膜
化学
氢键
溶剂
生物物理学
分子
自组装
分子动力学
合理设计
细胞膜
脂质双层
纳米技术
有机化学
计算化学
材料科学
生物化学
生物
作者
Pavel Banerjee,Dipankar Mondal,Meghna Ghosh,Devdeep Mukherjee,Pratyush Kiran Nandi,Tapas K. Maiti,Nilmoni Sarkar
出处
期刊:Langmuir
[American Chemical Society]
日期:2020-02-25
卷期号:36 (10): 2707-2719
被引量:10
标识
DOI:10.1021/acs.langmuir.9b03544
摘要
Controllable self-assembly and understanding of the interaction between single metabolite fibrils and live-cell membranes have paramount importance in providing minimal treatment in several neurodegenerative disorders. Here, utilizing the nonlinear nature and peculiar hydrogen bonding behavior of the dimethyl sulfoxide (DMSO)–water mixture, the selective self-assembly of a single metabolite 5-fluorouracil (5-FU) is achieved. A direct correlation between water availability and selective self-assembly of 5-FU is ratified from the excited-state dynamics. The specific fibrillar structures of 5-FU exhibit a great potential to modulate live cell membrane fluidity and model membrane lipid distribution. After 5-FU fibril addition, a disorder of H-bonded water molecules arises several layers beyond the first hydration shell of the polar headgroups, which essentially modifies interfacial water structure and dynamics. Overall, our results shed light on the role of solvent to govern specific self-assembly and also lay the foundation accounting for the earlier stage of several diseases and multidrug resistance.
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