Patent Application
20100248268
The present invention generally relates to methods and compositions for utilizing chemosensory proteins sourced from invertebrates in detectors, sensors, biosensors, and other sensor devices. As part of this set of applications, the invention also relates to methods for utilizing chemosensory proteins in collections or arrays in order to identify specific chemosensory cues or analytes to be detected. Furthermore, the invention provides the methods and means necessary to construct purification devices capable of detecting, isolating and purifying an analyte of interest from a complex mixture in the atmosphere or in solution. The technologies presented are feasible in a variety of applications where detection of an analyte or the absence of an analyte is desirable.
This invention can be incorporated into biosensors or other devices used for industrial, domestic, food safety, pharmaceutical, military, security, purification, and other applications.
The Electronic Nose is a chemical sensor system that detects volatile compounds or analytes. Electronic Nose technology is being utilized or developed for a wide variety of applications, from medical diagnostics to environmental monitoring.1-5 For example, the development of inexpensive, reliable detectors for the presence of volatile organic compounds (VOCs) is a particularly acute issue. Volatile organic compounds are emitted as gases from certain solids or liquids; VOCs include chemicals that have short- and long-term adverse health effects and/or are environmental risks, and their concentrations are consistently higher indoors (up to five times higher) than outdoors. Potentially harmful chemicals are emitted by a wide array of products numbering in the thousands (paints and lacquers, paint strippers, cleaning supplies, pesticides, building materials and furnishings, office equipment such as copiers and printers, correction fluids and carbonless copy paper, graphics and craft materials including glues and adhesives, permanent markers, photographic solutions, etc.). VOCs have also been demonstrated to be reliable markers of human diseases.6-13
A key limitation of the present generation of chemical sensors is the recognition elements that bind the compound being detected (
Biosensors are analytical tools that measure the presence of a single molecular species in complex mixtures by combining the exquisite molecular recognition properties of biological macromolecules with the generation of a detectable signal. Thus, biosensors overcome a critical drawback of the previously mentioned, non-biological sensor technologies—lack of analyte specificity. To date biosensors have incorporated enzymes or antibodies.19-22
This invention provides the means and methods necessary to overcome current sensor limitations by utilizing the diversity, versatility and specificity of the biomolecules comprising the invertebrate chemosensory system; this includes the olfactory and gustatory systems that comprise similar proteins and effectors.23 The invention also relates to the selective purification, identification, or exclusion of a desired or undesired analyte from a mixture, solution, or the atmosphere.
The rich molecular diversity present in insect chemosensory systems is an untapped yet valuable resource with applications in a wide range of areas including pharmaceutical screening, medical diagnostics, and chemical detection.4,5,24,25 The insect chemosensory machinery can be adapted to construct biosensor devices capable of detecting and isolating environmental contaminants or impurities in industrial processes, of detecting compounds or molecules in the environment or water and of screening pharmaceutical candidates. Additional applications for efficient compound detectors include the detection of diagnostic breath components in patients with cancer and other diseases.5,6,24
Unless otherwise stated, all scientific and technical terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Generally, the nomenclature used herein and the laboratory procedures in molecular biology, molecular genetics, biochemistry, physical chemistry, cell culture, protein chemistry, and nucleic acid chemistry described below are those well known and commonly employed in the art. Standard techniques are used for recombinant nucleic acid methods, eukaryotic transformation, and microbial culture and transformation. Enzymatic reactions and purification steps are performed according to the manufacturer's instructions unless otherwise noted. Techniques and procedures are generally performed according to conventional methods in the art. General references include Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd Ed. (1989) Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., USA, and Ashburner, M., Drosophila: A Laboratory Manual (1989) Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., USA. The laboratory procedures described in combinatorial chemistry, synthetic chemistry, and electrophysiology, and the nomenclature used are those well known and commonly employed in the art. As employed throughout the disclosure, the following terms, unless otherwise indicated, shall be understood to have the following meanings:
“Allomone” refers to a chemical signal sent from a member of one species to a member of another, with the intent to alter the latter's behavior in favor of the former. Allomones are commonly produced by plant species to affect insect species' behavior.
“Analyte” refers to a substance, molecule, compound, chemical constituent, or other form of matter that is undergoing analysis or detection. An analyte may consist of a single compound or a mixture of compounds.
“Bioinformatics” refers to the discipline that integrates biotechnology and modern computational, statistical, and analytical or mathematical methods.
“cDNA” refers to complementary DNA, which is a DNA copy of the mRNA or messenger RNA expressed in the cell. The term “cDNA” therefore represents gene products or transcripts.
“Chemosensome” refers to the collection of proteins and effectors that enable an insect species to detect chemosensory cues such as scents and/or tastes.
“Chemosensory protein” refers to a protein component of the chemosensory system including the olfactory and gustatory system. Chemosensory proteins can be soluble, insoluble, membrane-bound, extracellular, secreted, or intracellular.
“Domain” refers to an area of a protein with a specific function or exhibiting a specific structural motif.
“Effectors” refers to naturally occurring or synthetic molecules, or compounds capable of interacting with a chemosensory protein under study. Effectors can be agonists, antagonists, or neither.
“Genomics” refers to the cloning and molecular characterization of entire genomes.
“Genetically Modified Organism (GMO)” refers to an organism that has been genetically engineered using gene splicing or molecular biology techniques (vs. a traditional breeding approach) to exhibit specific genetic traits.
“G-protein coupled receptors (GPCRs)” refers to pheromone or odorant serpentine receptors that bind trimeric G-proteins within the cell. Also called odorant receptors (ORs).
“Gustatory receptor” or “GR” refers to the subcellular structures located in the plasma membrane of insect neuronal cells that are responsible for initiating the organism's perception of a specific taste—that is, they allow the organism to taste various flavors or tastes. Also called a GPCR.
“Homologs” refers to genes that have a common ancestry. Homologs are divided into orthologs, which are homologs with the same function as the ancestral gene, and paralogs, that are homologs with a different function from the ancestral gene.
“Homology” refers to the extent of similarity between the DNA sequences encoding two or more genes, or the amino acid sequences comprising two or more proteins, as in a gene or protein family.
“Hydrophobicity” refers to the solubility of a particular protein or molecule in water.
“IPM” refers to integrated pest management, a modern approach to controlling undesirable species by combining natural enemy species such as predators and parasites with other natural control methods and balanced chemical insecticide use.
“Mating disruption” refers to a method of pest control most commonly found in agriculture; it involves saturating the crop environment with a sex pheromone in order to confuse the males and prevent them from locating females.
“Odorant Binding Proteins” or “OBPs” refers to proteins in sensory tissues believed to bind odors, that are typically hydrophobic, and escort them across the hydrophilic extracellular matrix to the cell surface, where odorant receptors are located.
“Odorant Degrading Enzymes” or “ODEs” refers to enzymes that degrade semiochemicals, odors, scents, tastes, or other chemical stimuli in order to re-potentiate the invertebrate chemosensory system.
“Odorant Receptor” or OR refers to the subcellular structures located in the plasma membrane of insect neuronal cells that are responsible for initiating the organism's perception of a specific odor—that is, they allow the organism to smell various scents and odors. Also called a GPCR.
