SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Blakeley J.)
 

Search: WFRF:(Blakeley J.) > "To Be or Not to Be...

  • Kovalevsky, AndreyOak Ridge National Laboratory (author)

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

  • Article/chapterEnglish2018

Publisher, publication year, extent ...

  • Elsevier BV,2018

Numbers

  • LIBRIS-ID:oai:lup.lub.lu.se:1a0633a3-594e-4e4d-b8be-8c256cce745d
  • https://lup.lub.lu.se/record/1a0633a3-594e-4e4d-b8be-8c256cce745dURI
  • https://doi.org/10.1016/j.str.2018.01.006DOI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:art swepub-publicationtype
  • Subject category:ref swepub-contenttype

Notes

  • 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 and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Aggarwal, MayankOak Ridge National Laboratory (author)
  • Velazquez, HectorUniversity of Tennessee (author)
  • Cuneo, Matthew J.Oak Ridge National Laboratory (author)
  • Blakeley, Matthew P.Institut Laue Langevin (author)
  • Weiss, Kevin L.Oak Ridge National Laboratory (author)
  • Smith, Jeremy C.University of Tennessee (author)
  • Fisher, S. ZoëLund University,Lunds universitet,Molekylär cellbiologi,Biologiska institutionen,Naturvetenskapliga fakulteten,Molecular Cell Biology,Department of Biology,Faculty of Science,European Spallation Source ESS AB(Swepub:lu)biol-zfh (author)
  • McKenna, RobertUniversity of Florida (author)
  • Oak Ridge National LaboratoryUniversity of Tennessee (creator_code:org_t)

Related titles

  • In:Structure: Elsevier BV26:3, s. 3-3900969-2126

Internet link

Find in a library

  • Structure (Search for host publication in LIBRIS)

To the university's database

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view