Patent Application
20240261763
The present invention is concerned with methods of producing an activated substrate and a scaffold for isolation of a biomolecule. The invention is also concerned with the activated substrate and the scaffold per se. Finally, the application discloses a method of using the scaffold to isolate a biomolecule, for example in affinity chromatography.
Isolation of highly pure biomolecules is a requirement of a number of fields including biotechnology applications and the manufacture of biopharmaceutical products. Chromatography is used extensively in industry for purification of biopharmaceuticals including therapeutic proteins, nucleic acids, and cells etc. The downstream process for purification of biomolecules using traditional chromatography and alternative isolation methods such as the Cohn Process is inefficient and costly especially at large scale. The use of affinity chromatography in the purification of target biomolecules affords potential for far greater specificity than traditional separation methods allowing more efficient and cost-effective downstream bioprocesses.
WO 2018/011600 discloses a process for preparing a functionalised polymeric chromatography medium, including a functionalisation in which:
WO00/67900 discloses triazine-based detoxification agents.
The performance of affinity adsorbents on repeated use in terms of maintained selectivity and capacity is dependent on cleaning the solid phase matrix to restore it ready for subsequent use by means of a clean in place (CIP) step in the chromatography process. Sanitisation of the matrix is also necessary to avoid contamination from bacteria, viruses, and endotoxin. The conditions typically used for this cleaning and sanitisation is aqueous NaOH (0.1 M to 1.0 M NaOH) which means exposure of the matrix to solutions in excess of pH 13. NaOH is favoured for this purpose as it is cheap, non-toxic, freely available, and relatively easy to dispose of.
However, high pH conditions used in CIP and sanitisation steps are detrimental to the stability of some affinity ligands, notably protein-based ligands. High pH can affect the tertiary structure of the affinity ligand and in some cases cleavage of the ligand by hydrolysis which may diminish the performance of the adsorbent. This degradation can limit the re-use potential of an adsorbent and therefore increase the cost of bioprocesses and in turn the products manufactured with them.
Affinity ligands which have improved caustic stability are known in the art. The modification of asparagine residues in protein ligands to improve alkali stability is discussed in U.S. Pat. No. 6,831,161 B1. Patent WO 03/080655 also discusses the mutation of asparagine residues to amino acids other than glutamine or aspartic acid in immunoglobulin binding protein ligands to improve caustic stability. The use of functional protein fragments such as domain C from Staphylococcus protein A to provide adsorbents with improved stability to high pH is captured in US20140135476A1. Use of peptide ligands with improved caustic stability compared to protein-based ligands for immunoglobulin purification is described in U.S. Pat. No. 9,162,223B2.
The availability of highly stable, cost effective affinity chromatography adsorbents with low toxicological risk is therefore of particular interest in bioprocessing to achieve affordable therapeutics.
Further, it is desirable for activated adsorbents used for covalent attachment of affinity ligands to possess a high density of chemically reactive groups. High activation densities on solid supports afford increased reaction rates for ligand coupling which in turn allows reduction in ligand concentration required to drive the coupling reaction, manufacturing process time and reduction in reaction temperatures. This is particularly important for costly ligands and fragile ligands that require mild immobilisation reaction conditions to avoid degradation. Another advantage to high activation density is achievement of higher immobilised ligand concentrations. This affords the possibility of increasing the binding capacity for target biomolecules. Triazine adsorbents disclosed in the prior art, for example WO2004052870A1, describe the use of activating agents such as epichlorohydrin for epoxide activation. This type of activation chemistry, whist offering caustic stability, is limited in terms of the possible density of chemically reactive groups achievable on beaded agarose supports.
The present invention arises from the inventors' attempts to overcome the problems associated with the prior art.
Therefore, in accordance with a first aspect of the invention, there is provided a method of producing an activated substrate, the method comprising:
The activated substrate, also referred to herein as the activated base matrix, may be understood to be activated in that it is configured to further react with a molecule comprising a ligand to provide a scaffold for isolation of a biomolecule. Advantageously, therefore, the method provides an activated substrate, which can be further reacted with a molecule comprising a ligand to provide a scaffold for isolation of a biomolecule.
Activation of a substrate as described herein may achieve a high surface concentration of chemically active groups which may be conveniently converted to a high concentration of more highly reactive groups
The substrate may be a solid support. The solid support may be selected from the group consisting of a controlled pore glass, a magnetic controlled pore glass, a silica-containing particle, a polymer, and a controlled pore glass grafted with a polymer. The solid support may comprise a polymer. The polymer may be a natural polymer or a synthetic polymer. The polymer may be a polysaccharide, a polymethacrylate, a polymer of styrene, a copolymer of styrene and divinylbenzene, a copolymer of styrene and divinylbenzene grafted with polyethyleneglycol or a copolymer of dimethylacrylamide and N,N,-bisacryloylethylenediamine. The polysaccharide may be agarose, cellulose, hemicellulose, dextran, carrageenan or chitin.
The substrate may be a fibre, a fibre mat, a membrane, a solid bead, a porous bead, a monolith or a solid gel.
Preferably, the substrate comprises a nucleophilic moiety. The nucleophilic moiety may be an —OH, SH or —NH2 group. Preferably, the nucleophilic moiety is a hydroxyl moiety.
The method preferably comprises modifying the substrate to form a base matrix comprising a leaving group. The leaving group may be a halogen.
Modifying the substrate to form a base matrix comprising a leaving group may comprise:
Alternatively, the method may comprise modifying the substrate to form a base matrix comprising an optionally substituted heterocyclic ring. may be a 3 membered ring. The optionally substituted heterocyclic ring may be an optionally substituted epoxide.
Modifying the substrate to form a base matrix comprising an optionally substituted heterocyclic ring comprises contacting the substrate with an electrophile, wherein the electrophile comprises an optionally substituted heterocyclic ring, to thereby provide a base matrix comprising an optionally substituted heterocyclic ring.
Accordingly, both of the above methods comprise contacting the substrate with an electrophile.
The electrophile may comprise 1 to 24 carbon atoms, more preferably the electrophile comprises 2 to 12 carbon atoms or 3 to 10 carbon atoms, and most preferably 4 to 8 carbon atoms, or 5 to 7 carbon atoms.
The electrophile may comprise a C2-12 unsaturated hydrocarbon chain, more preferably a C2-6 unsaturated hydrocarbon chain, and most preferably a C2-3 unsaturated hydrocarbon chain. The unsaturated hydrocarbon chain may be an allyl group.
The electrophile may comprise an ether group.
The electrophile may be a compound of formula (I):
R1—L1—X1—L2—R2 (I)
The term “alkyl”, as used herein, unless otherwise specified, refers to a saturated straight or branched hydrocarbon. An alkyl group can be unsubstituted or substituted with one or more of halogen, OH, SH, COOH, NH2 or oxo.
“Alkenyl” refers to olefinically unsaturated hydrocarbon groups which can be unbranched or branched. An alkenyl group can be unsubstituted or substituted with one or more of halogen, OH, SH, COOH, NH2, oxo or an optionally substituted C1-6 alkynyl.
“Alkynyl” refers to acetylenically unsaturated hydrocarbon groups which can be unbranched or branched. An alkenyl group can be unsubstituted or substituted with one or more of halogen, OH, SH, COOH, NH2, oxo or an optionally substituted C1-6 alkenyl.
The term “alkylene”, as used herein, unless otherwise specified, refers to a bivalent saturated straight or branched hydrocarbon. An alkylene group can be unsubstituted or substituted with one or more of halogen, OH, SH, NH2, COOH or oxo.
