Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of polymer microsphere and its preparation and application

A polymer and microsphere technology, applied in the field of glycoprotein enrichment, can solve the problems of low efficiency of post-modification grafting strategy, cumbersome steps, unfavorable pretreatment of large-scale protein samples, etc., to achieve selective enrichment and reaction efficiency High, clean effect of polymer particles

Active Publication Date: 2017-02-08
DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the adopted post-modification grafting strategy is inefficient and the steps are extremely cumbersome
Some studies have prepared boric acid functionalized monolithic columns by means of copolymerization (L Ren, Y Liu, M Dong, Z. Liu. J. Chromatogr. A. 2009, 1216, 8421-8425; Z Lin, J Pang, H Yang , Z Cai, L Zhang, G.Chen, Chem.Commun.2011, 47, 9675-9677; Y Liu, L Ren, Z Liu.Chem.Commun.2011, 47, 5067-5069), although the boronic acid bonding efficiency Improvement and good glycoprotein enrichment effect, but the limitation of the column capacity of the monolithic column itself makes this kind of material unfavorable for the pretreatment of large-scale protein samples

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of polymer microsphere and its preparation and application
  • A kind of polymer microsphere and its preparation and application
  • A kind of polymer microsphere and its preparation and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] 1. Preparation of monodisperse core-shell polymer nanoparticles

[0023] In a 150 mL round bottom flask, add 80 mL of acetonitrile, add 105 mg of methacrylic acid (MAA), 755 mg of N, N'-methylenebisacrylamide (MBAA) and 17 mg of azobisisobutyronitrile (AIBN), and sonicate for 1 minute , so that the added reagents were dissolved to form a uniform solution, a Dean-Stark receiver was mounted on the flask, and a condenser was connected to it, after which nitrogen gas was passed for 15 minutes, a magnetic stirrer was added, and the magnetic stirrer was maintained at a speed of 300 rad / min. The reaction device was placed in an oil bath and heated evenly and slowly, and the reactor rose from room temperature to 115° C. within 30 minutes. Under the condition of maintaining 115° C., half of the solvent in the reaction system was distilled off within 2 hours, the reaction was stopped, and cooled to room temperature. Then use a high-speed centrifuge to centrifuge at a speed of 10...

Embodiment 2

[0028] Glycoprotein (horseradish peroxidase, HRP) and non-glycoprotein (bovine serum albumin, BSA) were mixed at a mass ratio of 1:1, and dissolved in 50 mM ammonium bicarbonate buffer solution (pH9.0), thereby A protein mixture solution with a concentration of 100 ng / μL was prepared.

[0029] Weigh 1 mg of the poly(MBAA-co-MAA)@(MBAA-co-APBA) core-shell polymer nanoparticles prepared in Example 1, disperse them in 200 μL of the above protein solution, and incubate at room temperature for 2 hours, Centrifuge after the reaction, and save the supernatant for identification by mass spectrometry. The material was washed several times with 50mM ammonium bicarbonate buffer solution (pH9.0), and the supernatant was discarded by centrifugation. Add 20 μL of acetonitrile:water:trifluoroacetic acid mixed solution with a volume ratio of 50:49:1 to the separated material, incubate at room temperature for 1 hour, and centrifuge to remove the enriched product. The protein stock solution, ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
particle diameteraaaaaaaaaa
particle diameteraaaaaaaaaa
particle diameteraaaaaaaaaa
Login to View More

Abstract

The invention relates to a polymer nanoparticle with monodisperse core-shell structure and its preparation and application. The polymer particles prepared by polymerization of monoene functional monomers and polyene crosslinking monomers are used as the core, and then 3-acrylamidophenylboronic acid is coated on the surface of the core by reversible addition-fragmentation chain transfer (RAFT) polymerization technology (APBA) and polyene cross-linked monomers to form polymer nanoparticles with a smooth surface and a core-shell structure with boric acid functional groups. The present invention introduces phenylboronic acid functional groups on the surface of the material through the RAFT method, which not only overcomes the shortcomings of traditional post-modification methods such as cumbersome steps, low reaction efficiency, and unstable product morphology during direct polymerization, but also enables APBA to polymerize more stably and improve the surface Amount of boric acid bonded. The polymer nanoparticle of the present invention can be used for separating or enriching glycoproteins with 1,2-cis-diol structure, and has good practical value and application prospect in the fields of proteomics and the like.

Description

technical field [0001] The invention relates to enriching glycoproteins, in particular to a monodisperse core-shell structure polymer nanoparticle and its preparation and application in glycoprotein enrichment. Background technique [0002] With the end of human genome sequencing, proteomics has gradually become the focus of attention. As we all know, the composition of proteins is extremely complex and constantly changing in organisms, even in different cells of the same species or in different stages of the same cell, there are significant differences in the composition of proteins. Among these proteins, post-translational modified proteins often become hot spots and difficulties in proteomics research due to their low abundance and complexity. [0003] As a class of important post-translational modification proteins, glycoproteins play an important role in biological processes such as signal transduction, immunity and tumorigenesis. Therefore, the discovery and identifi...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C08F267/10C08F222/38C08F220/58C08F220/06B01J20/26B01D15/08G01N1/28G01N1/40C07K1/14C12N9/08
Inventor 张丽华刘键熙杨开广曲焱焱张玉奎
Owner DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products