In spite of the high similarity in amino acid sequence between rod vis
ual pigment rhodopsin and gecko blue-sensitive pigment (gecko blue), n
ot only the spectral sensitivities but also the thermal decay rates of
the meta II- and III-intermediates are noticeably different from one
another [Kojima et al. (1995) Biochemistry 34, 1096-1106]. In order to
identify the protein region(s) that contain(s) key residues being res
ponsible for the functional difference, we constructed six chimerical
mutants derived from gecko blue and bovine rhodopsin, with the aid of
protein production in a human embryonic kidney cell line (2933). While
the absorption maximum of every mutant was located in between gecko b
lue (466 nm) and bovine rhodopsin (500 nm), a large blue-shift (18 nm)
was observed when the helices I-III of rhodopsin were replaced with t
hose of gecko blue. A lime-resolved spectroscopic study demonstrated t
hat this replacement also accelerated the decay rate of the meta II-in
termediate. The decay of the meta III-intermediate of the mutants beca
me faster as the compartment of gecko blue was increased. Thus, the fa
ster decay of the meta II-intermediate of gecko blue is largely attrib
uted to residues within helices I-III, while the decay of the meta III
-intermediate apparently depends on the overall structure of the prote
in.