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α1-抗胰蛋白酶Mmalton(缺失苯丙氨酸52)在体内形成环片层聚合物。聚合作用的C片层机制的证据。

alpha 1-Antitrypsin Mmalton (Phe52-deleted) forms loop-sheet polymers in vivo. Evidence for the C sheet mechanism of polymerization.

作者信息

Lomas D A, Elliott P R, Sidhar S K, Foreman R C, Finch J T, Cox D W, Whisstock J C, Carrell R W

机构信息

Department of Haematology, University of Cambridge, United Kingdom.

出版信息

J Biol Chem. 1995 Jul 14;270(28):16864-70. doi: 10.1074/jbc.270.28.16864.

Abstract

The Z (Glu342-->Lys) and Siiyama (Ser53-->Phe) deficiency variants of alpha 1-antitrypsin result in the retention of protein in the endoplasmic reticulum of the hepatocyte by loop-sheet polymerization in which the reactive center loop of one molecule is inserted into a beta-pleated sheet of a second. We show here that antitrypsin Mmalton (Phe52-deleted), which is associated with the same liver inclusions, is also retained at an endoglycosidase H-sensitive stage of processing in the Xenopus oocyte and spontaneously forms polymers in vivo. These polymers, obtained from the plasma of an Mmalton/QO (null) bolton heterozygote, were much shorter than other antitrypsin polymers and contained a reactive center loop-cleaved species. Monomeric mutant antitrypsin was also isolated from the plasma. The monomeric component had a normal unfolding transition on transverse urea gradient gel electrophoresis and formed polymers in vitro more readily than M, but less readily than Z, antitrypsin. The A beta-sheet accommodated a reactive center loop peptide much less readily than Z antitrypsin, which in turn was less receptive than native M antitrypsin. The nonreceptive conformation of the A sheet in antitrypsin Mmalton had little effect on kinetic parameters, the formation of SDS-stable complexes, the S to R transition, and the formation of the latent conformation. Comparison of the results with similar findings of short chain polymers associated with the antithrombin variant Rouen VI (Bruce, D., Perry, D., Borg, J.-Y., Carrell, R. W., and Wardell, M. R. (1994) J. Clin. Invest. 94, 2265-2274) suggests that polymerization is more complicated than the mechanism proposed earlier. The Z, Siiyama, and Mmalton mutations favor a conformational change in the antitrypsin molecule to an intermediate between the native and latent forms. This would involve a partial overinsertion of the reactive loop into the A sheet with displacement of strand 1C and consequent loop-C sheet polymerization.

摘要

α1 - 抗胰蛋白酶的Z(Glu342→Lys)和石山(Ser53→Phe)缺陷变体通过环 - 片层聚合导致蛋白质保留在肝细胞的内质网中,其中一个分子的反应中心环插入到第二个分子的β - 折叠片中。我们在此表明,与相同肝脏包涵体相关的抗胰蛋白酶Mmalton(Phe52缺失)在非洲爪蟾卵母细胞加工的内切糖苷酶H敏感阶段也被保留,并在体内自发形成聚合物。这些聚合物取自Mmalton/QO(无效)博尔顿杂合子的血浆,比其他抗胰蛋白酶聚合物短得多,并且包含一个反应中心环裂解物种。单体突变抗胰蛋白酶也从血浆中分离出来。该单体成分在横向尿素梯度凝胶电泳上具有正常的解折叠转变,并且在体外比M抗胰蛋白酶更容易形成聚合物,但比Z抗胰蛋白酶形成聚合物的难度小。与Z抗胰蛋白酶相比,Aβ - 折叠容纳反应中心环肽的能力要弱得多,而Z抗胰蛋白酶又比天然M抗胰蛋白酶的接受能力弱。抗胰蛋白酶Mmalton中A片层的非接受构象对动力学参数、SDS稳定复合物的形成、S到R转变以及潜在构象的形成影响很小。将这些结果与抗凝血酶变体鲁昂VI相关的短链聚合物的类似发现(布鲁斯,D.,佩里,D.,博格,J.-Y.,卡雷尔,R.W.,和沃德尔,M.R.(1994年)《临床研究杂志》94,2265 - 2274)进行比较表明,聚合过程比早期提出的机制更为复杂。Z、石山和Mmalton突变有利于抗胰蛋白酶分子构象转变为天然形式和潜在形式之间的中间状态。这将涉及反应环部分过度插入A片层,导致1C链移位,进而发生环 - C片层聚合。

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