The term “alkenylene”, as used herein, unless otherwise specified, refers to a bivalent olefinically unsaturated straight or branched hydrocarbon. An alkenylene group can be unsubstituted or substituted with one or more of halogen, OH, SH, COOH, NH2, oxo or an optionally substituted C1-6 alkynyl.
The term “alkynylene”, as used herein, unless otherwise specified, refers to a bivalent acetylenically unsaturated straight or branched hydrocarbon. An alkynylene group can be unsubstituted or substituted with one or more of halogen, OH, SH, COOH, NH2, oxo or an optionally substituted C1-6 alkenyl.
A “heterocyclic ring” may refer to 3 membered monocyclic rings in which at least one ring atom is a heteroatom. The or each heteroatom may be independently selected from the group consisting of oxygen, sulfur and nitrogen. A heterocyclic ring may be saturated or partially saturated. A heterocyclic group can be unsubstituted or substituted with one or more of halogen, OH, SH, COOH, NH2, oxo, optionally substituted C1-C6 alkyl, optionally substituted C2-C6 alkenyl or optionally substituted C2-C6 alkynyl.
“Heteroaryl” and “heteroaromatic ring” refers to a monocyclic or fused, e.g. bicyclic, aromatic 5 to 10 membered ring system in which at least one ring atom is a heteroatom. The or each heteroatom may be independently selected from the group consisting of oxygen, sulfur and nitrogen.
“Aryl”, “arylene” and “aromatic ring” refers to a monocyclic or fused, e.g. bicyclic, aromatic 6-12 membered aromatic ring system.
An optionally substituted aromatic or heteroaromatic group as described anywhere herein can be unsubstituted or substituted with one or more of halogen, OH, SH, COOH, NH2, oxo, optionally substituted C1-C6 alkyl, optionally substituted C2-C6 alkenyl or optionally substituted C2-C6 alkynyl.
A “heteroatom” may be O, NR4 or S, wherein R4 is H, an optionally substituted C1-C6 alkyl, an optionally substituted C2-C6 alkenyl or an optionally substituted C2-C6 alkynyl.
A “halogen” may be fluorine, chlorine, bromine or iodine.
R1 may be an optionally substituted 3 membered heterocyclic ring.
Accordingly, R1 may be
Accordingly, in a preferred embodiment, the compound of formula (I) is a compound of formula (Ia):
Preferably, R5, R6 and R7 are independently H, a C1-C3 alkyl, a C2-C3 alkenyl or a C2-C3 alkynyl. Preferably, R5, R6 and R7 are each H.
X2 is preferably O.
Accordingly, in a more preferred embodiment, the compound of formula (I) is a compound of formula (Iai):
In embodiments where R1 is a leaving group, the leaving group may be a halogen.
L1 may be absent, a C1-6 alkylene, a C2-6 alkenylene or a C2-6 alkynylene. Preferably, L1 is absent or a C1-3 alkylene, more preferably is absent, —CH2— or —CH2CH2—, and most preferably is —CH2—.
X1 is preferably O.
L2 may be absent, a C1-6 alkylene, a C2-6 alkenylene or a C2-6 alkynylene. Preferably, L2 is absent or a C1-3 alkylene, more preferably is absent, —CH2— or —CH2CH2—, and most preferably is absent or —CH2—.
In one embodiment, R2 may be an optionally substituted C2-C6 alkenyl or an optionally substituted C2-C6 alkynyl. More preferably, R2 is a C2-C3 alkenyl or an optionally substituted C2-C3 alkynyl. Most preferably, R2 is —CH2CHCH2.
Accordingly, the electrophile may by allyl glycidyl ether (AGE).
In an alternative embodiment, R2 may be an optionally substituted 3 membered heterocyclic ring.
Accordingly, R2 may be
Preferably, R11, R12 and R13 are independently H, a C1-C3 alkyl, a C2-C3 alkenyl or a C2-C3 alkynyl. Preferably, R11, R12 and R13 are each H.
X3 may be O.
Accordingly, the electrophile may by diglycidyl ether.
The substrate and the electrophile may be contacted in a weight ratio of between 100:1 and 1:100, between 50:1 and 1:50, between 25:1 and 1:25, more preferably between 20:1 and 1:10, between 15:1 and 1:5 or between 10:1 and 1:1, and most preferably between 8:1 and 2:1, between 6:1 and 3:1 or between 5:1 and 3.5:1.
The substrate and the electrophile may be contacted in a weight ratio sufficient to provide a base matrix comprising between 1 and 500 μg allyl groups or epoxide groups per gram, more preferably between 5 and 250 μg allyl groups or epoxide groups per gram or between 10 and 100 μg allyl groups or epoxide groups per gram, and most preferably between 20 and 70 μg allyl groups or epoxide groups per gram or between 30 and 80 μg allyl groups or epoxide groups per gram.
The substrate and the electrophile may be contacted in a solvent. The solvent may comprise water and/or an alcohol. The alcohol may be ethanol, propan-1-ol and/or propan-2-ol. In some embodiments, the solvent is water.
The substrate and the electrophile may be contacted under alkaline conditions. Accordingly, the substrate and the electrophile may be contacted in the presence of a base. The base may be sodium hydroxide (NaOH). The base may be present at a concentration between 0.001 and 15 M, more preferably between 0.005 and 10 M, between 0.01 and 5 M or between 0.05 and 2 M, and most preferably between 0.1 and 1 M, between 0.2 and 0.75 M or between 0.3 and 0.5 M.
The substrate and the electrophile may be contacted in the presence of an emulsifying agent. The emulsifying agent could be sodium sulphate.
The weight ratio of the substrate to the emulsifying agent may be between 100,000:1 and 1:1,000, between 10,000:1 and 1:500 or between 1,000:1 and 1:100, more preferably is between 500:1 and 1:50, between 100:1 and 1:25, between 50:1 and 1:10 or between 25:1 and 1:1, and most preferably between 10:1 and 2:1 or between 5:1 and 3:1.
The substrate and the electrophile may be contacted in the presence of a reducing agent. The reducing agent may be sodium borohydride.
The weight ratio of the substrate to the reducing agent may be between 100,000:1 and 1:1, between 10,000:1 and 10:1 or between 1,000:1 and 100:1, more preferably is between 900:1 and 150:1, between 800:1 and 200:1, between 700:1 and 250:1 or between 600:1 and 300:1, and most preferably between 500:1 and 350:1 or between 450: 1 and 375:1.
The substrate and the electrophile may be contacted at a temperature between 0 and 100° C., more preferably between 10 and 90° C., between 20 and 80° C. or between 30 and 70° C., and most preferably between 40 and 60° C. or between 45 and 55° C.
The substrate and the electrophile may be contacted for at least 1 minute, at least 30 minutes, at least 1 hour or at least 2 hours, and more preferably for at least 5 hours, at least 10 hours or at least 15 hours. The substrate and the electrophile may be contacted for between 1 minute and 100 hours, between 1 hour and 50 hours or between 2 and 40 hours, more preferably between 5 and 30 hours, between 10 and 25 hours, between 15 and 20 hours or between 17 and 18 hours.
In some embodiments, the method comprises contacting a base matrix comprising an unsaturated hydrocarbon chain with a halogenating matrix.
Prior to contacting the halogenating agent, the base matrix comprising an unsaturated hydrocarbon chain may be washed with a solvent. The solvent may be water and/or an alcohol. The alcohol may be ethanol.
The halogenating agent may be a fluorinating agent, a chlorinating agent or a brominating agent. Preferably, the halogenating agent is a brominating agent.
