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WO2003035672A1 - Nouveau procede de recuperation de mono esters d'acide squarique en chimie de conjugaison biologique - Google Patents

Nouveau procede de recuperation de mono esters d'acide squarique en chimie de conjugaison biologique Download PDF

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Publication number
WO2003035672A1
WO2003035672A1 PCT/SE2002/001892 SE0201892W WO03035672A1 WO 2003035672 A1 WO2003035672 A1 WO 2003035672A1 SE 0201892 W SE0201892 W SE 0201892W WO 03035672 A1 WO03035672 A1 WO 03035672A1
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WIPO (PCT)
Prior art keywords
group
amino
decyloxy
ethyl
dioxocyclobut
Prior art date
Application number
PCT/SE2002/001892
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English (en)
Inventor
Ulf Nilsson
Anders Bergh
Original Assignee
Lundonia Biotech Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lundonia Biotech Ab filed Critical Lundonia Biotech Ab
Priority to EP02802077A priority Critical patent/EP1438328A1/fr
Publication of WO2003035672A1 publication Critical patent/WO2003035672A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/18—Acyclic radicals, substituted by carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/14—Extraction; Separation; Purification
    • C07K1/16—Extraction; Separation; Purification by chromatography
    • C07K1/22—Affinity chromatography or related techniques based upon selective absorption processes

Definitions

  • the present invention relates to a method for non- polar extraction of novel biomolecule squaric acid monoamide conjugates of formula (I) , as presented below, ob- tained after a bioconjugation reaction.
  • bioconjugation or biocon - jugate chemistry
  • jbio- conjuga te The properties of the biological molecule and the carrier molecule or moiety are combined, thus creat- ing "designed" and unique characteristics of the biocon- jugate.
  • bioconjugates for example in assaying of small amount of molecules in biological samples, in drug delivery, or in modulation of biological activity, are well-know to practitioners skilled in the art and of fundamental importance for virtually every discipline within life sciences. Many biological assays, including pre-clinical drug trials, today involve the use of bioconjugates .
  • cross-linking reagent possesses two reactive functional groups, of which one reacts with the biomolecule and the other with the carrier molecule or moiety. Numerous such cross-linking reagents are well known to one skilled in the art and many are commercially available 1 .
  • Squaric acid diethyl ester is a highly efficient ho- mobifunctional amine-reactive cross-linking reagent that has found widespread use for bioconjugations in general ⁇ and in glycoconjugation (bioconjugation of carbohydrates) in particular.
  • Gl ⁇ senkamp et al disclosed a process for bioconjugation based on squaric acid esters (DE4341524 and DE14990550) .
  • the use of squaric acid diethyl ester in the preparation of glycoconjugates was pioneered by Ti- etze 3 and Hindsgaul 4 and later used many others. Additional publications describe squaric acid diester in conjugation chemistry.5-16
  • biomolecule- squaric acid monoamide intermediate (Fig. 1)
  • This intermediate is subsequently reacted with the carrier molecules or moiety chosen.
  • the biomolecule- squaric acid monoamide intermediate is commonly used in large molar excess to the carrier molecules or moiety. Biomolecules are typically isolated or synthesized in minute amounts and thus are very valuable. Consequently, the recovery of unreacted excess of biomolecule-squaric acid monoamide intermediate is of significant importance.
  • the squaric acid diethyl ester is an efficient amino-reactive cross-linking reagent
  • a major disadvantage is that the biomolecule-squaric acid monoamide ethyl ester intermediate is complicated to purify, which renders recovery of unreacted biomolecule-squaric acid monoamide ethyl ester intermediate a time-consuming and complex procedure.
  • Recovery/purification of carbohy- drate-squaric acid monoamide intermediates based on C18 solid-phase extraction has been reported 4 ' 15 .
  • the present invention relates to a method for non- polar extraction of a biomolecule squaric acid monoamide conjugate of formula (I) obtained after a bioconjugation reaction
  • X, Y and Z are, independently, selected from the group consisting of 0 and S;
  • R 1 is selected from the group consisting of an alkyl, an alkenyl, an alkynyl and an aryl group comprising at least 6 carbon atoms;
  • R 2 is a biomolecule;
  • R 3 is selected from the group consisting of hydro- gen, an alkyl, an alkenyl, an alkynyl group comprising from 6 to 30 carbon atoms, and an aryl group comprising from 6 to 18 carbon atoms; wherein said extraction comprises; recovering said intermediate by non-polar means.
  • Fig. 1 Schematic procedure for conjugation of a biomolecule to a carrier molecule/matrix using squaric acid esters as homobifunctional amine-reactive cross- linking reagents.
  • Fig. 4 MALDI-TOF MS of BSA before (a) and after (b) conjugation reaction with 1 showing the successful average conjugation of 5 ⁇ -D-mannopyranoside moieties per BSA molecule .
  • Fig. 5 Schematic procedure for the recovery of biomolecule intermediates of formula (I) subsequent biocon- jugation to an amino-functionalized microtiter plate.
  • the method further comprises, preceding said recovering, collecting a reaction solution after said bioconjugation reaction, and bringing said reaction solution, optionally after a change, concentration, dilution and/or addition of solvent, into contact with said non-polar means.
  • said non- polar means is selected from the group consisting of a non-polar solid phase and a non-polar solution.
  • said biomolecule is selected from the group consisting of a car- bohydrate, a protein, a peptide, a nucleoside, a nucleotide, a steroid, a lipid, an alkaloid, a secondary metabolite, a saccharide, a saccharide-substituted alkyl group, and a saccharide-substituted sulfur-containing alkyl group .
  • a car- bohydrate a protein, a peptide, a nucleoside, a nucleotide, a steroid, a lipid, an alkaloid, a secondary metabolite, a saccharide, a saccharide-substituted alkyl group, and a saccharide-substituted sulfur-containing alkyl group .
  • said saccharide is selected from the group consisting of glucose, mannose, galactose, glucosamine, galactosamine, fucose, fructose, xylose, neuraminic acid, glucoronic acid, idu- ronic acid, a disaccharide, an oligosaccharide comprising at least two of the above monosaccharides, and derivatives thereof .
  • Any other saccharide known to a person skilled within the art may obviously be used as an alternative to the above mentioned saccharides .
  • the bio- molecule intermediate of the above mentioned formula (I) comprises a saccharide in the form of a glycoside with an amino-functionalized aglycon or an amino-functionalized and sulfur-containing aglycon, which saccharide is selected from the group consisting of glucose, mannose, ga- lactose, glucosamine, galactosamine, fucose, fructose, xylose, neuraminic acid, glucoronic acid, iduronic acid, a disaccharide or an oligosaccharide comprising at least two of the above monosaccharides, and derivatives thereof. Any other saccharide known to a person skilled within the art may obviously be used as an alternative to the above mentioned saccharides.
