EP1487862A2 - Reactifs supportes par des polymeres pour la purification de produits naturels - Google Patents

Reactifs supportes par des polymeres pour la purification de produits naturels

Info

Publication number
EP1487862A2
EP1487862A2 EP03712004A EP03712004A EP1487862A2 EP 1487862 A2 EP1487862 A2 EP 1487862A2 EP 03712004 A EP03712004 A EP 03712004A EP 03712004 A EP03712004 A EP 03712004A EP 1487862 A2 EP1487862 A2 EP 1487862A2
Authority
EP
European Patent Office
Prior art keywords
polymer supported
reagents
reagent
bio
spacer
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP03712004A
Other languages
German (de)
English (en)
Inventor
Florian Thaler
Moreno Zamai
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Italia SRL
Original Assignee
Pharmacia Italia SpA
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 Pharmacia Italia SpA filed Critical Pharmacia Italia SpA
Priority to EP03712004A priority Critical patent/EP1487862A2/fr
Publication of EP1487862A2 publication Critical patent/EP1487862A2/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K17/00—Carrier-bound or immobilised peptides; Preparation thereof
    • C07K17/02—Peptides being immobilised on, or in, an organic carrier
    • C07K17/06—Peptides being immobilised on, or in, an organic carrier attached to the carrier via a bridging agent
    • 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

