uncharacterized protein
Citrus lemon	V4SY93	Uncharacterized protein
Citrus lemon	V4SYH9	Uncharacterized protein
Citrus lemon	V4SYK6	Uncharacterized protein
Citrus lemon	V4SZ03	Uncharacterized protein
Citrus lemon	V4SZ73	Uncharacterized protein
Citrus lemon	V4SZI9	Uncharacterized protein
Citrus lemon	V4SZX7	Uncharacterized protein
Citrus lemon	V4T057	Ribosomal protein L15
Citrus lemon	V4T0V5	Eukaryotic translation initiation factor 3 subunit A (eIF3a)
		(Eukaryotic translation initiation factor 3 subunit 10)
Citrus lemon	V4T0Y1	Uncharacterized protein
Citrus lemon	V4T1Q6	Uncharacterized protein
Citrus lemon	V4T1U7	Uncharacterized protein
Citrus lemon	V4T2D9	Uncharacterized protein
Citrus lemon	V4T2M6	Tubulin beta chain
Citrus lemon	V4T3G2	Uncharacterized protein
Citrus lemon	V4T3P3	6-phosphogluconate dehydrogenase, decarboxylating (EC
		1.1.1.44)
Citrus lemon	V4T3V9	Uncharacterized protein
Citrus lemon	V4T3Y6	Uncharacterized protein
Citrus lemon	V4T4H3	Uncharacterized protein
Citrus lemon	V4T4I7	Uncharacterized protein
Citrus lemon	V4T4M7	Superoxide dismutase [Cu—Zn] (EC 1.15.1.1)
Citrus lemon	V4T539	Uncharacterized protein
Citrus lemon	V4T541	Uncharacterized protein
Citrus lemon	V4T576	Uncharacterized protein
Citrus lemon	V4T5E1	Uncharacterized protein
Citrus lemon	V4T5I3	Uncharacterized protein
Citrus lemon	V4T5W7	Uncharacterized protein
Citrus lemon	V4T6T5	60S acidic ribosomal protein P0
Citrus lemon	V4T722	Uncharacterized protein
Citrus lemon	V4T785	Uncharacterized protein
Citrus lemon	V4T7E2	Uncharacterized protein
Citrus lemon	V4T7I7	Uncharacterized protein
Citrus lemon	V4T7N0	Proteasome subunit beta type (EC 3.4.25.1)
Citrus lemon	V4T7N4	Uncharacterized protein
Citrus lemon	V4T7T2	Uncharacterized protein
Citrus lemon	V4T7W5	Uncharacterized protein
Citrus lemon	V4T825	Uncharacterized protein
Citrus lemon	V4T846	Uncharacterized protein
Citrus lemon	V4T8E9	S-acyltransferase (EC 2.3.1.225) (Palmitoyltransferase)
Citrus lemon	V4T8G2	Uncharacterized protein
Citrus lemon	V4T8G9	Chorismate synthase (EC 4.2.3.5)
Citrus lemon	V4T8Y6	Uncharacterized protein
Citrus lemon	V4T8Y8	Uncharacterized protein
Citrus lemon	V4T939	Carboxypeptidase (EC 3.4.16.—)
Citrus lemon	V4T957	Uncharacterized protein
Citrus lemon	V4T998	Uncharacterized protein
Citrus lemon	V4T9B9	Uncharacterized protein
Citrus lemon	V4T9Y7	Uncharacterized protein
Citrus lemon	V4TA70	Uncharacterized protein
Citrus lemon	V4TAF6	Uncharacterized protein
Citrus lemon	V4TB09	Uncharacterized protein
Citrus lemon	V4TB32	Uncharacterized protein
Citrus lemon	V4TB89	Uncharacterized protein
Citrus lemon	V4TBN7	Phosphoinositide phospholipase C (EC 3.1.4.11)
Citrus lemon	V4TBQ3	Uncharacterized protein
Citrus lemon	V4TBS4	Uncharacterized protein
Citrus lemon	V4TBU3	Uncharacterized protein
Citrus lemon	V4TCA6	Uncharacterized protein
Citrus lemon	V4TCL3	Uncharacterized protein
Citrus lemon	V4TCS5	Pectate lyase (EC 4.2.2.2)
Citrus lemon	V4TD99	Uncharacterized protein
Citrus lemon	V4TDB5	Uncharacterized protein
Citrus lemon	V4TDI2	Uncharacterized protein
Citrus lemon	V4TDY3	Serine/threonine-protein kinase (EC 2.7.11.1)
Citrus lemon	V4TE72	Uncharacterized protein
Citrus lemon	V4TE95	Uncharacterized protein
Citrus lemon	V4TEC0	Uncharacterized protein
Citrus lemon	V4TED8	Uncharacterized protein
Citrus lemon	V4TES4	Uncharacterized protein
Citrus lemon	V4TEY9	Uncharacterized protein
Citrus lemon	V4TF24	Proteasome subunit alpha type (EC 3.4.25.1)
Citrus lemon	V4TF52	Uricase (EC 1.7.3.3) (Urate oxidase)
Citrus lemon	V4TFV8	Catalase (EC 1.11.1.6)
Citrus lemon	V4TGU1	Uncharacterized protein
Citrus lemon	V4TH28	Uncharacterized protein
Citrus lemon	V4TH78	Reticulon-like protein
Citrus lemon	V4THM9	Uncharacterized protein
Citrus lemon	V4TIU2	Ribulose-phosphate 3-epimerase (EC 5.1.3.1)
Citrus lemon	V4TIW6	Uncharacterized protein
Citrus lemon	V4TIY6	Uncharacterized protein
Citrus lemon	V4TIZ5	Uncharacterized protein
Citrus lemon	V4TJ75	Uncharacterized protein
Citrus lemon	V4TJC3	Uncharacterized protein
Citrus lemon	V4TJQ9	Uncharacterized protein
Citrus lemon	V4TK29	NEDD8-activating enzyme E1 regulatory subunit
Citrus lemon	V4TL04	Uncharacterized protein
Citrus lemon	V4TLL5	Uncharacterized protein
Citrus lemon	V4TLP6	Uncharacterized protein
Citrus lemon	V4TM00	Uncharacterized protein
Citrus lemon	V4TM19	Uncharacterized protein
Citrus lemon	V4TMB7	Uncharacterized protein (Fragment)
Citrus lemon	V4TMD1	Uncharacterized protein
Citrus lemon	V4TMD6	Uncharacterized protein
Citrus lemon	V4TMV4	Uncharacterized protein
Citrus lemon	V4TN30	Uncharacterized protein
Citrus lemon	V4TN38	Uncharacterized protein
Citrus lemon	V4TNY8	Uncharacterized protein
Citrus lemon	V4TP87	Carbonic anhydrase (EC 4.2.1.1) (Carbonate dehydratase)
Citrus lemon	V4TPM1	Homoserine dehydrogenase (HDH) (EC 1.1.1.3)
Citrus lemon	V4TQB6	Uncharacterized protein
Citrus lemon	V4TQM7	Uncharacterized protein
Citrus lemon	V4TQR2	Uncharacterized protein
Citrus lemon	V4TQV9	Uncharacterized protein
Citrus lemon	V4TS21	Proteasome subunit beta type (EC 3.4.25.1)
Citrus lemon	V4TS28	Annexin
Citrus lemon	V4TSD8	Uncharacterized protein (Fragment)
Citrus lemon	V4TSF8	Uncharacterized protein
Citrus lemon	V4TSI9	Uncharacterized protein
Citrus lemon	V4TT89	Uncharacterized protein
Citrus lemon	V4TTA0	Uncharacterized protein
Citrus lemon	V4TTR8	Uncharacterized protein
Citrus lemon	V4TTV4	Uncharacterized protein
Citrus lemon	V4TTZ7	Uncharacterized protein
Citrus lemon	V4TU54	Uncharacterized protein
Citrus lemon	V4TVB6	Uncharacterized protein
Citrus lemon	V4TVG1	Eukaryotic translation initiation factor 5A (eIF-5A)
Citrus lemon	V4TVJ4	Profilin
Citrus lemon	V4TVM6	Uncharacterized protein
Citrus lemon	V4TVM9	Uncharacterized protein
Citrus lemon	V4TVP7	Uncharacterized protein
Citrus lemon	V4TVT8	Uncharacterized protein
Citrus lemon	V4TW14	Uncharacterized protein
Citrus lemon	V4TWG9	T-complex protein 1 subunit delta
Citrus lemon	V4TWU1	Probable bifunctional methylthioribulose-1-phosphate
		dehydratase/enolase-phosphatase E1 [Includes: Enolase-phosphatase
		E1 (EC 3.1.3.77) (2,3-diketo-5-methylthio-1-phosphopentane
		phosphatase); Methylthioribulose-1-phosphate dehydratase
		(MTRu-1-P dehydratase) (EC 4.2.1.109)]
