Abstract
Difference absorption spectra were recorded during the formation and decay of metarhodopsin III after sonicated membrane suspensions of rhodopsin were bleached at 37°C. The data were analyzed using SVD, spectral decomposition and global exponential fitting. By comparison of the results in the presence or absence of 70 μM NADPH and those for bovine or human rhodopsin, a single comprehensive scheme was fit to all the data, including reduction of retinal to retinol by the intrinsic retinol dehydrogenase. On the time scale studied the mechanism involves two 382 nm absorbing species and two 468 nm, absorbing species, supporting the notion that human metarhodopsin III is not a homogeneous species. The results confirm that metarhodopsin III forms and persists sufficiently long in the human retina under physiological conditions that it could undergo secondary photoisomerization. Copyright (C) 2000 Elsevier Science Ltd.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3039-3048 |
| Number of pages | 10 |
| Journal | Vision Research |
| Volume | 40 |
| Issue number | 22 |
| DOIs | |
| State | Published - Oct 2000 |
Keywords
- Dark adaptation
- Human rhodopsin
- Metarhodopsin III
- NADPH
- Photoregeneration
- Retinol dehydrogenase
ASJC Scopus subject areas
- Ophthalmology
- Sensory Systems
Fingerprint
Dive into the research topics of 'Effect of NADPH on formation and decay of human metarhodopsin III at physiological temperatures'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS