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用于测定原始无膜聚酯微滴盐分摄取差异的光谱和生物物理方法。

Spectroscopic and Biophysical Methods to Determine Differential Salt-Uptake by Primitive Membraneless Polyester Microdroplets.

作者信息

Chen Chen, Yi Ruiqin, Igisu Motoko, Sakaguchi Chie, Afrin Rehana, Potiszil Christian, Kunihiro Tak, Kobayashi Katsura, Nakamura Eizo, Ueno Yuichiro, Antunes André, Wang Anna, Chandru Kuhan, Hao Jihua, Jia Tony Z

机构信息

Earth-Life Science Institute, Tokyo Institute of Technology, Meguro-ku, Tokyo, 152-8550, Japan.

Institute for Extra-cutting-edge Science and Technology Avant-garde Research (X-star), Japan Agency for Marine-Earth Science and Technology (JAMSTEC), Yokosuka, Kanagawa, 237-0061, Japan.

出版信息

Small Methods. 2023 Dec;7(12):e2300119. doi: 10.1002/smtd.202300119. Epub 2023 May 18.

Abstract

α-Hydroxy acids are prebiotic monomers that undergo dehydration synthesis to form polyester gels, which assemble into membraneless microdroplets upon aqueous rehydration. These microdroplets are proposed as protocells that can segregate and compartmentalize primitive molecules/reactions. Different primitive aqueous environments with a variety of salts could have hosted chemistries that formed polyester microdroplets. These salts could be essential cofactors of compartmentalized prebiotic reactions or even directly affect protocell structure. However, fully understanding polyester-salt interactions remains elusive, partially due to technical challenges of quantitative measurements in condensed phases. Here, spectroscopic and biophysical methods are applied to analyze salt uptake by polyester microdroplets. Inductively coupled plasma mass spectrometry is applied to measure the cation concentration within polyester microdroplets after addition of chloride salts. Combined with methods to determine the effects of salt uptake on droplet turbidity, size, surface potential and internal water distribution, it was observed that polyester microdroplets can selectively partition salt cations, leading to differential microdroplet coalescence due to ionic screening effects reducing electrostatic repulsion forces between microdroplets. Through applying existing techniques to novel analyses related to primitive compartment chemistry and biophysics, this study suggests that even minor differences in analyte uptake can lead to significant protocellular structural change.

摘要

α-羟基酸是益生元单体,它们通过脱水合成形成聚酯凝胶,在水合后组装成无膜微滴。这些微滴被认为是原细胞,能够分离和分隔原始分子/反应。不同的含有各种盐的原始水环境可能承载了形成聚酯微滴的化学反应。这些盐可能是分隔的益生元反应的必需辅助因子,甚至直接影响原细胞结构。然而,由于凝聚相定量测量的技术挑战,全面理解聚酯-盐相互作用仍然难以实现。在此,应用光谱和生物物理方法分析聚酯微滴对盐的摄取。添加氯盐后,采用电感耦合等离子体质谱法测量聚酯微滴内的阳离子浓度。结合确定盐摄取对液滴浊度、大小、表面电位和内部水分布影响的方法,观察到聚酯微滴可以选择性地分配盐阳离子,由于离子屏蔽效应降低了微滴之间的静电排斥力,导致微滴发生不同程度的聚并。通过将现有技术应用于与原始分隔化学和生物物理学相关的新分析,本研究表明,即使分析物摄取的微小差异也可能导致原细胞结构的显著变化。

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