Scorpion Toxin BeKm-1 Prevents Low K+ Induced Internalization of Cell-Surface hERG Channels

dc.contributor.authorHan, Xien
dc.contributor.departmentPhysiologyen
dc.contributor.supervisorZhang, Shetuanen
dc.date2015-08-07 10:52:03.487
dc.date.accessioned2015-08-07T15:36:35Z
dc.date.issued2015-08-07
dc.degree.grantorQueen's University at Kingstonen
dc.descriptionThesis (Master, Physiology) -- Queen's University, 2015-08-07 10:52:03.487en
dc.description.abstractThe human ether-à-go-go related gene (hERG) encoded the pore forming subunit of a K+ channel that conducts an important current for the repolarization of the cardiac action potential. Dysfunction of the hERG channel leads to abnormal cardiac activities characterized by prolongation of the QT interval, clinically known as long QT syndrome (LQTS), which can cause lethal tachyarrhythmias and sudden death. We have previously shown that hypokalemia induces a conformational change that leads to degradation of hERG channels from the plasma membrane (Guo et al., 2009). However, the molecular mechanisms for low K+ effect on hERG channels are not known and it is also unknown whether low K+-induced internalization of hERG channels can be prevented. Using various compounds that interact with hERG channels by binding to different regions of channels has been a field of interest to investigate the channel structure-function relationships. Moreover, certain high affinity hERG channel blockers such as E-4031 can rescue trafficking-detective hERG mutants (Gong et al., 2006). The hERG channel has an unusually long extracellular S5-pore linker to which the scorpion toxin BeKm-1 selectively binds. I hypothesized that the S5-pore linker contributes to the unique sensitivity of hERG channels to extracellular K+, and that BeKm-1 prevents the internalization of hERG channels induced by 0 mM [K+]o through binding to S5-pore linker. In the present study, I investigated the protective effects of the scorpion toxin, BeKm-1, on low K+-induced hERG internalization using whole-cell patch-clamp, and Western blot analysis. Our data demonstrate that BeKm-1 effectively prevents low K+-induced hERG current loss and protein degradation. Since BeKm-1 blocks hERG channels, its protective effect on low K+-induced hERG internalization has limited clinical potential. Thus, we designed ten BeKm-1 mutants to screen for peptides that can prevent hERG from low K+-induced internalization without blocking hERG conductance. Our data show that two mutants were able to rescue hERG channels in 0 mM [K+]o but do not block hERG conductance. This study extends our understanding of the structure-function relationship of hERG channels and revealed a potential novel way to protect hERG channels from low K+-induced internalization.en
dc.description.degreeM.Sc.en
dc.description.restricted-thesisData is in a paper to be published.en
dc.embargo.liftdate2020-08-05
dc.embargo.terms1825en
dc.identifier.urihttp://hdl.handle.net/1974/13485
dc.language.isoengen
dc.relation.ispartofseriesCanadian thesesen
dc.rightsQueen's University's Thesis/Dissertation Non-Exclusive License for Deposit to QSpace and Library and Archives Canadaen
dc.rightsProQuest PhD and Master's Theses International Dissemination Agreementen
dc.rightsIntellectual Property Guidelines at Queen's Universityen
dc.rightsCopying and Preserving Your Thesisen
dc.rightsThis publication is made available by the authority of the copyright owner solely for the purpose of private study and research and may not be copied or reproduced except as permitted by the copyright laws without written authority from the copyright owner.en
dc.subjecthERG K+ channelen
dc.subjectLQTSen
dc.subjectHypokalemiaen
dc.titleScorpion Toxin BeKm-1 Prevents Low K+ Induced Internalization of Cell-Surface hERG Channelsen
dc.typethesisen
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