Effect of Divalent Cations on Polarity and Hydration at the Lipid/Water Interface Probed by 4-Aminophthalimide-Based Dyes.

IF 2.9 2区 化学 Q3 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry B Pub Date : 2025-01-23 Epub Date: 2025-01-10 DOI:10.1021/acs.jpcb.4c05404
Parvez Alam, Pramod Kumar, Harsh Sahu, Deepika Sardana, Pronab Kundu, Ajay Kumar Chand, Sobhan Sen
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Abstract

The ion binding to the lipid/water interface can substantially influence the structural, functional, and dynamic properties of the cell membrane. Despite extensive research on ion-lipid interactions, the specific effects of ion binding on the polarity and hydration at the lipid/water interface remain poorly understood. This study explores the influence of three biologically relevant divalent cations─Mg2+, Ca2+, and Zn2+─on the depth-dependent interfacial polarity and hydration of zwitterionic DPPC lipid in its gel phase at room temperature. To measure these depth-dependent properties, we use a series of solvatochromic fluorescent probes synthesized based on 4-aminophthalimide with varying alkyl chain lengths (4AP-Cn; n = 5, 7, and 9). Employing steady-state fluorescence experiments and all-atom molecular dynamics (MD) simulations, we quantify changes in interfacial polarity and hydration induced by the cations binding to the lipid/water interface. Our results reveal that Zn2+ induces a significant blue shift in the fluorescence spectra of all 4AP-Cn dyes, indicating a marked decrease in local polarity (ETN ≤ 0.05) at the lipid/water interface compared to Mg2+ and Ca2+, which results in a higher polarity (ETN ≥ 0.2). The depth-dependent fluorescence spectra of dyes at the interface in the presence of Mg2+ and Ca2+ remain similar to those in the absence of cations, with only a minor red shift observed for Mg2+, implying a slight hydration effect. MD simulations show that cations primarily bind to the headgroup and glycerol regions of lipid. Simulations also reveal that Zn2+ causes substantial dehydration at the lipid/water interface, as detected by the 4AP-Cn dyes, while Mg2+ and Ca2+ have less pronounced effects, with only slight hydration induced by Mg2+. This study highlights the distinct positional effects of cations probed by 4AP-Cn probes at the lipid-water interface, underscoring the potential of 4AP-Cn dyes for monitoring depth-dependent changes in membrane properties induced by external agents or environmental conditions.

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二价阳离子对4-氨基酰亚胺染料探测的脂/水界面极性和水合作用的影响。
离子与脂/水界面的结合可以极大地影响细胞膜的结构、功能和动态特性。尽管对离子-脂质相互作用进行了广泛的研究,但离子结合对脂质/水界面极性和水合作用的具体影响仍然知之甚少。本研究探讨了三种生物相关的二价阳离子──Mg2+、Ca2+和Zn2+──在室温下对两性离子DPPC脂质凝胶相中深度依赖的界面极性和水化的影响。为了测量这些与深度相关的性质,我们使用了一系列基于不同烷基链长的4-氨基酞酰亚胺合成的溶剂致变色荧光探针(4AP-Cn;n = 5,7,和9)。采用稳态荧光实验和全原子分子动力学(MD)模拟,我们量化了由阳离子结合到脂质/水界面引起的界面极性和水合作用的变化。我们的研究结果表明,Zn2+在所有4AP-Cn染料的荧光光谱中引起了显著的蓝移,表明与Mg2+和Ca2+相比,脂质/水界面的局部极性(ETN≤0.05)明显降低,从而导致更高的极性(ETN≥0.2)。在Mg2+和Ca2+存在的情况下,染料在界面处的深度依赖荧光光谱与没有阳离子的情况相似,Mg2+只观察到轻微的红移,这意味着轻微的水化作用。MD模拟表明,阳离子主要结合到脂质的头基和甘油区域。模拟还显示,正如4AP-Cn染料检测到的那样,Zn2+在脂/水界面引起大量脱水,而Mg2+和Ca2+的作用不那么明显,Mg2+只引起轻微的水化。本研究强调了由4AP-Cn探针探测的阳离子在脂-水界面上的独特位置效应,强调了4AP-Cn染料在监测由外部介质或环境条件引起的膜性质深度依赖性变化方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
9.10%
发文量
965
审稿时长
1.6 months
期刊介绍: An essential criterion for acceptance of research articles in the journal is that they provide new physical insight. Please refer to the New Physical Insights virtual issue on what constitutes new physical insight. Manuscripts that are essentially reporting data or applications of data are, in general, not suitable for publication in JPC B.
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