衍生化
蛋白质水解
蛋白质组
蛋白质组学
肽
分子
溶解
色谱法
化学
试剂
定量蛋白质组学
小分子
组合化学
质谱法
生物化学
有机化学
酶
基因
作者
Cecil J. Howard,Brendan M. Floyd,Angela M. Bardo,Jagannath Swaminathan,Edward M. Marcotte,Eric V. Anslyn
标识
DOI:10.1021/acschembio.0c00040
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.
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