The halogenating agent may be N-bromosuccinimide, N-chlorosuccinimide, bromine or chlorine. Preferably, the halogenating agent is N-bromosuccinimide.
The weight ratio of the substrate to the halogenating agent may be between 100,000:1 and 1:100 or between 10,000:1 and 1:10, more preferably is between 1,000:1 and 1:1, between 500:1 and 5:1 or between 250:1 and 10:1, and most preferably between 100:1 and 20:1 or between 100:2 and 100:3.
The base matrix comprising an unsaturated hydrocarbon chain may be contacted with the halogenating agent at a temperature between −20 and 100° C., more preferably between 0 and 75° C., between 5 and 50° C. or between 10 and 30° C., and most preferably between 15 and 25° C.
The base matrix comprising an unsaturated hydrocarbon chain may be contacted with the halogenating agent in a solvent. The solvent may be water.
The base matrix comprising an unsaturated hydrocarbon chain may be contacted with the halogenating agent under acidic conditions. The base matrix comprising an unsaturated hydrocarbon chain may be contacted at a pH between 1 and 7, more preferably between 2 and 6 or between 3 and 5, and most preferably between 3.5 and 4.5.
The base matrix comprising an unsaturated hydrocarbon chain may be contacted for at least 1 minute, at least 10 minutes, at least 20 minutes or at least 30 minutes, and more preferably for at least 40 minutes, at least 50 minutes or at least 1 hour. The base matrix comprising an unsaturated hydrocarbon chain may be contacted for between 1 minute and 24 hours, between 10 minutes and 12 hours or between 30 minutes and 6 hours, more preferably between 40 minutes and 3 hours, between 50 minutes and 2 hours or between 60 and 90 minutes.
Prior to contacting the aminating agent, the halogenated base matrix may be washed with a solvent. The solvent may be water.
The aminating agent may be NH2R16 or
wherein R16 and R17 are independently H, an optionally substituted C1-24 alkyl, an optionally substituted C2-24 alkenyl or an optionally substituted C2-24 alkynyl and L3 is an optionally substituted C1-12 alkylene, an optionally substituted C2-12 alkenylene or an optionally substituted C2-12 alkynylene, where the backbone of the alkylene, alkenylene or alkynlene is optionally interrupted by one or more heteroatoms.
Preferably, R16 and R17 are both H.
Preferably, L3 is a C1-6 alkylene, a C2-6 alkenylene or a C2-6 alkynylene. More preferably, L3 is a C1-3 alkylene, most preferably is —CH2— or —CH2CH2—.
Preferably, the aminating agent is ammonia.
The halogenated base matrix and the aminating agent may be contacted in a solvent. The solvent may be water.
The halogenated base matrix and the aminating agent may be contacted in a weight ratio of between 100:1 and 1:100, between 50:1 and 1:50, between 25:1 and 1:25, more preferably between 20:1 and 1:20, between 15:1 and 1:10 or between 10:1 and 1:5, and most preferably between 8:1 and 1:2, between 5:1 and 1:1 or between 3:1 and 2:1.
The halogenated base matrix and the aminating agent may be contacted at a temperature between 0 and 100° C., more preferably between 10 and 90° C., between 20 and 80° C. or between 30 and 75° C., and most preferably between 45 and 70° C. or between 55 and 65° C.
The halogenated base matrix and the aminating agent may be contacted for at least 1 minute, at least 30 minutes, at least 1 hour or at least 2 hours, and more preferably for at least 5 hours, at least 10 hours, at least 15 hours or at least 20 hours. The halogenated base matrix and the aminating agent may be contacted for between 1 minute and 100 hours, between 1 hour and 50 hours or between 2 and 45 hours, more preferably between 5 and 40 hours, between 10 and 35 hours, between 15 and 30 hours or between 20 and 24 hours.
Prior to contacting the heteroaromatic compound, the aminated base matrix may be washed with a solvent. The solvent may be water and/or a pH neutral solution. The aminated base matrix is preferably washed with water and then a pH neutral solution. The pH neutral solution may be an aqueous solution. The pH neutral solution may comprise alkali metal ions, alkaline earth metal ions, phosphate ions, sulphate ions and/or halogen ions. The pH neutral solution may comprise sodium phosphate, potassium phosphate and/or sodium chloride.
The heteroaromatic compound is a heteroaromatic ring which is substituted with at least two halogens, and optionally one or more further substituents. The heteroaromatic ring may be a 5 to 10 membered heteroaromatic ring, more preferably a 5 or 6 membered heteroaromatic ring, and most preferably a 6 membered heteroaromatic ring.
The heteroaromatic ring may be a pyridine ring, a pyridazine ring, a pyrimidine ring, a pyrazine ring, a 1,2,4-triazine ring or a 1,3,5-triazine ring. Preferably, the heteroaromatic group comprises a 1,2,4-triazine ring or a 1,3,5-triazine ring and most preferably a 1,3,5-triazine ring.
The heteroaromatic ring is substituted with at least two halogen atoms, and may be substituted with 2, 3, 4 or 5 halogen atoms. Preferably, the heteroaromatic ring is substituted with 2 or 3 halogen atoms, most preferably 3 halogen atoms.
The or each halogen may be fluorine, chlorine, bromine or iodine. Preferably, the or each halogen is chlorine or bromine. In one embodiment, each halogen is chlorine.
The heteroaromatic ring may be substituted with one or more further substituents. The or each further substituent may be independently selected from the group consisting of OH, SH, COOH, NH2, optionally substituted C1-C24 alkyl, optionally substituted C2-C24 alkenyl and optionally substituted C2-C24 alkynyl.
The heteroaromatic compound may be dichloro-triazine or cyanuric chloride, and is preferably cyanuric chloride.
The aminated base matrix and the heteroaromatic compound may be contacted in a solvent. The solvent may be water and/or acetone.
The aminated base matrix and the heteroaromatic compound may be contacted in the presence of a buffer. The buffer may be potassium phosphate. The buffer may be present at a concentration of between 0.01 and 100 M, more preferably between 0.05 and 10 M or between 0.1 and 5 M, and most preferably between 0.5 and 2 M or between 0.75 and 1.5 M.
The weight ratio of the aminated base matrix to the heteroaromatic compound may be between 1,000:1 and 1:50 or between 500:1 and 1:25, more preferably is between 200:1 and 1:10, between 100:1 and 1:1, between 75:1 and 10:1 or between 50:1 and 20:1, and most preferably between 40:1 and 25:1 or between 35:1 and 30:1.
The aminated base matrix and the heteroaromatic compound may be contacted at a temperature between −50 and 50° C., more preferably between −30 and 30° C., between −20 and 20° C. or between −10 and 10° C., and most preferably between −5 and 7° C., between 0 and 5° C. or between 1 and 3° C.
The aminated base matrix and the heteroaromatic compound may be contacted for at least 1 minute, at least 10 minutes, at least 20 minutes or at least 30 minutes, and more preferably for at least 40 minutes, at least 50 minutes or at least 1 hour. The aminated base matrix and the heteroaromatic compound may be contacted for between 1 minute and 24 hours, between 10 minutes and 12 hours or between 30 minutes and 6 hours, more preferably between 40 minutes and 3 hours, between 50 minutes and 2 hours or between 60 and 90 minutes.
The activated substrate may be washed with a solvent. The solvent may be water and/or acetone. The activated substrate is preferably washed with a water and acetone solution and then water.
In accordance with a second aspect, there is provided the activated substrate obtained or obtainable by the method of the first aspect.
