Assay of protein kinases using radiolabeled ATP: a protocol

被引:198
作者
Hastie, C. James
McLauchlan, Hilary J.
Cohen, Philip
机构
[1] Univ Dundee, Inst Med Sci, Wellcome Trust Bioctr Complex, Div Signal Transduct Therapy, Dundee DD1 5EH, Scotland
[2] Univ Dundee, Wellcome Bioctr Complex, Inst Med Sci, Med Res Council Protein Phosphorylat Unit, Dundee DD1 5EH, Scotland
基金
英国医学研究理事会;
关键词
D O I
10.1038/nprot.2006.149
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein kinase activity results in the incorporation of radiolabeled phosphate from [gamma-P-32] ATP into a peptide or protein substrate. The measurement of the amount of radioactivity incorporated into a substrate as a function of time and enzyme concentration allows enzyme activity to be quantified. The activity is expressed as a 'unit', where 1 unit corresponds to the amount of protein kinase that catalyzes the incorporation of 1 nanomole of phosphate into the standard substrate in 1 minute. Specific activity is defined as units of activity per milligram protein. The assay format described here is quick, simple, inexpensive, sensitive and accurate, provides a direct measurement of activity and remains the 'gold standard' for the quantification of protein kinase activity. Up to 40 samples can be assayed manually at one time, and the assay takes one person less than 1 hour to complete.
引用
收藏
页码:968 / 971
页数:4
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