“Odorant” refers to smell, scent, or odor.
“Ortholog” refers to a gene or gene product sharing sequence elements and function with a related gene from another organism. See also “homolog” above.
“PCR” refers to the Polymerase Chain Reaction, a method of amplifying nucleic acid sequences in vitro in order to obtain larger amounts of DNA.
“Pheromone” refers to an odorant chemical released by an insect that causes a specific interaction with another insect of the same species.
“Reagents” refers to chemicals and compounds (either naturally occurring or synthetic) or enzymes used in a chemical reaction to measure or yield other substances.
“Reporter Gene” refers to a gene used in biological or biochemical experiments in order to monitor an interaction. Reported genes respond to protein-protein interactions by triggering an effect that is easily detectable, e.g., the emission of fluorescent light or the production of an assayable product.
“RFID” refers to Radio Frequency Identification, a radio-frequency-based, remote data collection technology that uses electronic tags to store data. The tags and the data they contain can be administered (altered) and observed remotely.
“Semiochemicals” refers to chemicals (scents, odors, tastes, pheromones, pheromone-like compounds, or other chemosensory compounds) that mediate interactions between organisms.
“Sensory appendage proteins” or SAPs refers to soluble proteins in sensory tissues believed to bind odors, which are typically hydrophobic, and escort them across the hydrophilic extracellular matrix to the cell surface, where odorant receptors are located.
“Serpentine receptors” refers to GPCRs including GRs or ORs; this term is based on the actual structure of the protein in the cell membrane (seven transmembrane passes in a serpentine shape).
“Signal transduction cascade” refers to a series of molecules in a cell that transduces or converts an external signal (e.g. a pheromone) into a downstream response within the cell (e.g. a change in gene activity).
“Takeout-Like” or “TOL” refers to orthologs of protein encoded by the Drosophila melanogaster gene, takeout. These proteins may be involved in the regulation of circadian rhythms, in mating, and in feeding behaviors.
“Trans-gene” refers to a gene that has been introduced into the genome of a cell or organism by transformation.
“Transmembrane Domains” refers to hydrophobic domains of a protein that penetrate the cell membrane.
The present invention recognizes the need to construct novel biosensors, novel filtration devices, and novel purification devices, and provides the methods and means to do so by utilizing insect or invertebrate chemosensory proteins in arrays of multiple proteins, smaller arrays or groups of several proteins, or individually. Since insect chemosensory proteins are known to bind a wide array of ligands, the invention provides for the use of numerous proteins sourced from many different insect species in order to maximize the total number of ligands or analytes an array of these proteins is capable of recognizing. The invention also recognizes that despite the tremendous diversity of ligand binding possibilities afforded by insect chemosensory protein arrays, some analytes may not be recognizable by these arrays; furthermore, the characteristics of binding between chemosensory proteins and certain analytes may need to be manipulated. Thus, the invention provides the means and methods necessary to construct chemosensory proteins in vitro that feature novel binding characteristics or the ability to bind novel analytes, or to bind known analytes in novel ways with respect to the affinity and/or the kinetics of the interaction. The invention provides distinct advantages over existing methods to identify, concentrate, or purify analytes, since it takes advantage of the diverse ligand binding capabilities and high sensitivity of insect chemosensory proteins.
What follows is a non-limiting introduction to the breadth of the invention, including several general and useful aspects:
Insects use a variety of specialized chemosensory organs or tissues, in which chemosensory proteins are expressed and function. These tissues include the antennae, bristles and other sensory organs throughout the body (including appendages such as the legs or wings), and structures in the head such as the labial and maxillary palps.23,26 Since chemosensory proteins are enriched in these tissues, dissecting the tissues and using them to generate cDNA libraries will result in libraries that are enriched for genes expressing chemosensory proteins. Furthermore, gender-specific libraries can be generated from the chemosensory tissues of a particular species, allowing for the rapid identification of gender-specific chemosensory genes such as those genes involved in the mating response. These approaches can be used to rapidly isolate sequences encoding chemosensory proteins from a particular species.23,26,27 Chemosensory proteins also can be identified using a variety of other means. One method relies on bioinformatic analysis. For example, OBPs and SAPs have characteristic domains, motifs, and sequence features that are conserved across species boundaries.23,26,28 Thus, novel members of these protein families can be identified on the basis of these characteristics by using bioinformatics to compare the sequences of known members expressed in one species to sequences from another species.23,26
Combined, the above approaches can rapidly identify and isolate a wide variety of chemosensory genes from any number of insect species. Given the large number of insect species extant,29 the number of potential chemosensory genes can exceed thousands. These genes can be expressed in vitro using a variety of methods common in the art39-34 to generate large collections of chemosensory proteins capable of interacting with a wide variety of analytes. These collections are chemosensory arrays and have a variety of applications. The present invention recognizes the need for such chemosensory arrays, and provides means and procedures necessary to incorporate these arrays in devices or biosensors capable of distinguishing or detecting known or unknown analytes or mixtures of analytes; the array can be combined with any number of reporter mechanisms common in the art (enzymatic, electronic, optical, etc.) depending on the goals of the specific application.
As described above, a chemosensory array can be constructed by expressing a large number of chemosensory proteins expressed in vitro using methods common in the art.30-34 When coupled to a reporter system (enzymatic, fluorescent, optical, electrical, and so on) such an array is potentially capable of recognizing a wide variety of analytes or chemosensory stimuli. The specific response generated by the array in the presence of a particular analyte is the chemosensory profile for that particular analyte; for example, a pheromone such as codlemone35 would be recognized by an array containing chemosensory proteins derived from Cydia pomonella, the codling moth, since this organism recognizes the pheromone in vivo. In addition to the chemosensory proteins from the codling moth in the chemosensory array, chemosensory proteins derived from other species may also recognize codlemone. By observing the response pattern (yes/no binding for each protein in the array) generated by the reporter system employed in the array, a chemosensory profile specific for codlemone can be generated. This profile is characteristic of the presence of codlemone in any given analyte, and can be used to identify codlemone as a result. (
In order to identify which protein(s) in the chemosensory protein array can bind to a given substance or molecule, several methods can be used. For example, a dye, such as N-phenyl-1-naphthylamine (1-NPN)36,37 or (+/−)-12-(9-anthroyloxy)stearic acid (ASA)34 will fluoresce when captured by the ligand-binding pocket of a chemosensory protein and this fluorescence is quenched when the dye is displaced by another molecule. Therefore, spectroscopy or flow cytometry can be used to detect fluorescence quenching and thus identify which chemosensory protein(s) in the array interact with the chemicals of interest.
The same method can be used to identify unknown analytes by generating a characteristic chemosensory profile for them. The array is exposed to the unknown analyte, and the resulting profile recorded for future comparison with other samples potentially containing that same unknown analyte. If the analyte is present, the characteristic chemosensory profile will be generated by the array. This method does not require knowing the identity of the analyte detected.
