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类病毒与组蛋白及其他蛋白质的复合物。

Complexes of viroids with histones and other proteins.

作者信息

Wolff P, Gilz R, Schumacher J, Riesner D

出版信息

Nucleic Acids Res. 1985 Jan 25;13(2):355-67. doi: 10.1093/nar/13.2.355.

Abstract

Complexes of potato spindle tuber viroid (PSTV) with nuclear proteins have been studied by in vitro reconstitution of the complexes and by isolation and characterization of in vivo complexes under non-dissociating conditions. For in vitro reconstitution, nuclear proteins were separated by SDS-gel-electrophoresis, renatured and blotted onto nitrocellulose filters, and incubated with viroid. The viroid-protein complexes were crosslinked covalently, and the viroid containing protein bands were detected by northern hybridization with a radioactive cDNA probe. The histones, a 41,000 dalton protein and to a small extent a 31,000 dalton protein were found in complexes with viroids. Raising the strength to 0.4 M NaCl destroys the complexes with the 41,000 dalton proteins but not those with the histones. From nucleoli, which are known to obtain the majority of viroids under non-dissociating conditions (Schumacher et al., (1983) EMBO J. 2, 1549-1555), a nucleosomal fraction was prepared. Viroids were found predominantly in this nucleosomal fraction. They are bound in a complex of 12-15 svedberg units.

摘要

通过体外复合物重组以及在非解离条件下对体内复合物进行分离和表征,对马铃薯纺锤块茎类病毒(PSTV)与核蛋白的复合物进行了研究。对于体外重组,通过SDS凝胶电泳分离核蛋白,使其复性并印迹到硝酸纤维素滤膜上,然后与类病毒一起孵育。将类病毒 - 蛋白质复合物进行共价交联,并用放射性cDNA探针通过Northern杂交检测含类病毒的蛋白条带。发现组蛋白、一种41,000道尔顿的蛋白质以及少量31,000道尔顿的蛋白质与类病毒形成复合物。将NaCl浓度提高到0.4M会破坏与41,000道尔顿蛋白质形成的复合物,但不会破坏与组蛋白形成的复合物。从已知在非解离条件下能获得大部分类病毒的核仁中制备了核小体组分(舒马赫等人,(1983年)《欧洲分子生物学组织杂志》2,1549 - 1555)。类病毒主要存在于该核小体组分中。它们以12 - 15斯维德伯格单位的复合物形式结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00df/341000/a00a97906e1c/nar00296-0052-a.jpg

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