LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

SSO and other inhibitors of putative fatty acid (FA) transport do not affect FA transport but disrupt FA metabolism.

Photo from wikipedia

Membrane-bound proteins have been proposed to mediate the transport of long-chain fatty acid (LCFA) transport through the plasma membrane (PM). These proposals are based largely on reports that PM transport… Click to show full abstract

Membrane-bound proteins have been proposed to mediate the transport of long-chain fatty acid (LCFA) transport through the plasma membrane (PM). These proposals are based largely on reports that PM transport of LCFA can be blocked by a number of enzymes and purported inhibitors of LCFA transport. Here, using the ratiometric pH indicator (2',7'-bis-(2-carboxyethyl)-5-and-6-)-carboxyfluorescein (BCECF) and acrylodated intestinal fatty acid-binding protein (ADIFAB)-based dual fluorescence assays, we investigated the effects of nine inhibitors of the putative FA transporter protein CD36 on the binding and transmembrane movement of LCFA.  We particularly focused on sulfosuccidimidyl oleate (SSO), reported to be a competitive inhibitor of CD36-mediated LCFA transport. Using these assays in adipocytes and inhibitor-treated protein-free lipid vesicles, we demonstrate that rapid LCFA transport across model and biological membranes remains unchanged in the presence of these purported inhibitors. We have previously shown in live cells that CD36 does not accelerate the transport of unesterified LCFA across the PM. Our present experiments indicated disruption of LCFA metabolism inside the cell within minutes upon treatment with many of the "inhibitors", previously assumed to inhibit LCFA transport across the PM. Furthermore, using confocal microscopy and a specific anti-SSO antibody, we found that numerous intracellular and PM-bound proteins are SSO-modified in addition to CD36. Our results support the hypothesis that LCFAs diffuse rapidly across biological membranes and do not require an active protein transporter for their transmembrane movement.

Keywords: metabolism; fatty acid; transport; lcfa transport; inhibitors putative; sso

Journal Title: Journal of lipid research
Year Published: 2020

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.