Linked Life Data

9875368

Source:http://linkedlifedata.com/resource/pubmed/id/9875368

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
1999-1-14
pubmed:abstractText
Various types of voltage gated potassium channels (Kv) are responsible for setting the resting potential and shaping the membrane potential waveform in the subcellular domains of neurons. In order to visualize the expression behaviour of recombinant Kv channels, we have fused green fluorescent protein (GFP) to the N-terminal of the alpha subunits Kv1.3 and Kv1.4. In transiently transfected HEK 293 cells the GFP-Kv chimeras localize to the plasma membrane. Whole-cell voltage clamp recordings demonstrate that they form functional potassium channels. Kinetic analysis reveals that the gating kinetics of GFP-Kv1.3 are virtually indistinguishable from those displayed by its wild-type correlate. For GFP-Kv1.4 channels we find that their gating is modified in an expected manner. In response to short depolarizing voltage pulses they do not inactivate, indicating that the attached GFP interferes with the fast N-type inactivation mechanism present in wild type Kv1.4 channels. We suggest that GFP tagging of Kv channels might be a useful tool to monitor the spatiotemporal distribution of recombinant potassium channels expressed in living neurons.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0953-816X
pubmed:author
pubmed:issnType
Print
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3908-12
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1998
pubmed:articleTitle
Functional expression of GFP-tagged Kv1.3 and Kv1.4 channels in HEK 293 cells.
pubmed:affiliation
Max-Planck-Institute for Biochemistry, Department of Membrane- and Neurophysics, Martinsried, Germany. kupper@biochem.mpg.de
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't