Reconciliation of the X-ray and NMR structures of the thrombin-binding aptamer d(GGTTGGTGTGGTTGG)

被引:174
作者
Kelly, JA
Feigon, J
Yeates, TO
机构
[1] UNIV CALIF LOS ANGELES, DEPT CHEM & BIOCHEM, LOS ANGELES, CA 90095 USA
[2] UNIV CALIF LOS ANGELES, INST MOLEC BIOL, LOS ANGELES, CA 90095 USA
关键词
thrombin; protein structure; nucleic acid structure; crystallography; aptamers; OXYTRICHA TELOMERIC DNA; EXPONENTIAL ENRICHMENT; SYSTEMATIC EVOLUTION; QUADRUPLEX STRUCTURE; SELECTION; MOLECULES; INVITRO; LIGANDS;
D O I
10.1006/jmbi.1996.0097
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The thrombin-binding aptamer d(GGTTGGTGTGGTTGG) is one of a family of DNA oligonucleotldes that were identified by in vitro selection to bind specifically and with high affinity to thrombin. Two groups independently determined the tertiary structure in solution by NMR and at about the same time, the X-ray crystal structure of the aptamer in complex with thrombin was reported. In all cases, the thrombin-binding aptamer was found to fold into a structure containing two planar guanine quartets as its core. The NMR and crystal structures, however, have fundamentally different folding patterns owing to differences in the way these central bases are connected. We discuss the distinctions between the refined crystal and solution structures and show that the NMR model is consistent with the X-ray diffraction data. (C) 1996 Academic Press Limited
引用
收藏
页码:417 / 422
页数:6
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