  • said R 1 in the biomolecule squaric acid monoamide conjugate of formula (I) comprises from 6 to 30 carbon atoms, preferably from 10 to 20 carbon atoms. It is very convenient that R 1 may be chosen independently of the structure of the biomolecule .
  • the non- polar solid phase, which the intermediate is brought into contact with according to the method of the invention is selected from the group consisting of alkylated silica (e.g. C2 , C4, C6, C8, C18, cyclohexyl, cyanopropyl) , ary- lated silica (e.g. phenyl), resin-based solid-phase extraction sorbents (e.g. polystyrene resin, co-polymer resins), and mixed mode solid-phase extraction sorbents.
  • alkylated silica e.g. C2 , C4, C6, C8, C18, cyclohexyl, cyanopropyl
  • ary- lated silica e.g. phenyl
  • resin-based solid-phase extraction sorbents e.g. polystyrene resin, co-polymer resins
  • mixed mode solid-phase extraction sorbents e.g. polystyrene resin, co
  • the invention relates to an easy, manual or automated, purification and recovery of unreacted excesses of biomolecule squaric acid monoamide conjugates of the general formula (I) , subsequent bioconjugation to a carrier molecule, moiety, or a matrix.
  • the present invention re- lates to the discovery that biomolecule squaric acid monoamide conjugates of formula I can readily be extracted into hydrophobic solution or solid phases, exemplified by, but not limited to, alkylated silica (e.g. C2, C4, C6, C8, C18, cyclohexyl, cyanopropyl etc), ary- lated silica (e.g. phenyl etc.), resin-based solid-phase extraction sorbents (e.g. polystyrene resin, co-polymer resins etc.), and mixed mode solid-phase extraction sorbents (i.e. sorbents comprising a mixture of 2 or more of the above mentioned sorbents) .
  • alkylated silica e.g. C2, C4, C6, C8, C18, cyclohexyl, cyanopropyl etc
  • ary- lated silica e.g. phenyl etc.
  • biomolecule squaric acid monoamide conjugates of formula (I) can thus be recovered from complex reactions mixtures subsequent a bioconjugation reaction to amino-group containing carrier molecules or matrixes, exemplified by, but not limited to, proteins, peptides, fluorescence markers, solid poly- mer beads, microtiter plates, test tubes, glass surfaces, and chromatographic matrices such as silica, dextran, starch, cellulose, agarose etc.
  • the extraction of bio- molecule squaric acid monoamide conjugates of formula (I) into hydrophobic solution or solid phases is enabled by the hydrophobic properties of R 1 . The simplicity of extraction procedure renders it suitable for automation.
  • said X is O
  • said Y is 0, said Z is 0, and said R 1 is a decyl group.
  • the biomolecule squaric acid monoamide conjugate of formula (I) is selected from, but not limited to, the group consisting of 2- [ (2-decyloxy-3 , 4-dioxocyclobut-l- enyl) amino] ethyl ⁇ -D-mannopyranoside (1), 2- [ (2-decyloxy- 3, 4-dioxocyclobut-l-enyl) amino] ethyl ( ⁇ -D- galactopyranosyl) - (l-»4) - ⁇ -D-glucopyranoside (2), 2-[(2- decyloxy-3 , 4-dioxocyclobut-l-enyl) amino] ethyl ( ⁇ -D- galactopyranosyl) - (1—»4) - ( ⁇ -D- galactopyranosyl) - (1—»4) - ⁇ -D-glucopyranoside (3), 2- [ (2-decyloxy-3
  • alkyl group is meant to comprise from 6 to 30 carbon atoms, preferably from 10 to 20 carbon atoms. Said alkyl group may be straight or branched. Said alkyl group may also form a cycle comprising from 6 to 30 carbon atoms, preferably from 10 to 20 carbon atoms. For example hexyl, heptyl , octyl etc ..
  • alkenyl group is meant to comprise from 6 to 30 carbon atoms, preferably from 10 to 20 carbon atoms. Said alkenyl group comprises at least one double bond. For example hexenyl, heptenyl, octenyl etc ..
  • alkynyl group is meant to comprise from 6 to 30 carbon atoms, preferably from 10 to 20 carbon atoms. Said alkynyl group comprises at least one triple bond. For example hexynyl, heptynyl, octynyl etc ..
  • aryl group is meant to comprise from 6 to 18 carbon atoms.
  • aryl group is meant to comprise from 6 to 18 carbon atoms.
  • phenyl, naphtyl, anthracenyl etc. are examples of aryl group.
  • the above mentioned groups may naturally be substituted with any other known substituent within the art of organic chemistry.
  • the groups may also be substituted with two or more of the substituents.
  • the invention relates to the recovery of a biomolecule squaric acid monoamide conjugate of the above mentioned formula after conjugation to a natural or artificial carrier molecule or moiety, for example, but not limited to, a polymer bead, a microtiter well, a protein, a fluorescence tag, an affinity matrix.
  • the present invention relates to the recovery of a biomolecule squaric acid monoamide conjugate of the above mentioned formula after conjugation to an amino-functionalized natural or artificial carrier molecule or moiety, for example, but not limited to, a polymer bead, a microtiter well, a protein, a fluorescence tag, an affinity matrix.
  • an amino-functionalized natural or artificial carrier molecule or moiety for example, but not limited to, a polymer bead, a microtiter well, a protein, a fluorescence tag, an affinity matrix.
  • the present invention originates in the discovery that the use of squaric acid esters of hydrophobic alcohols in bioconjugation chemistry results in squaric acid ester monoamides carrying a hydrophobic tag that is released during the bioconjugation reaction (see fig. 1) , i.e. the tag is traceless (hydrofobic tags may interfere with biological activity of the biomolecule) , thus avoiding the necessity of tagging each individual biomolecule as the hydrophobic tag is present in the squaric acid es- ter reagent.
