| Literature DB >> 26695040 |
Abstract
Voltage clamp fluorometry has become a powerful tool to compare partial reactions of P-type ATPases such as the Na(+),K(+)-ATPase and H(+),K(+)-ATPase with conformational dynamics of these ion pumps. Here, we describe the methodology to heterologously express membrane proteins in X. laevis oocytes and site-specifically label these proteins with one or more fluorophores. Fluorescence changes are measured simultaneously with current measurements under two-electrode voltage clamp conditions.Entities:
Keywords: Distance constraints; Donor photobleaching; Fluorescence
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Year: 2016 PMID: 26695040 PMCID: PMC4717471 DOI: 10.1007/978-1-4939-3179-8_25
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745