Citrus lemon	V4TWX8	Uncharacterized protein
Citrus lemon	V4TXH0	Glutamate decarboxylase (EC 4.1.1.15)
Citrus lemon	V4TXK9	Uncharacterized protein
Citrus lemon	V4TXU9	Thiamine thiazole synthase, chloroplastic (Thiazole
		biosynthetic enzyme)
Citrus lemon	V4TY40	Uncharacterized protein
Citrus lemon	V4TYJ6	Uncharacterized protein
Citrus lemon	V4TYP5	60S ribosomal protein L13
Citrus lemon	V4TYP6	Uncharacterized protein
Citrus lemon	V4TYR6	Uncharacterized protein
Citrus lemon	V4TYZ8	Tubulin alpha chain
Citrus lemon	V4TZ91	Guanosine nucleotide diphosphate dissociation inhibitor
Citrus lemon	V4TZA8	Uncharacterized protein
Citrus lemon	V4TZJ1	Uncharacterized protein
Citrus lemon	V4TZK5	Uncharacterized protein
Citrus lemon	V4TZP2	Uncharacterized protein
Citrus lemon	V4TZT8	Uncharacterized protein
Citrus lemon	V4TZU3	Mitogen-activated protein kinase (EC 2.7.11.24)
Citrus lemon	V4TZU5	Dihydrolipoyl dehydrogenase (EC 1.8.1.4)
Citrus lemon	V4TZZ0	Uncharacterized protein
Citrus lemon	V4U003	Eukaryotic translation initiation factor 3 subunit K (eIF3k)
		(eIF-3 p25)
Citrus lemon	V4U068	Uncharacterized protein
Citrus lemon	V4U088	Uncharacterized protein
Citrus lemon	V4U0J7	Uncharacterized protein
Citrus lemon	V4U133	Uncharacterized protein
Citrus lemon	V4U1A8	Uncharacterized protein
Citrus lemon	V4U1K1	Xylose isomerase (EC 5.3.1.5)
Citrus lemon	V4U1M1	Uncharacterized protein
Citrus lemon	V4U1V0	Uncharacterized protein
Citrus lemon	V4U1X7	Uncharacterized protein
Citrus lemon	V4U1X9	Proteasome subunit beta type (EC 3.4.25.1)
Citrus lemon	V4U251	Uncharacterized protein
Citrus lemon	V4U283	Uncharacterized protein
Citrus lemon	V4U2E4	Uncharacterized protein
Citrus lemon	V4U2F7	Uncharacterized protein
Citrus lemon	V4U2H8	Uncharacterized protein
Citrus lemon	V4U2L0	Malate dehydrogenase (EC 1.1.1.37)
Citrus lemon	V4U2L2	Uncharacterized protein
Citrus lemon	V4U2W4	V-type proton ATPase subunit C
Citrus lemon	V4U3L2	Uncharacterized protein
Citrus lemon	V4U3W8	Uncharacterized protein
Citrus lemon	V4U412	Uncharacterized protein
Citrus lemon	V4U4K2	Uncharacterized protein
Citrus lemon	V4U4M4	Uncharacterized protein
Citrus lemon	V4U4N5	Eukaryotic translation initiation factor 6 (eIF-6)
Citrus lemon	V4U4S9	Uncharacterized protein
Citrus lemon	V4U4X3	Serine hydroxymethyltransferase (EC 2.1.2.1)
Citrus lemon	V4U4Z9	Uncharacterized protein
Citrus lemon	V4U500	Uncharacterized protein
Citrus lemon	V4U5B0	Eukaryotic translation initiation factor 3 subunit E (eIF3e)
		(Eukaryotic translation initiation factor 3 subunit 6)
Citrus lemon	V4U5B8	Glutathione peroxidase
Citrus lemon	V4U5R5	Citrate synthase
Citrus lemon	V4U5Y8	Uncharacterized protein
Citrus lemon	V4U6I5	ATP synthase subunit beta (EC 3.6.3.14)
Citrus lemon	V4U6Q8	Uncharacterized protein
Citrus lemon	V4U706	Uncharacterized protein
Citrus lemon	V4U717	Uncharacterized protein
Citrus lemon	V4U726	Uncharacterized protein
Citrus lemon	V4U729	Uncharacterized protein
Citrus lemon	V4U734	Serine/threonine-protein phosphatase (EC 3.1.3.16)
Citrus lemon	V4U7G7	Uncharacterized protein
Citrus lemon	V4U7H5	Uncharacterized protein
Citrus lemon	V4U7R1	Potassium transporter
Citrus lemon	V4U7R7	Mitogen-activated protein kinase (EC 2.7.11.24)
Citrus lemon	V4U833	Malic enzyme
Citrus lemon	V4U840	Uncharacterized protein
Citrus lemon	V4U8C3	Uncharacterized protein
Citrus lemon	V4U8J1	3-phosphoshikimate 1-carboxyvinyltransferase (EC 2.5.1.19)
Citrus lemon	V4U8J8	T-complex protein 1 subunit gamma
Citrus lemon	V4U995	Uncharacterized protein
Citrus lemon	V4U999	Uncharacterized protein
Citrus lemon	V4U9C7	Eukaryotic translation initiation factor 3 subunit D (eIF3d)
		(Eukaryotic translation initiation factor 3 subunit 7) (eIF-3-zeta)
Citrus lemon	V4U9G8	Proline iminopeptidase (EC 3.4.11.5)
Citrus lemon	V4U9L1	Uncharacterized protein
Citrus lemon	V4UA63	Phytochrome
Citrus lemon	V4UAC8	Uncharacterized protein
Citrus lemon	V4UAR4	Uncharacterized protein
Citrus lemon	V4UB30	Uncharacterized protein
Citrus lemon	V4UBK8	V-type proton ATPase subunit a
Citrus lemon	V4UBL3	Coatomer subunit alpha
Citrus lemon	V4UBL5	Uncharacterized protein (Fragment)
Citrus lemon	V4UBM0	Uncharacterized protein
Citrus lemon	V4UBZ8	Aspartate aminotransferase (EC 2.6.1.1)
Citrus lemon	V4UC72	Uncharacterized protein
Citrus lemon	V4UC97	Beta-glucosidase (EC 3.2.1.21)
Citrus lemon	V4UCE2	Uncharacterized protein
Citrus lemon	V4UCT9	Acetyl-coenzyme A synthetase (EC 6.2.1.1)
Citrus lemon	V4UCZ1	Uncharacterized protein
Citrus lemon	V4UE34	Uncharacterized protein
Citrus lemon	V4UE78	Uncharacterized protein
Citrus lemon	V4UER3	Uncharacterized protein
Citrus lemon	V4UET6	Uncharacterized protein
Citrus lemon	V4UEZ6	Uncharacterized protein
Citrus lemon	V4UFD0	Uncharacterized protein
Citrus lemon	V4UFG8	Uncharacterized protein
Citrus lemon	V4UFK1	Uncharacterized protein
Citrus lemon	V4UG68	Eukaryotic translation initiation factor 3 subunit I (eIF3i)
Citrus lemon	V4UGB0	Uncharacterized protein
Citrus lemon	V4UGH4	Uncharacterized protein
Citrus lemon	V4UGL9	Uncharacterized protein
Citrus lemon	V4UGQ0	Ubiquitinyl hydrolase 1 (EC 3.4.19.12)
Citrus lemon	V4UH00	Uncharacterized protein
Citrus lemon	V4UH48	Uncharacterized protein
Citrus lemon	V4UH77	Proteasome subunit alpha type (EC 3.4.25.1)
Citrus lemon	V4UHD8	Uncharacterized protein
Citrus lemon	V4UHD9	Uncharacterized protein
Citrus lemon	V4UHF1	Uncharacterized protein
Citrus lemon	V4UHZ5	Uncharacterized protein
Citrus lemon	V4UI07	40S ribosomal protein S8
Citrus lemon	V4UI34	Eukaryotic translation initiation factor 3 subunit L (eIF3I)
Citrus lemon	V4UIF1	Uncharacterized protein
Citrus lemon	V4UIN5	Uncharacterized protein
Citrus lemon	V4UIX8	Uncharacterized protein
Citrus lemon	V4UJ12	Uncharacterized protein
Citrus lemon	V4UJ42	Uncharacterized protein
Citrus lemon	V4UJ63	Uncharacterized protein
Citrus lemon	V4UJB7	Uncharacterized protein (Fragment)
Citrus lemon	V4UJC4	Uncharacterized protein
Citrus lemon	V4UJX0	Phosphotransferase (EC 2.7.1.—)
Citrus lemon	V4UJY5	Uncharacterized protein
Citrus lemon	V4UK18	Uncharacterized protein
Citrus lemon	V4UK52	Uncharacterized protein
Citrus lemon	V4UKM9	Uncharacterized protein
Citrus lemon	V4UKS4	Uncharacterized protein
Citrus lemon	V4UKV6	40S ribosomal protein SA
