Adaptive Ligand Binding by the Purine Riboswitch in the Recognition of Guanine and Adenine Analogs

被引:111
作者
Gilbert, Sunny D. [1 ]
Reyes, Francis E. [1 ]
Edwards, Andrea L. [1 ]
Batey, Robert T. [1 ]
机构
[1] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
STRUCTURAL BASIS; INDUCED FIT; GENE-EXPRESSION; RNA; TARGETS;
D O I
10.1016/j.str.2009.04.009
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
Purine riboswitches; discriminate between guanine and adenine by at least 10,000-fold based on the identity of a single pyrimidine (Y74) that forms a Watson-Crick base pair with the ligand. To understand how this high degree of specificity for closely related compounds is achieved through simple pairing, we investigated their interaction with purine analogs with varying functional groups at the 2- and 6-positions that have the potential to alter interactions with Y74. Using a combination of crystallographic and calorimetric approaches, we find that binding these purines is often facilitated by either small structural changes in the RNA or tautomeric changes in the ligand. This work also reveals that, along with base pairing, conformational restriction of Y74 significantly contributes to nucleobase selectivity. These results reveal that compounds that exploit the inherent local flexibility within riboswitch binding pockets can alter their ligand specificity.
引用
收藏
页码:857 / 868
页数:12
相关论文
共 43 条
[1]   Mechanisms of resistance to an amino acid antibiotic that targets translation [J].
Ataide, Sandro F. ;
Wilson, Shamise N. ;
Dang, Sandy ;
Rogers, Theresa E. ;
Roy, Bappaditya ;
Banerjee, Rajat ;
Henkin, Tina M. ;
Ibba, Michael .
ACS CHEMICAL BIOLOGY, 2007, 2 (12) :819-827
[2]   Halogen bonds in biological molecules [J].
Auffinger, P ;
Hays, FA ;
Westhof, E ;
Ho, PS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (48) :16789-16794
[3]   Antibacterial lysine analogs that target lysine riboswitches [J].
Blount, Kenneth F. ;
Wang, Joy Xin ;
Lim, Jinsoo ;
Sudarsan, Narasimhan ;
Breaker, Ronald R. .
NATURE CHEMICAL BIOLOGY, 2007, 3 (01) :44-49
[4]   Riboswitches as antibacterial drug targets [J].
Blount, Kenneth F. ;
Breaker, Ronald R. .
NATURE BIOTECHNOLOGY, 2006, 24 (12) :1558-1564
[5]   Crystallography & NMR system:: A new software suite for macromolecular structure determination [J].
Brunger, AT ;
Adams, PD ;
Clore, GM ;
DeLano, WL ;
Gros, P ;
Grosse-Kunstleve, RW ;
Jiang, JS ;
Kuszewski, J ;
Nilges, M ;
Pannu, NS ;
Read, RJ ;
Rice, LM ;
Simonson, T ;
Warren, GL .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1998, 54 :905-921
[6]   General acid catalysis by the hepatitis delta virus ribozyme [J].
Das, SR ;
Piccirilli, JA .
NATURE CHEMICAL BIOLOGY, 2005, 1 (01) :45-52
[7]   A Structural Basis for the Recognition of 2′-Deoxyguanosine by the Purine Riboswitch [J].
Edwards, Andrea L. ;
Batey, Robert T. .
JOURNAL OF MOLECULAR BIOLOGY, 2009, 385 (03) :938-948
[8]   Crystal structures of the thi-box riboswitch bound to thiamine pyrophosphate analogs reveal adaptive RNA-small molecule recognition [J].
Edwards, Thomas E. ;
Ferre-D'Amare, Adrian R. .
STRUCTURE, 2006, 14 (09) :1459-1468
[9]   Crystal structure of the lysine riboswitch regulatory mRNA element [J].
Garst, Andrew D. ;
Heroux, Annie ;
Rambo, Robert P. ;
Batey, Robert T. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (33) :22347-22351
[10]  
GAUTHERET D, 1995, RNA, V1, P807