As described previously in this document, a chemosensory array can be constructed by expressing a large number of chemosensory proteins expressed in vitro using methods common in the art.30,34 When coupled to a reporter system (enzymatic, fluorescent, optical, electrical, and so on) such an array is potentially capable of recognizing a wide variety of analytes or chemosensory stimuli. The specific response generated by the array in the presence of a particular analyte is the chemosensory profile for that particular analyte. The proteins involved in the chemosensory profile for any given analyte can be incorporated into a detection device that relies on chemosensory proteins for analyte “recognition” and is coupled to a reporter mechanism (electrical, mechanical, enzymatic, or other). In this manner, the invention provides the means necessary to construct a biosensor to detect a given analyte in the atmosphere or in an aqueous solution.
IV. Methods to Increase the Diversity of Chemosensory Protein Recognition by Utilizing Peptides or Derivatives in Order to Construct Hybrid Chemosensory Proteins In Vitro and Employ these Hybrid Proteins in a Chemosensory Array
Chemosensory proteins and their potential ligands have been studied extensively, and in several cases structural studies have been performed or crystal structures have been determined.31-33,38-43 To date, chemosensory proteins such as OBPs have been associated with a specific binding partner44 or a range of potential binding partners that share structural motifs37 and the specificity of the chemosensory protein:ligand association is conferred by the ligand binding pocket on the chemosensory protein.32,38,45,46 Manipulating the binding pocket:ligand interaction can confer novel functionality to the chemosensory protein; this approach has potential uses in biosensors, purification devices, and signal transduction cascades.47,48 OBP structure is characterized by conserved domains separated by variable regions, and this overall structure is maintained across species boundaries.41 Despite the potentially enormous diversity afforded by the large number of chemosensory proteins from the millions of insect species29 there are potentially analytes that are not recognized by any available chemosensory proteins. Furthermore, it may be desirable to manipulate the specificity, strength of ligand binding, or other characteristics of ligand binding between chemosensory protein(s) and an analyte. The present invention provides the means to do so by utilizing peptides or derivatives of chemosensory proteins in order to construct novel, hybrid chemosensory proteins in vitro.
DNA sequences encoding fragments of known chemosensory proteins can be cloned from sensory-tissue-specific cDNA libraries23,26 or synthesized chemically using a variety of methods, including PCR-based DNA synthesis.49 By utilizing linker sequences at the end of each fragment, longer DNA fragments can be assembled into novel sequences encoding proteins with motifs or domains from a variety of sources; this novel motif combination can include complex structures.49 The present invention utilizes these methods to generate chemosensory proteins with novel ligand binding domains; these hybrid chemosensory proteins can then be used in chemosensory arrays to recognize novel analytes (
V. Methods for Developing Devices to Isolate or Detect By-Products of Chemical Synthesis, or to Isolate or Detect Desired Products of Chemical Synthesis; Also, Methods for Developing Devices for Purification or Concentration of an Analyte from a Mixture or Solution
Invertebrate chemosensory proteins are very diverse and are capable of detecting millions of scents, odors, tastes, semiochemicals, or molecules based on their ability to interact with these targets.23 Chemosensory proteins can be identified and expressed in vitro using methods common in the art;23,26-28 the expression of numerous such proteins results in a chemosensory protein array as described above. This array can be used to examine a given substance—an odor, scent, or chemical, for example—and identify which available insect chemosensory proteins are capable of binding the substance in question.
Thus, chemosensory proteins can be used in the construction of selective filtering devices that are capable of distinguishing a specific component or intermediate compound in biochemical or industrial processes. Depending on the desired level of selectivity and specificity, a filtering device can be designed to identify classes of related chemicals or it can be designed to be much more selective, to the point of distinguishing stereoisomers of molecules that have identical chemical structures. Or, chemosensory proteins capable of selectively binding to a specific compounds such as a water pollutant compound can be expressed in bacterial cells (e.g., E. coli cells) and linked to the bacterial cell membranes such that the chemosensory proteins are present on the outer surface of the bacterial cell membrane. These bacteria can then be used in applications requiring the selective removal of a pollutant compound from water, such as in water purification facilities. The high level of selectivity of insect chemosensory proteins toward analytes has been documented in the Gypsy Moth, Lemantria dispar;44 this moth's chemosensory system can reliably distinguish stereoisomers of a pheromone.
The invention recognizes the need to develop devices capable of detecting specific analytes, present in small quantities in the atmosphere or in solution, that are associated with explosives. To accomplish this, a chemosensory array is used to generate a chemosensory profile for each analyte or for commonly used combinations of analytes as described previously, and the portions of the chemosensory array (the chemosensory proteins) that participate in this chemosensory profile are incorporated into a detecting device while coupled to a reporter mechanism.
Analytes of particular interest to this application of the invention include but are not limited to ammonium nitrate (NH4NO3); black powder (a mixture of charcoal, sulfur, and saltpeter—nitrates of potassium or sodium); smokeless powder (primarily composed of nitrocellulose); RDX (cyclotrimethylenetrinitramine; also known as cyclonite); C4 (Composition C-4, comprising the explosive, typically RDX or cyclonite; the plasticizer, di(2-ethylhexyl) or dioctyl sebacate; the plastic binder, polyisobutylene; and a tag or marker such as 2,3-dimethyl-2,3-dinitrobutane or DMDNB); other nitroamines such as HMX (cyclotetramethylene-tetranitramine); PETN (Penthrite or Pentaerythritol Tetranitrat); dynamite; TNT (CH3C6H2(NO2)3 or trinitrotoluene; a common substance present in military-grade TNT is 2,4-DNT or 2,4-dinitrotoluene); Semtex (a mixture of PETN, RDX, N-phenyl-2-naphthylamine as an antioxidant, a plasticizer such as di-n-octyl phthalate, and a styrene-butadiene rubber binder; later stocks have an ethylene glycol dinitrate tag); TATP (acetone peroxide or triacetone triperoxide); and others.
Insects are known to recognize several of these substances from behavioral assays and from attempts to train honeybees to detect landmines and/or unexploded ordinance (UXO), and for general environmental monitoring.50-52 The present invention provides the methods to develop detection devices based on the chemosensory proteins that enable honeybees and other insects to detect explosives; the invention is novel in that it does not require live insects and merely relies on in vitro expression of recombinant chemosensory proteins as described previously in this document. The chemosensory proteins from honeybees and other insects capable of detecting analytes of interest are used to construct an explosives-specific chemosensory array that is coupled to an enzymatic, electric, mechanical, or other form of reporter mechanism to comprise a biosensor for detecting explosives.
The invention can also be used to generate a detector mechanism specifically designed to detect a known marker compound that is incorporated into explosive formulations by manufacturers. This arrangement is intended to aid in the rapid identification of the source of a tested explosive sample.
