小泡
化学
肺表面活性物质
肽
双层
三肽
堆积
背景(考古学)
分子
氢键
疏水
部分
疏水效应
组合化学
生物物理学
膜
立体化学
有机化学
生物化学
古生物学
生物
作者
Smriti Mukherjee,Ganesh Shanmugam
出处
期刊:Small
[Wiley]
日期:2023-02-17
卷期号:19 (19)
被引量:5
标识
DOI:10.1002/smll.202206906
摘要
Abstract Surfactant molecules typically have a long hydrophobic tail and a short hydrophilic head group. It remains unexplored if surfactants can have a short hydrophobic head group and a long hydrophilic tail. Designing such surfactants is a challenge as a lengthy hydrophilic tail would completely solubilize the molecules. In this context, herein, the Fmoc‐functionalized Gly‐Pro‐Hyp (GPO) tripeptide repeat‐based molecule (Fm‐GPO) with fluorenyl moiety as a short hydrophobic head and peptide as a long hydrophilic tail is demonstrated as a reverse surfactant at physiological pH, for the first time. π–π stacking of the fluorenyl moieties and intermolecular hydrogen bonding between the peptide chains with extended polyproline‐II structure promoted the self‐assembly into spherical vesicles with a unique feature of a large hydrophilic area in the interior and exterior of the bilayer. The current Fm‐GPO system offers a new class of surfactants with unique features that can aid in the design of drug‐loaded vehicles, which can be target‐specific as the peptide chain can be manipulated with different functional ultra‐short peptide sequences.
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