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Updated: Sep 29, 2026

A Rhodopsin Transport Assay by High-Content Imaging Analysis
Published on: January 16, 2019
Retinitis pigmentosa-associated rhodopsin mutations in three membrane-located cysteine residues present three
Githa Breikers1, Margriet J M Portier-VandeLuytgaarden, Petra H M Bovee-Geurts
1Department of Biochemistry, Nijmegen Center for Molecular Life Sciences, University of Nijmegen, 6500 HB Nijmegen, Netherlands.
Abstract:
A large number of mutations in rhodopsin are associated with autosomal dominant retinitis pigmentosa (ADRP). We analyzed the biochemical phenotypes of the ADRP-associated cysteine mutants C167R, C222R, and C264del. C222R behaved as wild type in every aspect testable and is classified as a class I mutant. C167R produced intact protein but did not regenerate with 11-cis retinal and was not transported to the plasma membrane. We confirm its classification as a class IIa mutant. C264del represents a novel phenotype, which we propose to call class III. It produced a truncated protein of 27kDa that failed to regenerate with 11-cis retinal and was not targeted to the plasma membrane.
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