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  Over-expression of a mammalian small-conductance calcium-activated K+ channel in Pichia pastoris: Effects of trafficking signals and subunit fusions

Licata, L., Haase, W., Eckhardt-Strelau, L., & Parcej, D. N. (2006). Over-expression of a mammalian small-conductance calcium-activated K+ channel in Pichia pastoris: Effects of trafficking signals and subunit fusions. Protein Expression and Purification, 47, 171-178. doi:10.1016/j.pep.2005.10.010.

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 Creators:
Licata, Luana1, Author           
Haase, Winfried1, 2, Author           
Eckhardt-Strelau, Luise1, Author           
Parcej, David N.1, Author           
Affiliations:
1Department of Structural Biology, Max Planck Institute of Biophysics, Max Planck Society, ou_2068291              
2Department of Physiology, Max Planck Institute of Biophysics, Max Planck Society, ou_2068297              

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Free keywords: Potassium channel; Mammalian; Pichia pastoris
 Abstract: Mammalian SK proteins are Ca2+-activated K+ channels, which show a sub-20 pS conductance. We have expressed the SK2 variant gene in Pichia pastoris and found protein to be produced at considerably higher levels than in brain tissue. The channel was correctly folded as evidenced by its high affinity interaction with apamin, a specific ligand from bee venom. However, the protein was largely unable to reach the plasma membrane, its normal destination, instead remaining in the endoplasmic reticulum. Adding a putative translocation sequence altered the intracellular distribution significantly with enhanced trafficking out of the endoplamic reticulum. Fusion of SK2 with the associated protein calmodulin also altered the channel localisation but in a different manner with channels now found mainly in transit between endoplasmic reticulum and Golgi compartments.

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Language(s): eng - English
 Dates: 2006-05
 Publication Status: Issued
 Pages: 8
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 305041
DOI: 10.1016/j.pep.2005.10.010
 Degree: -

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Title: Protein Expression and Purification
Source Genre: Journal
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Affiliations:
Publ. Info: San Diego : Academic Press
Pages: - Volume / Issue: 47 Sequence Number: - Start / End Page: 171 - 178 Identifier: ISSN: 1046-5928
CoNE: https://pure.mpg.de/cone/journals/resource/954922650158