In accordance with a third aspect, there is provided an activated substrate of formula (II):
It may be appreciated that the circle in formula (II) represents a substrate. The substrate may be as defined in relation to the first aspect.
L4 may be an optionally substituted C3-12 alkylene, an optionally substituted C3-12 alkenylene or an optionally substituted C3-12 alkynylene, where the backbone of the alkylene, alkenylene or alkynlene is optionally interrupted by one or more heteroatoms. Preferably, L4 is an optionally substituted C5-10 alkylene, an optionally substituted C5-10 alkenylene or an optionally substituted C5-10 alkynylene, where the backbone of the alkylene, alkenylene or alkynlene is optionally interrupted by one or more heteroatoms. More preferably, L4 is an optionally substituted C6-8 alkylene, an optionally substituted C6-8 alkenylene or an optionally substituted C6-8 alkynylene, where the backbone of the alkylene, alkenylene or alkynlene is optionally interrupted by one or more heteroatoms. Most preferably, L4 is an optionally substituted C7 alkylene, an optionally substituted C7 alkenylene or an optionally substituted C7 alkynylene, where the backbone of the alkylene, alkenylene or alkynlene is optionally interrupted by one or more heteroatoms. The alkylene, alkenylene or alkynlene may be substituted with one or more hydroxyl groups. The alkylene, alkenylene or alkynlene may be substituted with between 1 and 5 hydroxyl groups, between 1 and 4 hydroxyl groups or between 2 and 3 hydroxyl groups. Preferably the alkylene, alkenylene or alkynlene is substituted with two hydroxyl groups.
Preferably, the backbone of the alkylene, alkenylene or alkynlene is interrupted with at least one heteroatom. The backbone of the alkylene, alkenylene or alkynlene may be interrupted with between 1 and 5 heteroatoms, between 1 and 4 heteroatoms or between 2 and 3 heteroatoms. Preferably, the backbone of the alkylene, alkenylene or alkynlene is interrupted with two heteroatoms. The one or more heteroatoms may each be O, NR11 or S, wherein R11 is H, an optionally substituted C1-C6 alkyl, an optionally substituted C2-C6 alkenyl or an optionally substituted C2-C6 alkynyl. Preferably, the or each heteroatom is oxygen. Preferably, the backbone is interrupted with at least two oxygen atoms.
Accordingly, L4 may be
R18 may be a 5 to 10 membered heteroaryl group substituted with at least one halogen, and optionally substituted with further substituents, more preferably a 5 or 6 membered heteroaryl group substituted with at least one halogen, and optionally substituted with further substituents, and most preferably a 6 membered heteroaryl group substituted with at least one halogen, and optionally substituted with further substituents.
The heteroaryl group which is substituted with at least one halogen, and optionally one or more further substituents, may be a pyridinyl, a pyridazinyl, a pyrimidinyl, a pyrazinyl, a 1,2,4-triazinyl or a 1,3,5-triazinyl. Preferably, the heteroaryl group is a 1,2,4-triazinyl or a 1,3,5-triazinyl substituted with at least one halogen, and optionally one or more further substituents and most preferably 1,3,5-triazinyl substituted with at least one halogen, and optionally one or more further substituents.
The heteroaryl group is substituted with at least one halogen atom, and may be substituted with 1, 2, 3 or 4 halogen atoms. Preferably, the heteroaryl group is substituted with 1 or 2 halogen atoms, most preferably 2 halogen atoms.
The or each halogen may be fluorine, chlorine, bromine or iodine. Preferably, the or each halogen is chlorine or bromine. In one embodiment, each halogen is chlorine.
The heteroaryl group may be substituted with one or more further substituents. The one or more further substituents may be OH, SH, COOH, NH2, optionally substituted C1-C24 alkyl, optionally substituted C2-C24 alkenyl or optionally substituted C2-C24 alkynyl.
Accordingly, R18 may be
wherein R19 is a halogen and R20 is a halogen, H, OH, SH, COOH, NH2, optionally substituted C1-C24 alkyl, optionally substituted C2-C24 alkenyl or optionally substituted C2-C24 alkynyl. Preferably, R20 is a halogen or H.
Accordingly, in a preferring embodiment, the compound of formula (II) is a compound of formula (IIa):
In accordance with a fourth aspect, there is provided a method of producing a scaffold for isolation of a biomolecule, the method comprising:
It will be understood that the ligand may be selected according to the biomolecule to be isolated.
Advantageously, the method provides an alkaline-stable structure which can be used as an affinity medium or ligand for bioprocessing, where sanitisation with caustic solutions is highly desirable.
The biomolecule may be selected from the group consisting of an amino acid, a peptide, an affimer, a protein, an enzyme, a glycoprotein, a lipopolysaccharide, an antibody or a fragment thereof, a nucleic acid, an organic polymer, a virus, a bacterium, a cell, and a cell-related structure. The antibody may be an isoagglutinin. The virus may be adeno-associated virus (AAV) or Lentivirus. The cell may be an animal cell.
The molecule for forming the ligand attached to the activated substrate may be a compound of formula (IV):
X4—L5—X5 (IV)
X4 may be NH2 or SH. Preferably, X4 is NH2.
L5 may be an optionally substituted C3-20 alkylene, an optionally substituted C3-20 alkenylene or an optionally substituted C3-20 alkynylene, where the backbone of the alkylene, alkenylene or alkynlene is optionally interrupted by one or more heteroatoms.
More preferably, L5 is an optionally substituted C5-15 alkylene, an optionally substituted C5-15 alkenylene or an optionally substituted C5-15 alkynylene, where the backbone of the alkylene, alkenylene or alkynlene is optionally interrupted by one or more heteroatoms. Most preferably, L5 is an optionally substituted C8-12 alkylene, an optionally substituted C8-12 alkenylene or an optionally substituted C8-12 alkynylene, where the backbone of the alkylene, alkenylene or alkynlene is optionally interrupted by one or more heteroatoms.
L5 may be an alkylene, an alkenylene or an alkynylene where the alkylene, alkenylene or alkynylene is substituted with one or more oxo groups. Preferably, the alkylene, alkenylene or alkynylene is substituted with an oxo group.
L5 may be an alkylene, an alkenylene or an alkynylene wherein the backbone of the alkylene, alkenylene or alkynylene is interrupted by one or more heteroatoms selected from NR28, O or S, wherein R28 is H, an optionally substituted C1-6 alkyl, an optionally substituted C2-6 alkenyl or an optionally substituted C2-6 alkenyl. More preferably, L5 is an alkylene, an alkenylene or an alkynylene wherein the backbone of the alkylene, alkenylene or alkynylene is interrupted by an NH group.
The ligand may comprise an optionally derivatized saccharide molecule, an optionally derivatized amino acid, an optionally derivatized peptide, an optionally derivatized affimer or an optionally derivatized protein. The optionally derivatized saccharide molecule may be an optionally derivatives polysaccharide molecule.
The ligand may be derivatised with one or more functional groups. The one or more functional groups may replace a hydrogen or hydroxyl group in the ligand. In embodiments where the ligand is a polysaccharide, one or more of the saccharide monomers may be derivatized. The one or more functional groups may be an optionally substituted C1-6 alkyl, an optionally substituted C2-6 alkenyl, an optionally substituted C2-6 alkenyl, OR26, SR26, C(O)R26, NR26R27, NR26C(O)R27 or SO3R26, wherein R26 and R27 are independently H, an optionally substituted C1-6 alkyl, an optionally substituted C2-6 alkenyl or an optionally substituted C2-6 alkenyl.
