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A method and apparatus for the sequential degradation of protein or peptide molecules by successive coupling and cleavage reactions. Such molecules are immobilized on a macroporous reaction support surface and placed in a flowthrough reaction chamber which is mounted in a sequencer. In the Edman sequencing technique, reagents driven by pressurized inert gas are passed through the reaction chamber as follows: (a) liquid or vapor coupling reagent, (b) coupling base vapor, (c) washing solvent, (d) inert gas to partially dry the support surface, (e) cleavage reagent vapor to cleave amino acid derivatives from the immobilized coupled protein or peptide chains, (f) liquid extracting solvent to withdraw the cleaved amino acid derivative. An automated sequencer to carry out said method.

InventorWilliam J. Dreyer
Original AssigneeDurrum Instrument Corporation
Current U.S. Classification525/54.1; 422/129; 436/89; 525/54.11; 530/345; 930/10; 930/DIG.621
International Classification: C08L 3700

View patent at USPTO
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Citations

Cited PatentFiling dateIssue dateOriginal AssigneeTitle
US3725010Apr 8, 1969Apr 3, 1973APPARATUS FOR AUTOMATICALLY PERFORMING CHEMICAL PROCESSES

Referenced by

Citing PatentFiling dateIssue dateOriginal AssigneeTitle
US4155714Mar 31, 1978May 22, 1979Process and apparatus for conversion of atz to pth amino acid derivatives of proteins
US4552922Jun 24, 1983Nov 12, 1985Yeda Research & Development Co. Ltd.Method for multipolymer synthesis of organic compounds
US4603114Apr 20, 1984Jul 29, 1986California Institute of TechnologyMethod for the sequential performance of chemical processes
US4610847Apr 23, 1984Sep 9, 1986California Institute of TechnologyConversion flask for sequential performance apparatus
US4665037Apr 28, 1986May 12, 1987Analytichem International, Inc.Method of sequencing peptides
US4668476Mar 23, 1984May 26, 1987Applied Biosystems, Inc.Automated polypeptide synthesis apparatus
US4698208Jun 10, 1985Oct 6, 1987Yeda Research and Development Co., Ltd.Apparatus for multipolymer synthesis of organic compounds
US4701419Nov 26, 1985Oct 20, 1987M-Scan LimitedAnalysis of polymeric protein and protein products
US4704256Nov 10, 1982Nov 3, 1987California Institute of TechnologyApparatus for the sequential performance of chemical processes
US4746490Feb 6, 1986May 24, 1988Solid phase peptide synthesizer
US4816513May 22, 1987Mar 28, 1989Applied Biosystems, Inc.Automated polypeptide synthesis process
US4837165Apr 20, 1988Jun 6, 1989Beckman Research Institute, City of HopeMethod for sequencing of peptides by carboxyl terminus degradation
US4861726Mar 10, 1988Aug 29, 1989Bio-Affinity Systems, Inc.Method of thioacylation peptide sequencing with acylation of thiazoloinones
US4861866Jan 21, 1987Aug 29, 1989Eldex Laboratories, Inc.Continuous flow peptide synthesizer
US4865994Apr 19, 1988Sep 12, 1989Seiko Instruments & Electronics Ltd.Detection method for amino acid derivatives
US5008372Feb 12, 1990Apr 16, 1991Cornell Research Foundation, Inc.Deblocking amino terminal N-acetyl serine and N-acetyl threonine residues in peptides and proteins to allow sequencing
US5011861Jun 28, 1988Apr 30, 1991Millipore CorporationMembranes for solid phase protein sequencing
US5039488Sep 4, 1990Aug 13, 1991Genentech, Inc.Devices for amino acid sequence determination
US5053454Feb 15, 1989Oct 1, 1991SRI InternationalMultiple polymer synthesizer
US5082788Aug 22, 1989Jan 21, 1992Porton Instruments, Inc.Method of sequencing peptides and proteins using a valve block assembly
US5147608Apr 29, 1988Sep 15, 1992Millipore CorporationApparatus and process for performing repetitive chemical processing
US5156809Sep 16, 1991Oct 20, 1992Hewlett Packard CompanyApparatus for the stepwise performance of chemical reactions
US5223435Oct 25, 1991Jun 29, 1993Genetech, Inc.Amino acid sequence determination with mobile peptide
US5254476Jun 5, 1992Oct 19, 1993Millipore CorporationMethod and system for analysis of peptides and proteins
US5316034Jan 14, 1992May 31, 1994Porton Instruments, Inc.Valve block assembly
US5334536Jun 12, 1992Aug 2, 1994Apparatus for the photometric determination of gas concentrations
US5431882Nov 19, 1993Jul 11, 1995Shimadzu CorporationApparatus for collecting peptide fragment
US5516698Apr 30, 1992May 14, 1996Ludwig Institute For Cancer ResearchMethods and apparatus allowing sequential chemical reactions
US5604298Dec 7, 1995Feb 18, 1997In USA, Inc.Gas measurement system
US5605839May 29, 1992Feb 25, 1997Ludwig Institute for Cancer ResearchMethods and apparatus for use in sequential chemical reactions
US5824556Jun 11, 1997Oct 20, 1998Peptide mass ladders generated using carbon disulfide
US6277644Mar 22, 1999Aug 21, 2001Beckman Coulter, Inc.Method for compositional tag sequencing