Definitions

  • the introduction of polymer-supported scavengers opened the possibility of a simple and efficient method to facilitate the purification of a desired product from un-reacted reagents and/or byproducts. Once reacted with the solid support, it can be removed from the reaction mixture, e.g. by filtration or extraction.
  • a series of applications of scavengers bound on a solid support and their application in the practice of organic synthesis, combinatorial synthesis and automated organic synthesis have been developed.
  • the solid support are polystyrene resins, Merrifield resins, polyamine resins, poly(styrene-divinylbenzene) / poly(ethyleneglycol) grafted copolymer.
  • the polymeric support in the covalent chromatography must react with the desired product in a reaction mixture in the presence of other (undesired) compounds and the bound product has to be cleavable and retrieved from the polymer.
  • the present invention provides a method for the purification of bio-molecules after their chemical modification using one or more insoluble polymer supported reagents. Said polymer supported reagents are put in contact with the mixture containing the desired chemically modified bio-molecule in order to react covalently with excess of reagents and/or unwanted byproducts.
  • Bio-molecules are substances originated by living organisms. They can be proteins, peptides, DNA, RNA, lipids, small molecules, all originated by living organisms.
  • the polymer supported reagent reacts with byproducts or reactants, leaving the desired pure product in solution.
  • the use of polymer supported reagents also named scavenger resins
  • the purification is carried out by incubating the polymer supported reagents with the mixture containing the desired bio-molecule and undesired byproducts and educts and removing the solid support.
  • the solid support after incubation can be filtered from the solution or separated from the solution by aspiration.
  • scavenger resins can be used packed in columns or in a batch system.
  • the incubation and the separation of the reaction mixture from the insoluble polymeric support can be repeated one or more times.
  • the method of purification of this invention is performed under non- denaturing conditions.
  • the bio-molecule maintains its three dimensional structure during the treatment with the scavenger resin. Therefore it does not have to be re- natured in a second step.
  • the method of the present invention can be applied as an alternative and/or in combination with other purification steps, like ion exchange chromatography, affinity chromatography and gel filtration.
  • the invention also comprises the combination with other purification material such as ion-exchange resin; gel-filtration resin; NH 2 -reactive resins, (such as Actigel B, N-hydroxy succinimide esters activated columns, CNBr activated columns, Epoxy-activated columns, Carbonyl diimidazole activated columns, but not limited to these resins); SH- reactive resins (such as Iodoacetyl, Bromoacetyl, maleimide, pyridyl disulfide columns, but not limited to it) chelating resins, desalting columns, reverse-phase adsorbants.
  • the invention comprises the incubation of the reaction mixture with the scavenger resins combined with no, one or more of the other purification materials in one or in more subsequent steps.
  • a further embodiment of this invention includes the automatic performance of the process and the setup for a parallel purification array.
  • high concentrations of the reacting groups are present on the solid support, so an addition of a small amount of polymer is required.
  • the present invention is relating to a method for the fast purification of labeled bio-molecules using an insoluble polymer supported quenching reagent.
  • the labeling of the bio-molecules can be, for example, biotinylation or the introduction of fluorescent tags.
  • the present invention provides a method of removing biotinylating and/or fluorescent agent from a reaction mixture containing labeled bio-molecules, such as for example proteins, protein mixtures and/or peptides, which are either obtained by cellular expression or by chemical or enzymatic cleavage from proteins.
  • labeled bio-molecules such as for example proteins, protein mixtures and/or peptides, which are either obtained by cellular expression or by chemical or enzymatic cleavage from proteins.
  • this invention is addressed to the improvement of the purity of a modified bio-molecule by trapping unwanted byproducts and/or un-reacted starting material.
  • Bio-molecules can be proteins, peptides obtained by enzymatic and/or chemical cleavage from proteins and/or produced by cellular systems.
  • proteins and peptides can contain post-translational modifications, such as phosphorylations, glycosylations, myristolations and palmitoylations.
  • the bio-molecules can also be DNA, RNA, oligonucleotides, lipids, nucleotides, nucleosides, phospholipids. carbohydrates, small molecules (like NAD, NADH, ATP, ADP, AMP, GTP, GDP, GMP, but not limited to it) originated from living organisms.
  • the chemical modification of these bio-molecules can be the tagging with biotinylating or fluorescent agents.
  • the biotinylating and fluorescent agents contain three parts: biotin and/or the fluorescent tag; no, one or more linkers and a chemical group, which permits the binding to the bio-molecule.
  • the linker is expected to be chemically robust at the conditions the binding and quenching step is carried out.
