首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Reconstitution of protein translocation from detergent-solubilized Escherichia coli inverted vesicles: PrlA protein-deficient vesicles efficiently translocate precursor proteins.
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Reconstitution of protein translocation from detergent-solubilized Escherichia coli inverted vesicles: PrlA protein-deficient vesicles efficiently translocate precursor proteins.

机译:从去污剂溶解的大肠杆菌倒置囊泡中重建蛋白转运蛋白:缺乏PrlA蛋白的囊泡可有效地转运前体蛋白。

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摘要

Proteoliposomes were reconstituted by detergent dialysis of a sodium cholate extract of inverted vesicles derived from Escherichia coli plasma membrane. The translocation of precursor proteins into reconstituted vesicles occurred at high efficiency and was SecB dependent. The protein composition of the reconstituted vesicles differed markedly from that of native vesicles. Immunoblot analysis of the sodium cholate extract and of the reconstituted vesicles indicated that PrlA (SecY) protein remained largely unsolubilized under the described conditions and was virtually absent from the reconstituted vesicles, suggesting that PrlA may not be required for in vitro translocation.
机译:通过去污剂透析衍生自大肠杆菌质膜的倒置囊泡的胆酸钠提取物来重构蛋白脂质体。前体蛋白向重组囊泡的转运效率很高,并且是SecB依赖性的。重组囊泡的蛋白质组成与天然囊泡的蛋白质组成明显不同。胆酸钠提取物和重组囊泡的免疫印迹分析表明,在上述条件下,PrlA(SecY)蛋白仍然大部分不溶,并且重组囊泡中实际上不存在该蛋白,表明体外转运可能不需要PrlA。

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