SEMISYNTHESIS OF K+ CHANNELS

被引:4
作者
Komarov, Alexander G. [1 ]
Linn, Kellie M. [1 ]
Devereaux, Jordan J. [1 ]
Valiyaveetil, Francis I. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Program Chem Biol, Portland, OR 97201 USA
来源
METHODS IN ENZYMOLOGY: NON-NATURAL AMINO ACIDS | 2009年 / 462卷
关键词
EXPRESSED PROTEIN LIGATION; TOTAL CHEMICAL-SYNTHESIS; POTASSIUM CHANNEL; SELECTIVITY FILTER; CRYSTAL-STRUCTURE; GENETIC-CODE; KCSA; MUTAGENESIS; CONDUCTION; CHEMISTRY;
D O I
10.1016/S0076-6879(09)62007-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The ability to selectively conduct K+ ions is central to the function of K+ channels. Selection for K+ and rejection of Na+ takes place in a conserved structural element referred to as the selectivity filter. The selectivity filter consists of four K+-specific ion binding sites that are created using predominantly the backbone carbonyl oxygen atoms. Due to the involvement of the protein backbone, experimental manipulation of the ion binding sites in the selectivity filter is not possible using traditional site directed mutagenesis. The limited suitability of the site-directed mutagenesis for studies on the selectivity filter has motivated the development of a semisynthesis approach, which enables the use of chemical synthesis to manipulate the selectivity filter. In this chapter, we describe the protocols that are presently used in our laboratory for the semisynthesis of the bacterial K+ channel, KcsA. We show the introduction of a spectroscopic probe into the KcsA channel using semisynthesis. We also review previous applications of semisynthesis in investigations of K+ channels. While the protocols described in this chapter are for the KcsA K+ channel, we anticipate that similar protocols will also be applicable for the semisynthesis of other integral membrane proteins.
引用
收藏
页码:135 / +
页数:18
相关论文
共 34 条
[1]   Unnatural amino acid mutagenesis in mapping ion channel function [J].
Beene, DL ;
Dougherty, DA ;
Lester, HA .
CURRENT OPINION IN NEUROBIOLOGY, 2003, 13 (03) :264-270
[2]   Engineering and chemical synthesis of a transmembrane protein: The HCV protease cofactor protein NS4A [J].
Bianchi, E ;
Ingenito, R ;
Simon, RJ ;
Pessi, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (33) :7698-7699
[3]   Protein engineering by expressed protein ligation [J].
Blaschke, UK ;
Silberstein, J ;
Muir, TW .
APPLICATIONS OF CHIMERIC GENES AND HYBRID PROTEINS, PT C: PROTEIN-PROTEIN INTERACTIONS AND GENOMICS, 2000, 328 :478-496
[4]   Total chemical synthesis and electrophysiological characterization of mechanosensitive channels from Escherichia coli and Mycobacterium tuberculosis [J].
Clayton, D ;
Shapovalov, G ;
Maurer, JA ;
Dougherty, DA ;
Lester, HA ;
Kochendoerfer, GG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :4764-4769
[5]   SYNTHESIS OF PROTEINS BY NATIVE CHEMICAL LIGATION [J].
DAWSON, PE ;
MUIR, TW ;
CLARKLEWIS, I ;
KENT, SBH .
SCIENCE, 1994, 266 (5186) :776-779
[6]   Synthesis of native proteins by chemical ligation [J].
Dawson, PE ;
Kent, SBH .
ANNUAL REVIEW OF BIOCHEMISTRY, 2000, 69 :923-960
[7]   The structure of the potassium channel:: Molecular basis of K+ conduction and selectivity [J].
Doyle, DA ;
Cabral, JM ;
Pfuetzner, RA ;
Kuo, AL ;
Gulbis, JM ;
Cohen, SL ;
Chait, BT ;
MacKinnon, R .
SCIENCE, 1998, 280 (5360) :69-77
[8]   E-olefin dipeptide isostere incorporation into a polypeptide backbone enables hydrogen bond perturbation:: Probing the requirements for Alzheimer's amyloidogenesis [J].
Fu, YW ;
Bieschke, J ;
Kelly, JW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (44) :15366-15367
[9]   Functional reconstitution of a prokaryotic K+ channel [J].
Heginbotham, L ;
Kolmakova-Partensky, L ;
Miller, C .
JOURNAL OF GENERAL PHYSIOLOGY, 1998, 111 (06) :741-749
[10]  
Hille B., 2001, Ion Channels of Excitable Membranes, V3rd