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神经丝中分子量为145 kDa的亚基氨基末端头部结构域的磷酸化。由第二信使依赖性蛋白激酶调控的证据。

Phosphorylation of the amino-terminal head domain of the middle molecular mass 145-kDa subunit of neurofilaments. Evidence for regulation by second messenger-dependent protein kinases.

作者信息

Sihag R K, Nixon R A

机构信息

Ralph Lowell Laboratories, Mailman Research Center, McLean Hospital, Belmont, Massachusetts 02178.

出版信息

J Biol Chem. 1990 Mar 5;265(7):4166-71.

PMID:2105960
Abstract

To begin to understand the regulation and roles of neurofilament phosphorylation, we localized the phosphorylated domains on the 140-145-kDa neurofilament subunit (NF-M) and identified the protein kinases that may specifically phosphorylate the sites within these domains in vivo. Mouse retinal ganglion cells were labeled in vivo by injecting mice intravitreally with [32P]orthophosphate, and neurofilament-enriched fractions were obtained from the optic axons. Two-dimensional phosphopeptide map analysis of NF-M after digestion with alpha-chymotrypsin and trypsin revealed seven major (M8-M14) and at least eight minor (M1-M7 and M15) phosphopeptides. Two-dimensional phosphopeptide map analyses of NF-M phosphorylated in vitro by individual purified or endogenous axonal cytoskeleton-associated protein kinases showed that five peptides (M9-M13) were substrates for the heparin-sensitive second messenger-independent protein kinase(s). Protein kinase A and/or protein kinase C phosphorylated eight other peptides (M1-M8). Two alpha-chymotryptic peptides (C1 and C2) that were phosphorylated by protein kinase A but not by the endogenous independent kinase(s) were isolated by high performance liquid chromatography on a reverse-phase C8 column. Partial sequence analysis of peptides C1 (S R V S G P S ...) and C2 (S R G S P S T V S ...) showed that the peptides were localized on the head domain of NF-M at 25 and 41 residues from the amino terminus, respectively. Tryptic digest of peptide C1 (less than 12 kDa) generated the phosphopeptides M1-M6. Peptide C2 was a breakdown product of peptide C1. Since the polypeptide sites targeted by second messenger-independent kinase(s) associated with neurofilaments are localized on the carboxyl-terminal domain, separate aspects of NF-M function appear to be regulated by separate kinase systems that selectively phosphorylate head or tail domains of the polypeptide.

摘要

为了开始理解神经丝磷酸化的调控及其作用,我们定位了140 - 145 kDa神经丝亚基(NF - M)上的磷酸化结构域,并确定了在体内可能特异性磷酸化这些结构域内位点的蛋白激酶。通过向小鼠玻璃体内注射[32P]正磷酸盐在体内标记小鼠视网膜神经节细胞,然后从视神经轴突中获得富含神经丝的组分。用α - 胰凝乳蛋白酶和胰蛋白酶消化后对NF - M进行二维磷酸肽图谱分析,揭示了七个主要(M8 - M14)和至少八个次要(M1 - M7和M15)磷酸肽。对由单个纯化的或内源性轴突细胞骨架相关蛋白激酶在体外磷酸化的NF - M进行二维磷酸肽图谱分析表明,五个肽段(M9 - M13)是肝素敏感的不依赖第二信使的蛋白激酶的底物。蛋白激酶A和/或蛋白激酶C使另外八个肽段(M1 - M8)磷酸化。通过反相C8柱上的高效液相色谱法分离出两个被蛋白激酶A磷酸化但未被内源性不依赖激酶磷酸化的α - 胰凝乳蛋白酶肽段(C1和C2)。肽段C1(S R V S G P S...)和C2(S R G S P S T V S...)的部分序列分析表明,这些肽段分别位于NF - M头部结构域,距离氨基末端25和41个残基处。肽段C1(小于12 kDa)的胰蛋白酶消化产生了磷酸肽M1 - M6。肽段C2是肽段C1的降解产物。由于与神经丝相关的不依赖第二信使的激酶作用的多肽位点位于羧基末端结构域,因此NF - M功能的不同方面似乎由选择性磷酸化多肽头部或尾部结构域的不同激酶系统调控。

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