Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2006-1-31
pubmed:abstractText
The HERG potassium channel might have a non-canonical drug binding site, distinct from the channel's inner cavity, that could be responsible for elements of closed-state pharmacological inhibition of the channel. The macrolide antibiotic erythromycin is a drug that may block unconventionally because of its size. Here we used whole-cell patch-clamp recording at 37 degrees C from heterologously expressed HERG channels in a mammalian cell line to show that erythromycin either produces a rapid open-state-dependent HERG channel inhibition, or components of both open-state-dependent and closed-state-dependent inhibition. Alanine-substitution of HERG's canonical determinants of blockade revealed that Y652 was not important as a molecular determinant of blockade, and that mutation of F656 resulted in only weak attenuation of inhibition. In computer models of the channel, erythromycin could make several direct contacts with F656, but not with Y652, in the open-state model, and erythromycin was unable to fit into a closed-state channel model.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0006-291X
pubmed:author
pubmed:issnType
Print
pubmed:day
10
pubmed:volume
341
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
500-6
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:16446155-Cell Line, pubmed-meshheading:16446155-Dose-Response Relationship, Drug, pubmed-meshheading:16446155-Electrophysiology, pubmed-meshheading:16446155-Erythromycin, pubmed-meshheading:16446155-Ether-A-Go-Go Potassium Channels, pubmed-meshheading:16446155-Humans, pubmed-meshheading:16446155-Inhibitory Concentration 50, pubmed-meshheading:16446155-Models, Biological, pubmed-meshheading:16446155-Models, Chemical, pubmed-meshheading:16446155-Models, Molecular, pubmed-meshheading:16446155-Mutation, pubmed-meshheading:16446155-Patch-Clamp Techniques, pubmed-meshheading:16446155-Potassium Channels, Voltage-Gated, pubmed-meshheading:16446155-Protein Conformation, pubmed-meshheading:16446155-Protein Synthesis Inhibitors, pubmed-meshheading:16446155-Software, pubmed-meshheading:16446155-Temperature, pubmed-meshheading:16446155-Time Factors
pubmed:year
2006
pubmed:articleTitle
Erythromycin block of the HERG K+ channel: accessibility to F656 and Y652.
pubmed:affiliation
Department of Physiology and Cardiovascular Research Laboratories, School of Medical Sciences, University of Bristol, University Walk, Bristol BS8 1TD, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't