Pearson L, Chen C B, Gaynor R P, Sigman D S
Department of Biological Chemistry, School of Medicine, University of California, Los Angeles 90024-1570.
Nucleic Acids Res. 1994 Jun 25;22(12):2255-63. doi: 10.1093/nar/22.12.2255.
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.
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。