Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/16349
Title: Comparative molecular dynamics simulation study of aquaporin Z.
Authors: Ching, April Shi Min.
Keywords: DRNTU::Science::Biological sciences::Molecular biology
Issue Date: 2009
Abstract: The structural and functional divergence between two 30 ns simulations of aquaporin Z in a solvated membrane, one using the General AMBER force field and the other a modified GROMOS-87 force field, ffgmx, was determined. The protein in the AMBER run displayed water transport activity and typical water-protein interaction. The simulation using ffgmx, despite an outwardly normal structure, did not have any water transport activity as a result of channel occlusion. The channel was blocked essentially permanently at the cytoplasmic end by a deformed loop B, due to a loss of constraining hydrogen bonds. Reversible and transient constrictions also arise at the selectivity filter as a result of artificially elevated side chain motion of its constituent residues and loss of important stabilising Van der Waals contacts – most significant is the aromatic side chain of Phe-43 whose face becomes perpendicular to the channel axis. These observations highlighted the deficiencies of the ffgmx/Berger force field combination in preserving critical hydrophobic contacts and hydrogen bonds in flexible moieties.
URI: http://hdl.handle.net/10356/16349
Rights: Nanyang Technological University
Fulltext Permission: restricted
Fulltext Availability: With Fulltext
Appears in Collections:SBS Student Reports (FYP/IA/PA/PI)

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