  • the group reacting with the bio-molecule can be iodoalkyl, bromoalkyl, maleimido, dithiopyridine, disulphides, isothiocyanat, suc ⁇ nimidyl esters, sulphosuccinimidyl esters, aldehydes, ketones, dichlorotriazines, diazoles carboxylic acids, sulphonyl chlorides, acyl azides, acyl nitriles, acid chlorides, amino groups, hydra-zines, hydrazides, hydroxylamines, alcohol, carbodiimides and combinations thereof.
  • the fluorescent tags include all molecules, which are able to emit photons after having been excited by light or heat Examples are fluorescem, eosm, dimtrophenyl, naphthalene and substituted naphtalenes (such as dansyl), couma ⁇ n, [Ru(b ⁇ py) 3 ] 2+ , BODIPY® fluorophores, rhodamme, Texas RedTM, Indocarbocyanine (Cy3) or mdodicarbocyanme (Cy5), Alexa Fluor®, Nile Red, allophycocyanme, Oregon Green®, mdot ⁇ carbocyamne (CY7), Europium trisbipy ⁇ dine cryptate, N-[7-mtrobenz-2-oxa-l,3- d ⁇ azol-4-yl]
  • the method of the present invention is particularly attractive for the nanotechnological approach, owing to two characteristics It is a simple one step approach, in which the desired product does not have to bind or interact with a solid support Second, high concentrations of the quenching groups on the solid support allow the addition of a small amount of quenching polymer
  • the insoluble polymer supported reagents to be used in the present purification method are consisting of a polymer bearing at least one reagent residue
  • at least 0 01 mmoles of reagent residues, more preferably at least 0 05 mmoles are covalently bonded or immobilized on 1 gram of resin
  • there are two synthetic strategies by which the preferred high loading of quenching functionality on polymeric supports is achieved In the first strategy, a polymer with existing functionalities of greater than 0 01 mmol per gram of polymer is
  • polymeric supports known in the art can be conveniently used in the present invention, such as for example polyamide, polyamide/polyethylene glycol copolymer, polysulfone, latex, polyester, paper, polypropylene, polyethylene, nitrocellulose.
  • TentaGel is a trade mark of Rapp Polymere GmbH.
  • TentaGel resins are grafted copolymers consisting of a low cross linked polystyrene matrix on which polyethylene glycol (PEG or POE) is grafted.
  • Another classes of polymeric supports are polysaccharide resins like Sepharose, agarose (non cross-linked and cross-linked), cellulose, polysaccharides copolymerized with acrylamide (for example N,N'-methylene-bis(acrylamide), N-acryloyl-2-amino-2- hydroxymethyl- 1,3 -propane diol, but not limited to these two compounds). Even though these last compounds do not show such a high stability as those above, they keep being the mostly used resins in the purification procedures for proteins.
  • the reagent residue may be linked to the polymeric supports by means of a spacer.
  • a spacer can be linked to one or more reagent residues, and can also be linked to another spacer, of the same formula or different.
  • the insoluble polymer supported reagents to be used in the method of this invention may be prepared by converting a polymeric starting material into a polymer supported reagent in one to four synthetic steps, rinsing thoroughly with one or more solvents after each synthetic step, for example as described in WO-A-9742230. The preparation of the polymer supported reagents starts from known polymers.
  • Polymer supported reagents are made in one to four synthetic steps from readily available starting materials, such as for example, insoluble polymers or derivatives thereof which contain convenient linker functionality, and one or more polyfunctional reagents which bear a compatible connecting functionality and one or more functionalities used in the purification or quenching reaction process.
  • the preferred polymeric starting materials are well-known to those skilled in the art of solid-phase peptide or solid-phase organic synthesis.
  • the present invention also provides polymer supported reagent of the formula I:
  • Rs-Sp-Re I wherein Rs is insoluble polymer selected from polysaccharide resins, cellulose, polysaccharides copolymerized with acrylamide; Re is one or more reagent residues that are capable of selective covalent reaction with unwanted byproducts, or excess reagents; and Sp is one or more chemically robust spacer that join Rs and Re.
  • the reagent residue Re is selected from the group consisting of thiol, hydroxyl , carboxyl, formyl, keto, guanidino, amino groups and derivative thereof as defined above, azlactone and the spacer Sp is as defined above.
  • the starting materials are well-known to or those skilled in the art of purification of bio- molecules. They are commercially available or are known in the scientific literature.
  • Actigel B resin (1 ml, 150 mmoles/1) was washed for 3 times with 0.1 M K 2 CO and incubated with 333 ⁇ l of ethylenediamin (300 mg, 5 mmoles) in 4.5 ml of 0.1 M K 2 CO 3 overnight at 4°C.
  • Actigel B resin (1 ml, 150 mmoles/1) was washed for 3 times with 0.1 M K. 2 CO 3 and incubated with 500 ⁇ l propanedithiol (540 mg, 5 mmoles) in 4.5 ml 0.1 M 2 CO 3 overnight at 4°C.
  • the resin was washed with 0.1 M K 2 CO 3 (3 x 5 ml), PBS (3 x 5 ml) and for storage with PBS /20% ethanol (3 x 5 ml).
  • the supernatant solution was injected in a HP 1090 separation system using a RP-C4 column (Vydac 4.6x250 mm, 30 ⁇ Apore size, 7.5 ⁇ ). The efficiency was monitored by comparing the absorption of the traces at wavelengths of 220 and 280 nm. A reduction of 90% of EZ Link PEO-Biotin could be observed, whereas the recovery of the protein was >90%.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Peptides Or Proteins (AREA)