Citrus lemon	V4UL30	Pyrophosphate--fructose 6-phosphate 1-phosphotransferase
		subunit beta (PFP) (EC 2.7.1.90) (6-phosphofructokinase,
		pyrophosphate dependent) (PPi-PFK)
		(Pyrophosphate-dependent 6-phosphofructose-1-kinase)
Citrus lemon	V4UL39	Uncharacterized protein
Citrus lemon	V4ULH9	Uncharacterized protein
Citrus lemon	V4ULL2	Uncharacterized protein
Citrus lemon	V4ULS0	Uncharacterized protein
Citrus lemon	V4UMU7	Uncharacterized protein
Citrus lemon	V4UN36	Uncharacterized protein
Citrus lemon	V4UNT5	Uncharacterized protein
Citrus lemon	V4UNW1	Uncharacterized protein
Citrus lemon	V4UP89	Uncharacterized protein
Citrus lemon	V4UPE4	Uncharacterized protein
Citrus lemon	V4UPF7	Uncharacterized protein
Citrus lemon	V4UPK0	Uncharacterized protein
Citrus lemon	V4UPX5	Uncharacterized protein
Citrus lemon	V4UQ58	Uncharacterized protein
Citrus lemon	V4UQF6	Uncharacterized protein
Citrus lemon	V4UR21	Uncharacterized protein
Citrus lemon	V4UR80	Uncharacterized protein
Citrus lemon	V4URK3	Uncharacterized protein
Citrus lemon	V4URT3	Uncharacterized protein
Citrus lemon	V4US96	Uncharacterized protein
Citrus lemon	V4USQ8	Uncharacterized protein
Citrus lemon	V4UT16	Uncharacterized protein
Citrus lemon	V4UTC6	Uncharacterized protein
Citrus lemon	V4UTC8	Uncharacterized protein
Citrus lemon	V4UTP6	Uncharacterized protein
Citrus lemon	V4UTY0	Proteasome subunit alpha type (EC 3.4.25.1)
Citrus lemon	V4UU96	Uncharacterized protein
Citrus lemon	V4UUB6	Uncharacterized protein
Citrus lemon	V4UUJ9	Aminopeptidase (EC 3.4.11.—)
Citrus lemon	V4UUK6	Uncharacterized protein
Citrus lemon	V4UV09	Uncharacterized protein
Citrus lemon	V4UV83	Lysine--tRNA ligase (EC 6.1.1.6) (Lysyl-tRNA synthetase)
Citrus lemon	V4UVJ5	Diacylglycerol kinase (DAG kinase) (EC 2.7.1.107)
Citrus lemon	V4UW03	Uncharacterized protein
Citrus lemon	V4UW04	Uncharacterized protein
Citrus lemon	V4UWR1	Uncharacterized protein
Citrus lemon	V4UWV8	Uncharacterized protein
Citrus lemon	V4UX36	Uncharacterized protein
Citrus lemon	V4V003	Uncharacterized protein
Citrus lemon	V4V0J0	40S ribosomal protein S26
Citrus lemon	V4V1P8	Uncharacterized protein
Citrus lemon	V4V4V0	Uncharacterized protein
Citrus lemon	V4V5T8	Ubiquitin-fold modifier 1
Citrus lemon	V4V600	Uncharacterized protein
Citrus lemon	V4V622	Aldehyde dehydrogenase
Citrus lemon	V4V6W1	Uncharacterized protein
Citrus lemon	V4V6Z2	Uncharacterized protein
Citrus lemon	V4V738	Uncharacterized protein
Citrus lemon	V4V8H5	Vacuolar protein sorting-associated protein 35
Citrus lemon	V4V9P6	Eukaryotic translation initiation factor 3 subunit F (eIF3f)
		(eIF-3-epsilon)
Citrus lemon	V4V9V7	Clathrin heavy chain
Citrus lemon	V4V9X3	Uncharacterized protein
Citrus lemon	V4VAA3	Superoxide dismutase (EC 1.15.1.1)
Citrus lemon	V4VAF3	Uncharacterized protein
Citrus lemon	V4VBQ0	Uncharacterized protein (Fragment)
Citrus lemon	V4VCL1	Proteasome subunit beta type (EC 3.4.25.1)
Citrus lemon	V4VCZ9	Uncharacterized protein
Citrus lemon	V4VDK1	Peptidylprolyl isomerase (EC 5.2.1.8)
Citrus lemon	V4VEA1	Uncharacterized protein
Citrus lemon	V4VEB3	Alanine--tRNA ligase (EC 6.1.1.7) (Alanyl-tRNA synthetase)
		(AlaRS)
Citrus lemon	V4VEE3	Glutamine synthetase (EC 6.3.1.2)
Citrus lemon	V4VFM3	Uncharacterized protein
Citrus lemon	V4VFN5	Proteasome subunit beta type (EC 3.4.25.1)
Citrus lemon	V4VGD6	Uncharacterized protein
Citrus lemon	V4VGL9	Uncharacterized protein
Citrus lemon	V4VHI6	Uncharacterized protein
Citrus lemon	V4VIP4	Uncharacterized protein
Citrus lemon	V4VJT4	Uncharacterized protein
Citrus lemon	V4VK14	Uncharacterized protein
Citrus lemon	V4VKI5	Protein-L-isoaspartate O-methyltransferase (EC 2.1.1.77)
Citrus lemon	V4VKP2	Glyceraldehyde-3-phosphate dehydrogenase (EC 1.2.1.—)
Citrus lemon	V4VL73	Acyl-coenzyme A oxidase
Citrus lemon	V4VLL7	Uncharacterized protein
Citrus lemon	V4VN43	Uncharacterized protein (Fragment)
Citrus lemon	V4VQH3	Methylenetetrahydrofolate reductase (EC 1.5.1.20)
Citrus lemon	V4VTC9	Uncharacterized protein (Fragment)
Citrus lemon	V4VTT4	Uncharacterized protein
Citrus lemon	V4VTY7	Uncharacterized protein
Citrus lemon	V4VU14	Uncharacterized protein
Citrus lemon	V4VU32	Uncharacterized protein
Citrus lemon	V4VUK6	S-(hydroxymethyl)glutathione dehydrogenase (EC 1.1.1.284)
Citrus lemon	V4VVR8	Uncharacterized protein
Citrus lemon	V4VXE2	Uncharacterized protein
Citrus lemon	V4VY37	Phosphomannomutase (EC 5.4.2.8)
Citrus lemon	V4VYC0	Uncharacterized protein
Citrus lemon	V4VYV1	Uncharacterized protein
Citrus lemon	V4VZ80	Uncharacterized protein
Citrus lemon	V4VZJ7	Uncharacterized protein
Citrus lemon	V4W2P2	Alpha-mannosidase (EC 3.2.1.—)
Citrus lemon	V4W2Z9	Chloride channel protein
Citrus lemon	V4W378	Uncharacterized protein
Citrus lemon	V4W4G3	Uncharacterized protein
Citrus lemon	V4W5F1	Uncharacterized protein
Citrus lemon	V4W5N8	Uncharacterized protein
Citrus lemon	V4W5U2	Uncharacterized protein
Citrus lemon	V4W6G1	Uncharacterized protein
Citrus lemon	V4W730	Uncharacterized protein
Citrus lemon	V4W7J4	Obg-like ATPase 1
Citrus lemon	V4W7L5	Uncharacterized protein
Citrus lemon	V4W8C5	Uncharacterized protein
Citrus lemon	V4W8C9	Uncharacterized protein
Citrus lemon	V4W8D3	Uncharacterized protein
Citrus lemon	V4W951	Uncharacterized protein
Citrus lemon	V4W9F6	60S ribosomal protein L18a
Citrus lemon	V4W9G2	Uncharacterized protein (Fragment)
Citrus lemon	V4W9L3	Uncharacterized protein
Citrus lemon	V4W9Y8	Uncharacterized protein
Citrus lemon	V4WAP9	Coatomer subunit beta (Beta-coat protein)
Citrus lemon	V4WBK6	Cytochrome b-c1 complex subunit 7
Citrus lemon	V4WC15	Malic enzyme
Citrus lemon	V4WC19	Uncharacterized protein
Citrus lemon	V4WC74	Uncharacterized protein
Citrus lemon	V4WC86	Serine/threonine-protein phosphatase 2A 55 kDa regulatory
		subunit B
Citrus lemon	V4WCS4	GTP-binding nuclear protein
Citrus lemon	V4WD80	Aspartate aminotransferase (EC 2.6.1.1)
Citrus lemon	V4WDK0	Uncharacterized protein
Citrus lemon	V4WDK3	ATP-dependent 6-phosphofructokinase (ATP-PFK)
		(Phosphofructokinase) (EC 2.7.1.11) (Phosphohexokinase)
Citrus lemon	V4WE00	Uncharacterized protein
Citrus lemon	V4WEE3	Uncharacterized protein
Citrus lemon	V4WEN2	Uncharacterized protein
Citrus lemon	V4WG97	Autophagy-related protein
Citrus lemon	V4WGV2	Uncharacterized protein
