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通过免疫金标记法在甜菜坏死黄脉病毒颗粒一端附近检测P75通读蛋白。

Detection by immunogold labelling of P75 readthrough protein near an extremity of beet necrotic yellow vein virus particles.

作者信息

Haeberlé A M, Stussi-Garaud C, Schmitt C, Garaud J C, Richards K E, Guilley H, Jonard G

机构信息

INRA, Laboratorie de Pathologie Végétale, Colmar, France.

出版信息

Arch Virol. 1994;134(1-2):195-203. doi: 10.1007/BF01379118.

Abstract

RNA 2 of beet necrotic yellow vein virus carries the cistron for the 21 kd coat protein at its 5'-extremity. During translation, the coat protein cistron termination codon is suppressed about 10% of the time so that translation continues into the adjacent open reading frame to produce a 75 kd species, known as P75, which contains the coat protein sequence at its N-terminus. Immunoblotting experiments with a P75-specific antiserum showed that P75 is present in only trace amounts in purified virus preparations. Electron microscopic visualization of immunogold-labelled virions in crude tissue extracts has provided evidence for an association between P75 and at least a fraction of the BNYVV particles, with P75 being predominantly located near one end of the rod-shaped virions. This finding is discussed in the context of the current model for the role of P75 in virus assembly and vector transmission.

摘要

甜菜坏死黄脉病毒的RNA 2在其5'末端携带21kd外壳蛋白的顺反子。在翻译过程中,外壳蛋白顺反子的终止密码子约有10%的时间被抑制,从而使翻译继续进入相邻的开放阅读框,产生一种75kd的蛋白,称为P75,其N端包含外壳蛋白序列。用P75特异性抗血清进行的免疫印迹实验表明,P75在纯化的病毒制剂中仅以痕量存在。对粗组织提取物中免疫金标记病毒粒子的电子显微镜观察为P75与至少一部分BNYVV粒子之间的关联提供了证据,P75主要位于杆状病毒粒子的一端附近。本文结合当前关于P75在病毒组装和介体传播中作用的模型对这一发现进行了讨论。

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