Critchley A D, Haneef I, Cousens D J, Stockley P G
Department of Genetics, University of Leeds, UK.
J Mol Graph. 1993 Jun;11(2):92-7, 124. doi: 10.1016/0263-7855(93)87002-m.
We present a model for the three-dimensional structure of the HIV TAR stem-loop, based on a modeling algorithm which makes use of the known X-ray coordinates of tRNAs to generate a model structure, which has then been tested experimentally in solution by enzymatic and chemical structure probing of ribo-oligonucleotides encompassing the TAR sequence. The modeling suggested that the structure of TAR was similar to that of the anti-codon loop of tRNA(Asp), having a loop of just three single-stranded residues with a mismatched adenine excluded from the helical stem on the 3' side of the loop. The structural probing is consistent with such a structure for the loop, and reveals an unusual structure around the 5' uridine-rich bulge, which is the binding target for the transactivator protein Tat. These data may be useful in understanding the interaction of TAR with the Tat protein and may aid in the design of anti-AIDS drugs. The coordinates of the model are available on request.
我们基于一种建模算法提出了HIV TAR茎环三维结构的模型,该算法利用已知的tRNA的X射线坐标来生成模型结构,然后通过对包含TAR序列的核糖寡核苷酸进行酶促和化学结构探测,在溶液中对该模型结构进行了实验测试。建模表明,TAR的结构与tRNA(Asp)的反密码子环相似,有一个仅由三个单链残基组成的环,环3'侧螺旋茎上有一个错配的腺嘌呤被排除在外。结构探测与环的这种结构一致,并揭示了富含5'尿苷的凸起周围的异常结构,该凸起是反式激活蛋白Tat的结合靶点。这些数据可能有助于理解TAR与Tat蛋白的相互作用,并可能有助于抗艾滋病药物的设计。模型的坐标可应要求提供。