Literature DB >> 23529419

Use of Escherichia coli for the production and purification of membrane proteins.

Vincent G L Postis1, Andrea E Rawlings, Amelia Lesiuk, Stephen A Baldwin.   

Abstract

Individual types of ion channels and other membrane proteins are typically expressed only at low levels in their native membranes, rendering their isolation by conventional purification techniques difficult. The heterologous over-expression of such proteins is therefore usually a prerequisite for their purification in amounts suitable for structural and for many functional investigations. The most straightforward expression host, suitable for prokaryote membrane proteins and some proteins from eukaryotes, is the bacterium Escherichia coli. Here we describe the use of this expression system for production of functionally active polytopic membrane proteins and methods for their purification by affinity chromatography in amounts up to tens of milligrams.

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Year:  2013        PMID: 23529419     DOI: 10.1007/978-1-62703-351-0_3

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Functional Characterization of the γ-Aminobutyric Acid Transporter from Mycobacterium smegmatis MC2 155 Reveals Sodium-Driven GABA Transport.

Authors:  Ana Pavić; Yurui Ji; Agnese Serafini; Acely Garza-Garcia; Martin J McPhillie; Alexandra O M Holmes; Luiz Pedro Sório de Carvalho; Yingying Wang; Mark Bartlam; Adrian Goldman; Vincent L G Postis
Journal:  J Bacteriol       Date:  2021-01-25       Impact factor: 3.490

2.  Styrene maleic-acid lipid particles (SMALPs) into detergent or amphipols: An exchange protocol for membrane protein characterisation.

Authors:  Sophie J Hesketh; David P Klebl; Anna J Higgins; Maren Thomsen; Isabelle B Pickles; Frank Sobott; Asipu Sivaprasadarao; Vincent L G Postis; Stephen P Muench
Journal:  Biochim Biophys Acta Biomembr       Date:  2020-01-13       Impact factor: 3.747

  2 in total

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