Comparison of protein characterization using In solution and S-Trap digestion methods for proteomics

被引:12
作者
Bang, Geul [1 ,2 ]
Lee, Hayoung [1 ,3 ]
Kim, Hyejin [1 ]
Han, Eun Hee [1 ]
Park, Youngja Hwang [2 ]
Kim, Jin Young [1 ]
机构
[1] Korea Basic Sci Inst, Res Ctr Bioconvergence Anal, Chungbuk 28119, South Korea
[2] Korea Univ, Coll Pharm, Metabol Lab, Sejong 30019, South Korea
[3] Univ Sci & Technol, Dept Bioanalyt Sci, Daejeon 34113, South Korea
关键词
Shotgun proteomics; Sodium dodecyl sulfate; S-Trap digestion; Pellet S-Trap digestion; SAMPLE PREPARATION METHOD; IDENTIFICATION; EXCHANGE; REMOVAL;
D O I
10.1016/j.bbrc.2021.12.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein extraction and digestion are important analytical steps in the study of proteomics. The use of sodium dodecyl sulfate (SDS) buffer makes it possible to effectively analyze various proteins. Its use was evaluated using the S-Trap digestion method and compared to the traditional In solution digestion method. Differences in protein composition were examined for each protein preparation method. S-Trap digestion followed by SDS buffer extraction clearly increased the number of identified proteins, including more mitochondrial and membrane-related proteins. The S-Trap digestion method with 5% SDS buffer was applied to the pellet remaining from the removal of RIPA buffer-soluble proteins, which identified more extracellular space proteins than the conventional S-Trap digestion method. S-Trap digestion of the pellet was particularly advantageous for identifying proteins located inside multilayer membranes. (c) 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:197 / 203
页数:7
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