VII. Methods for Developing a Biosensor with Industrial Food Preparation Applications
The invention recognizes the need to detect byproducts of food decomposition in order to ensure safe food processing in applications such as meat packaging and other food preparation applications. Thus, the invention provides the methods necessary to identify analytes commonly associated with food decay or food quality problems. To accomplish this, a chemosensory array is used to generate a chemosensory profile for each analyte or for commonly occurring combinations of analytes as described previously in this document, and the portions of the chemosensory array (the chemosensory proteins) that participate in this chemosensory profile are incorporated into a detecting device while coupled to a reporter mechanism. These devices can be used in packaging plants, other industrial food preparation plants, food preparation applications (restaurants, mess halls, etc.), or, in a portable format, by health inspectors or other food service professionals.
This aspect of the invention can be incorporated directly into packaging materials and coupled to a reporter mechanism such as an enzymatically triggered color change or other mechanism, to allow end users or consumers to quickly determine if a particular food article is spoiled. If this aspect of the invention is coupled to a Radio Frequency Identification (RFID) mechanism, it will enable shipments of food or other perishable items to be monitored remotely for spoilage.
Analytes of particular interest to this application of the invention include but are not limited to fermentation products such as alcohol(s) produced by microorganisms, byproducts such as lactic acid, and ptomaines (nitrogenous organics resulting from bacterial putrefaction of protein) including putrescine, cadaverine, parvolin, and sepsin. The invention also provides the methods necessary to detect common invertebrate infestations in food products, again using a chemosensory array profile approach to determine which chemosensory proteins can detect compounds for a particular species.
The devices described in this method could also include functionality from the following method, “Methods to develop a portable device capable of detecting the presence of insect pests” in order to extent their application to the detection of pest-infested fruits and vegetables. This application is of interest to food packers, food exporters, agricultural inspectors, and customs agencies.
The invention also recognizes the need to monitor food quality to ensure product consistency while producing foodstuffs such as coffee and wine, where the aroma of the final product is critical to commercial success and trained humans capable of detecting specific odors or odor combinations have traditionally been charged with the task of monitoring the quality of production based on aroma. The method described here can also be used in this instance; the invention provides the means necessary to identify the key volatile components of a coffee or wine that contribute toward a desirable aroma by using a chemosensory protein array to develop a scent fingerprint for that coffee or wine. Production quality is monitored by checking samples of the coffee or wine using a biosensor with insect chemosensory proteins that recognize the volatiles emitted by a control or reference coffee or wine sample to ensure the aroma emitted by tested samples corresponds to the fingerprint of the reference.
VIII. Methods to Develop a Portable Device Capable of Detecting Human Corpses within Rubble or in Disaster Areas; Also, Methods to Develop a Portable Device Capable of Detecting Surviving Humans within Rubble or in Disaster Areas
The invention recognizes the need to detect byproducts of corpse decomposition in order to locate human remains. Thus, the invention provides the methods necessary to identify analytes commonly associated with tissue decay or tissue decomposition. To accomplish this, a chemosensory array is used to generate a chemosensory profile for each analyte or for commonly occurring combinations of analytes as described previously in this document, and the portions of the chemosensory array (the chemosensory proteins) that participate in this chemosensory profile are incorporated into a detecting device while coupled to a reporter mechanism. These devices can be used in portable detection mechanisms that can be transported to the site of an accident, attack, bombing, natural disaster, or other incident with multiple casualties, and used in lieu of or in addition to canine search units.
Analytes of particular interest to this application of the invention include but are not limited to fermentation products such as alcohol(s) produced by microorganisms; byproducts such as lactic acid, and ptomaines (nitrogenous organics resulting from bacterial putrefaction of protein) including putrescine, cadaverine, parvolin, and sepsin.
Similar methodology can be used to develop a chemosensory profile for living humans; analytes that are of interest in this application are the volatiles in the breath and those emitted from the skin of living humans.53 This chemosensory array can be coupled to a reporter mechanism in order to generate a device to detect survivors in disaster areas.
Many insect species employ chemical communication and emit scents or odors in order to communicate with other individuals of their species, or as signals that can be recognized by other species for a variety of reasons.29,37,53-57 Plants also interact with insects using chemical signaling; plant species are known to emit allomones or other chemical signals to attract beneficial insects.58 These chemical signals regulate critical aspects of insect behavior, such as feeding, foraging, oviposition, or mating.23 Due to the importance of chemical communication, insects have developed highly sensitive chemosensory systems; insect chemosensory proteins are thus ideally suited to recognize these chemical signals.
The present invention provides the means necessary to develop a detector device capable of identifying a particular species of insect based on detecting the chemical signals characteristic of that particular insect species. The applications of this aspect of the invention are mainly in pest control, whether agricultural, domestic, Homeland Security, or public health related. To accomplish this, a chemosensory array is used to generate a chemosensory profile for each analyte or for commonly occurring combinations of analytes as described previously, and the portions of the chemosensory array (the chemosensory proteins) that participate in this chemosensory profile are incorporated into a detecting device coupled to a reporter mechanism. The chemosensory array may be presented with a pheromone or other semiochemicals characteristic of a species of interest, or simply with extracts from ground specimens of the species of interest. This aspect of the invention can also be coupled to a Radio Frequency Identification (RFID) mechanism to allow remote monitoring of infestations.
One group of insects that potentially represent a promising source of chemosensory proteins is parasitoids such as parasitic wasps. These insects specialize in locating host organisms such as moths, and are thus often used in integrated pest management (IPM) schemes as a means of controlling insect pest populations.59,60 The invention provides for isolating chemosensory proteins from parasitoid wasp species, and other species that specialize in the chemical identification of pests; the chemosensory proteins can be expressed in vitro and used to assemble a chemosensory array capable of detecting the pest species in question when coupled to a reporter mechanism. Such a construct can be incorporated into a detection device to be used commercially.
X. Methods to Develop a Device Capable of Detecting Disease In humans
Sensors to detect disease in humans have been the topic of numerous investigations, with recent emphasis on the development of the “electronic nose”.5,10 The presence of specific volatiles has been associated with numerous diseases in humans. For example, cancerous cells on the skin or inside the body emit volatile compounds into the blood, the atmosphere or body fluids that are then expelled; the volatiles can be detected in order to speed the identification or diagnosis of disease. This is the case with a diverse set of human diseases such as prostate cancer,61-63 bladder cancer,64 pulmonary tuberculosis,65 breast cancer,6 lung cancer,66,67 melanoma,68 angina,67 and diabetes.9,69-71 In addition, anecdotal evidence suggests the emission of volatiles from the human body that are detectable by animal chemosensory systems in the case of imminent epileptic seizures; epileptic owners of service dogs often report their canines have developed the ability to sense an imminent seizure event before the patients can detect physiological changes themselves.
The invention recognizes the need to enhance the sensitivity and versatility of electronic nose-type biosensor devices, and provides the means necessary to do so. To accomplish this, the volatiles associated with a particular disease in humans are introduced as analytes into the insect chemosensory protein array described elsewhere in this document. The chemosensory array is used to generate a chemosensory profile for each analyte or for commonly occurring combinations of analytes as described previously in this document. As a control, the volatiles associated with healthy humans are used; the chemosensory fingerprint or profile generated by the analytes emitted by healthy humans is compared to that from diseased humans in order to identify those analytes positively associated with a particular disease. The portions of the chemosensory array (the chemosensory proteins) that participate in the chemosensory profile of a disease are incorporated into a detecting device while coupled to a reporter mechanism. These devices can be used in clinics, hospitals, portable health care labs, field hospitals, humanitarian relief efforts, and other health care or diagnostic applications.
