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Method of thioacylation peptide sequencing with alcoholysis of thiazolinones

Assignee: BIO-AFFINITY SYSTEMS Inc A CORP OF CA
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Filing: 1988-03-10
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Granted: 1989-09-05
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Expires: 2008-03-10
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Abstract

Abstract A sequencing method which exploits the thioacylation degradation of polypeptides and proteins is disclosed. The process involves reaction of the N-terminal amino acid of a polypeptide with an excess of a thioacylating reagent. After sufficient time to insure quantitative coupling and removal of excess reagent, the N-thioacyl polypeptide is subjected to cleavage by acid which affords a 2-substituted-5(4H)-thiazolinone of the N-terminal amino acid. Subsequent addition of a large excess of an aliphatic primary or secondary alcohol, either directly to the cleavage acid or after its removal, yields the corresponding N-thioacyl amino acid ester, a stable compound suitable for chromatographic separation and subsequent detection by contemporary methods of high pressure liquid chromatography.

Inventors

  • 👤 Mark L. Stolowitz
  • 👤 Beth A. Paape
  • 👤 Anne E. DeVaux

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 17:47
CPC Classifications
G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/68; G01N33/6803; G01N33/6842; C; C07; C07K; C07K1/00; C07K1/12; C07K1/122; C07K1/128; G01N33/6818; G01N33/6824; Y; Y10; Y10T; Y10T436/00; Y10T436/14; Y10T436/141111

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 163 words
A method for determining the identity of an N-terminal amino acid of a polypeptide comprising the steps of: (a) providing a starting polypeptide having an N-terminal amino acid; (b) reacting said polypeptide with a thioacylating reagent of the form X-C(S)W wherein X is aryl or aryl-alkyl and W is a leaving group, to form a compound having the formula IV, wherein R represents an amino acid side chain and -(peptide) represents the starting peptide, not including the N-terminal amino acid; ##STR7## (c) cleaving the compound of formula IV with a volatile anhydrous acid to form a residual polypeptide, which comprises the starting polypeptide with the N-terminal amino acid removed, and a 2-substituted-5(4H)-thiazolinone compound of general formula V; ##STR8## (d) reacting the compound of general formula V with an aliphatic primary or secondary alcohol to yield a corresponding N-thioacyl amino acid ester of general formula VI wherein R' is an alkyl substituent; ##STR9## (e) identifying the N-thioacyl amino acid ester of general formula VI.
Claim 2
Independent Claim 163 words
A method for determining the identity of an N-terminal amino acid of a polypeptide comprising the steps of: (a) providing a starting polypeptide having an N-terminal amino acid; (b) reacting said polypeptide with a thioacylating reagent of the form X-C(S)W wherein X is aryl or aryl-alkyl and W is a leaving group, to form a compound having the formula IV, wherein R represents an amino acid side chain and -(peptide) represents the starting peptide, not including the N-terminal amino acid; ##STR7## (c) cleaving the compound of formula IV with a volatile anhydrous acid to form a residual polypeptide, which comprises the starting polypeptide with the N-terminal amino acid removed, and a 2-substituted-5(4H)-thiazolinone compound of general formula V; ##STR8## (d) reacting the compound of general formula V with an aliphatic primary or secondary alcohol to yield a corresponding N-thioacyl amino acid ester of general formula VI wherein R' is an alkyl substituent; ##STR9## (e) identifying the N-thioacyl amino acid ester of general formula VI.
Claim 3
Dependent Claim 18 words
The method of claim 1 wherein said polypeptide is immobilized on a solid support prior to step b.
Claim 4
Dependent Claim 32 words
The method of claim 1, wherein said thioacylating reagent is selected from the group consisting of X-C(S)SR', X-C(S)OR' and X-C(S)NR'R" wherein R' and R" are alkyl, aryl, acyl or substituted derivatives thereof.
Claim 5
Dependent Claim 25 words
The method of claim 3 wherein said thioacylating reagent is selected from the group consisting of carboxymethyl dithiobenzoic acid, cyanomethyl dithiobenzoate and carboxymethyl dithiophenylacetic acid.
Claim 6
Dependent Claim 16 words
The method of claim 1 wherein step b occurs in the presence of excess thioacylating reagent.
Claim 7
Dependent Claim 15 words
The method of claim 5 further comprising removing excess thioacylating reagent prior to step c.
Claim 8
Dependent Claim 25 words
The method of claim 1 wherein step b occurs in the presence of an acid scavenger in an alkaline aqueous solvent or an anhydrous solvent.
Claim 9
Dependent Claim 13 words
The method of claim 1 wherein said volatile anhydrous acid is trifluoroacetic acid.
Claim 10
Dependent Claim 27 words
The method of claim 1 further comprising separating the compound of formula V from said residual polypeptide and separating said acid from said compound of formula V.
Claim 11
Dependent Claim 24 words
The method of claim 1 wherein said aliphatic primary or secondary alcohol is selected from the group consisting of methanol, ethanol, 2-propanol and n-propanol.
Claim 12
Dependent Claim 14 words
The method of claim 10 wherein said aliphatic primary or secondary alcohol is methanol.
Claim 13
Dependent Claim 13 words
The method of claim 1 wherein X is phenyl, m-nitrophenyl, benzyl or p-nitrobenzyl.
Claim 14
Dependent Claim 9 words
The method of claim 12 wherein X is phenyl.

References Cited (Backward Citations)

US3975155A Cited
US4110378A Cited
US4548904A Cited
US4652530A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1992-09-04 1993-03-06 1993-09-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1996-09-04 1997-03-06 1997-09-05 $3760.00 Window Closed / Lapsed
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