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US5049507A
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Method of C-terminal peptide sequencing
Assignee: Applied Biosystems LLC
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Filing: 1989-12-21
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Granted: 1991-09-17
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Expires: 2009-12-21
Abstract
Abstract A method of C-terminal peptide sequencing. The peptide is reacted with a mixed anhydride of isothiocyanic acid and a carboxylic, carbonic, or sulfonic acid, under basic conditions, to produce a C-terminal peptidyl thiohydantoin. The C-terminal amino acid can be identified by cleaving the thiohydantoin from the peptide and identifying the free amino acid thiohydantoin.
Inventors
- 👤 David H. Hawke
- 👤 Victoria L. Boyd
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-10 01:35
CPC Classifications
C; C07; C07K; C07K1/00; C07K1/12; C07K1/122; C07K1/10; C07K1/128; G; G01; G01N; G01N33/00; G01N33/48; G01N33/50; G01N33/68; G01N33/6803; G01N33/6818; G01N33/6821
Claims Analysis
Total Claims: 15
Claim 1
Independent Claim
117 words
A method of determining the C-terminal amino acid residue of a peptide, comprising reacting the peptide with a mixed anhydride of isothiocyanic acid and an acid selected from the group consisting of carboxylic, carbonic, and sulfonic acid, under basic conditions in which the C-terminal acid group of the amino acid is deprotonated, to form a peptidyl thiohydantoin in which the C-terminal amino acid has been converted to a C-terminal amino acid thiohydantoin which is linked to the next-in amino acid in the peptide through an amide bond, treating the peptidyl thiohydantoin under conditions effective to cleave said amide bond, thereby releasing a C-terminal amino acid thiohydantoin and a reduced-length peptide, and identifying the released amino acid thiohydantoin.
Claim 2
Independent Claim
117 words
A method of determining the C-terminal amino acid residue of a peptide, comprising reacting the peptide with a mixed anhydride of isothiocyanic acid and an acid selected from the group consisting of carboxylic, carbonic, and sulfonic acid, under basic conditions in which the C-terminal acid group of the amino acid is deprotonated, to form a peptidyl thiohydantoin in which the C-terminal amino acid has been converted to a C-terminal amino acid thiohydantoin which is linked to the next-in amino acid in the peptide through an amide bond, treating the peptidyl thiohydantoin under conditions effective to cleave said amide bond, thereby releasing a C-terminal amino acid thiohydantoin and a reduced-length peptide, and identifying the released amino acid thiohydantoin.
Claim 3
Dependent Claim
21 words
The method of claim 1, wherein said mixed anhydride has the form: ##STR4## where R is an alkyl or aryl group.
Claim 4
Dependent Claim
13 words
The method of claim 2, wherein said mixed anhydride is a benzoyl isothiocyanate.
Claim 5
Dependent Claim
13 words
The method of claim 1, wherein said mixed anyhydride is an alkyl acylisothiocyanate.
Claim 6
Dependent Claim
16 words
The method of claim 1, wherein said reacting is carried out in the presence of pyridine.
Claim 7
Dependent Claim
28 words
The method of claim 1, wherein said reacting is carried out at a temperature between about 50°-70° C., for a reaction time between about 10 and 60 minutes.
Claim 8
Dependent Claim
21 words
The method of claim 1, wherein said treating is carried out in a 5-10 % solution of trialkyl amine in acetonitrile.
Claim 9
Dependent Claim
27 words
The method of claim 1, wherein said treating is carried out in a 5-15 % solution of tripropylamine in acetonitrile for about 15 minutes at room temperature.
Claim 10
Dependent Claim
49 words
The method of claim 1, wherein said peptide is attached at a non C-terminal residue to a solid support, and which further includes repeating said reacting, treating and identifying steps one or more times to identify the sequence of amino acids in the peptide, from the C-terminal peptide end.
Claim 11
Dependent Claim
50 words
The method of claim 9, which is carried out in an automated fashion, by alternately and successively exposing the solid support to (i) a fresh solution of the mixed anhydride in a basic solution, and (ii) fresh treating solution, and isolating the amino acid released into each successive treating solution.
Claim 12
Independent Claim
66 words
A method of producing a thiohydantoin (TH) of a protected amino acid having a free carboxylic acid group, comprising contacting the amino acid in solution with a mixed anhydride of isothiocyanic acid and carboxylic, carbonic or sulfonic acid, under basic conditions in which the carboxylic acid group of the amino acid is deprotonated, and by said contacting, forming the TH of the amino acid in solution.
Claim 13
Independent Claim
66 words
A method of producing a thiohydantoin (TH) of a protected amino acid having a free carboxylic acid group, comprising contacting the amino acid in solution with a mixed anhydride of isothiocyanic acid and carboxylic, carbonic or sulfonic acid, under basic conditions in which the carboxylic acid group of the amino acid is deprotonated, and by said contacting, forming the TH of the amino acid in solution.
Claim 14
Dependent Claim
23 words
The method of claim 11, wherein the mixed anhydride has the form: ##STR5## where A is an alkyl, alkoxyl, aryl or aryloxy group.
Claim 15
Dependent Claim
15 words
The method of claim 11, wherein said contacting is performed in the presence of pyridine.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1994-09-16 | 1995-03-18 | 1995-09-17 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1998-09-16 | 1999-03-18 | 1999-09-17 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2002-09-16 | 2003-03-18 | 2003-09-17 | $7700.00 | Window Closed / Lapsed |