Citrus lemon	V4WGW5	Uridine kinase (EC 2.7.1.48)
Citrus lemon	V4WHD4	Uncharacterized protein
Citrus lemon	V4WHF8	Sucrose synthase (EC 2.4.1.13)
Citrus lemon	V4WHK2	Pectinesterase (EC 3.1.1.11)
Citrus lemon	V4WHQ4	Uncharacterized protein
Citrus lemon	V4WHT6	Uncharacterized protein
Citrus lemon	V4WJ93	Uncharacterized protein
Citrus lemon	V4WJA9	Uncharacterized protein
Citrus lemon	V4WJB1	Uncharacterized protein
Citrus lemon	V9HXG3	Protein disulfide-isomerase (EC 5.3.4.1)
Citrus lemon	W8Q8K1	Putative inorganic pyrophosphatase
Citrus lemon	W8QJL0	Putative isopentenyl pyrophosphate isomerase
Grape	Accession Number	Identified Proteins
Grape	A5C5K3 (+2)	Adenosylhomocysteinase
Grape	Q9M6B5	Alcohol dehydrogenase 6
Grape	A3FA65 (+1)	Aquaporin PIP1; 3
Grape	Q0MX13 (+2)	Aquaporin PIP2; 2
Grape	A3FA69 (+4)	Aquaporin PIP2; 4
Grape	A5AFS1 (+2)	Elongation factor 1-alpha
Grape	UPI0001985702	elongation factor 2
Grape	D7T227	Enolase
Grape	D7TJ12	Enolase
Grape	A5B118 (+1)	Fructose-bisphosphate aldolase
Grape	E0CQ39	Glucose-6-phosphate isomerase
Grape	D7TW04	Glutathione peroxidase
Grape	A1YW90 (+3)	Glutathione S-transferase
Grape	A5BEW0	Histone H4
Grape	UPI00015C9A6A	HSC70-1 (heat shock cognate 70 kDa protein 1); ATP
		binding isoform 1
Grape	D7FBC0 (+1)	Malate dehydrogenase
Grape	D7TBH4	Malic enzyme
Grape	A5ATB7 (+1)	Methylenetetrahydrofolate reductase
Grape	A5JPK7 (+1)	Monodehydroascorbate reductase
Grape	A5AKD8	Peptidyl-prolyl cis-trans isomerase
Grape	A5BQN6	Peptidyl-prolyl cis-trans isomerase
Grape	A5CAF6	Phosphoglycerate kinase
Grape	Q09VU3 (+1)	Phospholipase D
Grape	D7SK33	Phosphorylase
Grape	A5AQ89	Profilin
Grape	C5DB50 (+2)	Putative 2,3-bisphosphoglycerate-independent
		phosphoglycerate mutase
Grape	D7TIZ5	Pyruvate kinase
Grape	A5BV65	Triosephosphate isomerase
Grapefruit	G8Z362 (+1)	(E)-beta-farnesene synthase
Grapefruit	Q5CD81	(E)-beta-ocimene synthase
Grapefruit	D0UZK1 (+2)	1,2 rhamnosyltransferase
Grapefruit	A7ISD3	1,6-rhamnosyltransferase
Grapefruit	Q80H98	280 kDa protein
Grapefruit	Q15GA4 (+2)	286 kDa polyprotein
Grapefruit	D7NHW9	2-phospho-D-glycerate hydrolase
Grapefruit	D0EAL9	349 kDa polyprotein
Grapefruit	Q9DTG5	349-kDa polyprotein
Grapefruit	O22297	Acidic cellulase
Grapefruit	Q8H986	Acidic class I chitinase
Grapefruit	D3GQL0	Aconitate hydratase 1
Grapefruit	K7N8A0	Actin
Grapefruit	A8W8Y0	Alcohol acyl transferase
Grapefruit	Q84V85	Allene oxide synthase
Grapefruit	F8WL79	Aminopeptidase
Grapefruit	Q09MG5	Apocytochrome f
Grapefruit	J7EIR8	Ascorbate peroxidase
Grapefruit	B9VRH6	Ascorbate peroxidase
Grapefruit	G9I820	Auxin-response factor
Grapefruit	J7ICW8	Beta-amylase
Grapefruit	Q8L5Q9	Beta-galactosidase
Grapefruit	A7BG60	Beta-pinene synthase
Grapefruit	C0KLD1	Beta-tubulin
Grapefruit	Q91QZ1	Capsid protein
Grapefruit	Q3SAK9	Capsid protein
Grapefruit	D2U833	Cation chloride cotransporter
Grapefruit	C3VPJ0 (+3)	Chaicone synthase
Grapefruit	D5LM39	Chloride channel protein
Grapefruit	Q9M4U0	Cinnamate 4-hydroxylase CYP73
Grapefruit	Q39627	Citrin
Grapefruit	G2XKD3	Coat protein
Grapefruit	Q3L2I6	Coat protein
Grapefruit	D5FV16	CRT/DRE binding factor
Grapefruit	Q8H6S5	CTV.2
Grapefruit	Q8H6Q8	CTV.20
Grapefruit	Q8H6Q7	CTV.22
Grapefruit	Q1I1D7	Cytochrome P450
Grapefruit	Q7Y045	Dehydrin
Grapefruit	F8WLD2	DNA excision repair protein
Grapefruit	Q09MI8	DNA-directed RNA polymerase subunit beta″
Grapefruit	D2WKC9	Ethylene response 1
Grapefruit	D2WKD2	Ethylene response sensor 1
Grapefruit	D7PVG7	Ethylene-insensitive 3-like 1 protein
Grapefruit	G3CHK8	Eukaryotic translation initiation factor 3 subunit E
Grapefruit	A9NJG4 (+3)	Fatty acid hydroperoxide lyase
Grapefruit	B8Y9B5	F-box family protein
Grapefruit	Q000W4	Fe(III)-chelate reductase
Grapefruit	Q6Q3H4	Fructokinase
Grapefruit	F8WL95	Gag-pol polyprotein
Grapefruit	Q8L5K4	Gamma-terpinene synthase, chloroplastic
Grapefruit	Q9SP43	Glucose-1-phosphate adenylyltransferase
Grapefruit	Q3HM93	Glutathione S-transferase
Grapefruit	D0VEW6	GRAS family transcription factor
Grapefruit	F8WL87	Heat shock protein
Grapefruit	H9NHK0	Hsp90
Grapefruit	Q8H6R4	Jp18
Grapefruit	G3CHK6	Leucine-rich repeat family protein
Grapefruit	B2YGX9 (+1)	Limonoid UDP-glucosyltransferase
Grapefruit	Q05KK0	MADS-box protein
Grapefruit	F8WLB4	Mechanosensitive ion channel domain-containing protein
Grapefruit	Q5CD82	Monoterpene synthase
Grapefruit	F8WLC4	MYB transcription factor
Grapefruit	A5YWA9	NAC domain protein
Grapefruit	Q09MC9	NAD(P)H-quinone oxidoreductase subunit 5, chloroplastic
Grapefruit	Q8H6R9	NBS-LRR type disease resistance protein
Grapefruit	Q8H6S0	NBS-LRR type disease resistance protein
Grapefruit	Q8H6R6	NBS-LRR type disease resistance protein
Grapefruit	J9WR93	p1a
Grapefruit	Q1X8V8	P23
Grapefruit	E7DSS0 (+4)	P23
Grapefruit	G0Z9I6	p27
Grapefruit	I3XHN0	p33
Grapefruit	B8YDL3	p33 protein
Grapefruit	B9VB22	p33 protein
Grapefruit	P87587	P346
Grapefruit	B9VB56	p349 protein
Grapefruit	I3RWW7	p349 protein
Grapefruit	B9VB20	p349 protein
Grapefruit	Q9WID7	p349 protein
Grapefruit	Q2XP16	P353
Grapefruit	O04886 (+1)	Pectinesterase 1
Grapefruit	F8WL74	Peptidyl-prolyl cis-trans isomerase
Grapefruit	Q0ZA67	Peroxidase
Grapefruit	F1CT41	Phosphoenolpyruvate carboxylase
Grapefruit	B1PBV7 (+2)	Phytoene synthase
Grapefruit	Q9ZWQ8	Plastid-lipid-associated protein, chloroplastic
Grapefruit	Q94FM1	Pol polyprotein
Grapefruit	Q94FM0	Pol polyprotein
Grapefruit	G9I825	Poly C-binding protein
Grapefruit	O64460 (+7)	Polygalacturonase inhibitor
Grapefruit	I3XHM8	Polyprotein
Grapefruit	C0STR9	Polyprotein
Grapefruit	H6U1F0	Polyprotein
Grapefruit	B8QHP8	Polyprotein
Grapefruit	I3V6C0	Polyprotein
Grapefruit	C0STS0	Polyprotein
Grapefruit	K0FGH5	Polyprotein
Grapefruit	Q3HWZ1	Polyprotein
Grapefruit	F8WLA5	PPR containing protein
Grapefruit	Q06652 (+1)	Probable phospholipid hydroperoxide glutathione
		peroxidase
Grapefruit	P84177	Profilin
Grapefruit	Q09MB4	Protein ycf2
Grapefruit	A8C183	PSI reaction center subunit II
Grapefruit	A5JVP6	Putative 2b protein
Grapefruit	D0EFM2	Putative eukaryotic translation initiation factor 1
Grapefruit	Q18L98	Putative gag-pol polyprotein
Grapefruit	B5AMI9	Putative movement protein
Grapefruit	A1ECK5	Putative multiple stress-responsive zinc-finger protein
Grapefruit	B5AMJ0	Putative replicase polyprotein