Some insect species rely on their ability to detect the byproducts of combustion. For example, jewel beetles (Melanophila spp.) must locate freshly burned forest areas in order to oviposit, as the larvae of this species can only develop in the wood of freshly burned trees.72 Thus, these insects may be able to locate burned or burning wood from distances of several km by detecting volatiles such as phenolic compounds typical of burnt forest areas; one example of such a compound is guaiacol72 (C7H8O2).
The invention provides the means to generate a chemosensory array comprising chemosensory proteins from numerous insect species, including species with a known sensitivity to phenolic compounds and/or combustion byproducts. This array can be used to isolate the specific chemosensory proteins responsible for insect sensitivity to burning wood, and these chemosensory proteins can be used in novel fire detection devices when coupled with an electric or electronic reporter system or alarm. The invention thus provides the means to replace or augment existing smoke detectors (based usually on the radioactive compound, americium oxide, AmO2). Other applications of the invention include forest fire detection systems, and commercial or industrial fire detection systems for use in warehouses, airports, schools, auditoria, sporting venues, public transport stations, convention centers, public gathering places, etc.
XII. Methods to Develop Compounds or Constructs that Mask Odors, Scents, or Other Semiochemicals
The present invention recognizes the need to develop compounds, devices, or constructs capable of masking semiochemicals in industrial, agricultural, and domestic environments. The invention therefore provides methods and means to incorporate chemosensory protein-based odor-masking technologies into a variety of commercial products or devices. Chemosensory proteins that can be used include OBPs, odorant degrading enzymes, sensory appendage proteins, or chemosensory receptors.
DNA sequences encoding OBPs or other chemosensory proteins can be expressed in vitro using tools common in the art. Devices incorporating these chemosensory proteins in a solid form, particulate form in suspension, or aqueous form in a gel have numerous commercial, agricultural, and domestic applications that include but are not limited to the following:
Products incorporating chemosensory proteins can mask the unpleasant odors associated with cigarette, cigar, and pipe smoke. The products can be introduced as an aerosol spray or can be incorporated directly into cigarettes, cigars, or smoking tobacco.
These methods can also be employed to target chemosensory proteins including sensory appendage proteins (SAPs), odorant binding proteins (OBPs), odorant degrading enzymes (ODEs), and other proteins involved in olfaction, gustation, chemosensation, or the regulation of chemosensory-mediated behavior.
Furthermore, products to mask or trap odors need not incorporate the entire chemosensory protein; they can instead incorporate peptide derivatives or fragments.
Many important aspects of insect behavior rely on chemosensory cues.23,73,74 Since chemosensation profoundly influences insect behavior, the molecules and processes involved in the chemosensory pathway have developed extreme sensitivity toward chemosensory stimuli or analytes. Insects are capable of recognizing a tremendously diverse number of analytes at very low concentrations. The molecular mechanism of analyte detection in insects has been extensively studied in various species.23,26,27,75-89 The chemosensory signal transduction cascade is facilitated by extracellular, transmembrane, and intracellular proteins.90-92 The major molecular participants are odorant binding proteins (OBPs), G-protein coupled receptors (GPCRs), sensory appendage proteins (SAPs), odorant degrading enzymes (ODEs), circadian rhythm proteins (such as TOLs), gustatory binding proteins, and gustatory receptors (GRs).
These proteins can be expressed in vitro using methods common in the art23,26,27 Numerous methods are available to identify and isolate chemosensory proteins from a wide array of species, including bioinformatic analysis to search for orthologs of known proteins across species boundaries, and the construction of chemosensory-specific cDNA libraries from the species of interest from which clones encoding chemosensory proteins can be expressed. By combining numerous chemosensory proteins from a number of species, an array of chemosensory proteins can be constructed. Since the array contains chemosensory proteins from numerous species, it is capable of recognizing more analytes than any one insect species alone. The array is linked to a reporter system common in the art, such as a mechanical, electrical, piezoelectric, enzymatic, or electronic system, and can report the presence of an analyte in a mixture of gases or in a liquid solution by exposing each protein in the array to the specimen and noting whether the reporter system registers an interaction (binding event) between any protein in the array and the analyte of interest.
Numerous insect chemosensory proteins have a list of known natural ligands, that is, analytes they interact with in vivp31,75,93-96 Arrays can be constructed with constituent proteins that emphasize recognition of analytes for a given purpose; for example, arrays that specialize in the recognition of alcohol analytes can be constructed using known chemosensory proteins that bind alcohols and their orthologs or structurally similar proteins from a wide variety of insect species. Furthermore, the known ligand binding partners serve as positive controls to test array and reporter system functionality.
As shown in Example 1, a chemosensory array comprising chemosensory proteins from a wide variety of insect species expressed in vivo and linked to a reporter system common in the art can be constructed. Such an array is capable of recognizing a wide variety of analytes either in solution or in the atmosphere, and array function can be tested using analytes known to interact with chemosensory proteins present in the array.
The location and identity of each chemosensory protein in the array is known. Since chemosensory proteins individually recognize (bind to) one or a small number of analytes, that is, since chemosensory proteins tend to have specific ligands,23 the reporter system used will generate a distinct pattern of recognition when the array is presented with an analyte of interest, and this pattern of recognition will be unique to that analyte (
These chemosensory fingerprints have numerous applications. For example, an analyte of interest can be recognized easily if the chemosensory array's reporter system generates a chemosensory fingerprint known to arise when that analyte is present. This is an efficient way of constructing diverse biosensors, and the underlying chemosensory array can be common (mass produced) yet used in devices that detect a wide array of analytes (from natural gas leaks to explosives to spoiled food to the presence of insect pests on the basis of released odors).
Chemosensory fingerprints are also useful in the efficient construction of detector devices that can reveal the presence of an analyte or mixture of analytes without necessarily knowing the source of those analytes. For example, if a novel mycobacterium or other species capable of causing disease in humans by infecting the lungs is introduced into the United States by an infected traveler from the developing world, the bacterial infection generates volatiles in the patient's breath5,65 that may be detectable by a chemosensory array like the ones described here. A chemosensory array with a reporter mechanism can be exposed to the patient's breath to generate a chemosensory fingerprint of the volatile present from that particular individual. Comparison to a fingerprint from uninfected individuals will reveal the chemosensory proteins that are responding to the volatiles in the patient's breath that are the product of the unknown pathogen. This chemosensory profile can then be used to design novel biosensors to rapidly diagnose the new disease; these biosensors may use an enzymatic, electric, mechanical, or other reporter system to alert the user to the presence of an infected individual that breaths into a mouthpiece. Knowledge of the identity of the pathogen is not necessary, nor is knowledge of the identify of the specific volatiles in the breath created by the pathogen in the lungs. Such a biosensor can be deployed at airports, ports of entry, health car clinics, hospitals, or other areas where infected individuals may be identified.