Claims

1. In a method for the sequential degradation of protein or peptide chains in a reaction chamber by successive coupling and cleavage reactions, the steps of:

a. immobilizing said protein or peptide on a macroporous reaction support surface disposed in the reaction chamber, said immobilization being performed either by nonchemical sorptive deposition onto said support surface or by chemical linkage to said support surface,
b. passing coupling reagent through the reaction chamber to contact said immobilized protein or peptide,
c. directing a pressurized vapor stream comprising coupling base vapor through the reaction chamber while said coupling reagent is in contact with said protein or peptide to provide basic environment for coupling of said coupling reagent to said chains,
d. flowing a liquid washing solvent through the reaction chamber to remove unreacted coupling reagent and other contaminants from the support surface,
e. directing a pressurized stream of inert carrier gas through the reaction chamber after step (d) to at least partially dry said support surface,
f. directing a pressurized vapor stream comprising cleavage reagent vapor through the reaction chamber for sufficient time to cleave amino acid derivatives from said coupled protein or peptide, and
g. flowing a liquid extracting solvent through the reaction chamber after step (f) to extract and withdraw said cleaved amino acid derivative.

2. The method of claim 1 in which the washing solvent is delivered to the reaction chamber under pressure from a source of pressurized gas.

3. The method of claim 1 in which the extracting solvent is delivered to the reaction chamber under pressure from a source of pressurized gas.

4. In a method for the sequential degradation of protein or peptide chains in a reaction chamber by successive coupling and cleavage reactions, the steps of:

a. immobilizing the protein or peptide on a macroporous reaction support surface disposed in the reaction chamber, said immobilization being performed either by nonchemical sorptive deposition onto said support surface or by chemical linkage to said support surface,
b. passing coupling reagent in liquid form through the reaction chamber to contact and deposit on said immobilized protein or peptide chains, and
c. directing a pressurized vapor stream comprising coupling base vapor through the reaction chamber while said protein or peptide chains are wet with coupling reagent liquid to provide a basic environment for coupling of said coupling reagent to said immobilized protein or peptide.

5. The method of claim 3 in which said pressurized vapor stream comprises coupling base vapor entrained in an inert carrier gas.

6. The method of claim 5 in which said coupling base is entrained in said carrier gas stream by bubbling said gas stream through a reservoir of said coupling base in liquid form.

7. The method of claim 6 in which said coupling reagent is urged through said reaction chamber in a liquid stream under pressure from a source of gas pressure.

8. The method of claim 3 in which said immobilization of step (a) is performed by nonchemical sorptive deposition of said chains.

9. The method of claim 3 in which said immobilization of step (a) is performed by chemical linkage of said chains to said reaction support surface.

10. The method of claim 3 together with the following step after step (c):

d. passing a pressurized vapor stream comprising cleavage reagent vapor through the reaction chamber for sufficient time to cleave amino acid derivatives from said coupled protein or peptide chains.