Grapefruit	I7CYN5	Putative RNA-dependent RNA polymerase
Grapefruit	Q8RVR2	Putative terpene synthase
Grapefruit	B5TE89	Putative uncharacterized protein
Grapefruit	Q8JVF3	Putative uncharacterized protein
Grapefruit	F8WLB0	Putative uncharacterized protein ORF43
Grapefruit	A5JVP4	Putative viral replicase
Grapefruit	M1JAW3	Replicase
Grapefruit	H6VXK8	Replicase polyprotein
Grapefruit	J9UF50 (+1)	Replicase protein 1a
Grapefruit	J9RV45	Replicase protein 2a
Grapefruit	Q5EGG5	Replicase-associated polyprotein
Grapefruit	G9I823	RNA recognition motif protein 1
Grapefruit	J7EPC0	RNA-dependent RNA polymerase
Grapefruit	Q6DN67	RNA-directed RNA polymerase L
Grapefruit	A9CQM4	SEPALLATA1 homolog
Grapefruit	Q9SLS2	Sucrose synthase
Grapefruit	Q9SLV8 (+1)	Sucrose synthase
Grapefruit	Q38JC1	Temperature-induced lipocalin
Grapefruit	D0ELH6	Tetratricopeptide domain-containing thioredoxin
Grapefruit	D2KU75	Thaumatin-like protein
Grapefruit	C3VIC2	Translation elongation factor
Grapefruit	D5LY07	Ubiquitin/ribosomal fusion protein
Grapefruit	C6KI43	UDP-glucosyltransferase family 1 protein
Grapefruit	A0FKR1	Vacuolar citrate/H+ symporter
Grapefruit	Q944C8	Vacuolar invertase
Grapefruit	Q9MB46	V-type proton ATPase subunit E
Grapefruit	F8WL82	WD-40 repeat family protein
Helianthuus annuus	HanXRQChr03g0080391	Hsp90
Helianthuus annuus	HanXRQChr13g0408351	Hsp90
Helianthuus annuus	HanXRQChr13g0408441	Hsp90
Helianthuus annuus	HanXRQChr14g0462551	Hsp90
Helianthuus annuus	HanXRQChr02g0044471	Hsp70
Helianthuus annuus	HanXRQChr02g0044481	Hsp70
Helianthuus annuus	HanXRQChr05g0132631	Hsp70
Helianthuus annuus	HanXRQChr05g0134631	Hsp70
Helianthuus annuus	HanXRQChr05g0134801	Hsp70
Helianthuus annuus	HanXRQChr10g0299441	glutathione S-transferase
Helianthuus annuus	HanXRQChr16g0516291	glutathione S-transferase
Helianthuus annuus	HanXRQChr03g0091431	lactate/malate dehydrogenase
Helianthuus annuus	HanXRQChr13g0421951	lactate/malate dehydrogenase
Helianthuus annuus	HanXRQChr10g0304821	lactate/malate dehydrogenase
Helianthuus annuus	HanXRQChr12g0373491	lactate/malate dehydrogenase
Helianthuus annuus	HanXRQChr01g0031071	small GTPase superfamily, Rab type
Helianthuus annuus	HanXRQChr01g0031091	small GTPase superfamily, Rab type
Helianthuus annuus	HanXRQChr02g0050791	small GTPase superfamily, Rab type
Helianthuus annuus	HanXRQChr11g0353711	small GTPase superfamily, Rab type
Helianthuus annuus	HanXRQChr13g0402771	small GTPase superfamily, Rab type
Helianthuus annuus	HanXRQChr07g0190171	isocitrate/isopropylmalate dehydrogenase
Helianthuus annuus	HanXRQChr16g0532251	isocitrate/isopropylmalate dehydrogenase
Helianthuus annuus	HanXRQChr03g0079131	phosphoenolpyruvate carboxylase
Helianthuus annuus	HanXRQChr15g0495261	phosphoenolpyruvate carboxylase
Helianthuus annuus	HanXRQChr13g0388931	phosphoenolpyruvate carboxylase
Helianthuus annuus	HanXRQChr14g0442731	phosphoenolpyruvate carboxylase
Helianthuus annuus	HanXRQChr15g0482381	UTP--glucose-1-phosphate uridylyltransferase
Helianthuus annuus	HanXRQChr16g0532261	UTP--glucose-1-phosphate uridylyltransferase
Helianthuus annuus	HanXRQChr05g0135591	tubulin
Helianthuus annuus	HanXRQChr06g0178921	tubulin
Helianthuus annuus	HanXRQChr08g0237071	tubulin
Helianthuus annuus	HanXRQChr11g0337991	tubulin
Helianthuus annuus	HanXRQChr13g0407921	tubulin
Helianthuus annuus	HanXRQChr05g0145191	tubulin
Helianthuus annuus	HanXRQChr07g0187021	tubulin
Helianthuus annuus	HanXRQChr07g0189811	tubulin
Helianthuus annuus	HanXRQChr09g0253681	tubulin
Helianthuus annuus	HanXRQChr10g0288911	tubulin
Helianthuus annuus	HanXRQChr11g0322631	tubulin
Helianthuus annuus	HanXRQChr12g0367231	tubulin
Helianthuus annuus	HanXRQChr13g0386681	tubulin
Helianthuus annuus	HanXRQChr13g0393261	tubulin
Helianthuus annuus	HanXRQChr12g0371591	ubiquitin
Helianthuus annuus	HanXRQChr12g0383641	ubiquitin
Helianthuus annuus	HanXRQChr17g0569881	ubiquitin
Helianthuus annuus	HanXRQChr06g0171511	photosystem II HCF136, stability/assembly factor
Helianthuus annuus	HanXRQChr17g0544921	photosystem II HCF136, stability/assembly factor
Helianthuus annuus	HanXRQChr16g0526461	proteasome B-type subunit
Helianthuus annuus	HanXRQChr17g0565551	proteasome B-type subunit
Helianthuus annuus	HanXRQChr05g0149801	proteasome B-type subunit
Helianthuus annuus	HanXRQChr09g0241421	proteasome B-type subunit
Helianthuus annuus	HanXRQChr11g0353161	proteasome B-type subunit
Helianthuus annuus	HanXRQChr16g0506311	proteinase inhibitor family I3 (Kunitz)
Helianthuus annuus	HanXRQChr16g0506331	proteinase inhibitor family I3 (Kunitz)
Helianthuus annuus	HanXRQChr09g0265401	metallopeptidase (M10 family)
Helianthuus annuus	HanXRQChr09g0265411	metallopeptidase (M10 family)
Helianthuus annuus	HanXRQChr05g0154561	ATPase, AAA-type
Helianthuus annuus	HanXRQChr08g0235061	ATPase, AAA-type
Helianthuus annuus	HanXRQChr09g0273921	ATPase, AAA-type
Helianthuus annuus	HanXRQChr16g0498881	ATPase, AAA-type
Helianthuus annuus	HanXRQChr02g0058711	oxoacid dehydrogenase acyltransferase
Helianthuus annuus	HanXRQChr08g0214191	oxoacid dehydrogenase acyltransferase
Helianthuus annuus	HanXRQChr08g0208631	small GTPase superfamily, SAR1-type
Helianthuus annuus	HanXRQChr11g0331441	small GTPase superfamily, SAR1-type
Helianthuus annuus	HanXRQChr12g0371571	small GTPase superfamily, SAR1-type
Helianthuus annuus	HanXRQChr12g0383571	small GTPase superfamily, SAR1-type
Helianthuus annuus	HanXRQChr14g0446771	small GTPase superfamily, SAR1-type
Helianthuus annuus	HanXRQChr17g0539461	small GTPase superfamily, SAR1-type
Helianthuus annuus	HanXRQChr17g0548271	small GTPase superfamily, SAR1-type
Helianthuus annuus	HanXRQChr17g0569871	small GTPase superfamily, SAR1-type
Helianthuus annuus	HanXRQChr10g0311201	ATPase, V1 complex, subunit A
Helianthuus annuus	HanXRQChr12g0359711	ATPase, V1 complex, subunit A
Helianthuus annuus	HanXRQChr04g0124671	fructose-1,6-bisphosphatase
Helianthuus annuus	HanXRQChr06g0176631	fructose-1,6-bisphosphatase
Helianthuus annuus	HanXRQCPg0579861	photosystem II PsbD/D2, reaction centre
Helianthuus annuus	HanXRQChr00c0439g0574731	photosystem II PsbD/D2, reaction centre
Helianthuus annuus	HanXRQChr04g0099321	photosystem II PsbD/D2, reaction centre
Helianthuus annuus	HanXRQChr08g0210231	photosystem II PsbD/D2, reaction centre
