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Title: Spatial arrangement of rhodopsin in retinal rod outer segment membranes studied by spin-labeling and pulsed electron double resonance

Journal Article · · Biochemical and Biophysical Research Communications
 [1];  [2];  [3];  [1]
  1. Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043 (Japan)
  2. Bruker Biospin, Yokohama, Kanagawa 215-0022 (Japan)
  3. Department of Space and Earth Sciences, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043 (Japan)

Highlights: Black-Right-Pointing-Pointer Use of spin labeling and PELDOR to measure inter-rhodopsin distance in ROS. Black-Right-Pointing-Pointer Strong decay of PELDOR signal indicated a high density (mM range) of rhodopsin. Black-Right-Pointing-Pointer The decay was modeled by rhodopsin monomers dispersed in a planar membrane. -- Abstract: We have determined the spatial arrangement of rhodopsin in the retinal rod outer segment (ROS) membrane by measuring the distances between rhodopsin molecules in which native cysteines were spin-labeled at {approx}1.0 mol/mol rhodopsin. The echo modulation decay of pulsed electron double resonance (PELDOR) from spin-labeled ROS curved slightly with strong background decay. This indicated that the rhodopsin was densely packed in the retina and that the rhodopsin molecules were not aligned well. The curve was simulated by a model in which rhodopsin is distributed randomly as monomers in a planar membrane.

OSTI ID:
22210195
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 425, Issue 2; Other Information: Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English

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