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内质网上水通道MIWC和CHIP28独特的生物合成机制。

Distinct biogenesis mechanisms for the water channels MIWC and CHIP28 at the endoplasmic reticulum.

作者信息

Shi L B, Skach W R, Ma T, Verkman A S

机构信息

Department of Medicine, University of California, San Francisco 94143-0521, USA.

出版信息

Biochemistry. 1995 Jul 4;34(26):8250-6. doi: 10.1021/bi00026a006.

Abstract

MIWC is a 32 kDa mercurial-insensitive water channel [Hasegawa et al. (1994) J. Biol. Chem. 269, 5497-5500] expressed in kidney collecting duct, brain ependymal cells, airways, and other tissues. We showed recently that the homologous water channel CHIP28 spanned the endoplasmic reticulum (ER) membrane 4 times with N- and C-termini in the cytoplasm [Skach et al., (1994) J. Cell Biol. 125, 803-815]. Hydropathy analysis of MIWC indicated up to eight hydrophobic regions (HRs) comprising potential membrane-spanning domains. To determine MIWC transmembrane topology at the ER, 10 cDNA chimeras were constructed which encoded increasing lengths of MIWC upstream from a reporter epitope (prolactin P-domain) at residues 13, 46, 73, 92, 120, 140, 164, 209, 276, and 2097, corresponding to putative polar extramembrane loops in the MIWC sequence. The chimeras were translated cell-free (rabbit reticulocyte lysate+ER-derived microsomes) and in Xenopus oocytes. Peptide chains were labeled with [35S]methionine and immunoprecipitated with a P-domain antibody. Transmembrane topology as determined by protease accessibility of the P-reporter indicated six membrane-spanning domains with N- and C-termini in the cytoplasm. The predicted topology was confirmed by demonstrating N-linked glycosylation at native residue N131 and an engineered consensus site at residue 197. Membrane integration of the nascent chain, as assayed by extractability at pH 11.5, occurred after synthesis of the first HR (residues 1-46). Translocation was terminated by a stop transfer sequence in the second HR (residues 32-73) as demonstrated by translation of the heterologous construct, [prolactin signal sequence]-[globin]-[HR2]-P.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

MIWC是一种32 kDa的汞不敏感水通道[长谷川等人(1994年),《生物化学杂志》269卷,5497 - 5500页],在肾集合管、脑室管膜细胞、气道及其他组织中表达。我们最近表明,同源水通道CHIP28在内质网(ER)膜中跨膜4次,N端和C端位于细胞质中[斯卡奇等人,(1994年),《细胞生物学杂志》125卷,803 - 815页]。对MIWC的亲水性分析表明,其包含多达八个疏水区域(HRs),这些区域构成潜在的跨膜结构域。为确定MIWC在内质网处的跨膜拓扑结构,构建了10个cDNA嵌合体,它们在残基13、46、73、92、120、140、164、209、276和2097处的报告表位(催乳素P结构域)上游编码越来越长的MIWC片段,这些残基对应于MIWC序列中假定的极性胞外环。这些嵌合体在无细胞体系(兔网织红细胞裂解物 + ER衍生微粒体)和非洲爪蟾卵母细胞中进行翻译。肽链用[35S]甲硫氨酸标记,并用P结构域抗体进行免疫沉淀。通过P报告基因的蛋白酶可及性确定的跨膜拓扑结构表明有六个跨膜结构域,N端和C端位于细胞质中。通过在天然残基N131和工程化的共有位点残基197处证明N - 连接糖基化,证实了预测的拓扑结构。通过在pH 11.5下的可提取性测定,新生链的膜整合在第一个HR(残基1 - 46)合成后发生。如通过异源构建体[催乳素信号序列]-[球蛋白]-[HR2]-P的翻译所证明的,转运在第二个HR(残基32 - 73)中的一个终止转移序列处终止。(摘要截断于250字)

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