ATP-citrate lyase as a substrate of protein histidine phosphatase in vertebrates

被引:63
作者
Klumpp, S
Bechmann, G
Mäurer, A
Selke, D
Krieglstein, J
机构
[1] Univ Munster, Inst Pharmazeut & Med Chem, D-48149 Munster, Germany
[2] Univ Marburg, Inst Pharmakol & Toxikol, D-35032 Marburg, Germany
关键词
D O I
10.1016/S0006-291X(03)00920-3
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 first protein histidine phosphatase from vertebrates discovered recently was found in a variety of tissues, however, a physiological substrate protein was missing. Phosphorylation of liver extracts in the presence of EDTA, followed by SDS-PAGE and autoradiography showed labeling of three proteins. Acid- and alkaline-treatment revealed the existence of N-phosphates. Addition of histidine phosphatase exclusively resulted in dephosphorylation of a 110 kDa protein (denaturing conditions). Gelfiltration revealed its native molecular mass of similar to450 kDa. That protein was purified and identified as ATP-citrate lyase. The results are in favor of histidine phosphatase playing an important yet unidentified role in metabolic processes. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:110 / 115
页数:6
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