Sulfur as an Acceptor to Bromine in Biomolecular Halogen Bonds

被引:27
作者
Ford, Melissa Coates [1 ]
Saxton, Matthew [1 ]
Ho, P. Shing [1 ]
机构
[1] Colorado State Univ, Dept Biochem & Mol Biol, 1870 Campus Delivery, Ft Collins, CO 80523 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-INTERACTIONS; MEDICINAL CHEMISTRY; CRYSTAL-STRUCTURES; COMPLEXES; ENERGIES; SEQUENCE; JUNCTION; BINDING; DESIGN; MODEL;
D O I
10.1021/acs.jpclett.7b01725
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The halogen bond (X-bond) has become an important design element in chemistry, including medicinal chemistry and biomolecular engineering. Although oxygen is the most prevalent and best characterized X-bond acceptor in biomolecules, the interaction is seen with nitrogen, sulfur, and aromatic systems as well. In this study, we characterize the structure and thermodynamics of a Br center dot center dot center dot S X-bond between a 5-bromouracil base and a phosphorothioate in a model DNA junction. The single-crystal structure of the junction shows the geometry of the Br center dot center dot center dot S to be variable, while calorimetric studies show that the anionic S acceptor is comparable to or slightly more stable than the analogous O acceptor, with a -3.5 kcal/mol difference in Delta Delta H25 degrees(C) and -0.4 kcal/mol Delta Delta G(25 degrees C) (including an entropic penalty Delta Delta S-25 degrees C of -10 cal/(mol K)). Thus sulfur is shown to be a favorable acceptor for bromine X-bonds, extending the application of this interaction for the design of inhibitors and biological materials.
引用
收藏
页码:4246 / 4252
页数:7
相关论文
共 50 条
[31]   Halogen bonds of halonium ions [J].
Turunen, Lotta ;
Erdelyi, Mate .
CHEMICAL SOCIETY REVIEWS, 2020, 49 (09) :2688-2700
[32]   Halogen Bonds in the Structure of Tetrabromophenylbutane [J].
Korablev, G. G. ;
Dorovatovskii, P. V. ;
Efremov, A. N. ;
Osipov, A. A. ;
Rajakumar, K. ;
Nayfert, S. A. ;
Zherebtsov, D. A. .
JOURNAL OF STRUCTURAL CHEMISTRY, 2024, 65 (01) :75-81
[33]   Straightening out halogen bonds [J].
Setter, Caitlin J. ;
Whittaker, Jacob J. ;
Brock, Aidan J. ;
Arachchige, Kasun S. Athukorala ;
McMurtrie, John C. ;
Clegg, Jack K. ;
Pfrunder, Michael C. .
CRYSTENGCOMM, 2020, 22 (10) :1687-1690
[34]   Supramolecular Synthesis Based on a Combination of Hydrogen and Halogen Bonds [J].
Aakeroey, Christer B. ;
Schultheiss, Nate C. ;
Rajbanshi, Arbin ;
Desper, John ;
Moore, Curtis .
CRYSTAL GROWTH & DESIGN, 2009, 9 (01) :432-441
[35]   Structure-Energy Relationships of Halogen Bonds in Proteins [J].
Scholfield, Matthew R. ;
Ford, Melissa Coates ;
Carlsson, Anna-Carin C. ;
Butta, Hawera ;
Mehl, Ryan A. ;
Ho, P. Shing .
BIOCHEMISTRY, 2017, 56 (22) :2794-2802
[36]   Ability of Peripheral H Bonds to Strengthen a Halogen Bond [J].
Scheiner, Steve .
JOURNAL OF PHYSICAL CHEMISTRY A, 2022, 126 (51) :9691-9698
[37]   Testing the reality of F..F halogen bonds☆ [J].
Scheiner, Steve .
CHEMICAL PHYSICS LETTERS, 2025, 860
[38]   The relative roles of electrostatics and dispersion in the stabilization of halogen bonds [J].
Riley, Kevin E. ;
Hobza, Pavel .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2013, 15 (41) :17742-17751
[39]   NX•••Y halogen bonds. Comparison with NH•••Y H-bonds and CX•••Y halogen bonds [J].
Nepal, Binod ;
Scheiner, Steve .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2016, 18 (27) :18015-18023
[40]   Activation of metal-involved halogen bonds and classical halogen bonds in gold(i) catalysis [J].
Li, Ying ;
Sun, Yuanyuan ;
Zhao, Chang ;
Zeng, Yanli .
DALTON TRANSACTIONS, 2023, 52 (14) :4517-4525