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大鼠脑蛋白激酶Cζ亚型:其结构、表达及特性

Protein kinase C zeta subspecies from rat brain: its structure, expression, and properties.

作者信息

Ono Y, Fujii T, Ogita K, Kikkawa U, Igarashi K, Nishizuka Y

机构信息

Central Research Division, Takeda Chemical Industries, Osaka, Japan.

出版信息

Proc Natl Acad Sci U S A. 1989 May;86(9):3099-103. doi: 10.1073/pnas.86.9.3099.

Abstract

The primary structure of the zeta subspecies of rat brain protein kinase C was deduced from its overlapping cDNAs. The zeta subspecies of protein kinase C consists of 592 amino acid residues with the calculated molecular mass of 67,740 Da and has regulatory and protein kinase domains in its amino- and carboxyl-terminal halves, respectively. Although all members of the protein kinase C family so far identified have a tandem repeat of the characteristic cysteine-rich zinc-finger-like sequence in the regulatory domain, the zeta subspecies contains only one set of this sequence. Northern (RNA)-blot hybridization analysis indicated that two major RNA transcripts of the zeta subspecies with different lengths may be generated by the use of different polyadenylylational signals. The enzyme was expressed in COS-7 cells by transfection with the cDNA construct encoding its whole sequence. It showed an approximate molecular mass of 64,000 Da upon SDS/PAGE. The enzyme activity was significantly dependent on phospholipid but was independent of the presence of Ca2+ or diacylglycerol, when assayed with calf thymus H1 histone as a phosphate acceptor protein. The zeta subspecies expressed in COS-7 cells did not appear to show binding activity of phorbol ester. The structural and biochemical properties indicate that the zeta subspecies is related to, but distinct from, other subspecies of protein kinase C. Perhaps, this subspecies belongs to another entity of the enzyme family.

摘要

大鼠脑蛋白激酶C的ζ亚型的一级结构由其重叠的cDNA推导得出。蛋白激酶C的ζ亚型由592个氨基酸残基组成,计算分子量为67,740道尔顿,在其氨基末端和羧基末端分别具有调节结构域和蛋白激酶结构域。尽管迄今为止鉴定出的蛋白激酶C家族的所有成员在调节结构域中都有富含半胱氨酸的锌指样序列的串联重复,但ζ亚型仅包含一组该序列。Northern(RNA)印迹杂交分析表明,ζ亚型的两种不同长度的主要RNA转录本可能是通过使用不同的聚腺苷酸化信号产生的。通过用编码其全序列的cDNA构建体转染,该酶在COS-7细胞中表达。在SDS/PAGE上显示其近似分子量为64,000道尔顿。当以小牛胸腺H1组蛋白作为磷酸受体蛋白进行测定时,该酶的活性明显依赖于磷脂,但不依赖于Ca2+或二酰基甘油的存在。在COS-7细胞中表达的ζ亚型似乎没有显示佛波酯的结合活性。其结构和生化特性表明,ζ亚型与蛋白激酶C的其他亚型相关,但又有所不同。也许,该亚型属于酶家族的另一个实体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be6c/287072/be6d7197ae55/pnas00249-0120-a.jpg

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