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3F32

Horse spleen apoferritin

Summary for 3F32
Entry DOI10.2210/pdb3f32/pdb
Related1XZ1 1XZ3 3F33 3F34 3F35 3F36 3F37 3F38 3F39
DescriptorFerritin light chain, CADMIUM ION, SULFATE ION, ... (4 entities in total)
Functional Keywords4-helix bundle, acetylation, iron, iron storage, metal-binding, metal binding protein
Biological sourceEquus caballus (domestic horse,equine)
Total number of polymer chains1
Total formula weight20626.61
Authors
Vedula, L.S.,Economou, N.J.,Rossi, M.J.,Eckenhoff, R.G.,Loll, P.J. (deposition date: 2008-10-30, release date: 2009-07-14, Last modification date: 2023-09-06)
Primary citationVedula, L.S.,Brannigan, G.,Economou, N.J.,Xi, J.,Hall, M.A.,Liu, R.,Rossi, M.J.,Dailey, W.P.,Grasty, K.C.,Klein, M.L.,Eckenhoff, R.G.,Loll, P.J.
A unitary anesthetic binding site at high resolution.
J.Biol.Chem., 284:24176-24184, 2009
Cited by
PubMed Abstract: Propofol is the most widely used injectable general anesthetic. Its targets include ligand-gated ion channels such as the GABA(A) receptor, but such receptor-channel complexes remain challenging to study at atomic resolution. Until structural biology methods advance to the point of being able to deal with systems such as the GABA(A) receptor, it will be necessary to use more tractable surrogates to probe the molecular details of anesthetic recognition. We have previously shown that recognition of inhalational general anesthetics by the model protein apoferritin closely mirrors recognition by more complex and clinically relevant protein targets; here we show that apoferritin also binds propofol and related GABAergic anesthetics, and that the same binding site mediates recognition of both inhalational and injectable anesthetics. Apoferritin binding affinities for a series of propofol analogs were found to be strongly correlated with the ability to potentiate GABA responses at GABA(A) receptors, validating this model system for injectable anesthetics. High resolution x-ray crystal structures reveal that, despite the presence of hydrogen bond donors and acceptors, anesthetic recognition is mediated largely by van der Waals forces and the hydrophobic effect. Molecular dynamics simulations indicate that the ligands undergo considerable fluctuations about their equilibrium positions. Finally, apoferritin displays both structural and dynamic responses to anesthetic binding, which may mimic changes elicited by anesthetics in physiologic targets like ion channels.
PubMed: 19605349
DOI: 10.1074/jbc.M109.017814
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.7 Å)
Structure validation

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