The saccharide molecule may comprise between 1 and 20 saccharide monomers, more preferably between 2 and m saccharide monomers or between 2 and 8 saccharide monomers, and most preferably between 3 and 6 saccharide monomers.
The or each optionally derivatized saccharide monomer may be selected from the group consisting of optionally derivatized glucose; optionally derivatized glucosamine; optionally derivatized galactose; optionally derivatized fructose; and optionally derivatized xylose, or a stereoisomer thereof.
In some embodiments, X5 is
More preferably, X5 is
The compound of Formula (IV) may be an antigen-A trisaccharide ligand, which has Formula (IVa):
The compound of Formula (IV) may be an antigen-B trisaccharide ligand, which has Formula (IVb):
The ligand may have an affinity for isoagglutinins.
The ligand may, in use, be cationic, preferably protonated.
An exemplary ligand which may be cationic in use is a ligand formed from a compound of formula (IVc):
H2N—L5—N(Ak—NH2)2 (IVc)
A preferred compound of formula (IVc) is formula (IVd):
The ligand formed from the compound of formula (IVd) may have an affinity to lipopolysaccharide and albumin.
X5 of formula (IV) may be a boronate group. A ligand comprising a boronate group may be formed from a compound of formula (IVe):
The ligand may have an affinity to glycosylated proteins.
X5 of the compound of Formula (IV) may be a naphthol ligand. An exemplary compound of formula (IV) comprising a naphthol ligand has Formula (IVf):
The ligand may have an affinity to insulin.
The method may comprise contacting the activated substrate and the molecule comprising the ligand in a solvent. The solvent may be water.
The activated substrate and the molecule comprising the ligand may be contacted in a weight ratio of between 1,000,000:1 and 1:1 or between 100,000:1 and 10:1, more preferably between 10,000:1 and 25:1 or between 5,000:1 and 50:1, and most preferably between 2,000:1 and 100:1, between 1,500:1 and 200:1 or between 1,000:1 and 1,000:3.
Alternatively, or additionally, the ligand may be present at a concentration of between 1 15 μg/ml and 750 mg/ml, between 10 μg/ml and 500 mg/ml or between 50 μg/ml and 250 mg/ml, more preferably between 100 μg/ml and 100 mg/ml, between 250 μg/ml and 50 mg/ml, between 500 μg/ml and 10 mg/ml or between 750 μg/ml and 5 mg/ml, most preferably between 1 and 3 mg/ml.
Alternatively or additionally, the ligand may be present at a concentration at least 40 μmol per gram of scaffold, optionally a concentration of at least 50 μmol/g, optionally up to 300 or 200 μmol/g.
The activated substrate and the molecule comprising the ligand may be contacted under alkaline conditions. The activated substrate and the molecule comprising the ligand may be contacted in solution at a pH between 6 and 14 at 20° C., more preferably at a pH between 7 and 13 at 20° C., and most preferably at a pH of between 8 and 12 at 20° C.
The activated substrate and the molecule comprising the ligand may be contacted at a temperature between −20 and 100° C., more preferably between 0 and 75° C., between 5 and 50° C. or between 10 and 30° C., and most preferably between 15 and 25° C.
The activated substrate and the ligand molecule comprising the may be contacted for at least 1 minute, at least 10 minutes, at least 20 minutes or at least 30 minutes, and more preferably at least 1 hour, at least 2 hours, at least 3 hours or at least 4 hour. The activated substrate and the molecule comprising the ligand may be contacted for between 1 minute and 48 hours, between 30 minutes and 24 hours or between 1 and 12 hours, more preferably between 2 and 10 hours, between 3 and 8 hours or between 4 to 6 hours.
The method may subsequently comprise contacting the scaffold with an alcohol, a hydroxide, ammonia, an amine or a thiol. The alcohol, hydroxide, ammonia, amine or thiol may be HOR24, —OH, HNR24R25 or HSR24, wherein R24 and R25 are independently H, optionally substituted C1-C12 alkyl, optionally substituted C2-C12 alkenyl or optionally substituted C2-C12 alkynyl. More preferably, R24 and R25 are independently H, optionally substituted C1-C6 alkyl, optionally substituted C2-C6 alkenyl or optionally substituted C2-C6 alkynyl. Most preferably, R24 and R25 are independently H, optionally substituted C1-C3 alkyl, optionally substituted C2-C3 alkenyl or optionally substituted C2-C3 alkynyl. The alkyl, alkenyl or alkynyl may be optionally substituted with —OH, NH2 or SH.
The alcohol, hydroxide, ammonia, amine or thiol may be selected from the group consisting of 2-aminoethanol, methylamine, ammonia, sodium hydroxide, glycine, alanine, dimethylamine, tris(hydroxymethyl)aminomethane or 2-mercaptoethanol. Advantageously, this step removes residual halogen sites after ligand coupling.
The scaffold and the alcohol, hydroxide, ammonia, amine or thiol may be contacted in a weight ratio of between 1:10 and 1,000:1 or between 1:1 and 500:1, more preferably between 2:1 and 250:1 or between 4:1 and 100:1, and most preferably between 10:1 and 50:1, between 25:2 and 25:1 or between 100:6 and 100:5.
The scaffold may be washed with a solvent. The solvent may be water.
In accordance with a fifth aspect, there is provided the scaffold for isolation of a biomolecule obtained or obtainable by the method of the fourth aspect.
In accordance with a sixth aspect, there is provided a scaffold for isolation of a biomolecule, wherein the scaffold is represented by formula (III):
The group comprising the ligand and biomolecule may be as defined in relation to the fourth aspect.
In particular, the group comprising the ligand may have formula —L6—L5—X5, wherein L5 and X5 are as defined in the fourth aspect and L6 is O, S or NH.
R21 may be a 5 to 10 membered heteroaryl group substituted with at least one group comprising the ligand specific for a biomolecule, and optionally substituted with one or more further substituents, more preferably a 5 or 6 membered heteroaryl group substituted with at least one group comprising the ligand specific for a biomolecule, and optionally substituted with one or more further substituents, and most preferably a 6 membered heteroaryl group substituted with at least one group comprising the ligand specific for a biomolecule, and optionally substituted with one or more further substituents.
The heteroaryl group which is substituted with at least one group comprising the ligand specific for a biomolecule, and optionally substituted with one or more further substituents, may be a pyridinyl, a pyridazinyl, a pyrimidinyl, a pyrazinyl, a 1,2,4-triazinyl or a 1,3,5-triazinyl. Preferably, the heteroaryl group is a 1,2,4-triazinyl or a 1,3,5-triazinyl substituted with at least one group comprising the ligand specific for a biomolecule, and optionally substituted with one or more further substituents and most preferably a 1,3,5-triazinyl substituted with at least one group comprising the ligand specific for a biomolecule, and optionally substituted with one or more further substituents.
The heteroaryl group is substituted with at least one group comprising the ligand, and may be substituted with 1, 2, 3 or 4 groups comprising the ligand. Preferably, the heteroaryl group is substituted with 1 or 2 group comprising the ligand, most preferably 2 group comprising the ligand.
The heteroaryl group may be substituted with one or more further substituents. The one or more further substituents may be a halogen, OR24, SR24, COOR24, NR24R25, optionally substituted C1-C24 alkyl, optionally substituted C2-C24 alkenyl or optionally substituted C2-C24 alkynyl, wherein R24 and R25 are independently H optionally substituted C1-C24 alkyl, optionally substituted C2-C24 alkenyl or optionally substituted C2-C24 alkynyl.
