Preparation and application of immobilized enzymatic reactors for consecutive digestion with two enzymes

被引:11
作者
Wang, Bingbing [1 ]
Shangguan, Lulu [1 ]
Wang, Shulei [1 ]
Zhang, Lingyi [1 ,2 ]
Zhang, Weibing [1 ]
Liu, Fan [2 ]
机构
[1] East China Univ Sci & Technol, Shanghai Key Lab Funct Mat Chem, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
[2] Nanchang Univ, Ctr Anal & Testing, Nanchang 330047, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Immobilized enzymatic reactor (IMER); Consecutive proteolytic digestion; Complex protein samples; Enzymatic characteristics; EFFICIENT SAMPLE PREPARATION; MASS-SPECTROMETRY; GRAPHENE OXIDE; TRYPSIN IMMOBILIZATION; PROTEOLYTIC DIGESTION; ALPHA-CHYMOTRYPSIN; SEQUENCE COVERAGE; HYBRID MONOLITH; BOTTOM-UP; NANOPARTICLES;
D O I
10.1016/j.chroma.2016.11.027
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The bottom up strategy has drawn much attention due to the high accuracy, reliability, and reproducibility in protein identification in which proteins are digested into peptides. However, conventional solution based digestion and enzymatic reactor with one protease immobilized cannot satisfy high throughput proteolysis of complex samples. Application of consecutive hydrolysis by enzymatic reactor can be anew strategy for high throughput proteolysis of complex samples by adjusting immobilization amount of the enzymes, enzyme ratio, as well as hydrolysis order of two enzymes. In this work, we propose immobilized enzymatic reactor for consecutive digestion with two enzymes by combining two enzyme reactors with trypsin and chymotrypsin immobilized, respectively. Each reactor was prepared individually by immobilizing only one protease (trypsin or chymotrypsin) to hybrid monolith with SBA-15 particles embedded. Proteolysis conditions including hydrolysis order and trypsin to chymotrypsin ratio etc. were studied using standard proteins. Best digestion performance was obtained when the proteins were digested by trypsin first with trypsin to chymotrypsin ratio of 1:1. When applying them to digestion of rat liver proteins, total 1651 proteins and 11011 peptides were identified by combining four enzymolysis strategies with two enzymes including proteolytic digestion in two consecutive enzymatic reactors, synergy enzymolysis with two enzymes in one immobilized enzymatic reactor and consecutive hydrolysis with two enzymes in-solution digestion respectively, in which consecutive enzymolysis in enzymatic reactors gave the best results with 1091 proteins and 5071 peptides identified. The reactors showed good digestion capability for proteins with different hydrophobicity and molecular weights, and will play an important role in high efficient and high throughput proteomics research. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:22 / 29
页数:8
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