Helianthuus annuus	HanXRQChr11g0326671	photosystem II PsbD/D2, reaction centre
Helianthuus annuus	HanXRQChr17g0549121	photosystem II PsbD/D2, reaction centre
Helianthuus annuus	HanXRQCPg0579731	photosystem II protein D1
Helianthuus annuus	HanXRQChr00c0126g0571821	photosystem II protein D1
Helianthuus annuus	HanXRQChr00c0165g0572191	photosystem II protein D1
Helianthuus annuus	HanXRQChr00c0368g0574171	photosystem II protein D1
Helianthuus annuus	HanXRQChr00c0454g0574931	photosystem II protein D1
Helianthuus annuus	HanXRQChr00c0524g0575441	photosystem II protein D1
Helianthuus annuus	HanXRQChr00c0572g0575941	photosystem II protein D1
Helianthuus annuus	HanXRQChr09g0257281	photosystem II protein D1
Helianthuus annuus	HanXRQChr11g0326571	photosystem II protein D1
Helianthuus annuus	HanXRQChr11g0327051	photosystem II protein D1
Helianthuus annuus	HanXRQChr16g0503941	photosystem II protein D1
Helianthuus annuus	HanXRQCPg0580061	photosystem II cytochrome b559
Helianthuus annuus	HanXRQChr01g0020331	photosystem II cytochrome b559
Helianthuus annuus	HanXRQChr10g0283581	photosystem II cytochrome b559
Helianthuus annuus	HanXRQChr10g0284271	photosystem II cytochrome b559
Helianthuus annuus	HanXRQChr10g0289291	photosystem II cytochrome b559
Helianthuus annuus	HanXRQChr10g0318171	photosystem II cytochrome b559
Helianthuus annuus	HanXRQChr11g0326851	photosystem II cytochrome b559
Helianthuus annuus	HanXRQChr16g0529011	photosystem II cytochrome b559
Helianthuus annuus	HanXRQChr08g0219051	chlorophyll A-B binding protein
Helianthuus annuus	HanXRQChr12g0370841	chlorophyll A-B binding protein
Helianthuus annuus	HanXRQChr02g0053151	chlorophyll A-B binding protein
Helianthuus annuus	HanXRQChr02g0053161	chlorophyll A-B binding protein
Helianthuus annuus	HanXRQCPg0580051	cytochrome f
Helianthuus annuus	HanXRQChr01g0020341	cytochrome f
Helianthuus annuus	HanXRQChr10g0283571	cytochrome f
Helianthuus annuus	HanXRQChr10g0284261	cytochrome f
Helianthuus annuus	HanXRQChr10g0289281	cytochrome f
Helianthuus annuus	HanXRQChr10g0318181	cytochrome f
Helianthuus annuus	HanXRQChr11g0326841	cytochrome f
Helianthuus annuus	HanXRQChr15g0497521	cytochrome f
Helianthuus annuus	HanXRQChr06g0163851	ribosomal protein
Helianthuus annuus	HanXRQChr09g0252071	ribosomal protein
Helianthuus annuus	HanXRQChr12g0374041	ribosomal protein
Helianthuus annuus	HanXRQChr04g0128141	ribosomal protein
Helianthuus annuus	HanXRQChr05g0163131	ribosomal protein
Helianthuus annuus	HanXRQChr03g0076971	ribosomal protein
Helianthuus annuus	HanXRQChr05g0159851	ribosomal protein
Helianthuus annuus	HanXRQChr05g0159971	ribosomal protein
Helianthuus annuus	HanXRQChr11g0324631	ribosomal protein
Helianthuus annuus	HanXRQChr13g0408051	ribosomal protein
Helianthuus annuus	HanXRQChr03g0089331	ribosomal protein
Helianthuus annuus	HanXRQChr13g0419951	ribosomal protein
Helianthuus annuus	HanXRQChr15g0497041	ribosomal protein
Helianthuus annuus	HanXRQChr16g0499761	ribosomal protein
Helianthuus annuus	HanXRQChr04g0106961	ribosomal protein
Helianthuus annuus	HanXRQChr06g0175811	ribosomal protein
Helianthuus annuus	HanXRQChr04g0122771	ribosomal protein
Helianthuus annuus	HanXRQChr09g0245691	ribosomal protein
Helianthuus annuus	HanXRQChr16g0520021	ribosomal protein
Helianthuus annuus	HanXRQChr03g0060471	ribosomal protein
Helianthuus annuus	HanXRQChr14g0429531	ribosomal protein
Helianthuus annuus	HanXRQChr06g0171911	ribosomal protein
Helianthuus annuus	HanXRQChr15g0479091	ribosomal protein
Helianthuus annuus	HanXRQChr15g0479101	ribosomal protein
Helianthuus annuus	HanXRQChr17g0543641	ribosomal protein
Helianthuus annuus	HanXRQChr17g0543661	ribosomal protein
Helianthuus annuus	HanXRQChr04g0105831	ribosomal protein
Helianthuus annuus	HanXRQChr09g0258341	ribosomal protein
Helianthuus annuus	HanXRQChr10g0287141	ribosomal protein
Helianthuus annuus	HanXRQChr15g0463911	ribosomal protein
Helianthuus annuus	HanXRQChr03g0076171	ribosomal protein
Helianthuus annuus	HanXRQChr05g0159291	ribosomal protein
Helianthuus annuus	HanXRQChr13g0407551	ribosomal protein
Helianthuus annuus	HanXRQChr12g0380701	ribosomal protein
Helianthuus annuus	HanXRQChr15g0477271	ribosomal protein
Helianthuus annuus	HanXRQChr17g0545211	ribosomal protein
Helianthuus annuus	HanXRQChr17g0570741	ribosomal protein
Helianthuus annuus	HanXRQChr17g0570761	ribosomal protein
Helianthuus annuus	HanXRQChr02g0044021	ribosomal protein
Helianthuus annuus	HanXRQChr05g0152871	ribosomal protein
Helianthuus annuus	HanXRQChr01g0012781	ribosomal protein
Helianthuus annuus	HanXRQChr08g0230861	ribosomal protein
Helianthuus annuus	HanXRQChr13g0391831	ribosomal protein
Helianthuus annuus	HanXRQChr11g0337791	bifunctional trypsin/alpha-amylase inhibitor
Helianthuus annuus	HanXRQChr10g0312371	2-oxoacid dehydrogenase acyltransferase
Helianthuus annuus	HanXRQChr09g0276191	acid phosphatase (class B)
Helianthuus annuus	HanXRQChr05g0142271	aldose-1-epimerase
Helianthuus annuus	HanXRQChr14g0439791	alpha-D-phosphohexomutase
Helianthuus annuus	HanXRQChr09g0251071	alpha-L-fucosidase
Helianthuus annuus	HanXRQChr05g0147371	annexin
Helianthuus annuus	HanXRQChr09g0247561	Asp protease (Peptidase family A1)
Helianthuus annuus	HanXRQChr13g0409681	berberine-bridge enzyme (S)-reticulin: oxygen oxido-reductase
Helianthuus annuus	HanXRQChr10g0295971	beta-hydroxyacyl-(acyl-carrier-protein) dehydratase
Helianthuus annuus	HanXRQChr13g0412571	carbohydrate esterase family 13 - CE13 (pectin acylesterase - PAE)
Helianthuus annuus	HanXRQChr12g0360101	carbohydrate esterase family 8 - CE8 (pectin methylesterase - PME)
Helianthuus annuus	HanXRQChr01g0019231	carbonic anhydrase
Helianthuus annuus	HanXRQChr02g0036611	cellular retinaldehyde binding/alpha-tocopherol transport
Helianthuus annuus	HanXRQChr10g0313581	chaperonin Cpn60
Helianthuus annuus	HanXRQChr09g0251791	chlathrin
Helianthuus annuus	HanXRQChr11g0329811	chlorophyll A-B binding protein
Helianthuus annuus	HanXRQChr13g0398861	cobalamin (vitamin B12)-independent methionine synthase
Helianthuus annuus	HanXRQChr10g0298981	cyclophilin
Helianthuus annuus	HanXRQChr04g0103281	Cys protease (papain family)
Helianthuus annuus	HanXRQChr09g0268361	cytochrome P450
Helianthuus annuus	HanXRQChr17g0535591	dirigent protein
