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抗原表位-抗原决定簇结合中的疏水、亲水及其他相互作用。

Hydrophobic, hydrophilic and other interactions in epitope-paratope binding.

作者信息

Van Oss C J

机构信息

Department of Microbiology, State University of New York at Buffalo 14214.

出版信息

Mol Immunol. 1995 Feb;32(3):199-211. doi: 10.1016/0161-5890(94)00124-j.

Abstract

Macroscopic, non-covalent, aspecific interactions between hydrophilic biopolymers, particles and cells in aqueous media tend to be repulsive; they are caused by Lifshitz-van der Waals (LW), Lewis acid-base (AB) and electrostatic (EL) forces. Microscopic scale specific interactions, e.g. between epitopes and paratopes, are also non-covalent and caused by attractive LW, AB and EL forces, which locally must be able to overcome the long- to medium-range macroscopic aspecific repulsive forces. Thus epitopes and paratopes need to be able to attract each other over a distance of at least 3 nm. The medium- and long-range specific attractive forces are mainly of hydrophobic (AB) and of EL origin; in aqueous media the medium- and long-range LW attractions are usually much weaker. It has been shown that hydrophobic (AB) interactions are as often enthalpic as entropic. Upon expulsion of interstitial water of hydration between epitope and paratope, a strong interfacial bond ultimately arises which is mainly caused by LW forces.

摘要

在水性介质中,亲水性生物聚合物、颗粒和细胞之间的宏观非共价非特异性相互作用往往具有排斥性;它们是由 Lifshitz-范德华力(LW)、路易斯酸碱力(AB)和静电力(EL)引起的。微观尺度的特异性相互作用,例如表位与互补位之间的相互作用,也是非共价的,由吸引力的LW、AB和EL力引起,这些力在局部必须能够克服长程到中程的宏观非特异性排斥力。因此,表位和互补位需要能够在至少3纳米的距离上相互吸引。中程和长程特异性吸引力主要源于疏水(AB)力和EL力;在水性介质中,中程和长程LW吸引力通常要弱得多。研究表明,疏水(AB)相互作用的焓效应和熵效应出现的频率相当。当表位和互补位之间的间隙水化水被排出时,最终会形成一种主要由LW力引起的强界面键。

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