Accordingly, R21 may be
wherein R22 is a group comprising a ligand specific for a biomolecule and R23 is a group comprising a ligand specific for a biomolecule, a halogen, H, OR24, COOR24, NR24R25, SR24, optionally substituted C1-C24 alkyl, optionally substituted C2-C24 alkenyl or optionally substituted C2-C24 alkynyl, wherein R24 and R25 are independently H optionally substituted C1-C24 alkyl, optionally substituted C2-C24 alkenyl or optionally substituted C2-C24 alkynyl. Preferably, R24 and R25 are independently H, optionally substituted C1-C12 alkyl, optionally substituted C2-C12 alkenyl or optionally substituted C2-C12 alkynyl. More preferably, R24 and R25 are independently H, optionally substituted C1-C6 alkyl, optionally substituted C2-C6 alkenyl or optionally substituted C2-C6 alkynyl. Most preferably, R24 and R25 are independently H, optionally substituted C1-C3 alkyl, optionally substituted C2-C36 alkenyl or optionally substituted C2-C3 alkynyl. The alkyl, alkenyl or alkynyl may be optionally substituted with —OH, NH2 or SH.
In a most preferred embodiment, the scaffold is represented by formula (IIIa):
R22 may be
Preferably, R23 is a group comprising a ligand specific for a biomolecule. Preferably, R23 is the same as R22.
In accordance with a seventh aspect, there is provided use of the scaffold of the fifth or sixth aspect to isolate a biomolecule.
In accordance with an eighth aspect, there is provided a method of isolating a biomolecule on a scaffold, the method comprising contacting a scaffold with a biomolecule, wherein the scaffold is as defined in either the fifth or sixth aspect.
It may be appreciated that the use of the seventh aspect is in affinity chromatography. The method of the eighth aspect is preferably a method of conducting affinity chromatography.
The biomolecule may be as defined in relation to the fourth aspect.
The method may comprise contacting the scaffold for isolation of a biomolecule with a solution comprising the biomolecule.
The biomolecule may be present in human intravenous immunoglobulin (IVIG) intermediate product. Accordingly, the method may comprise contacting the scaffold for isolation of a biomolecule with human IVIG intermediate product.
In accordance with a ninth aspect, there is provided a method of cleaning a scaffold, the method comprising contacting a scaffold with a caustic substance, wherein the scaffold is as defined in either the fifth or sixth aspect.
Advantageously, the scaffold may be cleaned to avoid contamination from bacteria, viruses, and endotoxin without loss of performance.
The caustic substance may be or comprise an alkaline solution.
The alkaline solution may have a pH of at least 7.5, at least 8, at least 9, at least 10, at least 11, at least 12 or at least 13 at 20° C. The alkaline solution may have a pH of between 8 and 14.5, between 9 and 14, between 10 and 13.75, between 11 and 13.5, between 12 and 13.25 or between 12.5 and 13 at 20° C.
The alkaline solution may comprise an alkali metal hydroxide or an alkaline earth metal hydroxide. Preferably, the alkaline solution comprises an alkali metal hydroxide. The alkaline solution may comprise lithium hydroxide, sodium hydroxide or potassium hydroxide. In some embodiments, the alkaline solution comprises sodium hydroxide. The alkaline solution may comprise the alkali metal hydroxide or the alkaline earth metal hydroxide at a concentration of between 0.01 and 10 M, between 0.05 and 5 M, between 0.1 and 2.5 M, between 0.2 and 1 M, between 0.3 and 0.75 M or between, between 0.4 and 0.6 M.
The method of the ninth aspect may be performed subsequent to the method of the eighth aspect. The scaffold may then be used in a further method of isolating a biomolecule. Accordingly, the method of the eighth aspect may be repeated after the method of the ninth aspect.
The methods of the eighth and ninth aspect may be cycled, one after the other. The methods of the eighth and ninth aspect may be repeated at least 2 times, at least 3 times at least 4 times or at least 5 times, more preferably at least 10 times, at least 20 times or at least 30 times, and most preferably at least 40 or 50 times.
All of the features described herein (including accompanying claims, abstract and drawings), and/or all of the steps of any method or process so disclosed, may be combined with any of the above aspects in any combination, except combinations where at least some of such features and/or steps are mutually exclusive.
For a better understanding of the invention, and to show how embodiments of the same may be carried into effect, reference will now be made, by way of example, to the accompanying drawings, in which:
A synthetic route for producing a dihalogentriazine scaffold is shown in
Approximately 1 kg of a solid support, such as beaded agarose, is slurried in water with up to 380 g, optionally approximately 250 g of sodium sulphate, 10 M NaOH, and 2.5 g of sodium borohydride. The slurry is heated to 45 to 55° C. before adding allyl glycidyl ether (up to 1800 mL, optionally 250 mL). The slurry is left to react for no more than 18 hours, after which the drained gel is washed with ethanol and water. The resulting material is an activated base matrix that contains up to about 200 μmol allyl groups per g adsorbent.
The allyl-activated base matrix is slurried at room temperature with an acidic solution of pH around 4, followed by the addition of N-bromosuccinimide, and incubation for at least one hour. The resulting brominated base matrix is then washed with water and left to settle.
The brominated base matrix is resuspended in water followed by the addition of 600 mL of an ammonia solution, and heating to no more than 65° C. under stirring for less than 24 hours. At the end of the reaction period, the reaction is drained and washed with water, then a pH-neutral solution, followed by settling.
1.4 Dichlorotriazine (DCT) Activation of the Aminated Base Matrix The aminated base matrix resulting from the previous step is then slurried in an aqueous solution of potassium phosphate (1M), followed by settling and re-suspension in the same solution, with the addition of 160 mL of acetone, under stirring at around 2° C. Approximately 1.4 molar equivalents of cyanuric chloride with respect to the precursor activation density dissolved in acetone is added to the slurried aminated base matrix, followed by incubation under refrigeration for approximately one hour, after which it is drained, washed with aqueous acetone solutions of decreasing concentration, then a final wash in water, after which the slurry is settled under gravity. The final product of this reaction is the DCT-activated base matrix.
A DCT-activated base matrix is suspended in water and set to stir at room temperature. A solution of A-antigen trisaccharide ligand comprising a flexible linker in water is added to the DCT gel slurry maintained under high pH at room temperature for 4 to 6 hours. The A-antigen trisaccharide ligand comprising the flexible linker is a compound of formula (IVa), as described herein. After reaction, the derivatised base matrix is blocked using mercaptoethanol and thoroughly washed with water before being allowed to settle under gravity.
This reaction results in a chromatographic scaffold material containing an affinity ligand which binds A-isoagglutinins (Scaffold Example 1).
A DCT-activated base matrix is suspended in water and set to stir at room temperature. A solution of B-antigen trisaccharide ligand comprising a flexible linker in water is added to the DCT gel slurry maintained under high pH conditions at room temperature for 4 to 6 hours. The B-antigen trisaccharide ligand comprising the flexible linker is a compound of formula (IVb), as described herein. After reaction, the derivatised base matrix is blocked using mercaptoethanol, thoroughly washed with water then settled under gravity.
This reaction results in a chromatographic scaffold material containing an affinity ligand which binds B-isoagglutinins (Scaffold Example 2).
3.1 Removal of A-Isoagglutinin from Human IVIG Intermediate Product Feedstock Using a Product of this Invention
A column containing the antigen A ligand (Scaffold Example 1) is packed, followed by the application of an IVIG solution containing isoagglutinins at a flow rate of 1 mL/min.
The flow-through from the loading process is collected. The load and flow-through samples are analysed for of A-isoagglutinins using a standard agglutination assay.
