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"To Be or Not to Be" Protonated : Atomic Details of Human Carbonic Anhydrase-Clinical Drug Complexes by Neutron Crystallography and Simulation

Kovalevsky, Andrey (author)
Oak Ridge National Laboratory
Aggarwal, Mayank (author)
Oak Ridge National Laboratory
Velazquez, Hector (author)
University of Tennessee
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Cuneo, Matthew J. (author)
Oak Ridge National Laboratory
Blakeley, Matthew P. (author)
Institut Laue Langevin
Weiss, Kevin L. (author)
Oak Ridge National Laboratory
Smith, Jeremy C. (author)
University of Tennessee
Fisher, S. Zoë (author)
Lund University,Lunds universitet,Molekylär cellbiologi,Biologiska institutionen,Naturvetenskapliga fakulteten,Molecular Cell Biology,Department of Biology,Faculty of Science,European Spallation Source ESS AB
McKenna, Robert (author)
University of Florida
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 (creator_code:org_t)
Elsevier BV, 2018
2018
English.
In: Structure. - : Elsevier BV. - 0969-2126. ; 26:3, s. 3-390
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Human carbonic anhydrases (hCAs) play various roles in cells, and have been drug targets for decades. Sequence similarities of hCA isoforms necessitate designing specific inhibitors, which requires detailed structural information for hCA-inhibitor complexes. We present room temperature neutron structures of hCA II in complex with three clinical drugs that provide in-depth analysis of drug binding, including protonation states of the inhibitors, hydration water structure, and direct visualization of hydrogen-bonding networks in the enzyme's active site. All sulfonamide inhibitors studied bind to the Zn metal center in the deprotonated, anionic, form. Other chemical groups of the drugs can remain neutral or be protonated when bound to hCA II. MD simulations have shown that flexible functional groups of the inhibitors may alter their conformations at room temperature and occupy different sub-sites. This study offers insights into the design of specific drugs to target cancer-related hCA isoform IX. Kovalevsky et al. used macromolecular neutron crystallography and molecular dynamics simulations to obtain a detailed picture of clinical inhibitors binding to human carbonic anhydrase II. The study visualized hydrogen atom positions, revealing protonation/deprotonation events and intricate hydrogen-bonding networks, providing insights for drug design.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

Brinzolamide
Dorzolamide
Drug binding
Ethoxzolamide
Human carbonic anhydrase
Hydrogen bonding
MD simulations
Neutron crystallography
Perdeuteration

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art (subject category)
ref (subject category)

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