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An RNA complex of the HIV-1 A-loop and tRNALys,3 is stabilized by nucleoside modifications
被引:21
作者
:
Bajji, AC
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
Bajji, AC
Sundaram, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
Sundaram, M
Myszka, DG
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
Myszka, DG
Davis, DR
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
Davis, DR
机构
:
[1]
Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
[2]
Univ Utah, Dept Oncol Sci, Salt Lake City, UT 84112 USA
来源
:
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
|
2002年
/ 124卷
/ 48期
关键词
:
D O I
:
10.1021/ja028015f
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
The HIV transcription initiation complex involves a putative interaction between the primer tRNA anticodon and a conserved A-rich loop in the HIV genome. Surface plasmon resonance was used to demonstrate that the hypermodified nucleosides in the tRNA anticodon stem loop (ASL) stabilize RNA-RNA interactions in a model for the anticodon/A-loop complex. tRNA ASL hairpins with the modifications of Escherchia coli tRNALys and human tRNALys,3 each form stable complexes. Partially modified tRNA ASLs bind the A-loop hairpin with lesser affinity, and it was found that the modifications of the bacterial and mammalian tRNAs make distinct contributions toward stabilizing the RNA complex. One model for the anticodon/A-loop RNA complex that is consistent with the known modification effects on tRNA structure and function is that of complementary tRNAs, as seen for the published crystal structure of tRNAAsp. Copyright © 2002 American Chemical Society.
引用
收藏
页码:14302 / 14303
页数:2
相关论文
共 21 条
[21]
TURNER DH, 1988, ANNU REV BIOPHYS BIO, V17, P167
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共 21 条
[21]
TURNER DH, 1988, ANNU REV BIOPHYS BIO, V17, P167
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