Human red blood cells are washed with PBS buffer by adding 2 mL red blood cells into a 5 mL centrifuge tube and centrifuging at 1400 rpm for 3 minutes. The supernatant from the centrifuged cells is removed before adding PBS buffer to the cell pellet to make the suspension up to a 2 mL volume and the cells mixed by inverting the tube. This PBS wash is repeated three times.
Freeze dried papain is reconstituted with PBS buffer (2 mL) before adding 200 μL to the cells after centrifugation and removal of the supernatant. These suspensions are then made up to 2 mL volume with PBS buffer before incubation with mixing for to minutes at 37° C.
At the end of this incubation period, the suspension is centrifuged for 3 minutes at 1400 rpm. The supernatant is removed from the centrifuged cells, then PBS buffer added to make the suspension up to a 2 mL volume. The cells are mixed by inverting the tube. This PBS wash is repeated three times.
The spun cells are mixed with inversion made up to 2 mL volume with 2 mg/mL BSA solution.
A sample of the feedstock from step 3.1 is diluted ½, ¼, ⅙, ⅛, 1/10, 1/12, 1/14 and 1/16 with a solution of 2 mg/mL BSA solution.
A sample of the non-bound from step 3.1 is diluted ½, ⅓, ¼, ⅕, ⅙, 1/7, ⅛ and 1/9 with a solution of 2 mg/mL BSA solution.
The feedstock and non-bound dilutions described above (20 μL) are transferred to a 96 well v-bottomed plate along with the blank 2 mg/mL BSA solution.
The red blood cells prepared in stage 3.2.1 are mixed by inversion before transferring to a pipette reservoir. The blood cell suspension (20 μL) is transferred to the plate using a multichannel pipette. The plate is agitated to mix the solutions for 30 seconds before centrifuging the plate at 1400 rpm for 3 minutes.
The plate is placed onto a stand at a 70° angle for 15 minutes. Each well of the plate is studied to determine the level of clearance of isoagglutinin from the red blood cells. This is achieved by assessing the sample dilution required to prevent agglutination, indicated by streaming of the red blood cells in the plate wells (
As shown in
Removal of B-Isoagglutinin from Human IVIG Intermediate Product Feedstock Using a Product of this Invention
A column containing the antigen B ligand (Scaffold Example 2) is packed followed by the application of an IVIG solution containing isoagglutinins at a flow rate of 1 mL/min. The flow-through from the loading process is collected. The load and flow-through samples are analysed for the content of B-isoagglutinins using a standard agglutination assay.
4.2 Agglutination Assay on Flow Through from Column Chromatography Purification of IVIG Feedstock with B-Antigen Beaded Agarose Adsorbent
To make the type-B red blood cells up in PBS buffer, the cells are washed with PBS buffer by adding 2 mL red blood cells into a 5 mL centrifuge tube and centrifuging at 1400 rpm for 3 minutes. The supernatant from the centrifuged cells is removed before adding PBS buffer to the cell pellet to make the suspension up to a 2 mL volume, and the cells are mixed by inverting the tube. This PBS wash is repeated three times.
Freeze dried papain was reconstituted with PBS buffer (2 mL) before adding 200 μL to the cells after centrifugation and removal of the supernatant. These suspensions are then made up to 2 mL volume with PBS buffer before incubation with mixing for 10 minutes at 37° C.
At the end of this incubation period, the suspension is centrifuged for 3 minutes at 1400 rpm. The supernatant is removed from the centrifuged cells, then PBS buffer added to make the suspension up to a 2 mL volume. The cells are mixed by inverting the tube. This PBS wash is repeated three times.
The spun cells are mixed with inversion made up to 2 mL volume with 2 mg/mL BSA solution.
A sample of the feedstock from step 4.1 is diluted ½, ¼, ⅙, ⅛, 1/10, 1/12, 1/14 and 1/16 with a solution of 2 mg/mL BSA solution.
A sample of the non-bound from step 4.1 is diluted ½, ⅓, ¼, ⅕, ⅙, 1/7, ⅛ and 1/9 with a solution of 2 mg/mL BSA solution.
The feedstock and non-bound dilutions described above (20 μL) are transferred to a 96 well v-bottomed plate along with the blank 2 mg/mL BSA solution.
The red blood cells prepared in stage 4.2.1 are mixed by inversion before transferring to a pipette reservoir. The blood cell suspension (20 μL) is transferred to the plate using a multichannel pipette. The plate is agitated to mix the solutions for 30 seconds before centrifuging the plate at 1400 rpm for 3 minutes.
The plate is placed onto a stand at a 70° angle for 15 minutes. Each well of the plate is studied to determine the level of clearance of isoagglutinin from the red blood cells. This is achieved by assessing the sample dilution required to prevent agglutination, indicated by streaming of the red blood cells in the plate wells (
As shown in
Two samples of the A-Antigen adsorbent were incubated in 0.5 M NaOH at 40° C. for 1 week, and subsequently tested for performance using a standard agglutination assay. The samples both showed reduction in agglutinin titres of 1/10 to ¼ before and after incubation under caustic conditions, indicating the stability of the adsorbent under those conditions.
In another experiment, a batch of the A-Antigen adsorbent was subjected to a cycling study, where a packed column of the adsorbent went through 51 cycles of a procedure containing a caustic-based cleaning-in-place (CIP) step using 0.5 M NaOH. The isoagglutinin titre of samples taken before and after the column run both showed a reduction of agglutinin titre from ⅛ to ½ after the first and 51st runs, demonstrating the stability of the material to caustic conditions.
A batch of the B-Antigen adsorbent was subjected to a cycling study, where a packed column of the adsorbent went through 51 cycles of a procedure containing a caustic-based cleaning-in-place (CIP) step using 0.5 M NaOH. The isoagglutinin titre of samples taken before and after the column run both showed a reduction of agglutinin titre from ¼ to 1/1 (neat) after the first and 51st runs, demonstrating the stability of the material to caustic conditions.
A range of DCT activated substrates with activation densities ranging from 30 μmol/g to 140 μmol/g were generated using the method described in Example 1.
A solution of A-antigen trisaccharide ligand comprising a flexible linker in water was added to the DCT gel slurries maintained under high pH at room temperature for 24 hours. The A-antigen trisaccharide ligand comprising the flexible linker is a compound of formula (IVa), as described herein. After 0, 0.5, 1, 2, 3, 5 and 24 hours, samples of the reaction supernatants were collected for quantitation of unreacted ligand.
As shown in
A synthetic route for producing a n-hydroxy succinimide scaffold is shown in Scheme 1. The steps are described in more detail below.
Approximately 1 kg of a solid support, such as beaded agarose, is suspended in water before heating to 40 to 50° C. Sodium chloroacetate (approximately 235 g) is added to the reaction slurry and left to react for no more than 18 hours, after which the drained gel is washed with water. The resulting material is an activated matrix that contains 20 to 30 μmol carboxy groups per g adsorbent.
The carboxylated support is acidified by washing with 0.1 M HCl and then washed free of water with acetone. The gel is then suspended in acetone before reacting with N-hydroxysuccinimide (NHS) (16 g per kg of support) and N-ethyl-N′-(3-(dimethylamino)propyl)carbodiimide (EDC) (10 g per kg of support) at ambient temperature for at least 16 hours. After the reaction, the gel is drained and washed with N,N-dimethylformamide. The resulting material is an activated matrix that contains 20 to 30 μmol NHS groups per g adsorbent.
