Method for preparing peptide fragments, kit for preparing peptide fragments to be used therein, and analysis method

US2020072846A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2020072846-A1
Application numberUS-201916683560-A
CountryUS
Kind codeA1
Filing dateNov 14, 2019
Priority dateSep 9, 2013
Publication dateMar 5, 2020
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method of proteolyzing a protein, including immobilizing a protein in at least one pore of a porous body, and contacting the protein immobilized in the pore and a protease immobilized on a solid surface such that the protease selectively accesses a site of the protein and proteolyzes the protein at the site.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method of proteolyzing a protein, comprising: immobilizing a protein in at least one pore of a porous body; and contacting the protein immobilized in the pore and a protease immobilized on a solid surface such that the protease selectively accesses a site of the protein and proteolyzes the protein at the site. 2 . The method of claim 1 , wherein the solid surface is a surface of at least one particle. 3 . The method of claim 2 , wherein the at least one pore is a plurality of pores, the at least one particle is a plurality of particles, and the plurality of particles has an average particle diameter larger than an average pore diameter of the plurality of pores. 4 . The method of claim 3 , wherein the contacting is performed in a liquid. 5 . The method of claim 1 , wherein the immobilizing comprises immobilizing the protein at a site different from the site of the protein at which the protein is proteolyzed. 6 . The method of claim 1 , wherein the immobilizing comprises immobilizing the protein in the pore through a linker molecule that site-specifically interacts with the protein. 7 . The method of claim 6 , wherein the immobilizing is performed such that the protein having the linker molecule bound thereto has a molecular size which is 0.5 times to 1.5 times greater than the average pore diameter of the pores. 8 . The method of claim 2 , wherein the protease is immobilized on the surface of the particle through a spacer molecule that binds with the protease. 9 . The method of claim 1 , wherein the protein is an antibody. 10 . The method of claim 9 , wherein the antibody is a monoclonal antibody. 11 . The method of claim 4 , wherein the protein is an antibody. 12 . The method of claim 11 , wherein the antibody is a monoclonal antibody. 13 . The method of claim 9 , wherein the immobilizing comprises immobilizing an Fc domain of the antibody, and the contacting is performed such that a Fab domain of the antibody is site-selectively proteolyzed by the protease. 14 . The method of claim 11 , wherein the immobilizing comprises immobilizing an Fc domain of the antibody, and contacting is performed such that a Fab domain of the antibody is site-selectively proteolyzed by the protease. 15 . The method of claim 1 , wherein the protease is trypsin. 16 . The method of claim 4 , wherein the protease is trypsin. 17 . The method of claim 4 , wherein the average particle diameter of the particles is 100 nm or greater and the average pore diameter of the pores is in a range of from 30 nm to 150 nm, provided that the average particle diameter is larger than the average pore diameter. 18 . The method of claim 11 , wherein the average particle diameter of the particles is 120 nm or greater, and the average pore diameter of the pores is in a range of from 50 nm to 100 nm. 19 . The method of claim 18 , wherein the average particle diameter of the particles is 150 nm or greater. 20 . The method of claim 18 , wherein the average particle diameter of the particles is 170 nm or greater. 21 . The method of claim 18 , wherein the average particle diameter of the particles is in a range of from 120 nm to 1 μm. 22 . The method of claim 20 , wherein the average particle diameter of the particles is in a range of from 170 nm to 300 nm.

Assignees

Inventors

Classifications

  • acting on peptide bonds (3.4) · CPC title

  • Trypsin; Chymotrypsin · CPC title

  • Carrier-bound or immobilised peptides (carrier-bound or immobilised enzymes C12N11/00); Preparation thereof · CPC title

  • by hydrolysis {, i.e. solvolysis in general} · CPC title

  • Methods of protein analysis involving laser desorption ionisation mass spectrometry · CPC title

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What does patent US2020072846A1 cover?
A method of proteolyzing a protein, including immobilizing a protein in at least one pore of a porous body, and contacting the protein immobilized in the pore and a protease immobilized on a solid surface such that the protease selectively accesses a site of the protein and proteolyzes the protein at the site.
Who is the assignee on this patent?
Shimadzu Corp
What technology area does this patent fall under?
Primary CPC classification G01N33/6857. Mapped technology areas include Physics.
When was this patent published?
Publication date Thu Mar 05 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).