Structure and function in rhodopsin: covalent crosslinking of the rhodopsin (metarhodopsin II) -transducin complex--the rhodopsin cytoplasmic face links to the transducin alpha subunit

Resek, J.F.; Farrens, D.; Khorana, H.G.

Proceedings of the National Academy of Sciences of the United States of America 91(16): 7643-7647


ISSN/ISBN: 0027-8424
PMID: 8052635
DOI: 10.1073/pnas.91.16.7643
Accession: 047455665

Download citation:  

Article/Abstract emailed within 0-6 h
Payments are secure & encrypted
Powered by Stripe
Powered by PayPal

We prepared rhodopsin mutants that contained a single reactive cysteine residue per rhodopsin molecule at position 65, 140, 240, or 316 on the cytoplasmic face. A carbene-generating photoactivatable group was linked by a disulfide bond to the cysteine sulfhydryl group of each of the rhodopsin mutants. The resulting derivative was then light-activated at lambda > 495 nm to form the metarhodopsin II intermediate, which bound transducin. Subsequent photoactivation (355 nm) of the carbene-generating group resulted in crosslinking of the rhodopsin mutant carrying a cysteine residue at position 240 to transducin. This crosslinking was determined to be specifically with the alpha subunit of transducin. An alternative reaction observed during photolysis of the rhodopsin mutants was intramolecular insertion of the carbene into rhodopsin.