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纺锤菌素和偏端霉素A与tRNA(苯丙氨酸)意外的大沟结合。

An unexpected major groove binding of netropsin and distamycin A to tRNA(phe).

作者信息

Rubin J, Sundaralingam M

机构信息

Department of Biochemistry, College of Agricultural and Life Sciences, University of Wisconsin-Madison 53706.

出版信息

J Biomol Struct Dyn. 1984 Aug;2(1):165-74. doi: 10.1080/07391102.1984.10507555.

Abstract

Crystalline complexes of yeast tRNA(phe) and the oligopeptide antibiotics netropsin and distamycin A were prepared by diffusing drugs into crystals of tRNA. X-ray structure analyses of these complexes reveal a single common binding site for both drugs which is located in the major or deep groove of the tRNA T-stem. The netropsin-tRNA complex is stabilized by specific hydrogen bonds between the amide groups of the drug and the tRNA bases G51 O(6), U52 O(4) and G53 N(7) on one strand, and is further stabilized by electrostatic interactions between the positively charges guanidino side chain of the drug and the tRNA phosphate P53 on the same strand and the positively charged amidino propyl side chain and the phosphates P61, P62 and P63 on the opposite strand of the double helix. These results are in contrast to the implicated minor groove binding of these drugs to non-guanine sequences in DNA. The binding to the GUG sequence in tRNA implies that major groove binding to certain DNA sequences is possible.

摘要

通过将药物扩散到酵母苯丙氨酸转运核糖核酸(tRNA(phe))晶体中,制备了tRNA(phe)与寡肽抗生素纺锤菌素和偏端霉素A的晶体复合物。对这些复合物的X射线结构分析揭示了两种药物的一个共同结合位点,该位点位于tRNA T形茎的大沟或深沟中。纺锤菌素-tRNA复合物通过药物酰胺基团与一条链上tRNA碱基G51的O(6)、U52的O(4)和G53的N(7)之间的特定氢键得以稳定,并且通过药物带正电荷的胍基侧链与同一条链上的tRNA磷酸基团P53以及双螺旋相反链上带正电荷的脒基丙基侧链与磷酸基团P61、P62和P63之间的静电相互作用进一步稳定。这些结果与这些药物与DNA中非鸟嘌呤序列的小沟结合的观点形成对比。与tRNA中GUG序列的结合表明,与某些DNA序列的大沟结合是可能的。

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