Abstract

La présente invention concerne un procédé pour la purification de molécules biologiques après modification chimique en utilisant un ou plusieurs réactifs supportés par des polymères. La présente invention concerne plus particulièrement un procédé pour la purification rapide de molécules biologiques marquées en utilisant des réactifs d'extinction supportés sur des polymères insolubles. L'invention concerne également de nouveaux réactifs supportés par des polymères représentés par la formulé suivante (I): Rs-Sp-Re, dans laquelle Rs est un polymère insoluble, Re est un ou plusieurs groupes fonctionnels du réactif, et Sp est un ou plusieurs intercalaires chimiquement cohérents qui réunissent Rs et Re. L'invention concerne enfin un procédé pour leur préparation.
EP03712004A 2002-03-20 2003-03-12 Reactifs supportes par des polymeres pour la purification de produits naturels Withdrawn EP1487862A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP03712004A EP1487862A2 (fr) 2002-03-20 2003-03-12 Reactifs supportes par des polymeres pour la purification de produits naturels

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP02076087 2002-03-20
EP02076087 2002-03-20
EP03712004A EP1487862A2 (fr) 2002-03-20 2003-03-12 Reactifs supportes par des polymeres pour la purification de produits naturels
PCT/EP2003/002635 WO2003078454A2 (fr) 2002-03-20 2003-03-12 Reactifs supportes par des polymeres pour la purification de produits naturels

Publications (1)

Publication Number Publication Date
EP1487862A2 true EP1487862A2 (fr) 2004-12-22

Family

ID=27838102

Family Applications (1)

Application Number Title Priority Date Filing Date
EP03712004A Withdrawn EP1487862A2 (fr) 2002-03-20 2003-03-12 Reactifs supportes par des polymeres pour la purification de produits naturels

Country Status (7)

Country Link
EP (1) EP1487862A2 (fr)
JP (1) JP2005535567A (fr)
AU (1) AU2003218755A1 (fr)
BR (1) BR0308577A (fr)
CA (1) CA2479355A1 (fr)
MX (1) MXPA04009084A (fr)
WO (1) WO2003078454A2 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1660519B1 (fr) * 2003-07-29 2014-05-14 Immunomedics, Inc. Conjugués comprenant le 2-[18F]-fluoro-2-désoxy-D-glucose et une molécule peptidique
IL212911A0 (en) * 2011-05-16 2011-07-31 Omrix Biopharmaceuticals Ltd Immunoglobulin reduced in thrombogenic contaminants and preparation thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0896590A1 (fr) * 1996-05-03 1999-02-17 Warner-Lambert Company Purification rapide par reactifs de refroidissement brusque supportes par des polymeres
JP2003509185A (ja) * 1999-09-13 2003-03-11 バイオタージ インコーポレイテッド 精製装置および精製方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO03078454A3 *

Also Published As

Publication number Publication date
AU2003218755A1 (en) 2003-09-29
BR0308577A (pt) 2005-01-04
WO2003078454A3 (fr) 2004-04-01
JP2005535567A (ja) 2005-11-24
CA2479355A1 (fr) 2003-09-25
WO2003078454A2 (fr) 2003-09-25
MXPA04009084A (es) 2004-12-06

Similar Documents

Publication Publication Date Title
Castro et al. CuAAC: An efficient click chemistry reaction on solid phase
CA3070407C (fr) Procede de modification chimique de surfaces plastiques
US7538192B2 (en) Process for preparing albumin protein conjugated oligonucleotide probes
WO2016165621A1 (fr) Procédé de synthèse en phase solide de bibliothèque chimique codée par adn
EP1397372A1 (fr) Compositions a affinite d'ions metalliques polymeres hydrosolubles et procedes d'utilisation afferents
AU2002315414A1 (en) Water-soluble polymeric metal ion affinity compositions and methods for using the same
JP2012211134A (ja) 糖鎖捕捉物質およびその用途
US7408023B2 (en) Peptoids incorporating chemoselective functionalities
WO2003078454A2 (fr) Reactifs supportes par des polymeres pour la purification de produits naturels
EP4232578A1 (fr) Bibliothèques codées par l'acide nucléique auto-purifié
KR100889587B1 (ko) 기질표면 처리 및 특이적 단백질 고정용 링커분자, 및 그제조방법
JP4689941B2 (ja) 固相合成担体および方法
JP3800245B2 (ja) 新規な機能性ペプチド核酸およびその製法
EP0675898A1 (fr) Utilisation de polymeres imprimes de maniere moleculaire dans la synthese stereospecifique et/ou regioselective
US5874589A (en) Methods for synthesizing diverse collections of tetramic acids and derivatives thereof
WO2021229013A1 (fr) Échafaudages peptidiques, leurs procédés de fabrication et leurs utilisations en tant que supports solubles
WO2023100976A1 (fr) Banque de billes immobilisée par un peptide
JP2004275140A (ja) Ｄｎａ又はｒｎａコンジュゲートの製造方法
WO2006126760A1 (fr) Resine a structure coeur-ecorce ('core-shell') de type gel
HK40030993B (en) Method of chemically modifying plastic surfaces
HK40030993A (en) Method of chemically modifying plastic surfaces
JPH11318488A (ja) 核酸固定化法及び固定化核酸
JP2008106005A (ja) アミノ酸残基又はペプチド残基を有する化合物、及びその製造方法

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20041019

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL LT LV MK

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20060829