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
  • [41] Characterization of hydrogen bond lengths in Watson-Crick base pairs by cross-correlated relaxation
    Riek, R
    JOURNAL OF MAGNETIC RESONANCE, 2001, 149 (01) : 149 - 153
  • [42] PtII coordination to guanine-N7:: enhancement of the stability of the Watson-Crick base pair with cytosine
    Sigel, RKO
    Lippert, B
    CHEMICAL COMMUNICATIONS, 1999, (21) : 2167 - 2168
  • [43] Single versus double proton-transfer reactions in Watson-Crick base pair radical cations.: A theoretical study
    Bertran, J
    Oliva, A
    Rodríguez-Santiago, L
    Sodupe, M
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (32) : 8159 - 8167
  • [44] Substituent effects of phthalimide-based nucleoside analogs on binding a CG Watson-Crick base pair
    Xiao, Z.
    Weisz, K.
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 2007, 20 (10) : 771 - 777
  • [45] Characterization of the Trans Watson-Crick GU Base Pair Located in the Catalytic Core of the Antigenomic HDV Ribozyme
    Levesque, Dominique
    Reymond, Cedric
    Perreault, Jean-Pierre
    PLOS ONE, 2012, 7 (06):
  • [46] Charge Transport Properties of DNA Aperiodic Molecule: The Role of Interbase Hopping in Watson-Crick Base Pair
    Sinurat, E. N.
    Yudiarsah, E.
    INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2016 (ISCPMS 2016), 2017, 1862
  • [47] Regulative effect of water molecules on the switches of guanine-cytosine (GC) Watson-Crick pair
    Ai, Hongqi
    Peng, Xian
    Li, Yun
    Zhang, Chong
    COMPUTATIONAL SCIENCE - ICCS 2007, PT 2, PROCEEDINGS, 2007, 4488 : 327 - +
  • [48] Substituent effif ects on hydrogen bonding in Watson-Crick base pairs. A theoretical study
    Guerra, CF
    van der Wijst, T
    Bickelhaupt, FM
    STRUCTURAL CHEMISTRY, 2005, 16 (03) : 211 - 221
  • [49] Metal-Mediated DNA Base Pairing: Alternatives to Hydrogen-Bonded Watson-Crick Base Pairs
    Takezawa, Yusuke
    Shionoya, Mitsuhiko
    ACCOUNTS OF CHEMICAL RESEARCH, 2012, 45 (12) : 2066 - 2076
  • [50] Discrimination among individual Watson-Crick base pairs at the termini of single DNA hairpin molecules
    Vercoutere, WA
    Winters-Hilt, S
    DeGuzman, VS
    Deamer, D
    Ridino, SE
    Rodgers, JT
    Olsen, HE
    Marziali, A
    Akeson, M
    NUCLEIC ACIDS RESEARCH, 2003, 31 (04) : 1311 - 1318