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克服离子识别与结合中的水合和溶剂化问题:仿生方法。

Overcoming the Hydration and Solvation Problem in Ion Recognition and Binding: The Biomimetic Approach.

作者信息

Anzenbacher Pavel, Prakash Anjusha, George Sandra M, Sartori Austin R, Zamkov Mikhail, Tarnovsky Alexander N

机构信息

Department of Chemistry, Bowling Green State University, Bowling Green, Ohio 43403, United States.

Department of Physics and Astronomy, Bowling Green State University, Bowling Green, Ohio 43403, United States.

出版信息

Acc Chem Res. 2025 Aug 21. doi: 10.1021/acs.accounts.5c00472.

Abstract

ConspectusArtificial receptors for cations and anions utilizing noncovalent binding, transport, sequestration, or sensing in aqueous media must address enthalpic factors such as electrostatic attraction, hydrogen bonding, van der Waals forces, and London dispersion forces. The entropic component also significantly contributes to the free energy of association, especially in polar environments like water, where binding may be entropy-driven due to the release of ordered solvent molecules from the solvation sphere, increasing system entropy and resulting in a negative free Gibbs energy. Over the years, chemists have focused on enthalpic criteria, such as size complementarity and functional group interactions, for designing artificial receptors. However, designing for the entropic component, particularly solvation/desolvation, remains challenging and often depends on fortunate circumstances.As shown by X-ray crystallography, enzymes and proteins can strip solvating water molecules from the ions. Inspired by phosphate-binding enzymes and transporters, we examined polymers comprising amide bonds, such as polyamides and polyurethanes, to mimic protein backbones. These hydrophilic polymers can be engineered to absorb specific amounts of water (10-100% or even more). We aimed to use hydrophilic polymers to remove water molecules from hydrated ions, rendering them "naked" ions, thus enabling better recognition by receptors based on enthalpic factors. To test this, we used copolymers with amide and urethane-amide moieties with different ratios of poly(ethylene oxide) and poly(butylene oxide) to control water uptake between 10% and 100%, along with embedded fluorescent sensors. We found that polymers with 30-50% water uptake showed the highest fluorescence response, while uptake below 20% resulted in small changes in fluorescence and 60-100% led to diminished responses. Low water uptake caused reduced ion co-transport, while high uptake formed large water pools within the polymers, isolating solvated ions from receptors. The optimal water uptake of 30-50% produced (semi)naked ions and a water-organic matrix similar to that of DMSO-water environments. Just like proteins, the structure impacts the recognition and internalization of anions, such as phosphate or sulfate; here too, the monomer composition and synthetic sequence greatly influence material responses to anions, with lipophilic ones eliciting lower responses. The data analysis of fluorescence responses enables the generation of sensor arrays for both cations and anions in water, buffers, saliva, urine, or blood plasma, both qualitative and quantitative analyses, for single analytes or as analyte mixtures. Overall, this biomimetic approach focused on the recovery of the enthalpic factor (by diminishing the impact of solvation and entropy) has proven remarkably successful in creating sensors and adsorbents for charged species in aqueous media and water and is expected to find applications in optical sensors, sensor arrays, ion-selective electrodes, and other analytical methods.

摘要

概述

在水介质中利用非共价结合、运输、螯合或传感作用的阳离子和阴离子人工受体,必须考虑焓因素,如静电吸引、氢键、范德华力和伦敦色散力。熵成分也对缔合自由能有显著贡献,特别是在像水这样的极性环境中,由于溶剂化球中有序溶剂分子的释放,结合可能是由熵驱动的,这会增加系统熵并导致吉布斯自由能为负。多年来,化学家们一直专注于焓标准,如尺寸互补性和官能团相互作用,来设计人工受体。然而,针对熵成分进行设计,特别是溶剂化/去溶剂化,仍然具有挑战性,而且往往取决于幸运的情况。

如X射线晶体学所示,酶和蛋白质可以从离子上剥离溶剂化水分子。受磷酸盐结合酶和转运蛋白的启发,我们研究了包含酰胺键的聚合物,如聚酰胺和聚氨酯,以模拟蛋白质主链。这些亲水性聚合物可以被设计成吸收特定量的水(10 - 100%甚至更多)。我们的目标是使用亲水性聚合物从水合离子中去除水分子,使其成为“裸”离子,从而使受体基于焓因素能够更好地识别。为了测试这一点,我们使用了具有酰胺和氨基甲酸酯 - 酰胺部分的共聚物,其聚(环氧乙烷)和聚(环氧丁烷)的比例不同,以控制吸水量在10%至100%之间,同时还嵌入了荧光传感器。我们发现,吸水量为30 - 50%的聚合物显示出最高的荧光响应,而吸水量低于20%时荧光变化较小,60 - 100%时响应减弱。低吸水量导致离子共运输减少,而高吸水量则在聚合物内形成大水池,将溶剂化离子与受体隔离开来。30 - 50%的最佳吸水量产生了(半)裸离子和类似于二甲基亚砜 - 水环境的水 - 有机基质。就像蛋白质一样,结构会影响阴离子(如磷酸盐或硫酸盐)的识别和内化;在这里,单体组成和合成序列也极大地影响材料对阴离子的响应,亲脂性阴离子引起的响应较低。荧光响应的数据分析能够生成用于水、缓冲液、唾液、尿液或血浆中阳离子和阴离子的传感器阵列,可进行定性和定量分析,用于单一分析物或分析物混合物。总体而言,这种专注于恢复焓因素(通过减少溶剂化和熵的影响)的仿生方法已被证明在创建用于水介质和水中带电物种的传感器和吸附剂方面非常成功,并有望在光学传感器、传感器阵列、离子选择性电极和其他分析方法中找到应用。

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