The concept of a chemosensory fingerprint as described in Example 2 has numerous applications, including the construction of a biosensor for detecting the presence of compounds in the environment or atmosphere. For example, a biosensor based on insect chemosensory proteins in an array that is linked to a reporter system such as an audible beeper or alarm can be constructed to detect molecules that are colorless and odorless to humans, thus making these compounds difficult for humans to detect.
Such a detector is particularly useful in the detection of toxic compounds in the atmosphere that pose a health risk to humans, as humans are often unable to sense them using their own chemosensory systems, or the chemicals are so toxic that they must be detected before they are smelt by humans. Examples of such chemicals are the nerve gases, tabun (GA), soman (GD), sarin (GB), cyclosarin (GF) and VX. These agents are used in chemical weapons and are extremely toxic to humans, making their detection important to security, military, and anti-terrorist applications.
In this example, the invention provides the means and methods necessary to detect the nerve gas, soman (1,2,2-Trimethylpropyl methylphosphonofluoridate). Soman is a volatile, colorless liquid classified as a weapon of mass destruction by United Nations Resolution 687. The stockpiling and production of soman has been banned by the Chemical Weapons Convention of 1993. A chemosensory array comprising chemosensory proteins from numerous insect species can be used to identify insect chemosensory proteins capable of detecting soman; these proteins are then incorporated into a specialized array that is linked to a reporter system such as a piezoelectric buzzer with a power source, and incorporated into portable devices. These devices are biosensors capable of detecting soman and can be used in military, homeland security, and government installations. Portable devices can be used in the field by armed forces personnel and weapons treaty compliance inspectors.
Insect chemosensory proteins have been shown to selectively bind to a particular stereoisomer of a ligand and not the another stereoisomer of the same ligand; for example, the moth, Lemantria dispar, can use its chemosensory system to select a specific stereoisomer of a pheromone.44 This extremely selective, highly specific binding activity of chemosensory proteins can be utilized to select for, concentrate, select against, or purify a specific analyte from a complex mixture, and has numerous applications in industry. For example, chemosensory proteins from a wide variety of insect species in an array linked to a reporter system can be exposed to diastereomers of ephedrine, a drug used in a variety of applications and sold over the counter as well as in prescription medications. Each diastereomer will generate a unique chemosensory profile, and those chemosensory proteins capable of binding one diastereomer but not the other(s) can be selected for inclusion into purification devices. These devices are then incorporated into synthesis pathways by pharmaceutical companies in order to efficiently isolate or purify desired products from mixtures containing their stereoisomers and/or by-products of chemical synthesis. Thus, a chemosensory protein with highly selective specificity of binding for the (1S,2S)-diastereomer of ephedrine, (called “pseudoephedrine” and available over the counter as a decongestant) is used to isolate and purify this stereoismoer from a mixture of compounds including (1R,2S)-ephedrine (banned for over the counter use in diet aids; used for asthma) and/or other structurally related amines. Likewise, selecting any dextrorotatory isomer from its levorotatory isomer, or vice versa, can be accomplished by using a highly selective chemosensory protein identified from the array and incorporated into a filtering mechanism in a pharmaceutical production line. For example, all molecules containing a characteristic structure such as the 17 carbon atoms arranged in four rings (hallmark of steroid molecules) can be rapidly identified, isolated, or concentrated by using chemosensory proteins capable of selectively binding them.
This aspect of the invention is also useful in applications such as environmental cleanup or any application requiring the selective removal of a class of compounds or a single compound.
Live insects are already in use to detect unexploded ordinance (UXO). Insects are known to recognize several explosive substances,50-52 and honeybees are being trained to detect land mines or other UXO. However, there are several serious drawbacks to using live insects for detecting UXO. Firstly, although insects have very sensitive chemosensory systems as a group, the variety of compounds any individual species can detect is less than the variety of compounds numerous species can detect. Secondly, insects must be available in large numbers, as most species have a short life span; this implies domesticated species such as the honey bee are easier to use in detection than other species that may have equally sensitive chemosensory systems, such as wasps. Thirdly, insects like honeybees must be trained to detect explosives, and must be observed detecting these explosives in order to identify the location of the UXO.
The present invention overcomes these difficulties and provides the methods to develop detection devices based on the chemosensory proteins to detect explosives without requiring live insects. The chemosensory proteins from honeybees and other insects capable of detecting analytes of interest are used to construct an explosives-specific chemosensory array that is coupled to an enzymatic, electric, mechanical, or other form of reporter mechanism to comprise a biosensor for detecting explosives. For example, a chemosensory array containing chemosensory proteins from several hundred insect species is used to develop a chemosensory profile for the commonly available explosive, Semtex. This substance is a commercially produced mixture of PETN, RDX, N-phenyl-2-naphthylamine, di-n-octyl phthalate, and a styrene-butadiene rubber binder. The array will provide chemosensory proteins capable of binding to each of these substances individually, or to mixtures of the component substances. These chemosensory proteins can be incorporated into a portable device and linked to a piezoelectric buzzer for use as an explosives alarm system in battlefields, airports, or other military or security applications.
Although insect chemosensory proteins represent a highly diverse group with a wide variety of binding properties there are potential analytes that may be unrecognized by existing expressed proteins. Furthermore, it may be desirable to manipulate the specificity, strength of ligand binding, or other characteristics of ligand binding between chemosensory protein(s) and analyte. This example shows how a modified OBP with a higher binding affinity to a given analyte can be can be isolated so that it can be used in a biosensor device to detect explosives.
The compound 2,4-DNT is a chemical degradation by-product of trinitrotoluene, a common component of many high explosives. Several groups have focused on detection of 2,4-DNT as a method to locate explosives, including underwater mines and land mines. At least one such study successfully used honeybees (Apis mellifera) trained to smell 2,4-DNT to locate land mines,50,97 indicating insects have chemosensory proteins that recognize this compound. The Apis genome has been sequenced and many of the genes encoding chemosensory proteins have been identified.
2,4-DNT would be screened using the chemosensory array described above. A variety of chemosensory proteins from the array would be identified that bind 2,4-DNT with a range of affinities. In order to isolate proteins with improved affinity, DNA sequences representing the individual functional domains of chemosensory proteins that bind 2,4-DNT are used to generate oligomers of approximately 60 bp. Since these genes are on average 300 bp long this means generating about 5 oligomers from each gene. In addition, linking oligomers of 30 bp are generated representing the reverse strand, these contain 15 bp from the end of two adjacent 60 bp oligomers. Both sets of oligomers are mixed together, allowed to anneal and a DNA polymerase is used to fill in the gap. This method is a novel and substantial improvement of the method detailed by Xiong et al. (“A simple, rapid high-fidelity and cost-effective PCR-based two-step DNA synthesis method for long gene sequences”).49 By mixing oligomers from the 2,4-DNT-binding chemosensory proteins with specific linking oligomers we can create novel gene chimeras containing functional domains from the different proteins. These novel genes are expressed and the resulting proteins screened for improved binding affinity to 2,4-DNT using an assay that has been previously described above.
