Spontaneous Reconstitution of Functional Transmembrane Proteins During Bioorthogonal Phospholipid Membrane Synthesis

被引:30
作者
Cole, Christian M. [1 ]
Brea, Roberto J. [1 ]
Kim, Young Hun [1 ]
Hardy, Michael D. [1 ]
Yang, Jerry [1 ]
Devaraj, Neal K. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
membrane proteins; phospholipids; proteoliposomes; self-assembly; synthetic biology; CYTOCHROME-C-OXIDASE; NATIVE CHEMICAL LIGATION; ESCHERICHIA-COLI MSBA; TERMINAL ALKYNES; CA2+ CHANNELS; ION-CHANNEL; CA2+-ATPASE; DETERGENTS; LIPOSOMES; MECHANISM;
D O I
10.1002/anie.201504339
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Transmembrane proteins are critical for signaling, transport, and metabolism, yet their reconstitution in synthetic membranes is often challenging. Non-enzymatic and chemo-selective methods to generate phospholipid membranes in situ would be powerful tools for the incorporation of membrane proteins. Herein, the spontaneous reconstitution of functional integral membrane proteins during the de novo synthesis of biomimetic phospholipid bilayers is described. The approach takes advantage of bioorthogonal coupling reactions to generate proteoliposomes from micelle-solubilized proteins. This method was successfully used to reconstitute three different transmembrane proteins into synthetic membranes. This is the first example of the use of non-enzymatic chemical synthesis of phospholipids to prepare proteoliposomes.
引用
收藏
页码:12738 / 12742
页数:5
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