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. 22, 2022

Filed:

Aug. 18, 2017
Applicant:

Public University Corporation Yokohama City University, Yokohama, JP;

Inventors:

Yuki Ohta, Yokohama, JP;

Nana Kawasaki, Yokohama, JP;

Daisuke Takakura, Yokohama, JP;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N 33/68 (2006.01); C07K 16/00 (2006.01); C12Q 1/44 (2006.01); G01N 30/72 (2006.01); G01N 30/86 (2006.01); H01J 49/00 (2006.01); G01N 30/02 (2006.01);
U.S. Cl.
CPC ...
G01N 33/6848 (2013.01); C07K 16/00 (2013.01); C12Q 1/44 (2013.01); G01N 30/7233 (2013.01); G01N 30/8696 (2013.01); H01J 49/004 (2013.01); H01J 49/0031 (2013.01); C07K 2317/41 (2013.01); G01N 2030/027 (2013.01); G01N 2400/00 (2013.01); G01N 2440/38 (2013.01);
Abstract

Disclosed is a novel means for accurate qualitative and quantitative analyses for each N-glycosylation site. The method of analyzing N-linked sugar chain(s) of glycoprotein according to the present invention comprises: treating a part of a glycopeptide-containing sample to be analyzed with endo-β-N-acetylglucosaminidases to cleave off sugar chains while leaving one GlcNAc of the chitobiose core on the Asn at the N-glycosylation site; subjecting the obtained sugar chain-cleaved sample to preliminary liquid chromatography/mass spectrometry; predicting the retention time of the glycopeptide of interest and the mass-to-charge ratio (m/z) of the precursor ion in main analysis based on the results of the preliminary liquid chromatography/mass spectrometry; and carrying out the main analysis. By this method, the binding sites and structures of N-linked sugar chains in a glycoprotein can be analyzed. By using the sugar chain-cleaved sample as an internal standard in the main analysis, quantitative analysis of sugar chains at each glycosylation site also becomes possible.


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