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Overview of the assays to probe O-linked β-N-acetylglucosamine transferase binding and activity
ID
Balsollier, Cyril
(
Avtor
),
ID
Pieters, Roland J.
(
Avtor
),
ID
Anderluh, Marko
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(5,14 MB)
MD5: 35B267780BEB1B4F5DB490F2412408E7
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/1420-3049/26/4/1037
Galerija slik
Izvleček
O-GlcNAcylation is a posttranslational modification that occurs at serine and threonine residues of protein substrates by the addition of O-linked β-D-N-acetylglucosamine (GlcNAc) moiety. Two enzymes are involved in this modification: O-GlcNac transferase (OGT), which attaches the GlcNAc residue to the protein substrate, and O-GlcNAcase (OGA), which removes it. This biological balance is important for many biological processes, such as protein expression, cell apoptosis, and regulation of enzyme activity. The extent of this modification has sparked interest in the medical community to explore OGA and OGT as therapeutic targets, particularly in degenerative diseases. While some OGA inhibitors are already in phase 1 clinical trials for the treatment of Alzheimer’s disease, OGT inhibitors still have a long way to go. Due to complex expression and instability, the discovery of potent OGT inhibitors is challenging. Over the years, the field has grappled with this problem, and scientists have developed a number of techniques and assays. In this review, we aim to highlight assays and techniques for OGT inhibitor discovery, evaluate their strength for the field, and give us direction for future bioassay methods.
Jezik:
Angleški jezik
Ključne besede:
OGT
,
GlcNAcylation
,
O-GlcNAc transferase
,
bioassay
,
OGT inhibitor
Vrsta gradiva:
Članek v reviji
Tipologija:
1.02 - Pregledni znanstveni članek
Organizacija:
FFA - Fakulteta za farmacijo
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2021
Št. strani:
20 str.
Številčenje:
Vol. 26, iss. 4, art. 1037
PID:
20.500.12556/RUL-135020
UDK:
615.4:54:616.894
ISSN pri članku:
1420-3049
DOI:
10.3390/molecules26041037
COBISS.SI-ID:
51829507
Datum objave v RUL:
17.02.2022
Število ogledov:
1357
Število prenosov:
129
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Molecules
Skrajšan naslov:
Molecules
Založnik:
MDPI
ISSN:
1420-3049
COBISS.SI-ID:
18462981
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:
16.02.2021
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
farmacevtska kemija
,
Alzheimerjeva bolezen
Projekti
Financer:
EC - European Commission
Program financ.:
H2020
Številka projekta:
765581
Naslov:
Multidisciplinary European Joint Doctorate in the Design and Development of Glyco Drugs
Akronim:
PhD4GlycoDrug
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