Intracellular localization and membrane topology of 11-cis retinol dehydrogenase in the retinal pigment epithelium suggest a compartmentalized synthesis of 11-cis retinaldehyde
A. Simon et al., Intracellular localization and membrane topology of 11-cis retinol dehydrogenase in the retinal pigment epithelium suggest a compartmentalized synthesis of 11-cis retinaldehyde, J CELL SCI, 112(4), 1999, pp. 549-558
11-cis retinol dehydrogenase (EC 1.1.1.105) catalyses the last step in the
biosynthetic pathway generating 11-cis retinaldehyde, the common chromophor
e of all visual pigments in higher animals. The enzyme is abundantly expres
sed in retinal pigment epithelium of the eye and is a member of the short c
hain dehydrogenase/reductase superfamily, In this work we demonstrate that
a majority of 11-cis retinol dehydrogenase is associated with the smooth ER
in retinal pigment epithelial cells and that the enzyme is an integral mem
brane protein, anchored to membranes by two hydrophobic peptide segments. T
he catalytic domain of the enzyme is confined to a lumenal compartment and
is not present on the cytosolic aspect of membranes. Thus, the subcellular
localization and the membrane topology of 11-cis retinol dehydrogenase sugg
est that generation of 11-cis retinaldehyde is a compartmentalized process.