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芜菁黄花叶病毒66K复制蛋白在受感染细胞中的检测与亚细胞定位

Detection and subcellular localization of the turnip yellow mosaic virus 66K replication protein in infected cells.

作者信息

Prod'homme D, Le Panse S, Drugeon G, Jupin I

机构信息

Laboratoire de Virologie Moléculaire, Institut Jacques Monod, UMR 7592, CNRS, Universités Paris 6-Paris 7, 2 place Jussieu, 75251 Paris Cedex 05, France.

出版信息

Virology. 2001 Mar 1;281(1):88-101. doi: 10.1006/viro.2000.0769.

Abstract

Turnip yellow mosaic virus (TYMV) encodes a 206-kDa (206K) polyprotein with domains of methyltransferase, proteinase, NTPase/helicase, and RNA-dependent RNA polymerase (RdRp). In vitro, the 206K protein has been shown to undergo proteolytic processing, giving rise to the synthesis of 140-kDa (140K) and 66-kDa (66K) proteins, the latter comprising the RdRp protein domain. Antibodies were raised against the 66K protein and were used to detect the corresponding viral protein in infected cells; both leaf tissues and protoplasts were examined. The antiserum specifically recognized a protein of approximately 66 kDa, indicating that the cleavage observed in vitro is also functional in vivo. The 66K protein accumulates transiently during protoplast infection and localizes to cellular membrane fractions. Indirect immunofluorescence assays and electron microscopy of immunogold-decorated ultrathin sections of infected leaf tissue using anti-66K-specific antibody revealed labeling of membrane vesicles located at the chloroplast envelope.

摘要

芜菁黄花叶病毒(TYMV)编码一种206千道尔顿(206K)的多聚蛋白,该多聚蛋白具有甲基转移酶、蛋白酶、NTP酶/解旋酶和RNA依赖性RNA聚合酶(RdRp)结构域。在体外,已证明206K蛋白会进行蛋白水解加工,从而合成140千道尔顿(140K)和66千道尔顿(66K)的蛋白,后者包含RdRp蛋白结构域。制备了针对66K蛋白的抗体,并用于检测受感染细胞中的相应病毒蛋白;对叶片组织和原生质体都进行了检测。抗血清特异性识别一种约66千道尔顿的蛋白,表明体外观察到的切割在体内也具有功能。66K蛋白在原生质体感染期间短暂积累,并定位于细胞膜部分。使用抗66K特异性抗体对受感染叶片组织的免疫金标记超薄切片进行间接免疫荧光测定和电子显微镜观察,结果显示叶绿体被膜处的膜泡有标记。

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