Document Detail


Two open states with progressive proton selectivities in the branched channelrhodopsin-2 photocycle.
MedLine Citation:
PMID:  20197028     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Channelrhodopsins are light-gated ion channels that mediate vision in phototactic green algae like Chlamydomonas. In neurosciences, channelrhodopsins are widely used to light-trigger action potentials in transfected cells. All known channelrhodopsins preferentially conduct H(+). Previous studies have indicated the existence of an early and a late conducting state within the channelrhodopsin photocycle. Here, we show that for channelrhodopsin-2 expressed in Xenopus oocytes and HEK cells, the two open states have different ion selectivities that cause changes in the channelrhodopsin-2 reversal voltage during a light pulse. An enzyme kinetic algorithm was applied to convert the reversal voltages in various ionic conditions to conductance ratios for H(+) and divalent cations (Ca(2+) and/or Mg(2+)), as compared to monovalent cations (Na(+) and/or K(+)). Compared to monovalent cation conductance, the H(+) conductance, alpha, is approximately 3 x 10(6) and the divalent cation conductance, beta, is approximately 0.01 in the early conducting state. In the stationary mixture of the early and late states, alpha is larger and beta smaller, both by a factor of approximately 2. The results suggest that the ionic basis of light perception in Chlamydomonas is relatively nonspecific in the beginning of a light pulse but becomes more selective for protons during longer light exposures.
Authors:
André Berndt; Matthias Prigge; Dietrich Gradmann; Peter Hegemann
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Biophysical journal     Volume:  98     ISSN:  1542-0086     ISO Abbreviation:  Biophys. J.     Publication Date:  2010 Mar 
Date Detail:
Created Date:  2010-03-03     Completed Date:  2010-05-19     Revised Date:  2011-07-26    
Medline Journal Info:
Nlm Unique ID:  0370626     Medline TA:  Biophys J     Country:  United States    
Other Details:
Languages:  eng     Pagination:  753-61     Citation Subset:  IM    
Copyright Information:
2010 Biophysical Society. Published by Elsevier Inc. All rights reserved.
Affiliation:
Institute for Biology, Humboldt-Universität zu Berlin, Germany.
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MeSH Terms
Descriptor/Qualifier:
Animals
Cations, Divalent / pharmacology
Cell Line
Humans
Ion Channel Gating / drug effects,  radiation effects*
Light*
Models, Biological
Oocytes / drug effects,  metabolism,  radiation effects
Protons*
Rhodopsin / metabolism*
Xenopus / metabolism
Chemical
Reg. No./Substance:
0/Cations, Divalent; 0/Protons; 9009-81-8/Rhodopsin
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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