Modeling fatty acid delivery from intestinal fatty acid binding protein to a membrane

Intestinal fatty acid binding protein (IFABP) interacts with biological membranes and delivers fatty acid (FA) into them via a collisional mechanism. However, the membrane‐bound structure of the protein and the pathway of FA transfer are not precisely known. We used molecular dynamics (MD) simulations with an implicit membrane model to determine the optimal orientation of apo‐ and holo‐IFABP (bound with palmitate) on an anionic membrane. In this orientation, the helical portal region, delimited by the αII helix and the βC‐βD and βE‐βF turns, is oriented toward the membrane whereas the putative β‐strand portal, delimited by the βB‐βC, βF‐βG, βH‐βI turns and the N terminus, is exposed to solvent. Starting from the MD structure of holo‐IFABP in the optimal orientation relative to the membrane, we examined the release of palmitate via both pathways. Although the domains can widen enough to allow the passage of palmitate, fatty acid release through the helical portal region incurs smaller conformational changes and a lower energetic cost.