Solid-Phase Peptide Capture and Release for Bulk and Single-Molecule Proteomics

被引:13
作者
Howard, Cecil J. [1 ]
Floyd, Brendan M. [2 ]
Bardo, Angela M. [2 ]
Swaminathan, Jagannath [2 ]
Marcotte, Edward M. [2 ]
Anslyn, Eric, V [1 ]
机构
[1] Univ Texas Austin, Dept Chem, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Mol Biosci, Austin, TX 78712 USA
关键词
MASS-SPECTROMETRY; PROTEIN; PURIFICATION;
D O I
10.1021/acschembio.0c00040
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
The field of proteomics has expanded recently with more sensitive techniques for the bulk measurement of peptides as well as single-molecule techniques. One limiting factor for some of these methods is the need for multiple chemical derivatizations and highly pure proteins free of contaminants. We demonstrate a solid-phase capture-release strategy suitable for the proteolysis, purification, and subsequent chemical modification of peptides. We use this resin on an HEK293T cell lysate and perform one-pot proteolysis, capture, and derivatization to survey peptide capture biases from over 40 000 unique peptides from a cellular proteome. We also show that this capture can be reversed in a traceless manner, such that it is amenable for single-molecule proteomics techniques. With this technique, we perform a fluorescent labeling and C-terminal derivatization on a peptide and subject it to fluorosequencing, demonstrating that washing the resin is sufficient to remove excess dyes and other reagents prior to single-molecule protein sequencing.
引用
收藏
页码:1401 / 1407
页数:7
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