The improved protein can then be produced and incorporated into a detecting device while coupled to a reporter mechanism.
The food and shipping industries require a reliable method to detect byproducts of food decomposition in order to ensure safe food processing in applications such as meat packaging and other food preparation applications. Meats and vegetables are often prepared in a central location such as a packing plant and shipped across country or even abroad as perishable cargo, and care must be taken that this cargo arrives at the destination still fit for human consumption.
Decomposing meat typically harbors bacteria and other microorganisms that produce characteristic substances such as alcohol(s), lactic acid, and nitrogenous organics resulting from bacterial putrefaction of protein including ptomaines, putrescine, cadaverine, parvolin, and sepsin. The invention can use insect chemosensory proteins to detect these substances. A chemosensory array composed of numerous chemosensory proteins from different insect pest species, particularly species known to be attracted to cadavers and carcasses, is used to generate a chemosensory profile for each analyte or for commonly occurring combinations. Those proteins from the chemosensory array that do recognize the analytes of interest are then incorporated into a detecting device while coupled to a reporter mechanism. Thus, the invention can be incorporated directly into packaging materials and coupled to a reporter mechanism such as an enzymatically triggered color change or other mechanism, to allow end users or consumers to quickly determine if a particular food article is spoiled. A Radio Frequency Identification (RFID) mechanism can also be linked to the biosensor, so as to enable shipments of food or other perishable items to be monitored remotely for spoilage while in transit on ships, trucks, trains, airplanes, or other means of transport. The RFID-linked spoilage biosensor can also monitor foodstuffs in storage in warehouses etc.
The invention recognizes the need to detect a specific aroma or combination of aromas or scents as an indicator of quality in certain foods or beverages. For example, the coffee and wine industries rely on humans that are trained to detect specific odors or aromas in these products; the quality of coffee or wine is directly associated to its aroma by consumers and producers alike. The invention provides the means necessary to identify the key volatile components of a coffee or wine that contribute toward a desirable aroma; once these volatiles are identified they are incorporated into a chemosensory fingerprint and the interested industry can then monitor coffee production to ensure current batches also emit the same volatile scents or odors in order to obtain a consistent aroma.
A sample of coffee with a highly desirable aroma (a reference coffee) is used to establish the chemosensory fingerprint of the “correct” or desirable aroma for subsequent production. A chemosensory protein array consisting of numerous insect chemosensory proteins linked to a reporter mechanism (see
The invention recognizes the need to detect byproducts of human respiration, scents or odors such as oils and sweat emitted from the skin, and other odors characteristics of living humans in order to construct a biosensor for the discovery of survivors of natural or wartime disasters that may be trapped under wreckage, rubble, mines, etc.
Numerous insect species have chemosensory proteins specialized for the detection of humans; for example, the malaria carrying mosquito, Anopheles gambiae, is anthropophilic and can locate humans in the dark by sensing volatiles in the human breath and emitted from the skin.23,98-100 The invention recognizes the application of chemosensory proteins from insects that can detect human-emitted volatiles in the construction of biosensor devices to detect humans. Thus, the invention provides the methods necessary to identify analytes commonly associated with the presence of living humans. To accomplish this, a chemosensory array is used to generate a chemosensory profile for each analyte or for commonly occurring combinations of analytes typically emitted by humans, such as carbon dioxide and lactic acid.23,98-100 As described previously in this document, the portions of the chemosensory array (the chemosensory proteins) that participate in this chemosensory profile are incorporated into a detecting device while coupled to a reporter mechanism. These devices can be used in portable detection mechanisms that can be transported to the site of an accident, attack, bombing, natural disaster, and used in lieu of or in addition to canine search units.
Insects are economically detrimental to many industries, such as the agriculture, food shipment, and housing industries. These industries invest large sums of money to control insect pests, primarily with insecticides and/or other forms of pest management such as IPM. This invention provides the means to construct a biosensor capable of detecting the presence of a particular insect pest species; such a device is useful in the field, in packaging plants, as well as in inspection stations such as those run by the government agriculture departments of many nations to control import/export of infected foods.
Numerous insect species employ chemical communication and emit scents or odors in order to communicate with other individuals of their species, or as signals that can be recognized by other species for a variety of reasons.29,37,53-57 Plants also interact with insects using chemical signaling; plant species are known to emit allomones or other chemical signals to attract beneficial insects.58 These chemical signals regulate critical aspects of insect behavior, such as feeding, foraging, oviposition, or mating.23 Due to the importance of chemical communication, insects have developed highly sensitive chemosensory systems; insect chemosensory proteins are thus ideally suited to recognize these chemical signals.
The codling moth, Cydia pomonella, is a pest of pome fruit in the United States. The codling moth utilizes a pheromone, codlemone, to allow individuals to locate one another for mating; the structure and function of codlemone are well characterized, and it is known that male moths respond to it.101-104 Currently, levels of codling moth infestation in apple orchards are monitored using traps combining a glue to hold male moths with artificial codlemone to attract them, and require human intervention. This invention provides the means to develop a codling moth biosensor that detects moths by identifying codlemone in the atmosphere. A chemosensory array containing chemosensory proteins from the codling moth is generated by expressing these proteins in vitro. The array can contain chemosensory proteins from other insect species, as it is likely several other species express proteins that can identify codlemone. For example, predators such as wasps that feed on codling moth are likely to express chemosensory proteins that can detect volatile scents or odors emitted by the moths; the protein array can thus include chemosensory proteins from wasp species. The array is used to generate a chemosensory profile for codlemone. The chemosensory proteins that participate in this chemosensory profile are incorporated into a detecting device while coupled to a reporter mechanism. This biosensor device can also be coupled to a Radio Frequency Identification (RFID) mechanism to allow remote monitoring of infestations.
Apples infested with codling moths are banned in several countries that import fruit from the United States. Thus, this aspect of the invention coupled to an RFID mechanism can be used to monitor fruit shipments for possible codling moth infestation during transit, ensuring no infested shipments are allowed to arrive.
Several human diseases cause the patient to emit detectable volatiles either through the skin, breath, or body fluids. One such disease is pulmonary tuberculosis,65 a contagious disease in humans that is caused by mycobacteria. Tuberculosis (TB) infection among humans in the developed world resurged in the 1990s as a result of immigration, relaxed TB control in countries where the disease had previously been eradicated, and an increase in the number of immunosuppressed patients as a result of AIDS.
The established method to test a human for exposure to the organism that causes TB was developed in the early 20th century and named after French physician, Charles Mantoux. The Mantoux test involves an intradermal injection of 10 Tuberculin units, usually performed on the inner forearm of the test subject. The subject is observed for visible reaction to the Tuberculin at the site of injection up to 72 hours later. One drawback to the Mantoux test is the lag period between injection and analysis. Another drawback is that the test does not confirm active tuberculosis; rather, it merely confirms the subject was at one point exposed to the microorganism. Furthermore, the results must be interpreted, essentially in a subjective manner, depending on the history of the subject. For example, induration (measured in millimeters) of 5 mm is positive in an HIV patient but negative in lab personnel, drug users, or diabetics; these latter persons are considered positive at 10 mm.
