Mg. Wootan et al., MECHANISM OF FLUORESCENT FATTY-ACID TRANSFER FROM ADIPOCYTE FATTY-ACID-BINDING PROTEIN TO MEMBRANES, Biochemistry, 32(33), 1993, pp. 8622-8627
Adipocyte fatty acid binding protein (A-FABP) is a 15-kDa protein foun
d in high abundance in the cytosol of adipose cells. To better underst
and the role of this protein in intracellular free fatty acid (ffa) tr
ansport, the mechanism of ffa transfer from A-FABP to model membranes
was examined by monitoring the transfer of fluorescent anthroyloxy ffa
(AOffa) to small unilamellar phospholipid vesicles, using a resonance
energy transfer assay. Structural features of ffa that increase aqueo
us solubility, such as shorter chain length and unsaturation, did not
increase the AOffa transfer rate. In addition, solution conditions tha
t increase the aqueous solubility of ffa, such as decreasing ionic str
ength and increasing pH, had little effect on AOffa transfer from A-FA
BP to membranes. These results suggest that AOffa do not transfer thro
ugh the aqueous phase. The small entropic contribution to the free ene
rgy of the transfer process provides further evidence that AOffa may n
ot travel through the surrounding aqueous environment when transferred
from A-FABP to phospholipid membranes. Finally, the rate of AOffa tra
nsfer from A-FABP was directly dependent on the concentration of the a
cceptor membranes. These studies suggest that AOffa transfer from A-FA
BP to phospholipid vesicles may occur via transient collisional intera
ctions between the protein and membranes. Such a mechanism is similar
to that found recently for AOffa transfer from heart FABP [Kim, H. K.,
& Storch, J. (1992) J. Biol. Chem. 267, 20051-20056], an FABP which p
ossesses a high degree of sequence homology (62% identity) with A-FABP
, but different from the aqueous diffusion mechanism described for the
more distantly related (20% homology) liver FABP [Kim, H. K., & Storc
h, J. (1992) J. Biol. Chem. 267, 77-82]. These differences indicate th
at structural divergence among FABP may be translated into functional
differences, as evidenced here by the mechanism of AOffa transfer to m
embranes.