Kinase-catalyzed biotinylation for phosphoprotein detection

Kinase-catalyzed biotinylation for phosphoprotein detection
复制标题

DOI:
10.1021/ja066828o
复制
发表时间:
2007-01-10
影响因子:
15
通讯作者:
Pflum, Mary Kay H.
Pflum, Mary Kay H.
中科院分区:
化学1区
文献类型:
--
作者:
Green, Keith D.;Pflum, Mary Kay H.

文献摘要

被引文献

相似文献

Protein phosphorylation plays a critical role in a variety of cellular functions. As a result, the monitoring of phosphoproteins in cells represents an important goal for proteomics research. To facilitate phosphoprotein detection, the first enzymatic phosphorylation-dependent biotinylation reaction of proteins is described. Specifically, kinase enzymes were coupled with an ATP-biotin conjugate to efficiently biotinylate substrate peptides and proteins after phosphate transfer. The kinase-mediated biotinylation reaction enables efficient detection of phosphoproteins in cell lysates or phosphopeptides after trypsin proteolysis, demonstrating its utility for proteomics research. Importantly, the studies reveal the cosubstrate promiscuity of kinase enzymes, laying the foundation for development of new chemical tools targeting the phosphoproteome.