11. The method of claim 9 together with the following steps performed between steps (c) and (d):

e. flowing a liquid washing solvent through the reaction chamber to remove unreacted coupling reagent and other contaminants from said surface,
f. directing a pressurized stream of inert carrier gas through the reaction chamber after step (e) for sufficient time to at least partially dry said reaction support surface.

12. The method of claim 3 in which said support surface is formed of a material selected from the group consisting of macroreticular cross-linked polystyrene and its derivatives and macroporous glass and its derivatives.

13. The method of claim 3 in which said reaction chamber is detachably disposed in an apparatus during performance of steps (b) and (c), and said peptides or proteins are immobilized on said reaction support surface in said reaction chamber prior to disposition of the same in said apparatus.

14. In a method for the sequential degradation of protein or peptide chains in a reaction chamber by successive coupling and cleavage reactions, the steps of:

a. immobilizing said peptide or protein chains on a macroporous reaction support surface disposed in the reaction chamber, said immobilization being performed either by nonchemical sorptive deposition onto said support surface or by chemical linkage to said support surface,
b. chemically coupling a coupling reagent to said protein or peptide chains,
c. passing a pressurized vapor stream comprising cleavage reagent vapor through the reaction chamber for sufficient time to cleave amino acid derivatives from said coupled protein or peptide chains, and
d. flowing a liquid extracting solvent through the reaction chamber to extract and withdraw said cleaved amino acid derivatives.

15. The method of claim 14 in which said pressurized vapor stream comprises cleavage reagent vapor entrained in an inert carrier gas.

16. The method of claim 13 in which said cleavage reagent is entrained in said carrier gas stream by bubbling said gas stream through a reservoir of said cleavage reagent in liquid form.

17. The method of claim 12 in which said immobilization of step (a) is performed by nonchemical sorptive deposition of said protein or peptide chains onto said support surface.

18. The method of claim 12 in which said immobilization of step (a) is performed by chemical linkage of said protein or peptide chains to said support surface.

19. The method of claim 12 in which the cleavage reagent is an anhydrous acid.

20. The method of claim 18 in which said extracting solvent is delivered to said reaction chamber under pressure from a source of pressurized inert gas.

21. The method of claim 12 together with the following steps performed between steps (b) and (c):

e. flowing a liquid washing solvent through the reaction chamber to remove unreacted coupling reagent and other contaminants from said support surface, and
f. directing a pressurized stream of inert carrier gas through the reaction chamber to at least partially dry said support surface.

22. The method of claim 21 in which said extracting solvent is delivered to said reaction chamber under pressure from a source of pressurized gas.

23. The method of claim 12 in which said support surface is formed of a material selected from the group consisting of macroreticular cross-linked polystyrene and its derivatives and macroporous glass and its derivatives.

24. The method of claim 12 in which said reaction surface comprises the surface of a bed of particles disposed in the path of said pressurized vapor stream flowing through the reaction chamber.

25. The method of claim 12 in which said reaction chamber is detachably disposed in an apparatus during performance of steps (b) and (c), and said protein or peptide chains are immobilized on said reaction support surface in said reaction chamber prior to disposition of the same in said apparatus.

26. In a method for the sequential degradation of protein or peptide chains in a reaction chamber by successive coupling and cleavage reactions, the steps of:

a. immobilizing said protein or peptide chains on a macroporous surface in said chamber by nonchemical sorptive deposition,
b. chemically coupling a coupling reagent to said protein or peptide chains in the presence of a coupling base, and
c. directing a cleavage reagent through the reaction chamber for sufficient time to cleave amino acid derivative from said coupled protein or peptide chains, and
d. flowing a liquid extracting solvent through the reaction chamber to extract and withdraw said cleaved amino acid derivative.

27. The method of claim 26 in which coupling base is directed through said reaction chamber in vapor form while the protein or peptide chains are wet with coupling reagent liquid.

28. The method of claim 23 in which step (c) is performed by passing through the reaction chamber a pressurized vapor stream comprising cleavage reagent vapor.

29. The method of claim 26 in which said pressurized vapor stream comprises said cleavage reagent vapor entrained in an inert carrier gas.