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A component of the chloroplastic protein import apparatus is targeted to the outer envelope membrane via a novel pathway.

机译:叶绿素蛋白输入装置的一个组成部分通过一种新颖的途径靶向于外壳膜。

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摘要

A chloroplastic outer envelope membrane protein of 75 kDa (OEP75) was identified previously as a component of the protein import machinery. Here we provide additional evidence that OEP75 is a component of protein import, present the isolation of a cDNA clone encoding this protein, briefly describe its developmental expression and tissue specificity, and characterize its insertion into the outer envelope membrane. OEP75 was synthesized as a higher molecular weight precursor (prOEP75) which bound to isolated chloroplasts in an in vitro import assay and subsequently was processed to the mature form (mOEP75). During this import assay, two proteins intermediate in size between prOEP75 and mOEP75 were detected. One of these intermediates was also detected in chloroplast envelopes isolated from young pea leaves. Binding and processing of prOEP75 required ATP and one or more surface-exposed proteinaceous components, and was competed by prSSU, a stromal-targeted protein. We propose that the N-terminus of the prOEP75 transit peptide acts as a stromal-targeting domain and a central, hydrophobic region of this transit peptide acts as a stop-transfer domain. A complex route of insertion and processing of prOEP75 may exist to ensure high fidelity targeting of this import component.
机译:75 kDa的叶绿体外壳膜蛋白(OEP75)先前已被确定为蛋白导入机制的组成部分。在这里,我们提供了其他证据,表明OEP75是蛋白质输入的组成部分,目前已分离出编码该蛋白质的cDNA克隆,简要描述了其发育表达和组织特异性,并表征了其插入外膜的能力。 OEP75被合成为较高分子量的前体(prOEP75),​​在体外导入测定中与分离的叶绿体结合,随后被加工成成熟形式(mOEP75)。在该导入测定过程中,检测到两种蛋白,大小介于prOEP75和mOEP75之间。从豌豆幼叶中分离出的叶绿体包膜中也检测到了这些中间体之一。 prOEP75的结合和加工需要ATP和一种或多种表面暴露的蛋白质成分,并与基质靶向蛋白质prSSU竞争。我们建议prOEP75转运肽的N末端充当基质靶向结构域,而该转运肽的中央疏水区域充当终止转运结构域。可能存在复杂的prOEP75插入和处理路径,以确保此导入组件具有高保真度。

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