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Biophys J, August 2000, p. 756-766, Vol. 79, No. 2


and
*Biomembrane Structure Unit, Department of Biochemistry, University
of Oxford, Oxford OX1 3QU, United Kingdom, and
Department of Biochemistry, Groningen Biomolecular
Sciences and Biotechnology Institute, University of Groningen,
9747 AG Groningen, the Netherlands
A single-cysteine mutant of the lactose transport protein
LacS(C320A/W399C) from Streptococcus thermophilus was
selectively labeled with a nitroxide spin label, and its mobility in
lipid membranes was studied as a function of its concentration in the membrane by saturation-transfer electron spin resonance. Bovine rhodopsin was also selectively spin-labeled and studied to aid the
interpretation of the measurements. Observations of spin-labeled proteins in macroscopically aligned bilayers indicated that the spin
label tends to orient so as to reflect the transmembrane orientation of
the protein. Rotational correlation times of 1-2 µs for purified
spin-labeled bovine rhodopsin in lipid membranes led to viscosities of
2.2 poise for bilayers of dimyristoylphosphatidylcholine (28°C) and
3.0 poise for the specific mixture of lipids used to reconstitute LacS
(30°C). The rotational correlation time for LacS did not vary
significantly over the range of low concentrations in lipid bilayers,
where optimal activity was seen to decrease sharply and was determined
to be 9 ± 1 µs (mean ± SD) for these samples. This
mobility was interpreted as being too low for a monomer but could
correspond to a dimer if the protein self-associates into an elongated
configuration within the membrane. Rather than changing its oligomeric
state, LacS appeared to become less ordered at the concentrations in
aligned membranes exceeding 1:100 (w/w) with respect to the lipid.
Biophys J, August 2000, p. 756-766, Vol. 79, No. 2
© 2000 by the Biophysical Society 0006-3495/00/08/756/11 $2.00
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