The invention provides the means to construct a biosensor for rapid diagnosis of active TB in humans based on detecting the volatiles associated with pulmonary TB in the breath of tested individuals. This device can be used at ports of entry, airports, health clinics, and other areas where high population densities dictate the need for careful public health screening (dorms, military bases, etc.). To accomplish this, the volatiles associated with pulmonary TB in humans tested using an insect chemosensory protein array containing insect chemosensory proteins expressed in vitro and sourced from numerous insect species. The chemosensory array is used to generate a chemosensory profile for active TB infection in humans as described previously in this document, and the portions of the chemosensory array (the chemosensory proteins) that participate in this chemosensory profile are incorporated into a detecting device while coupled to a reporter mechanism. The breath of non-infected humans is used as a control, to exclude chemosensory proteins that recognize normal analytes in human breath from the array in the TB biosensor. These devices can be used in clinics, hospitals, portable health care labs, field hospitals, humanitarian relief efforts, and other health care or diagnostic applications. The devices can also be coupled to a RFID mechanism to allow rapid data collection by public health agencies.
Jewel beetles (Melanophila spp.) must locate freshly burned forest areas in order to oviposit; thus, this species relies on its chemosensory system to detect forest fires.72 These beetles can detect burning wood from distances of several km by identifying phenolic compounds such as guaiacol72 (C7H8O2).
The invention provides the means to construct a biosensor based on insect chemosensory proteins that can be used to detect forest fires remotely and signal the appropriate authorities. A chemosensory array comprising chemosensory proteins from numerous insect species, including species with a known sensitivity to phenolic compounds and/or combustion byproducts, is used to identify the proteins responsive to the smoke generated from tree fires. These chemosensory proteins can be used in novel fire detection devices when coupled with an electric or electronic reporter system or alarm. For example, the array proteins are incorporated into a small device with a power supply and an electric reporter mechanism that activates an RFID transmitter when the array proteins detect smoke. The transmitter can be monitored by fire control agencies remotely. Other applications of this device include airports, warehouses or storage facilities, shipping, ports of entry, fuel storage facilities, and places of public gathering.
The present invention provides methods to quantify the amount of artificially applied pheromone in the field. This is particularly useful when attempting to control insect pest populations using mating disruption based on pheromone application. After an initial pheromone application, the present invention can indicate when another application is desirable. In this example, the present invention is used to monitor the application of codling moth codlemone.
The gene(s) encoding GPCR(s) responsible for codlemone102 detection in the codling moth is transformed into Drosophila, mammalian, yeast, or other eukaryotic cells incorporating a reporter gene cascade coupled to an ion channel. These cells are then embedded into silica gel capable of transmitting detectable current across two electrodes. If codling moth codlemone is present in the atmosphere, the GPCRs in the cells embedded in the silica gel bind to it, initiating the signaling cascade that results in ion flux (for example, calcium ions) across the plasma membrane. This ion flux causes a change in electrical current or potential that can be measured. In this manner, the present invention can be used to indicate whether further codlemone application is desirable.
Alternatively, an enzymatic reaction resulting in a color change on a strip can be used instead of ion flux for detecting codlemone. In this method, the chemosensory protein is coupled to an enzymatic reporter cascade which, when evoked, releases a colored product (for example, beta.-galactosidase105). The appearance of this product on the device indicates the presence of codlemone.
The present invention provides the compositions and methods desirable to develop highly effective products to inhibit odors. These products can be used in any environment where unpleasant odors need to be contained. To develop these products, odorant-binding proteins can be purified, enriched or identified using the methods provided by the present invention.
For example, DNA sequences encoding OBPs or peptide derivatives are expressed in vitro using tools common in the art. The OBPs or peptide derivatives are then incorporated into aqueous gels that can be deployed in environments where odor control is desirable. Odors, scents, or semiochemicals emanating from those environments will be bound by the OBP, or peptide derivatives of the OBP, that essentially act as odor traps. Detectable odors will thus be greatly reduced. These odor control gels incorporating OBPs or OBP peptide derivatives are useful in locations including but not limited to private or public lavatories, garages, kitchens, storage areas, or refuse containers.
Water purification or treatment plants focus on removing pollutants, waste, and other undesirable compounds from water collected in drain systems in order to make the water useable for a variety of applications, or simply to make the water safe enough to dispose of into rivers, lakes, or seas without contaminating the environment. For example, volatile organic compounds are highly undesirable in water, and treatment plants must purify the water of these compounds.
Undesirable volatile organic compounds (VOCs) are screened using an insect chemosensory protein array in order to identify those chemosensory proteins that are capable of recognizing the VOCs as described previously. DNA sequences encoding those chemosensory proteins are then cloned into bacterial expression and transformation vectors common in the art in order to transform E. coli bacteria. The bacterial cells will express the recombinant insect chemosensory proteins and incorporate the proteins into the cell membrane such that the proteins are present on the external cell surfaces. Cultures of these bacteria can be grown in water to be treated; the chemosensory proteins on the bacterial cell surfaces will bind to the undesirable VOCs and remove them from the solution. Thus, this aspect of the invention is suitable for use in water treatment plants.
All publications, including patent documents and scientific articles, referred to in this application and the bibliography and attachments are incorporated herein by reference in their entirety for all purposes to the same extent as if each individual publication were individually incorporated by reference. All headings are for the convenience of the reader and should not be used to limit the meaning of the text that follows the heading, unless so specified.
This application is a continuation-in-part of U.S. patent application Ser. No. 11/372,777, filed Mar. 10, 2006, entitled “Efficient Methods To Isolate Effectors of Proteins Involved In Olfactory Or Chemosensory Pathways and Efficient Methods To Use These Effectors To Alter Organism Olfaction, Chemosensation, or Behavior” which is incorporated herein by reference in its entirety, and which is a continuation-in-part of U.S. patent application Ser. No. 10/106,749, filed Mar. 26, 2002, entitled “Efficient methods for isolating functional G-protein coupled receptors and identifying active effectors and efficient methods to isolate proteins involved in olfaction and efficient methods to isolate and identify active effectors” which is incorporated herein by reference in its entirety, which claims benefit of priority of Provisional U.S. Patent Application Ser. No. 60/279,168, filed Mar. 27, 2001, entitled “Efficient methods for isolating functional G-protein coupled receptors and identifying active effectors,” which is incorporated herein by reference in its entirety. This application also claims benefit of priority of Provisional U.S. Patent Application Ser. No. 60/353,392, filed Jan. 31, 2002, entitled “Efficient methods for isolating functional G-protein coupled receptors and identifying active effectors and efficient methods to isolate proteins involved in olfaction and identify active effectors or interactors,” which is incorporated herein by reference in its entirety.
| Number | Date | Country | |
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| 60279168 | Mar 2001 | US | |
| 60353392 | Jan 2002 | US |
| Number | Date | Country | |
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| Parent | 11372777 | Mar 2006 | US |
| Child | 11581889 | US | |
| Parent | 10106749 | Mar 2002 | US |
| Child | 11372777 | US |
