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:
May. 09, 2017

Filed:

Apr. 24, 2013
Applicant:

Livzon Mabpharm Inc., Zhuhai, Guangdong, CN;

Inventors:

Baoguo Zhu, Guangdong, CN;

Yucai Peng, Guangdong, CN;

Jiaming Yang, Guangdong, CN;

Assignee:

LIVZON MABPHARM INC., Zhuhai, Guangdong Province, CN;

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N 33/68 (2006.01); G01N 30/06 (2006.01); G01N 30/72 (2006.01); G01N 30/88 (2006.01); G01N 30/02 (2006.01);
U.S. Cl.
CPC ...
G01N 33/6848 (2013.01); G01N 30/06 (2013.01); G01N 30/7233 (2013.01); G01N 33/6854 (2013.01); G01N 2030/027 (2013.01); G01N 2030/065 (2013.01); G01N 2030/067 (2013.01); G01N 2030/8831 (2013.01); G01N 2440/38 (2013.01); G01N 2560/00 (2013.01); Y10T 436/24 (2015.01);
Abstract

The present invention provides a method for determining glycosylation and terminal modifications of immunoglobulin during immunoglobulin purification process, which can simultaneously and rapidly determine glycosylation, N-terminal pyroglutamination and C-terminal de-lysination of immunoglobulin, including Step 1) separating immunoglobulin by using cation-exchange resin, and collecting different components in according to retention time; Step 2) denaturing the components of immunoglobulin obtained in step 1) with a denaturant, followed by reducing them with a reducing agent, to separate the light chain and heavy chain; Step 3) separating the light chain and heavy chain of immunoglobulin of step 2) by using reverse phase ultrahigh pressure liquid chromatography; Step 4) measuring the molecular weights of the light chain and heavy chain obtained in step 3) with mass spectrum; and Step 5) analyzing the chromatographic data obtained in step 3) and the mass spectrometric data obtained in step 4) to determine glycosylation and terminal modifications of the immunoglobulin.


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