Robust Chemical Synthesis of Membrane Proteins through a General Method of Removable Backbone Modification

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• 作者：Ji-Shen Zheng ; Yao He ; Chao Zuo ; Xiao-Ying Cai ; Shan Tang ; Zhipeng A. Wang ; Long-Hua Zhang ; Chang-Lin Tian ; Lei Liu
• 刊名：Journal of the American Chemical Society
• 出版年：2016
• 出版时间：March 16, 2016
• 年：2016
• 卷：138
• 期：10
• 页码：3553-3561
• 全文大小：604K
• ISSN：1520-5126

文摘

Chemical protein synthesis can provide access to proteins with post-translational modifications or site-specific labelings. Although this technology is finding increasing applications in the studies of water-soluble globular proteins, chemical synthesis of membrane proteins remains elusive. In this report, a general and robust removable backbone modification (RBM) method is developed for the chemical synthesis of membrane proteins. This method uses an activated O-to-N acyl transfer auxiliary to install in the Fmoc solid-phase peptide synthesis process a RBM group with switchable reactivity toward trifluoroacetic acid. The method can be applied to versatile membrane proteins because the RBM group can be placed at any primary amino acid. With RBM, the membrane proteins and their segments behave almost as if they were water-soluble peptides and can be easily handled in the process of ligation, purification, and mass characterizations. After the full-length protein is assembled, the RBM group can be readily removed by trifluoroacetic acid. The efficiency and usefulness of the new method has been demonstrated by the successful synthesis of a two-transmembrane-domain protein (HCV p7 ion channel) with site-specific isotopic labeling and a four-transmembrane-domain protein (multidrug resistance transporter EmrE). This method enables practical synthesis of small- to medium-sized membrane proteins or membrane protein domains for biochemical and biophysical studies.