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快速连续双重肟键合能够从水溶性前体物中从头形成功能性的合成膜。

Rapid and Sequential Dual Oxime Ligation Enables De Novo Formation of Functional Synthetic Membranes from Water-Soluble Precursors.

机构信息

Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, Natural Sciences Building 3328, La Jolla, CA 92093, USA.

Biomimetic Membrane Chemistry (BioMemChem) Group, Centro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña, Rúa As Carballeiras, 15701, A Coruña, Spain.

出版信息

Angew Chem Int Ed Engl. 2022 Jul 18;61(29):e202200549. doi: 10.1002/anie.202200549. Epub 2022 Jun 2.

Abstract

Cell membranes define the boundaries of life and primarily consist of phospholipids. Living organisms assemble phospholipids by enzymatically coupling two hydrophobic tails to a soluble polar head group. Previous studies have taken advantage of micellar assembly to couple single-chain precursors, forming non-canonical phospholipids. However, biomimetic nonenzymatic coupling of two alkyl tails to a polar head-group remains challenging, likely due to the sluggish reaction kinetics of the initial coupling step. Here we demonstrate rapid de novo formation of biomimetic liposomes in water using dual oxime bond formation between two alkyl chains and a phosphocholine head group. Membranes can be generated from non-amphiphilic, water-soluble precursors at physiological conditions using micromolar concentrations of precursors. We demonstrate that functional membrane proteins can be reconstituted into synthetic oxime liposomes from bacterial extracts in the absence of detergent-like molecules.

摘要

细胞膜定义了生命的边界,主要由磷脂组成。生物体通过酶促偶联两个疏水尾部到一个可溶性极性头部基团来组装磷脂。以前的研究利用胶束组装来偶联单链前体,形成非典型的磷脂。然而,将两个烷基尾部与极性头部基团进行仿生非酶偶联仍然具有挑战性,这可能是由于初始偶联步骤的缓慢反应动力学。在这里,我们展示了使用两个烷基链和一个磷酸胆碱头部基团之间的双重肟键形成,在水中快速从头形成仿生脂质体。可以使用毫摩尔浓度的前体,在生理条件下,从非两亲性、水溶性前体中生成膜。我们证明,功能膜蛋白可以从细菌提取物中重新组装到合成肟脂质体中,而无需去污剂样分子。

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