Overexpression of membrane proteins from higher eukaryotes in yeasts

被引:14
|
作者
Emmerstorfer, Anita [1 ]
Wriessnegger, Tamara [1 ]
Hirz, Melanie [2 ]
Pichler, Harald [1 ,2 ]
机构
[1] ACIB Austrian Ctr Ind Biotechnol, A-8010 Graz, Austria
[2] Graz Univ Technol, Inst Mol Biotechnol, A-8010 Graz, Austria
关键词
Yeast; Heterologous expression; Membrane protein; Protein interactions; Protein structure; HIGH-LEVEL EXPRESSION; MONOAMINE-OXIDASE-A; HISTAMINE H-1 RECEPTOR; HIGH-YIELD EXPRESSION; HOST-CELL RESPONSE; MU-OPIOID RECEPTOR; X-RAY-STRUCTURE; PICHIA-PASTORIS; CRYSTAL-STRUCTURE; SACCHAROMYCES-CEREVISIAE;
D O I
10.1007/s00253-014-5948-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Heterologous expression and characterisation of the membrane proteins of higher eukaryotes is of paramount interest in fundamental and applied research. Due to the rather simple and well-established methods for their genetic modification and cultivation, yeast cells are attractive host systems for recombinant protein production. This review provides an overview on the remarkable progress, and discusses pitfalls, in applying various yeast host strains for high-level expression of eukaryotic membrane proteins. In contrast to the cell lines of higher eukaryotes, yeasts permit efficient library screening methods. Modified yeasts are used as high-throughput screening tools for heterologous membrane protein functions or as benchmark for analysing drug-target relationships, e.g., by using yeasts as sensors. Furthermore, yeasts are powerful hosts for revealing interactions stabilising and/or activating membrane proteins. We also discuss the stress responses of yeasts upon heterologous expression of membrane proteins. Through co-expression of chaperones and/or optimising yeast cultivation and expression strategies, yield-optimised hosts have been created for membrane protein crystallography or efficient whole-cell production of fine chemicals.
引用
收藏
页码:7671 / 7698
页数:28
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