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蛋白激酶C-α的C1和C2结构域在其膜结合与激活过程中的相互作用。

Interplay of C1 and C2 domains of protein kinase C-alpha in its membrane binding and activation.

作者信息

Medkova M, Cho W

机构信息

Department of Chemistry, University of Illinois, Chicago, Illinois 60607-7061, USA.

出版信息

J Biol Chem. 1999 Jul 9;274(28):19852-61. doi: 10.1074/jbc.274.28.19852.

Abstract

The regulatory domain of conventional protein kinase C (PKC) contains two membrane-targeting modules, the C2 domain that is responsible for Ca2+-dependent membrane binding of protein, and the C1 domain composed of two cysteine-rich zinc fingers (C1a and C1b) that bind diacylglycerols and phorbol esters. To understand the individual roles and the interplay of the C1 and C2 domains in the membrane binding and activation of PKC, we functionally expressed isolated C1 and C2 domains of PKC-alpha and measured their vesicle binding and monolayer penetration. Results indicate that the C2 domain of PKC-alpha is responsible for the initial Ca2+- and phosphatidylserine-dependent electrostatic membrane binding of PKC-alpha, whereas the C1 domain is involved in subsequent membrane penetration and diacylglycerol binding, which eventually lead to enzyme activation. To determine the roles of individual zinc fingers in the C1 domain, we also mutated hydrophobic residues in the C1a (Trp58 and Phe60) and C1b (Tyr123 and Leu125) domains of the native PKC-alpha molecule and measured the effects of mutations on vesicle binding, enzyme activity and monolayer penetration. Results show that the hydrophobic residues in the C1a domain are essential for the membrane penetration and activation of PKC-alpha, whereas those in the C1b domain are not directly involved in these processes. Based on these results in conjunction with our previous structure-function studies of the C2 domain (Medkova, M., and Cho, W. (1998) J. Biol. Chem. 273, 17544-17552), we propose a mechanism for the in vitro membrane binding and activation of conventional PKC that accounts for the temporal and spatial sequences of PKC activation.

摘要

传统蛋白激酶C(PKC)的调节结构域包含两个膜靶向模块,即负责蛋白质Ca2+依赖性膜结合的C2结构域,以及由两个富含半胱氨酸的锌指(C1a和C1b)组成的C1结构域,该结构域可结合二酰基甘油和佛波酯。为了了解C1和C2结构域在PKC的膜结合和激活中的各自作用及相互作用,我们功能性表达了PKC-α的分离C1和C2结构域,并测量了它们与囊泡的结合及单层穿透情况。结果表明,PKC-α的C2结构域负责PKC-α最初的Ca2+和磷脂酰丝氨酸依赖性静电膜结合,而C1结构域参与随后的膜穿透和二酰基甘油结合,最终导致酶激活。为了确定C1结构域中各个锌指的作用,我们还对天然PKC-α分子的C1a(Trp58和Phe60)和C1b(Tyr123和Leu125)结构域中的疏水残基进行了突变,并测量了这些突变对囊泡结合、酶活性和单层穿透的影响。结果表明,C1a结构域中的疏水残基对于PKC-α的膜穿透和激活至关重要,而C1b结构域中的疏水残基不直接参与这些过程。基于这些结果并结合我们之前对C2结构域的结构-功能研究(Medkova,M.,和Cho,W.(1998)J. Biol. Chem. 273,17544-17552),我们提出了一种传统PKC体外膜结合和激活的机制,该机制解释了PKC激活的时间和空间顺序。

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