Daly T J, Rusche J R, Maione T E, Frankel A D
Repligen Corporation, Cambridge, Massachusetts 02139.
Biochemistry. 1990 Oct 23;29(42):9791-5. doi: 10.1021/bi00494a005.
The circular dichroism (CD) spectrum of the Rev protein from HIV-1 indicates that Rev contains about 50% alpha helix and 25% beta sheet at 5 degrees C in potassium phosphate buffer, pH 3, and 300 mM KF. The spectrum is independent of protein concentration over a 20-fold range. At neutral pH, Rev is relatively insoluble but can be brought into solution by binding to its specific RNA binding site, the Rev-responsive element (RRE), at a Rev:RNA ratio of about 3:1. Nonspecific binding to tRNA does not solubilize Rev. As judged by difference CD spectra, the conformation of Rev when bound to the RRE at neutral pH is similar to the conformation of unbound Rev at pH 3, although changes in the RNA may also contribute to the difference spectrum. Indeed, some difference is observed near 260 nm, consistent with a conformational change of the RRE upon Rev binding. Rev alone at pH 3 shows irreversible aggregation as the temperature is raised, while Rev bound to the RRE at neutral pH shows a reversible transition with a Tm of 68 degrees C.
来自HIV-1的Rev蛋白的圆二色性(CD)光谱表明,在5℃、pH 3的磷酸钾缓冲液和300 mM KF条件下,Rev含有约50%的α螺旋和25%的β折叠。该光谱在20倍的蛋白浓度范围内与蛋白浓度无关。在中性pH值下,Rev相对不溶,但通过以约3:1的Rev:RNA比例结合其特定的RNA结合位点——Rev反应元件(RRE),可以使其溶解。与tRNA的非特异性结合不能使Rev溶解。通过差示CD光谱判断,在中性pH值下与RRE结合时Rev的构象与在pH 3时未结合的Rev的构象相似,尽管RNA的变化也可能对差示光谱有贡献。实际上,在260 nm附近观察到了一些差异,这与Rev结合后RRE的构象变化一致。在pH 3时单独的Rev随着温度升高会发生不可逆聚集,而在中性pH值下与RRE结合的Rev显示出可逆转变,熔解温度为68℃。