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Title: Enzymes for carbon sequestration: neutron crystallographic studies of carbonic anhydrase

Journal Article · · Acta Crystallographica. Section D: Biological Crystallography
 [1];  [2];  [1];  [3];  [2];  [1]
  1. Bioscience Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)
  2. Department of Biochemistry and Molecular Biology, PO Box 100245, University of Florida, Gainesville, FL 32610 (United States)
  3. Department of Pharmacology and Therapeutics, PO Box 100267, University of Florida, Gainesville, FL 32610 (United States)

The first neutron crystal structure of carbonic anhydrase is presented. The structure reveals interesting and unexpected features of the active site that affect catalysis. Carbonic anhydrase (CA) is a ubiquitous metalloenzyme that catalyzes the reversible hydration of CO{sub 2} to form HCO{sub 3}{sup −} and H{sup +} using a Zn–hydroxide mechanism. The first part of catalysis involves CO{sub 2} hydration, while the second part deals with removing the excess proton that is formed during the first step. Proton transfer (PT) is thought to occur through a well ordered hydrogen-bonded network of waters that stretches from the metal center of CA to an internal proton shuttle, His64. These waters are oriented and ordered through a series of hydrogen-bonding interactions to hydrophilic residues that line the active site of CA. Neutron studies were conducted on wild-type human CA isoform II (HCA II) in order to better understand the nature and the orientation of the Zn-bound solvent (ZS), the charged state and conformation of His64, the hydrogen-bonding patterns and orientations of the water molecules that mediate PT and the ionization of hydrophilic residues in the active site that interact with the water network. Several interesting and unexpected features in the active site were observed which have implications for how PT proceeds in CA.

OSTI ID:
22351219
Journal Information:
Acta Crystallographica. Section D: Biological Crystallography, Vol. 66, Issue Pt 11; Other Information: PMCID: PMC2967421; PMID: 21041933; PUBLISHER-ID: dz5205; OAI: oai:pubmedcentral.nih.gov:2967421; Copyright (c) International Union of Crystallography 2010; Country of input: International Atomic Energy Agency (IAEA); ISSN 0907-4449
Country of Publication:
Denmark
Language:
English