The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 13, 2007

Filed:

Oct. 06, 2004
Applicants:

Takashi Nakazawa, Nara, JP;

Minoru Yamaguchi, Kyoto, JP;

Hiroki Kuyama, Kyoto, JP;

Eiji Ando, Kyoto, JP;

Norikazu Ueyama, Osaka, JP;

Taka-aki Okamura, Osaka, JP;

Shigemi Norioka, Ibaraki, JP;

Inventors:

Takashi Nakazawa, Nara, JP;

Minoru Yamaguchi, Kyoto, JP;

Hiroki Kuyama, Kyoto, JP;

Eiji Ando, Kyoto, JP;

Norikazu Ueyama, Osaka, JP;

Taka-aki Okamura, Osaka, JP;

Shigemi Norioka, Ibaraki, JP;

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07K 1/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

A simple and low-cost method of selectively modifying the C-terminal of a protein or peptide is provided. A method of modifying the C-terminal of a protein or peptide comprises forming an intramolecular oxazolone ring at the C-terminal of the protein or peptide that requires C-terminal modification, and then performing a ring-opening of the oxazolone ring to produce a protein or peptide with a modified C-terminal. Preferred forms include a method in which by reacting the oxazolone ring with a compound containing a nucleophilic group to effect an oxazolone ring-opening, a protein or peptide is produced in which the C-terminal is modified with the compound containing the nucleophilic group, as well as a method in which by reacting the oxazolone ring with an active esterifying agent to effect a ring-opening, the oxazolone is converted to an active ester, which by subsequent reaction with a compound containing a nucleophilic group, produces a protein or peptide in which the C-terminal has been modified with the compound containing the nucleophilic group.


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