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Using virtual AChE homology screening to identify small molecules with the ability to inhibit marine biofouling
ID
Arabshahi, Homayon John
(
Avtor
),
ID
Trobec, Tomaž
(
Avtor
),
ID
Foulon, Valentin
(
Avtor
),
ID
Hellio, Claire
(
Avtor
),
ID
Frangež, Robert
(
Avtor
),
ID
Sepčić, Kristina
(
Avtor
),
ID
Cahill, Patrick
(
Avtor
),
ID
Svenson, Johan
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(2,67 MB)
MD5: 8AEFD939B41784005C58CFB072C44B7C
URL - Izvorni URL, za dostop obiščite
https://www.frontiersin.org/articles/10.3389/fmars.2021.762287/full
Galerija slik
Izvleček
The search for effective yet environmentally friendly strategies to prevent marine biofouling is hampered by the large taxonomic diversity amongst fouling organisms and a lack of well-defined conserved molecular targets. The acetylcholinesterase enzyme catalyses the breakdown of the neurotransmitter acetylcholine, and several natural antifouling allelochemicals have been reported to display acetylcholinesterase inhibitory activity. Our study is focussed on establishing if acetylcholinesterase can be used as a well-defined molecular target to accelerate discovery and development of novel antifoulants via sequential high-throughput in silico screening, in vitro enzymatic studies of identified compound libraries, and in vivo assessment of the most promising lead compounds. Using this approach, we identified potent cholinesterase inhibitors with inhibitory concentrations down to 3 mM from a 10,000 compound library. The most potent inhibitors were screened against five microfouling marine bacteria and marine microalgae and the macrofouling tunicate Ciona savignyi. No activity was seen against the microfoulers but a potent novel inhibitor of tunicate settlement and metamorphosis was discovered. Although only one of the identified active cholinesterase inhibitors displayed antifouling activity suggesting the link between cholinesterase inhibition and antifouling is limited to certain compound classes, the study highlights how in silico screening employed regularly for drug discovery can also facilitate discovery of antifouling leads.
Jezik:
Angleški jezik
Ključne besede:
homology screening
,
in silico screening
,
in vitro enzymatic studies
,
cholinesterase
,
AChE inhibitor
,
antifouling
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
VF - Veterinarska fakulteta
BF - Biotehniška fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Datum objave:
13.12.2021
Leto izida:
2021
Št. strani:
12 str.
Številčenje:
Vol. 8, art. 762287
PID:
20.500.12556/RUL-133797
UDK:
636.09:575
ISSN pri članku:
2296-7745
DOI:
10.3389/fmars.2021.762287
COBISS.SI-ID:
89164547
Datum objave v RUL:
15.12.2021
Število ogledov:
1358
Število prenosov:
160
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Frontiers in marine science
Skrajšan naslov:
Front. mar. sci.
Založnik:
Frontiers Media
ISSN:
2296-7745
COBISS.SI-ID:
523094809
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:
15.12.2021
Projekti
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
CAWX1805 - New Zealand Ministry for Business Innovation and Employment
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P4-0053
Naslov:
Endokrini, imunski in encimski odzivi pri zdravih in bolnih živalih
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P1-0207
Naslov:
Toksini in biomembrane
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