  • the excesse of the unreacted squaric acid ester monoamide after bioconjugation reaction is easily recovered by use of the method of the invention and may be re-used in a further bioconjugation reaction.
  • NMR experiments were recorded either with a Bruker ARX 300 MHz, Bruker DRX 400 MHz, or a Varian Unity 400 MHz spectrometer at ambient temperature.
  • 1 H NMR assign- ments were derived from COSY experiments. Optical rotations were measured with a Perkin-Elmer 241 polarimeter.
  • High-resolution FAB mass spectra (HRMS) were recorded with a JEOL SX-120 instrument.
  • MALDI-TOF MS were recorded on a Bruker Biflex III instrument (run in positive mode) using gentisic acid ( , 5-dihydroxy benzoic acid) as matrix.
  • Lectin-peroxidase conjugates were purchased from Sigma-Aldrich ( Concavalin A (L6397) for 1, Arachis hypo- gaea (peanut agglutinin, L7759) for 2, Ricinus communis (Castorbean) Toxin RCA ⁇ 20 (L2758) for 2 and 4, Bandeira simplicifolia (L5391) for 3, and Tri ticum vulgaris (weat germ agglutinin, L3892) for 5 and 6) .
  • PBS buffer 24 g NaCl , 0.6 g KCl , 3.46 g NaH 2 P0 4 *H 2 0 and 0.6 g KH 2 P0 4 in 1000 mL H 2 0.
  • the pH was adjusted to 7.2.
  • Tween20/PBS solution 0.10 mL Tween20 in 200 mL PBS buffer.
  • Lectin solutions lmg of lectin in 1 mL Tween20/PBS solution and filtered through a 0.22 ⁇ m filter. The resulting solution was then diluted between 25-50 times in Tween20/PBS.
  • Cova buffert 117 g NaCl , 10 g MgS0 4 *7H 2 0 and 0.50 mL Tween20 in 1000 mL PBS buffer.
  • Citric acid buffer 7.98 g citric acid monohydrate and 9.46 g Na 2 HP0 4 in 1000 mL H 2 0. The pH was adjusted to 5.0.
  • O-Phenylendiamine substrate solution To 6.0 mg O- phenylendiamine in 10 mL citric acid buffer was added 5 ⁇ L H 2 0 2 . The solution was used immediately.
  • NaHC0 3 buffer 20 g NaHC0 3 in 1000 mL H 2 0. The pH was adjusted to 9.00.
  • 4-Nitrophenyl ⁇ -D-mannopyranoside was purchased from Sigma-Aldrich. Amino-functionalized Covalink microtiter plates were from Nalge Nunc International (Roskilde, Denmark) . Microtiter plates absorbencies were read on an In- terMed ImmunoReader NJ-2000. Isolute C-18 cartridges were from International Sorbent Technology. Synthesis of didecyl squarate (3, 4-Didecyloxy-cyclobut-3- ene-1,2- dione)
  • the reaction mixture was diluted with water (10 mL) and extracted with CH 2 C1 2 (2x30 mL) .
  • the organic phase was dried (MgS0 ) and con- centrated.
  • the residue was flash chromatographed (Si0 2 , heptane :ethylacetate 1:2) to afford 2-[2-(t- butoxycarbonylamino) ethylthio] ethyl 2,3,4, 6-tetra-O- acetyl ⁇ -D-mannopyranoside (191 mg, 87%) as a clear syrup.
  • Bovine serum albumin (BSA, 62 mg, 0.93 ⁇ mol) and 1 (2.5 mg, 5.44 ⁇ mol) were dissolved in NaHC0 3 buffer (2.5 mL) and stirred in room temperature for 24 hrs . The solution was then dialyzed against 5x25 mL water and ly- ophilized which afforded the ⁇ -D-mannopyranoside neogly - coprotein as a white powder. The average degree of incorporation was determined by MALDI-TOF MS using the center of the single charged protein peak (Fig. 4) . Typical procedure for the conjugation of squaric decyl ester glycosides (1-9) to Sepharose EAH 4B
  • the sulfur-containing squaric decyl ester 7 (5.0 mg) was added to a suspension of sedimented Sepharose EAH 4B (Pharmacia Amersham, 0.05 mL) in NaHC0 3 buffer (1.5 L) .
  • the sepharose beads were after 24 h filtered on a sintered glass funnel and washed thoroughly with water.
  • the sulfur atom present in 7 enabled differential sulfur com- bustion analysis: small samples of the sepharose beads were taken before and after conjugation with 7, lyophi- lized, and subjected to sulfur combustion analysis.
  • the increase in sulfur content subsequent conjugation corresponded to an ⁇ -D-mannopyranoside content of 3.1 ⁇ mol/mL sedimented sepharose beads.
  • a suspension of amino-functionalized polymer beads (500 ⁇ L, IDC amine polystyrene latex 3.0 ⁇ m, 4% aqueous suspension, Interfacial Dynamics Corporation, Portland, USA) was further suspended in NaHC0 3 buffer (2 mL) , mixed, centrifuged, where after the supernatant was discarded. This washing procedure was repeated 5 times. To the particles in NaHC0 3 buffer (2 mL) was added 8
  • the squaric decyl ester glycoside solution (150 ⁇ L/- well, 0.02 mM in NaHC0 3 buffer), was added to an amino- functionalized microtiter plate (CovaLink, NUNC A/S, Roskilde, Denmark) . After 24 hrs, the plates were emptied and washed three times with Cova buffert followed by a thorough washing with water. To the plates a solution of 20% acetic anhydride in water was added. After 2 hrs, the plates where thoroughly washed with water. Typical procedure for the recovery of squaric decyl ester glycosides (3, 5, and 6) after conjugation reaction (Fig.
  • reaction solutions were taken from the wells, combined, and passed through an Isolute C-18 column. The column was washed with 2x5 L H 2 0 and then eluted with
  • a solution (75 ⁇ L) of 4-nitrophenyl ⁇ -D- mannopyranoside (36 mM in T EEN20/PBS) was added to the first row.
  • Tween20 /PBS 50 ⁇ L was added to the rest of the wells.
  • a volume of 25 ⁇ L from the first row was then transferred to the second row and mixed. This procedure was repeated down the rows until the last row, from which 25 ⁇ L were discarded. This resulted in a dilution factor of three for every row.
  • the concavalin A-horseradish peroxidase conjugate was then added and the binding was detected as above.