Helianthuus annuus	HanXRQChr03g0065901	expansin
Helianthuus annuus	HanXRQChr11g0336761	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr10g0280931	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr10g0288971	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr12g0380361	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr09g0254381	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr04g0112711	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr07g0196131	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr10g0301281	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr10g0301931	expressed protein (cupin domain, seed storage protein domain)
Helianthuus annuus	HanXRQChr13g0404461	expressed protein (cupin domain)
Helianthuus annuus	HanXRQChr01g0015821	expressed protein (DUF642)
Helianthuus annuus	HanXRQChr03g0065301	expressed protein (Gnk2-homologous domain, antifungal
		protein of Ginkgo seeds)
Helianthuus annuus	HanXRQChr03g0068311	expressed protein (LRR domains)
Helianthuus annuus	HanXRQChr10g0291371	expressed protein (LRR domains)
Helianthuus annuus	HanXRQChr03g0075061	fasciclin-like arabinogalactan protein (FLA)
Helianthuus annuus	HanXRQChr08g0221961	ferritin
Helianthuus annuus	HanXRQChr09g0257521	FMN-dependent dehydrogenase
Helianthuus annuus	HanXRQChr14g0441641	fructose-bisphosphate aldolase
Helianthuus annuus	HanXRQChr10g0312621	germin
Helianthuus annuus	HanXRQChr09g0244271	glucose-methanol-choline oxidoreductase
Helianthuus annuus	HanXRQChr03g0061571	glutamate synthase
Helianthuus annuus	HanXRQChr05g0144801	glyceraldehyde 3-phosphate dehydrogenase
Helianthuus annuus	HanXRQChr17g0550211	glycerophosphoryl diester phosphodiesterase
Helianthuus annuus	HanXRQChr06g0175391	glycoside hydrolase family 16 - GH16 (endoxyloglucan
		transferase)
Helianthuus annuus	HanXRQChr11g0351571	glycoside hydrolase family 17 - GH17 (beta-1,3-glucosidase)
Helianthuus annuus	HanXRQChr05g0141461	glycoside hydrolase family 18 - GH18
Helianthuus annuus	HanXRQChr09g0276721	glycoside hydrolase family 19 - GH19
Helianthuus annuus	HanXRQChr02g0046191	glycoside hydrolase family 2 - GH2
Helianthuus annuus	HanXRQChr16g0524981	glycoside hydrolase family 20 - GH20
		(N-acetyl-beta-glucosaminidase)
Helianthuus annuus	HanXRQChr11g0322851	glycoside hydrolase family 27 - GH27
		(alpha-galactosidase/melibiase)
Helianthuus annuus	HanXRQChr10g0293191	glycoside hydrolase family 3 - GH3
Helianthuus annuus	HanXRQChr16g0511881	glycoside hydrolase family 31 - GH31 (alpha-xylosidase)
Helianthuus annuus	HanXRQChr14g0461441	glycoside hydrolase family 32 - GH32 (vacuolar invertase)
Helianthuus annuus	HanXRQChr13g0423671	glycoside hydrolase family 35 - GH35 (beta-galactosidase)
Helianthuus annuus	HanXRQChr10g0319301	glycoside hydrolase family 35 - GH35 (beta-galactosidase)
Helianthuus annuus	HanXRQChr09g0256531	glycoside hydrolase family 38 - GH38 (alpha-mannosidase)
Helianthuus annuus	HanXRQChr11g0320901	glycoside hydrolase family 5 - GH5 (glucan-1,3-beta
		glucosidase)
Helianthuus annuus	HanXRQChr05g0130491	glycoside hydrolase family 51 - GH51
		(alpha-arabinofuranosidase)
Helianthuus annuus	HanXRQChr10g0314191	glycoside hydrolase family 79 - GH79
		(endo-beta-glucuronidase/heparanase
Helianthuus annuus	HanXRQChr13g0397411	homologous to A. thaliana PMR5 (Powdery Mildew
		Resistant) (carbohydrate acylation)
Helianthuus annuus	HanXRQChr14g0444681	inhibitor family I3 (Kunitz-P family)
Helianthuus annuus	HanXRQChr14g0445181	lactate/malate dehydrogenase
Helianthuus annuus	HanXRQChr17g0564111	lectin (D-mannose)
Helianthuus annuus	HanXRQChr17g0558861	lectin (PAN-2 domain)
Helianthuus annuus	HanXRQChr02g0039251	lipase acylhydrolase (GDSL family)
Helianthuus annuus	HanXRQChr01g0000161	lipid transfer protein/trypsin-alpha amylase inhibitor
Helianthuus annuus	HanXRQChr02g0047121	mannose-binding lectin
Helianthuus annuus	HanXRQChr10g0303361	mitochondrial carrier protein
Helianthuus annuus	HanXRQChr15g0489551	multicopper oxidase
Helianthuus annuus	HanXRQChr05g0135581	neutral/alkaline nonlysosomal ceramidase
Helianthuus annuus	HanXRQChr01g0017621	nucleoside diphosphate kinase
Helianthuus annuus	HanXRQChr10g0295991	peroxidase
Helianthuus annuus	HanXRQChr13g0398251	peroxiredoxin
Helianthuus annuus	HanXRQChr11g0333171	phosphate-induced (phi) protein 1
Helianthuus annuus	HanXRQChr03g0060421	phosphodiesterase/nucleotide pyrophosphatase/phosphate
		transferase
Helianthuus annuus	HanXRQChr03g0078011	phosphofructokinase
Helianthuus annuus	HanXRQChr13g0408831	phosphoglycerate kinase
Helianthuus annuus	HanXRQChr10g0286701	phosphoglycerate mutase
Helianthuus annuus	HanXRQChr06g0171591	photosystem II PsbP, oxygen evolving complex
Helianthuus annuus	HanXRQChr14g0434951	plastid lipid-associated protein/fibrillin conserved domain
Helianthuus annuus	HanXRQChr05g0146621	plastocyanin (blue copper binding protein)
Helianthuus annuus	HanXRQChr11g0330251	polyphenol oxidase
Helianthuus annuus	HanXRQChr04g0094541	proteasome A-type subunit
Helianthuus annuus	HanXRQChr03g0081271	proteasome B-type subunit
Helianthuus annuus	HanXRQChr12g0356851	purple acid phosphatase
Helianthuus annuus	HanXRQChr15g0485781	pyridoxal phosphate-dependent transferase
Helianthuus annuus	HanXRQChr11g0336791	ribosomal protein
Helianthuus annuus	HanXRQChr11g0330521	ribosomal protein
Helianthuus annuus	HanXRQChr11g0326801	ribulose bisphosphate carboxylase, large subunit
Helianthuus annuus	HanXRQChr16g0523951	ribulose-1,5-bisphosphate carboxylase small subunit
Helianthuus annuus	HanXRQChr01g0022151	S-adenosyl-L-homocysteine hydrolase
Helianthuus annuus	HanXRQChr14g0454811	S-adenosylmethionine synthetase
Helianthuus annuus	HanXRQChr04g0109991	SCP-like extracellular protein (PR-1)
Helianthuus annuus	HanXRQChr03g0072241	Ser carboxypeptidase (Peptidase family S10)
Helianthuus annuus	HanXRQChr12g0377221	Ser protease (subtilisin) (Peptidase family S8)
Helianthuus annuus	HanXRQChr02g0055581	superoxide dismutase
Helianthuus annuus	HanXRQChr15g0493261	thaumatin (PR5)
Helianthuus annuus	HanXRQChr16g0532531	transketolase
Helianthuus annuus	HanXRQChr07g0197421	translation elongation factor EFTu/EF1A
Helianthuus annuus	HanXRQChr06g0173951	translationally controlled tumour protein

