Microscale immobilized enzyme reactors in proteomics: Latest developments

被引:74
作者
Safdar, Muhammad [1 ]
Spross, Jens [2 ]
Jaenis, Janne [1 ]
机构
[1] Univ Eastern Finland, Dept Chem, FI-80101 Joensuu, Finland
[2] Univ Bielefeld, Dept Chem, Inst Organ Chem 1, D-33615 Bielefeld, Germany
关键词
Proteomics; Microfluidics; Enzyme reactor; Enzyme immobilization; Miniaturization; Monolith; PHASE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; EFFICIENT PROTEIN DIGESTION; ORGANIC POLYMER MONOLITHS; STRONG CATION-EXCHANGE; TRYPSIN REACTOR; GRAPHENE OXIDE; MACROPOROUS POLYMER; STATIONARY PHASES; SEPARATION MEDIA;
D O I
10.1016/j.chroma.2013.11.045
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Enzymatic digestion of proteins is one of the key steps in proteomic analyses. There has been a steady progress in the applied digestion protocols in the past, starting from conventional time-consuming in-solution or in-gel digestion protocols to rapid and efficient methods utilizing different types of microscale enzyme reactors. Application of such microreactors has been proven beneficial due to lower sample consumption, higher sensitivity and straightforward coupling with LC-MS set-ups. Novel stationary phases, immobilization techniques and device formats are being constantly developed and tested to optimize digestion efficiency of proteolytic enzymes. This review focuses on the latest developments associated with the preparation and application of microscale enzyme reactors for proteomics applications since 2008 onwards. A special attention has been paid to the discussion of different stationary phases applied for immobilization purposes. (C) 2013 Elsevier B.V. All rights reserved.
引用
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页码:1 / 10
页数:10
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