Functionalisation of a Base Matrix with Tris 2-Aminoethyl Amine Ligand
The bromo activated base matrix produced as described in Example 1 is suspended in water before adding tris 2-aminoethyl amine ligand. The charge of tris 2-aminoethyl ligand is calculated with respect to the precursor allyl activation density to give an excess of 30 molar equivalents.
After addition of the amine, the reaction is left to react at 60° C. for at least 16 hours. At the end of the reaction period, the gel is drained and washed with water, 0.1 M HCl and 0.1 M NaCl before settling under gravity.
This reaction results in a chromatographic material containing an affinity ligand which binds bovine serum albumin.
The NHS activated base matrix produced as described in Example 7 is suspended in N,N-dimethylformamide before adding tris 2-aminoethyl ligand. The charge of tris 2-aminoethyl ligand is calculated with respect to the precursor NHS activation density to give an excess of 30 molar equivalents.
After addition of the amine, the reaction is left to react at ambient temperature for at least 16 hours. At the end of the reaction period, the gel is drained and washed with water, 0.1 M HCl and 0.1 M NaCl before settling under gravity.
This reaction results in a chromatographic material containing an affinity ligand which binds bovine serum albumin.
The DCT activated base matrix produced as described in Example 1 is suspended in water before adding tris 2-aminoethyl ligand. The amount of tris 2-aminoethyl ligand is calculated with respect to the precursor activation density to give an excess of 10 molar equivalents.
After addition of the amine, the reaction is left to react at 45° C. temperature for at least 16 hours. At the end of the reaction period, the gel is drained and washed with water, 0.1 M HCl and 0.1 M NaCl before settling under gravity.
This reaction results in a chromatographic material containing an affinity ligand which binds bovine serum albumin.
A sample of the tren adsorbent produced as described in Example 8.1 (bromo attachment, Comparative Scaffold 1), 8.2 (NHS attachment, Comparative Scaffold 2) and 8.3 (DCT attached product of the invention, Scaffold Example 3) were subjected to a cycling study, where packed columns of the adsorbents went through 21 cycles of a procedure containing a caustic-based cleaning-in-place (CIP) step using 0.5 M NaOH. On the first, 11th and 21st cycle, the column was loaded to 10% breakthrough with bovine serum albumin (BSA) and the binding capacity was calculated.
As shown in
The bromo attached Tren adsorbent of Comparative Scaffold 1 also showed good caustic stability however, as described in Example 8.1 this required much stronger reaction conditions compared to the triazine attachment process for Scaffold Example 3, including higher temperature and a three-fold excess of amine (Tren ligand).
Functionalisation of Activated Scaffolds with Blue Chromophore Ligand
A solution of 4.5 g of Mimetic Blue SA ligand available from Astrea Bioseparations (referred to herein as “Blue ligand”) per kg of adsorbent is prepared in water with adjustment to pH 12 with NaOH. The bromo activated base matrix produced as described in Example 1 is suspended in the Blue ligand solution and the reaction is left to react at 60° C. for at least 16 hours. At the end of the reaction period, any residual reactive sites on the gel are blocked by addition of ethanolamine followed by reaction at 60° C. for at least 16 hours. After the blocking reaction, the gel is drained and washed with water. This reaction results in a chromatographic material containing an affinity ligand at approximately 3.0 μmol ligand per g of adsorbent which binds human serum albumin.
A solution of 4.5 g of Blue ligand per kg of adsorbent is prepared in water with adjustment to pH 12 with NaOH. The NHS activated base matrix produced as described in Example 7 is suspended in the Blue ligand solution and the reaction is left to react at ambient temperature for at least 16 hours. At the end of the reaction period, any residual reactive sites on the gel are blocked by addition of ethanolamine followed by reaction at room temperature for at least 16 hours. After the blocking reaction, the gel is drained and washed with water. This reaction results in a chromatographic material containing an affinity ligand at approximately 3.4 μmol ligand per g of adsorbent which binds human serum albumin.
A solution of 4.5 g of Blue ligand per kg of adsorbent is prepared in water with adjustment to pH 12 with NaOH. The DCT activated base matrix produced as described in Example 1 is suspended in the Blue ligand solution and the reaction is left to react at ambient temperature for at least 16 hours. At the end of the reaction period, any residual reactive sites on the gel are blocked by addition of ethanolamine followed by reaction at 45° C. for at least 16 hours. After the blocking reaction, the gel is drained and washed with water. This reaction results in a chromatographic material containing an affinity ligand at approximately 6 μmol ligand per g of adsorbent which binds human serum albumin.
A sample of the Blue chromophore ligand scaffolds produced as described in Example 10.1 (bromo attachment, Comparative Scaffold 3), 10.2 (NHS attachment, Comparative Scaffold 4) and 10.3 (DCT attached product of the invention, Scaffold Example 4) were subjected to a cycling study, where a packed column of the adsorbents went through 21 cycles of a procedure containing a caustic-based cleaning-in-place (CIP) step using 0.5 M NaOH. On the first, 11th and 21st cycle, the columns were loaded to 10% breakthrough with human serum albumin (HSA) and the binding capacity was calculated.
As shown in
Despite being activated to the same density and having the same excess of ligand in the immobilisation reaction, the triazine adsorbent showed higher binding capacity than the bromo attached adsorbent. Without wishing to be bound by any theory, this is afforded by the higher reactivity of the chlorotriazine reactive group leading to increased ligand density of the adsorbent and demonstrating an advantage in efficiency of the synthesis process.
In another experiment, a sample of the Blue chromophore ligand adsorbents produced as described in Example 10.2 (NHS coupled Comparative Scaffold 4) and 10.3 (DCT attached product of the invention Scaffold Example 4), were incubated in 0.5 M NaOH at 40° C. for three days. Approximately every 24 hours, a supernatant sample was collected for quantitation of ligand leachate concentration by HPLC.
As shown in
The two adsorbents were tested for HSA binding capacity at 10% breakthrough before the stability study and after incubation in 0.5 M NaOH at 40° C. for 66 hours.
As shown in
12.1 Activation of Beaded Agarose with Epichlorohydrin
Approximately 1 kg of a beaded agarose solid support, is suspended in 0.9 L of water before addition of 166 mL of 10 M NaOH. Epichlorohydrin is added to the reaction slurry at 250 mL per kg of base matrix. The reaction is left to stir at 16° C. for at least 16 hours before adding an additional 125 mL portion of epichlorohydrin and 84 mL of 10 M NaOH. The reaction mixture is left to react for 3 hours before draining and washing with water. The resulting material is an activated matrix that contains up to 30 μmol epoxide groups per g adsorbent, demonstrating the limited activation density of epichlorohydrin activation method on beaded agarose support.
The inventors have shown that their functionalised solid support can be used to selectively isolate isoagglutinin. However, it will be appreciated that the scaffold could be functionalised with alternative ligands to enable the isolation of other biomolecules.
The inventors have also shown that the functionalised solid support is compatible with cleaning and sanitisation using sodium hydroxide, thereby preventing contamination thereof. The functionalised solid support is stable under these conditions, allowing repeated use thereof. This will significantly reduce the cost of isolating biomolecules, and in turn any products manufactured therewith.
In addition, the inventors have shown that their activated solid support can be functionalised under mild reaction conditions (low temperature, low molar excess of amine and short reaction times) by virtue of the high activation densities achievable by this invention and the high reactivity of the dichlorotriazine attachment chemistry. It will also be appreciated by those skilled in the art that this high potential activation density enables higher ligand densities which in turn can provide increased binding capacity of target biomolecules.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2107352.3 | May 2021 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/GB2022/051301 | 5/24/2022 | WO |