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

La présente invention concerne un conjugué monoamide d'acide squarique de biomolécule représenté par la formule (I), telle que présentée dans les revendications, et un procédé d'extraction non polaire d'un conjugué monoamide d'acide squarique de biomolécule représenté par la formule (I), telle que présentée dans les revendications, obtenu après une réaction de conjugaison biologique, cette extraction consistant à récupérer cet intermédiaire par un moyen non polaire.
PCT/SE2002/001892 2001-10-25 2002-10-25 Nouveau procede de recuperation de mono esters d'acide squarique en chimie de conjugaison biologique WO2003035672A1 (fr)

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EP02802077A EP1438328A1 (fr) 2001-10-25 2002-10-25 Nouveau procede de recuperation de mono esters d'acide squarique en chimie de conjugaison biologique

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SE0103558-3 2001-10-25
SE0103558A SE520256C2 (sv) 2001-10-25 2001-10-25 Biomolekylkvadratsyramonoamidkopplingsreagensintermediär

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003084982A3 (fr) * 2001-11-14 2004-09-10 Luminex Corp Compositions fonctionnalisees pour immobilisation amelioree
JP2011032206A (ja) * 2009-07-31 2011-02-17 National Institute Of Advanced Industrial Science & Technology Ｓｓｅａ系新規糖鎖化合物
CN110156844A (zh) * 2012-05-21 2019-08-23 安捷伦科技有限公司 组合物和缀合寡核苷酸的方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4523980A (en) * 1984-08-31 1985-06-18 The Halcon Sd Group, Inc. Process for the recovery of high purity squaric acid
WO2000023478A1 (fr) * 1998-10-16 2000-04-27 Amersham Pharmacia Biotech Ab Support active par acide squarique utilisable pour l'immobilisation de composes contenant des groupes amines

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4523980A (en) * 1984-08-31 1985-06-18 The Halcon Sd Group, Inc. Process for the recovery of high purity squaric acid
WO2000023478A1 (fr) * 1998-10-16 2000-04-27 Amersham Pharmacia Biotech Ab Support active par acide squarique utilisable pour l'immobilisation de composes contenant des groupes amines

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
BLIXT O. ET AL.: "Enzymatic glycosylation of reducing oligosaccharides linked to a solid phase or a lipid via a cleavable squarate linker", CARBOHYDRATE RESEARCH, vol. 319, 1999, pages 80 - 91, XP002965395 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003084982A3 (fr) * 2001-11-14 2004-09-10 Luminex Corp Compositions fonctionnalisees pour immobilisation amelioree
US7385053B2 (en) 2001-11-14 2008-06-10 Luminex Corporation Functionalized compositions for improved immobilization
US8188269B1 (en) 2001-11-14 2012-05-29 Luminex Corporation Functionalized compositions for improved immobilization
JP2011032206A (ja) * 2009-07-31 2011-02-17 National Institute Of Advanced Industrial Science & Technology Ｓｓｅａ系新規糖鎖化合物
CN110156844A (zh) * 2012-05-21 2019-08-23 安捷伦科技有限公司 组合物和缀合寡核苷酸的方法

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SE0103558L (sv) 2003-04-26
SE0103558D0 (sv) 2001-10-25
SE520256C2 (sv) 2003-06-17

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