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凝胶阻滞分析后对RNA-蛋白质复合物进行足迹分析:应用于R-17-前衣壳蛋白-RNA和反式激活因子-TAR相互作用

Footprinting RNA-protein complexes following gel retardation assays: application to the R-17-procoat-RNA and tat--TAR interactions.

作者信息

Pearson L, Chen C B, Gaynor R P, Sigman D S

机构信息

Department of Biological Chemistry, School of Medicine, University of California, Los Angeles 90024-1570.

出版信息

Nucleic Acids Res. 1994 Jun 25;22(12):2255-63. doi: 10.1093/nar/22.12.2255.

Abstract

RNA-protein complexes isolated following a gel retardation assay can be footprinted within the gel matrix using the chemical nuclease activities of 4,7-dimethyl-, 5,6-dimethyl-, and 3,4,7,8-tetramethyl-1,10-phenanthroline-copper. These complexes are more reactive than 1,10-phenanthroline-copper but share its reaction preference for bulges and loops. The interaction of the coat protein of R-17 with its viral RNA target and tat- and tat-derived peptides with HIV TAR RNA have been studied. In both cases, the RNA sequence opposite a 2-3 nucleotide bulge are protected. Tat-derived peptides inhibit cleavage at sites which intact tat does not protect. These results are consistent with transcription studies which have suggested that truncation of tat increases nonspecific binding.

摘要

通过凝胶阻滞试验分离得到的RNA-蛋白质复合物,可利用4,7-二甲基-、5,6-二甲基-和3,4,7,8-四甲基-1,10-菲咯啉铜的化学核酸酶活性在凝胶基质内进行足迹分析。这些复合物比1,10-菲咯啉铜更具反应活性,但在对凸起和环的反应偏好上与其相同。已经研究了R-17外壳蛋白与其病毒RNA靶标的相互作用,以及tat和tat衍生肽与HIV TAR RNA的相互作用。在这两种情况下,与2-3个核苷酸凸起相对的RNA序列都受到保护。tat衍生肽在完整tat不保护的位点抑制切割。这些结果与转录研究一致,转录研究表明tat的截短会增加非特异性结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/605f/523682/73e9ddfa5930/nar00036-0083-a.jpg

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