TY - JOUR
T1 - Virtual Screening of a Library of Naturally Occurring Anthraquinones for Potential Anti-Fouling Agents
AU - Preet, Gagan
AU - Astakala, Rishi Vachaspathy
AU - Gomez-Banderas, Jessica
AU - Rajakulendran, Joy Ebenezer
AU - Hasan, Ahlam Haj
AU - Ebel, Rainer
AU - Jaspars, Marcel
N1 - Acknowledgments
A sincere thanks to Mehak Sharma and Varship Creations, India, for their constructive suggestions. Additionally, thank you to Nidhan Singh Oberoi and Albrn Care, India.
Funding
This research received no external funding.
PY - 2023/1/19
Y1 - 2023/1/19
N2 - Marine biofouling is the undesired accumulation of organic molecules, microorganisms, macroalgae, marine invertebrates, and their by-products on submerged surfaces. It is a serious challenge for marine vessels and the oil, gas, and renewable energy industries, as biofouling can cause economic losses for these industries. Natural products have been an abundant source of therapeutics since the start of civilisation. Their use as novel anti-fouling agents is a promising approach for replacing currently used, harmful anti-fouling agents. Anthraquinones (AQs) have been used for centuries in the food, pharmaceutical, cosmetics, and paint industries. Citreorosein and emodin are typical additives used in the anti-fouling paint industry to help improve the global problem of biofouling. This study is based on our previous study, in which we presented the promising activity of structurally related anthraquinone compounds against biofilm-forming marine bacteria. To help uncover the anti-fouling potential of other AQ-related structures, 2194 compounds from the COCONUT natural products database were analysed. Molecular docking analysis was performed to assess the binding strength of these compounds to the LuxP protein in Vibrio carchariae. The LuxP protein is a vital binding protein responsible for the movements of autoinducers within the quorum sensing system; hence, interrupting the process at an early stage could be an effective strategy. Seventy-six AQ structures were found to be highly docked, and eight of these structures were used in structure-based pharmacophore modelling, resulting in six unique pharmacophore features.
AB - Marine biofouling is the undesired accumulation of organic molecules, microorganisms, macroalgae, marine invertebrates, and their by-products on submerged surfaces. It is a serious challenge for marine vessels and the oil, gas, and renewable energy industries, as biofouling can cause economic losses for these industries. Natural products have been an abundant source of therapeutics since the start of civilisation. Their use as novel anti-fouling agents is a promising approach for replacing currently used, harmful anti-fouling agents. Anthraquinones (AQs) have been used for centuries in the food, pharmaceutical, cosmetics, and paint industries. Citreorosein and emodin are typical additives used in the anti-fouling paint industry to help improve the global problem of biofouling. This study is based on our previous study, in which we presented the promising activity of structurally related anthraquinone compounds against biofilm-forming marine bacteria. To help uncover the anti-fouling potential of other AQ-related structures, 2194 compounds from the COCONUT natural products database were analysed. Molecular docking analysis was performed to assess the binding strength of these compounds to the LuxP protein in Vibrio carchariae. The LuxP protein is a vital binding protein responsible for the movements of autoinducers within the quorum sensing system; hence, interrupting the process at an early stage could be an effective strategy. Seventy-six AQ structures were found to be highly docked, and eight of these structures were used in structure-based pharmacophore modelling, resulting in six unique pharmacophore features.
KW - anthraquinones
KW - anti-fouling
KW - biofouling
KW - citreorosein
KW - emodin
KW - in silico
KW - marine
KW - molecular docking
KW - paints
KW - pharmacophore
KW - repurposing
KW - virtual screening
UR - https://www.mdpi.com/1420-3049/28/3/995
UR - http://www.scopus.com/inward/record.url?scp=85147894579&partnerID=8YFLogxK
U2 - 10.3390/molecules28030995
DO - 10.3390/molecules28030995
M3 - Article
C2 - 36770663
VL - 28
JO - Molecules
JF - Molecules
SN - 1420-3049
IS - 3
M1 - 995
ER -