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8GEW

H-FABP crystal soaked in a bromo palmitic acid solution

Summary for 8GEW
Entry DOI10.2210/pdb8gew/pdb
DescriptorFatty acid-binding protein, heart, 2-Bromopalmitic acid, OLEIC ACID, ... (4 entities in total)
Functional Keywordsh-fabp, br-palmitic acid, lipid binding protein
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight15425.72
Authors
Howard, E.,Cousido-Siah, A.,Alvarez, A.,Espinosa, Y.,Podjarny, A.,Mitschler, A.,Carlevaro, M. (deposition date: 2023-03-07, release date: 2023-08-30, Last modification date: 2024-04-17)
Primary citationAlvarez, H.A.,Cousido-Siah, A.,Espinosa, Y.R.,Podjarny, A.,Carlevaro, C.M.,Howard, E.
Lipid exchange in crystal-confined fatty acid binding proteins: X-ray evidence and molecular dynamics explanation.
Proteins, 91:1525-1534, 2023
Cited by
PubMed Abstract: Fatty acid binding proteins (FABPs) are responsible for the long-chain fatty acids (FAs) transport inside the cell. However, despite the years, since their structure is known and the many studies published, there is no definitive answer about the stages of the lipid entry-exit mechanism. Their structure forms a -barrel of 10 anti-parallel strands with a cap in a helix-turn-helix motif, and there is some consensus on the role of the so-called portal region, involving the second -helix from the cap ( 2), C- D, and E- F turns in FAs exchange. To test the idea of a lid that opens, we performed a soaking experiment on an h-FABP crystal in which the cap is part of the packing contacts, and its movement is strongly restricted. Even in these conditions, we observed the replacement of palmitic acid by 2-Bromohexadecanoic acid (Br-palmitic acid). Our MD simulations reveal a two-step lipid entry process: (i) The travel of the lipid head through the cavity in the order of tens of nanoseconds, and (ii) The accommodation of its hydrophobic tail in hundreds to thousands of nanoseconds. We observed this even in the cases in which the FAs enter the cavity by their tail. During this process, the FAs do not follow a single trajectory, but multiple ones through which they get into the protein cavity. Thanks to the complementary views between experiment and simulation, we can give an approach to a mechanistic view of the exchange process.
PubMed: 37462340
DOI: 10.1002/prot.26546
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (0.97 Å)
Structure validation

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