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Relevance of hydrogen bonds for the histamine H2 receptor-ligand interactions : a lesson from deuteration
ID Kržan, Mojca (Avtor), ID Keuschler, Jan (Avtor), ID Mavri, Janez (Avtor), ID Vianello, Robert (Avtor)

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Izvleček
We used a combination of density functional theory (DFT) calculations and the implicit quantization of the acidic N-H and O-H bonds to assess the effect of deuteration on the binding of agonists (2-methylhistamine and 4-methylhistamine) and antagonists (cimetidine and famotidine) to the histamine H2 receptor. The results show that deuteration significantly increases the affinity for 4-methylhistamine and reduces it for 2-methylhistamine, while leaving it unchanged for both antagonists, which is found in excellent agreement with experiments. The revealed trends are interpreted in the light of the altered strength of the hydrogen bonding upon deuteration, known as the Ubbelohde effect, which affects ligand interactions with both active sites residues and solvent molecules preceding the binding, thus providing strong evidence for the relevance of hydrogen bonding for this process. In addition, computations further underline an important role of the Tyr250 residue for the binding. The obtained insight is relevant for the therapy in the context of (per)deuterated drugs that are expected to enter therapeutic practice in the near future, while this approach may contribute towards understanding receptor activation and its discrimination between agonists and antagonists.

Jezik:Angleški jezik
Ključne besede:histamine receptor, receptor activation, hydrogen bonding, computational chemistry, DFT calculations, deuteration, heavy drugs
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:MF - Medicinska fakulteta
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2020
Št. strani:10 str.
Številčenje:Vol. 10, iss. 2, art. 196
PID:20.500.12556/RUL-133064 Povezava se odpre v novem oknu
UDK:615
ISSN pri članku:2218-273X
DOI:10.3390/biom10020196 Povezava se odpre v novem oknu
COBISS.SI-ID:34671833 Povezava se odpre v novem oknu
Datum objave v RUL:10.11.2021
Število ogledov:972
Število prenosov:134
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Gradivo je del revije

Naslov:Biomolecules
Skrajšan naslov:Biomolecules
Založnik:MDPI
ISSN:2218-273X
COBISS.SI-ID:519952921 Povezava se odpre v novem oknu

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:01.02.2020

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:histaminski receptor, aktivacija receptorjev, vodikove vezi, kromatografija

Projekti

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P1-0012
Naslov:Molekulske simulacije, bioinformatika in načrtovanje zdravilnih učinkovin

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P3-0067
Naslov:Farmakologija in farmakogenomika

Financer:HRZZ - Croatian Science Foundation
Številka projekta:IP-2014-09-3386
Naslov:Design and Synthesis of Novel Nitrogen-Containing Heterocyclic Fluorophores and Fluorescent Nanomaterials for pH and Metal-Ion Sensing

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