A Single Watson-Crick G•C Base Pair in Water: Aqueous Hydrogen Bonds in Hydrophobic Cavities

被引:76
|
作者
Sawada, Tomohisa [1 ]
Fujita, Makoto [1 ,2 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
[2] CREST JST, Bunkyo Ku, Tokyo 1138656, Japan
关键词
ANION-PI INTERACTIONS; NUCLEIC-ACID BASES; HELICAL ROSETTE NANOTUBES; MOLECULAR RECOGNITION; COORDINATION CAGE; CONFINED CAVITY; CRYSTALLOGRAPHIC OBSERVATION; SELECTIVE RECOGNITION; GEOMETRIC PARAMETERS; DISCRETE STACKING;
D O I
10.1021/ja101718c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen bond (H-bond) formation in water has been a challenging task because water molecules are constant competitors. In biological systems, however, stable H-bonds are formed by shielding the H-bonding sites from the competing water molecules within hydrophobic pockets. Inspired by the nature's elaborated way, we found that even mononucleotides (G and C) can form the minimal G center dot C Watson-Crick pair in water by simply providing a synthetic cavity that efficiently shields the Watson-Crick H-bonding sites. The minimal Watson-Crick structure in water was elucidated by NMR study and firmly characterized by crystallographic analysis. The crystal structure also displays that, within the cavity, coencapsulated anions and solvents efficiently mediate the minimal G center dot C Watson-Crick pair formation. Furthermore, the competition experiments with the other nucleobases clearly revealed the evident selectivity for the G center dot C base pairing in water. These results show the fact that a H-bonded nucleobase pair was effectively induced and stabilized in the local environment of an artificial hydrophobic cavity.
引用
收藏
页码:7194 / 7201
页数:8
相关论文
共 50 条
  • [1] Cooperative vibrational properties of hydrogen bonds in Watson-Crick DNA base pairs
    Shi, Yulei
    Jiang, Wanrun
    Zhang, Zhiyuan
    Wang, Zhigang
    NEW JOURNAL OF CHEMISTRY, 2017, 41 (20) : 12104 - 12109
  • [2] Detection of the G(-H)• Radical in the Electronic Deactivation of the G-C Watson-Crick Base Pair
    Roettger, Katharina
    Temps, Friedrich
    ULTRAFAST PHENOMENA XIX, 2015, 162 : 514 - 516
  • [3] A DNA hairpin with a single residue loop closed by a strongly distorted Watson-Crick G•C base-pair
    El Amri, C
    Mauffret, O
    Monnot, M
    Tevanian, G
    Lescot, E
    Porumb, H
    Fermandjian, S
    JOURNAL OF MOLECULAR BIOLOGY, 1999, 294 (02) : 427 - 442
  • [4] Reverse Watson-Crick G-G base pair in G-quadruplex formation
    Mondal, Soma
    Bhat, Jyotsna
    Jana, Jagannath
    Mukherjee, Meghomukta
    Chatterjee, Subhrangsu
    MOLECULAR BIOSYSTEMS, 2016, 12 (01) : 18 - 22
  • [5] Solvent effects on hydrogen bonds in Watson-Crick, mismatched, and modified DNA base pairs
    Poater, Jordi
    Swart, Marcel
    Guerra, Celia Fonseca
    Bickelhaupt, F. Matthias
    COMPUTATIONAL AND THEORETICAL CHEMISTRY, 2012, 998 : 57 - 63
  • [6] Theoretical ab initio study of the effects of methylation on structure and stability of G:C Watson-Crick base pair
    Forde, G
    Flood, A
    Salter, L
    Hill, G
    Gorb, L
    Leszczynski, J
    JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2003, 20 (06): : 811 - 817
  • [7] NMR scaler couplings across Watson-Crick base pair hydrogen bonds in DNA observed by transverse relaxation optimized spectroscopy
    Pervushin, K
    Ono, A
    Fernández, C
    Szyperski, T
    Kainosho, M
    Wüthrich, K
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (24) : 14147 - 14151
  • [8] Electron attachment to the microsolvated Watson-Crick guanine cytosine base pair
    Zhang, Jun D.
    Schaefer, Henry F., III
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 233 : 211 - 211
  • [9] Canonical Watson-Crick base pair interactions in π → π* type triplet states
    Noguera, M
    Blancafort, L
    Sodupe, M
    Bertran, J
    MOLECULAR PHYSICS, 2006, 104 (5-7) : 925 - 931
  • [10] Watson-Crick base pairs with thiocarbonyl groups: How sulfur changes the hydrogen bonds in DNA
    Guerra, Celia Fonseca
    Baerends, Evert Jan
    Bickelhaupt, F. Matthias
    CENTRAL EUROPEAN JOURNAL OF CHEMISTRY, 2008, 6 (01): : 15 - 21