Comparative Analysis of Click Chemistry Mediated Activity-Based Protein Profiling in Cell Lysates

Comparative Analysis of Click Chemistry Mediated Activity-Based Protein Profiling in Cell Lysates
复制标题

细胞裂解物中点击化学介导的基于活性的蛋白质分析的比较分析

DOI:
--
复制
发表时间:
2013
期刊:
影响因子:
4.6
通讯作者:
S. Verhelst
S. Verhelst
中科院分区:
化学2区
文献类型:
--
作者:
Yinliang Yang;Xiaomeng Yang;S. Verhelst

文献摘要

参考文献

被引文献

相似文献

基于活性的蛋白质分析使用共价连接到活性酶靶的化学探针。具有常规标签的探针具有缺点,例如有限的细胞渗透性或反应基团周围的空间位阻。串联标记策略与点击化学现在被广泛用于研究酶的目标在原位和在体内。在本文中,探针在活细胞中反应,而随后通过点击化学的检测发生在细胞裂解物中。我们在这里通过使用Cu(I)催化和应变促进的点击化学、不同配体和不同裂解条件来比较基于活性的串联标记策略的效率。
Activity-based protein profiling uses chemical probes that covalently attach to active enzyme targets. Probes with conventional tags have disadvantages, such as limited cell permeability or steric hindrance around the reactive group. A tandem labeling strategy with click chemistry is now widely used to study enzyme targets in situ and in vivo. Herein, the probes are reacted in live cells, whereas the ensuing detection by click chemistry takes place in cell lysates. We here make a comparison of the efficiency of the activity-based tandem labeling strategy by using Cu(I)-catalyzed and strain-promoted click chemistry, different ligands and different lysis conditions.
DOI: 10.1021/bc100272z
发表时间: 2010-10-20
影响因子: 4.7
作者:
Hong, Vu;Steinmetz, Nicole F.;Manchester, Marianne;Finn, M. G.
通讯作者: Finn, M. G.
DOI: 10.1074/mcp.m112.021014
发表时间: 2013-01-01
影响因子: 7
作者:
Yang, Yinliang;Hahne, Hannes;Verhelst, Steven H. L.
通讯作者: Verhelst, Steven H. L.
DOI: 10.1021/cb6003228
发表时间: 2006-01-01
影响因子: 4
作者:
Agard, Nicholas J.;Baskin, Jeremy M.;Bertozzi, Carolyn R.
通讯作者: Bertozzi, Carolyn R.
DOI: 10.1002/asia.201100385
发表时间: 2011-10-04
影响因子: 4.1
作者:
Wang, Wei;Hong, Senglian;Andrew Tran;Jiang, Hao;Triano, Rebecca;Liu, Yi;Chen, Xing;Wu, Peng
通讯作者: Wu, Peng
DOI: 10.1002/anie.200905087
发表时间: 2009
影响因子: 16.6
作者:
Hong, Vu;Presolski, Stanislav I.;Ma, Celia;Finn, M. G.
通讯作者: Finn, M. G.