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胰岛素分泌颗粒的胰岛素原加工内肽酶将前白蛋白转化为白蛋白。

Proalbumin to albumin conversion by a proinsulin processing endopeptidase of insulin secretory granules.

作者信息

Rhodes C J, Brennan S O, Hutton J C

机构信息

Department of Clinical Biochemistry, University of Cambridge, United Kingdom.

出版信息

J Biol Chem. 1989 Aug 25;264(24):14240-5.

PMID:2503514
Abstract

A lysate of purified insulin secretory granules, which contains two types of proinsulin processing activity (type 1, Arg-Arg-directed and type II, Lys-Arg-directed (Davidson, H.W., Rhodes, C.J., and Hutton, J. C. (1988) Nature 333, 93-96), was found to process proalbumin by specific proteolytic cleavage of the COOH-terminal side of the Arg-2-Arg-1 sequence. The subcellular distribution of proalbumin processing activity in insulinoma tissue paralleled that for proinsulin conversion and occurred principally in a secretory granule fraction. Cleavage appeared to result from the Arg-Arg-directed type 1 proinsulin processing endo-peptidase. It was Ca2+-dependent (K0.5 activation = 1.0-1.5 mM Ca2+), unaffected by group-specific inhibitors of serine, cysteinyl, or aspartyl proteinases, and had an acidic pH optimum (5.5). Active-site inhibitor studies showed this activity had a preference for dibasic over monobasic amino acid sequences and indicated that the sequence of the dibasic site was an important determinant of the susceptibility of the substrate to cleavage. The activity did not process the proalbumin Christchurch mutant (Arg-2-Arg-1 to Arg-2-Gln-1). It was inhibited by the variant alpha 1-antitrypsin Pittsburgh (Met358 to Arg358; K0.5 = 100 nM) but not by other related proteins normally co-secreted with albumin from hepatocytes, namely alpha 1-antitrypsin M, alpha 2-macroglobulin, or antithrombin III. The insulin secretory granule proalbumin processing activity was indistinguishable from a proalbumin endopeptidase reported in rat liver membranes and similar to the yeast KEX-2 protease. These findings suggest that a highly conserved set of proprotein endopeptidases exists, which are specific for a dibasic sequence but broadly specific for proprotein substrates. Such enzymic activities appear to be active within both the constitutive and regulated pathways of secretion. Intraorganellar Ca2+ and pH appear to play a key role in regulating their activities.

摘要

纯化的胰岛素分泌颗粒裂解物含有两种胰岛素原加工活性(1型,精氨酸 - 精氨酸导向型和II型,赖氨酸 - 精氨酸导向型(戴维森,H.W.,罗兹,C.J.,和赫顿,J.C.(1988年)《自然》333卷,93 - 96页)),经发现,其通过对精氨酸 - 2 - 精氨酸 - 1序列羧基末端的特异性蛋白水解切割来加工前清蛋白。胰岛素瘤组织中前清蛋白加工活性的亚细胞分布与胰岛素原转化的分布相似,主要发生在分泌颗粒部分。切割似乎是由精氨酸 - 精氨酸导向的1型胰岛素原加工内肽酶引起的。它依赖于Ca2 +(K0.5激活 = 1.0 - 1.5 mM Ca2 +),不受丝氨酸、半胱氨酸或天冬氨酸蛋白酶的基团特异性抑制剂的影响,并且最适pH值为酸性(5.5)。活性位点抑制剂研究表明,这种活性对双碱性氨基酸序列的偏好高于单碱性氨基酸序列,并表明双碱性位点的序列是底物易受切割的重要决定因素。该活性不能加工前清蛋白克赖斯特彻奇突变体(精氨酸 - 2 - 精氨酸 - 1变为精氨酸 - 2 - 谷氨酰胺 - 1)。它被变异的α1 - 抗胰蛋白酶匹兹堡型(甲硫氨酸358变为精氨酸358;K0.5 = 100 nM)抑制,但不被通常与白蛋白从肝细胞共同分泌的其他相关蛋白质抑制,即α1 - 抗胰蛋白酶M、α2 - 巨球蛋白或抗凝血酶III。胰岛素分泌颗粒前清蛋白加工活性与大鼠肝细胞膜中报道的一种前清蛋白内肽酶无法区分,并且与酵母KEX - 2蛋白酶相似。这些发现表明存在一组高度保守的前体蛋白内肽酶,它们对双碱性序列具有特异性,但对前体蛋白底物具有广泛的特异性。这种酶活性似乎在组成型和调节型分泌途径中均有活性。细胞内Ca2 +和pH似乎在调节它们的活性中起关键作用。

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