Structure of a pseudo-16-mer DNA with stacked guanines and two G-A mispairs complexed with the N-terminal fragment of Moloney murine leukemia virus reverse transcriptase

被引:17
作者
Coté, ML
Georgiadis, MM
机构
[1] Rutgers State Univ, Waksman Inst, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Dept Chem, Piscataway, NJ 08854 USA
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2001年 / 57卷
关键词
D O I
10.1107/S090744490100943X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The X-ray crystal structure at 2.0 Angstrom resolution of a DNA molecule complexed with the N-terminal fragment of Moloney murine leukemia virus reverse transcriptase (MMLV RT) has been determined. This method allows the study of nucleic acids in a unique and largely unfettered environment without the complicated lattice interactions typically observed in DNA-only crystal structures. Molecular-replacement phasing using only the protein provided readily interpretable electron density with no model bias for the DNA. The asymmetric unit of the structure consists of the protein molecule bound to the blunt end of a DNA 6/10-mer, which is composed of a six-base strand (5'-GTCGTC-3') and a ten-base strand (3'-CAGCAGGGCA-5'), resulting in a six-base-pair duplex with a four-base single-stranded overhang. In the crystal structure, the bases of the overhang reciprocally pair to yield a doubly nicked pseudo-hexadecamer primarily B-form DNA molecule. The pairing between the single strands gives two standard (G-C) Watson-Crick pairs and two G(anti)-A(anti) mispairs. The mispairs reside in a G-C-rich environment and the three consecutive guanines on the 10-mer impart interesting structural features to the pseudo-hexadecamer, such as the preference for a guanine stack, stretching the C-G base pairs flanking the mispair to the point of loss of intra-base-pair hydrogen bonding. The DNA was designed for the purpose of comparison with a previous structure, which was determined in the same crystal lattice. In all of the authors' previous fragment-DNA complexes, the nucleotide at the blunt-ended 3'-hydroxyl was a purine. Consistent with the proposed mechanistic role of interactions with the 3'-hydroxyl in processive DNA synthesis by RT, it was found that a pyrimidine at this position in the DNA makes indentical interactions with the strictly conserved Gly191 and the main chain of Leu115 of MMLV RT.
引用
收藏
页码:1238 / 1250
页数:13
相关论文
共 42 条
[1]   RECOGNITION OF A DNA OPERATOR BY THE REPRESSOR OF PHAGE-434 - A VIEW AT HIGH-RESOLUTION [J].
AGGARWAL, AK ;
RODGERS, DW ;
DROTTAR, M ;
PTASHNE, M ;
HARRISON, SC .
SCIENCE, 1988, 242 (4880) :899-907
[2]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[3]   CRYSTAL-STRUCTURE AND STABILITY OF A DNA DUPLEX CONTAINING A(ANTI).G(SYN) BASE-PAIRS [J].
BROWN, T ;
LEONARD, GA ;
BOOTH, ED ;
CHAMBERS, J .
JOURNAL OF MOLECULAR BIOLOGY, 1989, 207 (02) :455-457
[4]   MOLECULAR-STRUCTURE OF THE G-A BASE PAIR IN DNA AND ITS IMPLICATIONS FOR THE MECHANISM OF TRANSVERSION MUTATIONS [J].
BROWN, T ;
HUNTER, WN ;
KNEALE, G ;
KENNARD, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2402-2406
[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]   POSSIBLE CONFORMATIONS OF DOUBLE-HELICAL POLYNUCLEOTIDES CONTAINING INCORRECT BASE-PAIRS [J].
CHUPRINA, VP ;
POLTEV, VI .
NUCLEIC ACIDS RESEARCH, 1983, 11 (15) :5205-5222
[7]   Use of an N-terminal fragment from Moloney murine leukemia virus reverse transcriptase to facilitate crystallization and analysis of a pseudo-16-mer DNA molecule containing G-A mispairs [J].
Coté, ML ;
Yohannan, SJ ;
Georgiadis, MM .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2000, 56 :1120-1131
[8]   Two distinct modes of protein-induced bending in DNA [J].
El Hassan, MA ;
Calladine, CR .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 282 (02) :331-343
[9]   G(SYN).A(ANTI) MISMATCH FORMATION IN DNA DODECAMERS AT ACIDIC PH - PH-DEPENDENT CONFORMATIONAL TRANSITION OF G.A MISPAIRS DETECTED BY PROTON NMR [J].
GAO, XL ;
PATEL, DJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (15) :5178-5182
[10]   High-resolution A-DNA crystal structures of d(AGGGGCCCCT) -: An A-DNA model of poly(dG)•poly(dC) [J].
Gao, YG ;
Robinson, H ;
Wang, AHJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 261 (02) :413-420