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通过与羟胺的化学选择性酰胺形成连接快速形成非经典磷脂膜。

Rapid Formation of Non-canonical Phospholipid Membranes by Chemoselective Amide-Forming Ligations with Hydroxylamines.

机构信息

Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, Natural Sciences Building, La Jolla, CA 92093, USA.

Biomimetic Membrane Chemistry (BioMemChem) Group, CICA-Centro Interdisciplinar de Química e Bioloxía, Universidade da Coruña, Rúa As Carballeiras, 15701, A Coruña, Spain.

出版信息

Angew Chem Int Ed Engl. 2024 Jan 2;63(1):e202311635. doi: 10.1002/anie.202311635. Epub 2023 Nov 28.

Abstract

There has been increasing interest in methods to generate synthetic lipid membranes as key constituents of artificial cells or to develop new tools for remodeling membranes in living cells. However, the biosynthesis of phospholipids involves elaborate enzymatic pathways that are challenging to reconstitute in vitro. An alternative approach is to use chemical reactions to non-enzymatically generate natural or non-canonical phospholipids de novo. Previous reports have shown that synthetic lipid membranes can be formed in situ using various ligation chemistries, but these methods lack biocompatibility and/or suffer from slow kinetics at physiological pH. Thus, it would be valuable to develop chemoselective strategies for synthesizing phospholipids from water-soluble precursors that are compatible with synthetic or living cells Here, we demonstrate that amide-forming ligations between lipid precursors bearing hydroxylamines and α-ketoacids (KAs) or potassium acyltrifluoroborates (KATs) can be used to prepare non-canonical phospholipids at physiological pH conditions. The generated amide-linked phospholipids spontaneously self-assemble into cell-like micron-sized vesicles similar to natural phospholipid membranes. We show that lipid synthesis using KAT ligation proceeds extremely rapidly, and the high selectivity and biocompatibility of the approach facilitates the in situ synthesis of phospholipids and associated membranes in living cells.

摘要

人们对合成脂质膜的方法越来越感兴趣,这些方法是人工细胞的关键组成部分,或者是开发用于重塑活细胞中膜的新工具。然而,磷脂的生物合成涉及到复杂的酶促途径,这些途径很难在体外重建。另一种方法是使用化学反应非酶促地从头生成天然或非典型的磷脂。以前的报告表明,可以使用各种连接化学方法原位形成合成脂质膜,但这些方法缺乏生物相容性,并且在生理 pH 值下动力学较慢。因此,开发化学选择性策略从水溶性前体制备与合成或活细胞相容的磷脂将是有价值的。在这里,我们证明了带有羟胺的脂质前体与α-酮酸(KAs)或三氟硼酸钾酰基(KATs)之间的酰胺形成连接可以在生理 pH 条件下用于制备非典型的磷脂。生成的酰胺键连接的磷脂自发自组装成类似天然磷脂膜的细胞样微米大小的囊泡。我们表明,使用 KAT 连接进行脂质合成的速度极快,并且该方法的高选择性和生物相容性有助于在活细胞中进行磷脂原位合成和相关膜的合成。

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