Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, Colorado 80523-1870, USA.
Protein Sci. 2013 Feb;22(2):139-52. doi: 10.1002/pro.2201. Epub 2012 Dec 29.
The concept of the halogen bond (or X-bond) has become recognized as contributing significantly to the specificity in recognition of a large class of halogenated compounds. The interaction is most easily understood as primarily an electrostatically driven molecular interaction, where an electropositive crown, or σ-hole, serves as a Lewis acid to attract a variety of electron-rich Lewis bases, in analogous fashion to a classic hydrogen bonding (H-bond) interaction. We present here a broad overview of X-bonds from the perspective of a biologist who may not be familiar with this recently rediscovered class of interactions and, consequently, may be interested in how they can be applied as a highly directional and specific component of the molecular toolbox. This overview includes a discussion for where X-bonds are found in biomolecular structures, and how their structure-energy relationships are studied experimentally and modeled computationally. In total, our understanding of these basic concepts will allow X-bonds to be incorporated into strategies for the rational design of new halogenated inhibitors against biomolecular targets or toward molecular engineering of new biological-based materials.
卤键(或 X 键)的概念已被认为对一大类卤化化合物的特异性识别有重要贡献。这种相互作用最容易被理解为主要是静电驱动的分子相互作用,其中正电冠或 σ 空穴作为路易斯酸,以类似于经典氢键(H 键)相互作用的方式吸引各种富电子路易斯碱。我们从可能不熟悉这种最近重新发现的相互作用类别的生物学家的角度,在这里广泛概述 X 键,因此可能有兴趣了解如何将它们作为分子工具包的高度定向和特定组成部分应用。本综述包括讨论 X 键在生物分子结构中的位置,以及它们的结构-能量关系如何通过实验和计算建模进行研究。总的来说,我们对这些基本概念的理解将使 X 键能够被纳入针对生物分子靶标的新型卤化抑制剂的合理设计或新型基于生物的材料的分子工程的策略中。