O-glycoside orientation is an essential aspect of base J recognition by the kinetoplastid DNA-binding protein JBP1

被引:22
作者
Grover, Rajesh K.
Pond, Stephanie J. K.
Cui, Qizhi
Subramaniam, Prem
Case, David A.
Millar, David P.
Wentworth, Paul, Jr.
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[3] Univ Oxford, Dept Biochem, Scripps Oxford Lab, Oxford Glycobiol Inst, Oxford OX1 3QU, England
[4] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[5] Scripps Res Inst Florida, Dept Infectol, Jupiter, FL 32458 USA
关键词
DNA; glycosides; molecular dynamics; molecular recognition;
D O I
10.1002/anie.200604635
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A binding edge? Comparison of dissociation constants and molecular-dynamics snapshots of a panel of synthetic telomeric double-stranded DNA sequences containing HMdU O-glycosides has revealed that the DNA-binding protein of kinetoplastids, such as Leishmania and Trypanosoma, JBP1, recognizes a critical edge-on conformation of the pyranosyl ring of base J. If this conformation is perturbed, JBP1 binding is dramatically reduced.(Chemical Equation Presented). © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:2839 / 2843
页数:5
相关论文
共 26 条
[1]   Thermodynamic dissection of the polymerizing and editing modes of a DNA polymerase [J].
Bailey, MF ;
van der Schans, EJC ;
Millar, DP .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 336 (03) :673-693
[2]   Solvated ensemble averaging in the calculation of partial atomic charges [J].
Basma, M ;
Sundara, S ;
Çalgan, D ;
Vernali, T ;
Woods, RJ .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2001, 22 (11) :1125-1137
[3]   MODIFICATION OF TELOMERIC DNA IN TRYPANOSOMA-BRUCEI - A ROLE IN ANTIGENIC VARIATION [J].
BERNARDS, A ;
VANHARTENLOOSBROEK, N ;
BORST, P .
NUCLEIC ACIDS RESEARCH, 1984, 12 (10) :4153-4170
[4]   β-D-glucosyl-hydroxymethyluracil, a novel base in African trypanosomes and other Kinetoplastida [J].
Borst, P ;
van Leeuwen, F .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1997, 90 (01) :1-8
[5]   The Amber biomolecular simulation programs [J].
Case, DA ;
Cheatham, TE ;
Darden, T ;
Gohlke, H ;
Luo, R ;
Merz, KM ;
Onufriev, A ;
Simmerling, C ;
Wang, B ;
Woods, RJ .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2005, 26 (16) :1668-1688
[6]   A 2ND GENERATION FORCE-FIELD FOR THE SIMULATION OF PROTEINS, NUCLEIC-ACIDS, AND ORGANIC-MOLECULES [J].
CORNELL, WD ;
CIEPLAK, P ;
BAYLY, CI ;
GOULD, IR ;
MERZ, KM ;
FERGUSON, DM ;
SPELLMEYER, DC ;
FOX, T ;
CALDWELL, JW ;
KOLLMAN, PA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (19) :5179-5197
[7]   The modified base J is the target for a novel DNA-binding protein in kinetoplastid protozoans [J].
Cross, M ;
Kieft, R ;
Sabatini, R ;
Wilm, M ;
de Kort, M ;
van der Marel, GA ;
van Boom, JH ;
van Leeuwen, F ;
Borst, P .
EMBO JOURNAL, 1999, 18 (22) :6573-6581
[8]  
de Kort M, 1999, EUR J ORG CHEM, V1999, P2337
[9]   Base J originally found in kinetoplastida is also a minor constituent of nuclear DNA of Euglena gracilis [J].
Dooijes, D ;
Chaves, I ;
Kieft, R ;
Dirks-Mulder, A ;
Martin, W ;
Borst, P .
NUCLEIC ACIDS RESEARCH, 2000, 28 (16) :3017-3021
[10]   Binding of daunorubicin to beta-D-glucosylated DNA found in protozoa Trypanosoma brucei studied by X-ray crystallography [J].
Gao, YG ;
Robinson, H ;
Wijsman, ER ;
vanderMarel, GA ;
vanBoom, JH ;
Wang, AHJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (06) :1496-1497