Claims

1. A plant messenger pack (PMP) comprising one or more exogenous polypeptides, wherein the one or more exogenous polypeptides are mammalian therapeutic agents and are encapsulated by the PMP, and wherein the exogenous polypeptides are not pathogen control agents.

2. The PMP of claim 1, wherein the mammalian therapeutic agent is an enzyme.

3. The PMP of claim 2, wherein the enzyme is a recombination enzyme or an editing enzyme.

4. The PMP of claim 1, wherein the mammalian therapeutic agent is an antibody or an antibody fragment.

5. The PMP of claim 1, wherein the mammalian therapeutic agent is an Fc fusion protein.

6. The PMP of claim 1, wherein the mammalian therapeutic agent is a hormone.

7. The PMP of claim 6, wherein the mammalian therapeutic agent is insulin.

8. The PMP of claim 1, wherein the mammalian therapeutic agent is a peptide.

9. The PMP of claim 1, wherein the mammalian therapeutic agent is a receptor agonist or a receptor antagonist.

10. The PMP of any one of claims 1-9, wherein the mammalian therapeutic agent has a size of less than 100 kD.

11. The PMP of claim 10, wherein the mammalian therapeutic agent has a size of less than 50 kD.

12. The PMP of any one of claims 1-11, wherein the mammalian therapeutic agent has an overall charge that is neutral.

13. The PMP of claim 12, wherein the mammalian therapeutic agent has been modified to have a charge that is neutral.

14. The PMP of any one of claims 1-11, wherein the mammalian therapeutic agent has an overall charge that is positive.

15. The PMP of any one of claims 1-11, wherein the mammalian therapeutic agent has an overall charge that is negative.

16. The PMP of any one of claims 1-15, wherein the exogenous polypeptide is released from the PMP in a target cell with which the PMP is contacted.

17. The PMP of claim 16, wherein the exogenous polypeptide exerts activity in the cytoplasm of the target cell.

18. The PMP of claim 16, wherein the exogenous polypeptide is translocated to the nucleus of the target cell.

19. The PMP of claim 18, wherein the exogenous polypeptide exerts activity in the nucleus of the target cell.

20. The PMP of any one of claims 1-19, wherein uptake by a cell of the exogenous polypeptide encapsulated by the PMP is increased relative to uptake of the exogenous polypeptide not encapsulated by a PMP.

21. The PMP of any one of claims 1-20, wherein the effectiveness of the exogenous polypeptide encapsulated by the PMP is increased relative to the effectiveness of the exogenous polypeptide not encapsulated by a PMP.

22. The PMP of any one of claims 1-21, wherein the exogenous polypeptide comprises at least 50 amino acid residues.

23. The PMP of any one of claims 1-22, wherein the exogenous polypeptide is at least 5 kD in size.

24. The PMP of any one of claims 1-23, wherein the PMP comprises a purified plant extracellular vesicle (EV), or a segment or extract thereof.

25. The PMP of claim 24, wherein the EV or segment or extract thereof is obtained from a citrus fruit.

26. The PMP of claim 25, wherein the citrus fruit is a grapefruit or a lemon.

27. A composition comprising a plurality of the PMPs of any one of claims 1-26.

28. The composition of claim 27, wherein the PMPs in the composition are at a concentration effective to increase the fitness of a mammal.

29. The composition of claim 27 or 28, wherein the exogenous polypeptide is at a concentration of at least 0.01, 0.1, 0.2, 0.3, 0.4, 0.5, or 1 μg polypeptide/mL.

30. The composition of any one of claims 27-29, wherein at least 15% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide.

31. The composition of claim 30, wherein at least 50% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide.

32. The composition of claim 31, wherein at least 95% of PMPs in the plurality of PMPs encapsulate the exogenous polypeptide.

33. The composition of any one of claims 27-32, wherein the composition is formulated for administration to a mammal.

34. The composition of any one of claims 27-33, wherein the composition is formulated for administration to a mammalian cell.

35. The composition of any one of claims 27-34, further comprising a pharmaceutically acceptable vehicle, carrier, or excipient.

36. The composition of any one of claims 27-35, wherein the composition is stable for at least one day at room temperature, and/or stable for at least one week at 4° C.

37. The composition of any one of claims 27-36, wherein the PMPs are stable for at least 24 hours, 48 hours, seven days, or 30 days at 4° C.

38. The composition of claim 37, wherein the PMPs are further stable at a temperature of at least 20° C., 24° C., or 37° C.

39. A composition comprising a plurality of PMPs, wherein each of the PMPs is a plant EV, or a segment or extract thereof, wherein each of the plurality of PMPs encapsulate an exogenous polypeptide, wherein the exogenous polypeptide is a mammalian therapeutic agent, the exogenous polypeptide is not a pathogen control agent, and the composition is formulated for delivery to an animal.

40. A pharmaceutical composition comprising a composition according to any one of claims 1-26 and a pharmaceutically acceptable vehicle, carrier, or excipient.

41. A method of producing a PMP comprising an exogenous polypeptide, wherein the exogenous polypeptide is a mammalian therapeutic agent, and wherein the exogenous polypeptide is not a pathogen control agent, the method comprising: (a) providing a solution comprising the exogenous polypeptide; and(b) loading the PMP with the exogenous polypeptide, wherein the loading causes the exogenous polypeptide to be encapsulated by the PMP.

42. The method of claim 41, wherein the exogenous polypeptide is soluble in the solution.

43. The method of claim 41 or 42, wherein the loading comprises one or more of sonication, electroporation, and lipid extrusion.

44. The method of claim 43, wherein the loading comprises sonication and lipid extrusion.

45. The method of claim 43, wherein the loading comprises lipid extrusion.

46. The method of claim 45, wherein PMP lipids are isolated prior to lipid extrusion.

47. The method of claim 46, wherein the isolated PMP lipids comprise glycosylinositol phosphorylceramides (GIPCs).

48. A method for delivering a polypeptide to a mammalian cell, the method comprising: (a) providing a PMP comprising one or more exogenous polypeptides, wherein the one or more exogenous polypeptides are mammalian therapeutic agents and are encapsulated by the PMP, and wherein the exogenous polypeptides are not pathogen control agents; and(b) contacting the cell with the PMP, wherein the contacting is performed with an amount and for a time sufficient to allow uptake of the PMP by the cell.

49. The method of claim 48, wherein the cell is a cell in a subject.

50. The PMP, composition, pharmaceutical composition, or method of any of claims 1-49, wherein the mammal is a human.

51. A method for treating diabetes, the method comprising administering to a subject in need thereof an effective amount of a composition comprising a plurality of PMPs, wherein one or more exogenous polypeptides are encapsulated by the PMP.

52. The method of claim 51, wherein the administration of the plurality of PMPs lowers the blood sugar of the subject.

53. The method of claim 52, wherein the exogenous polypeptide is insulin.

54. The PMP, composition, pharmaceutical composition, or method of any of claims 1-53, wherein the PMP is not significantly degraded by gastric fluids.