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丝状噬菌体组装需要基因I和重叠的读码框基因XI的产物。

The products of gene I and the overlapping in-frame gene XI are required for filamentous phage assembly.

作者信息

Rapoza M P, Webster R E

机构信息

Department of Biochemistry, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

J Mol Biol. 1995 May 5;248(3):627-38. doi: 10.1006/jmbi.1995.0247.

Abstract

The class I filamentous bacteriophage are non-lytic single-stranded DNA phage, which are assembled at the cell envelope as they are extruded from the Gram-negative bacteria, Escherichia coli. The process requires the products of the phage genes I and IV, which reside in the inner and outer membrane, respectively, and are not present in the mature phage particle. Gene I encodes two proteins, the full length 348-residue pI and a smaller pI*, which this report shows is the result of an internal translation initiation event at methionine codon 241. Both pI and pI* are shown to be required for phage assembly. Therefore, pI* can be considered the product of an additional phage gene, XI, which is a separate in-frame gene that overlaps gene I. Both proteins contain a 13-residue region adjacent to the cytoplasmic face of the inner membrane that probably exists as a positively charged amphiphilic helix. Although this region is not required for membrane insertion of pI and pI*, it is shown to be required for phage assembly. Oligonucleotide-directed mutagenesis of this region, which removes positive charges or alters the hydrophobic face of the putative helix, renders pI and pI* unable to function in phage assembly. This region of pI and pI* is highly homologous in structure to the carboxyl-terminal 11 amino acids of pVIII, the main coat protein, which also reside adjacent to the cytoplasmic face of the inner membrane.

摘要

I类丝状噬菌体是非裂解性单链DNA噬菌体,它们在从革兰氏阴性细菌大肠杆菌中挤出时在细胞膜上组装。这个过程需要噬菌体基因I和IV的产物,它们分别位于内膜和外膜中,且不存在于成熟的噬菌体颗粒中。基因I编码两种蛋白质,全长348个氨基酸残基的pI和一个较小的pI*,本报告表明pI是甲硫氨酸密码子241处内部翻译起始事件的结果。pI和pI都被证明是噬菌体组装所必需的。因此,pI可被视为另一个噬菌体基因XI的产物,XI是一个与基因I重叠的独立读框内基因。这两种蛋白质都含有一个与内膜细胞质面相邻的13个氨基酸残基的区域,该区域可能以带正电荷的两亲性螺旋形式存在。虽然该区域不是pI和pI插入膜所必需的,但它被证明是噬菌体组装所必需的。对该区域进行寡核苷酸定向诱变,去除正电荷或改变推定螺旋的疏水面,会使pI和pI无法在噬菌体组装中发挥作用。pI和pI的这个区域在结构上与主要衣壳蛋白pVIII的羧基末端11个氨基酸高度同源,pVIII也位于内膜细胞质面附近。

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