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The mechanosensitive channel of large conductance MscL is a well-characterized mechanically gated non-selective ion channel, which often serves as a prototype mechanosensitive channel for mechanotransduction studies. However, there are some discrepancies between MscL constructs used in these studies, most notably unintended heterogeneous expression from some MscL expression constructs. In this study we investigate the possible cause of this expression pattern, and compare the original non-homogenously expressing constructs with our new homogeneously expressing one to confirm that there is little functional difference between them. In addition, a new MscL construct has been developed with an improved molar extinction coefficient at 280 nm, enabling more accurate protein quantification.

Original publication

DOI

10.1007/s00249-015-1062-5

Type

Journal article

Journal

European biophysics journal : EBJ

Publication Date

10/2015

Volume

44

Pages

589 - 598

Addresses

Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD, 4072, Australia.

Keywords

Escherichia coli, Escherichia coli Proteins, Ion Channels, Codon, Liposomes, Amino Acid Sequence, Protein Structure, Tertiary, Molecular Sequence Data