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探索水中大环合成受体动态组合库中扩增与结合之间的关系。

Exploring the relation between amplification and binding in dynamic combinatorial libraries of macrocyclic synthetic receptors in water.

作者信息

Corbett Peter T, Sanders Jeremy K M, Otto Sijbren

机构信息

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK.

出版信息

Chemistry. 2008;14(7):2153-66. doi: 10.1002/chem.200701413.

Abstract

Herein we describe an extensive study of the response of a set of closely related dynamic combinatorial libraries (DCLs) of macrocyclic receptors to the introduction of a focused range of guest molecules. We have determined the amplification of two sets of diastereomeric receptors induced by a series of neutral and cationic guests, including biologically relevant compounds such as acetylcholine and morphine. The host-guest binding affinities were investigated using isothermal titration calorimetry. The resulting dataset enabled a detailed analysis of the relationship between the amplification of selected receptors and host-guest Gibbs binding energies, giving insight into the factors affecting the design, simulation and interpretation of DCL experiments. In particular, two questions were addressed: Is amplification by a given guest selective for the best receptor? And does the best guest induce the largest amplification of a given receptor? Our experimental results and computer simulations showed that the relative levels of amplification of hosts by a guest are well-correlated with their relative affinities, and simulations have confirmed previous observations that amplification can be selective for the best receptor when only modest amounts of guest are used. In contrast, the correlation between guest binding and the extent of amplification of a given receptor across a wide range of guests tends to be poorer, because every guest has its own unique set of affinities for competing receptors in the DCL. This implies that the results of screening a DCL for selective receptors by comparing the response of the mixture to two different guests should be interpreted with caution. DCLs are complex mixtures in which all compounds are connected through a set of equilibria. Obtaining quantitative information about all host-guest binding constants from such systems will require the explicit and simultaneous consideration of all of the main equilibria within a DCL.

摘要

在此,我们描述了一项广泛的研究,该研究涉及一组紧密相关的大环受体动态组合库(DCLs)对一系列特定客体分子引入的响应。我们已经确定了由一系列中性和阳离子客体(包括生物相关化合物如乙酰胆碱和吗啡)诱导的两组非对映体受体的扩增情况。使用等温滴定量热法研究了主客体结合亲和力。所得数据集使得能够详细分析所选受体的扩增与主客体吉布斯结合能之间的关系,从而深入了解影响DCL实验设计、模拟和解释的因素。特别是,解决了两个问题:给定客体的扩增是否对最佳受体具有选择性?以及最佳客体是否能诱导给定受体的最大扩增?我们的实验结果和计算机模拟表明,客体对主体的相对扩增水平与其相对亲和力密切相关,并且模拟证实了先前的观察结果,即当仅使用适量客体时,扩增可以对最佳受体具有选择性。相比之下,在广泛的客体范围内,客体结合与给定受体的扩增程度之间的相关性往往较差,因为每个客体对DCL中竞争受体都有其独特的亲和力组合。这意味着通过比较混合物对两种不同客体的响应来筛选DCL中的选择性受体的结果应谨慎解释。DCL是复杂的混合物,其中所有化合物通过一组平衡相互连接。从这样的系统中获取所有主客体结合常数的定量信息将需要明确并同时考虑DCL内的所有主要平衡。

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