• Je něco špatně v tomto záznamu ?

In silico screening and molecular dynamics of phytochemicals from Indian cuisine against SARS-CoV-2 MPro

M. Rajendran, S. Roy, K. Ravichandran, B. Mishra, DK. Gupta, S. Nagarajan, RC. Arul Selvaraj, I. Provaznik

. 2022 ; 40 (7) : 3155-3169. [pub] 20201117

Jazyk angličtina Země Velká Británie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc22018990

SARS-CoV-2 cause fatal infection in 213 countries accounting for the death of millions of people globally. In the present study, phytochemicals from spices were assessed for their ability to interact with SARS-CoV-2 MPro. Structure based virtual screening was performed with 146 phytochemicals from spices using Autodock Vina. Phytochemicals with binding energy ≥ -8.0 kcal/mol were selected to understand their interaction with MPro. Virtual screening was further validated by performing molecular docking to generate favorable docked poses and the participation of important amino acid residues. Molecular dynamics simulation for the docked poses was performed to study thermodynamic properties of the protein, ligand and protein-ligand complexes. The finding shows that cinnamtannin B2 and cyanin showed favorable binding affinity values with SARS-CoV-2 MPro. The results are comparable in terms of docked poses, important amino acid participation and thermodynamic properties with the standard control drugs remdesivir, benazepril and hydroxychloroquine diphosphate. Prime MM-GBSA was employed for end-point binding energy calculation. Binding to domain I and II of MPro were mediated through the OH, SH, NH2 and non-polar side chain of amino acids. Cinnamtannin B2 and cyanin binds to MPro with many sub sites within the active site with RMSD and RMSF within 4 Å. The results computed using Prime MM-GBSA show that cinnamtannin B2 (-68.54940214 kcal/mol) and cyanin (-62.1902835 kcal/mol) have better binding affinity in comparison to hydroxychloroquine diphosphate (-54.00912412 kcal/mol) and benazepril (-53.70242369 kcal/mol). The results provide a basis for exploiting cinnamtannin B2 and cyanin as a starting point potential candidate for the development of drug against SARS-CoV-2.Communicated by Ramaswamy H. Sarma.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc22018990
003      
CZ-PrNML
005      
20220804135239.0
007      
ta
008      
220720s2022 xxk f 000 0|eng||
009      
AR
024    7_
$a 10.1080/07391102.2020.1845980 $2 doi
035    __
$a (PubMed)33200680
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxk
100    1_
$a Rajendran, Mala $u Department of Biotechnology, Mepco Schlenk Engineering College, Sivakasi, Tamil Nadu, India
245    10
$a In silico screening and molecular dynamics of phytochemicals from Indian cuisine against SARS-CoV-2 MPro / $c M. Rajendran, S. Roy, K. Ravichandran, B. Mishra, DK. Gupta, S. Nagarajan, RC. Arul Selvaraj, I. Provaznik
520    9_
$a SARS-CoV-2 cause fatal infection in 213 countries accounting for the death of millions of people globally. In the present study, phytochemicals from spices were assessed for their ability to interact with SARS-CoV-2 MPro. Structure based virtual screening was performed with 146 phytochemicals from spices using Autodock Vina. Phytochemicals with binding energy ≥ -8.0 kcal/mol were selected to understand their interaction with MPro. Virtual screening was further validated by performing molecular docking to generate favorable docked poses and the participation of important amino acid residues. Molecular dynamics simulation for the docked poses was performed to study thermodynamic properties of the protein, ligand and protein-ligand complexes. The finding shows that cinnamtannin B2 and cyanin showed favorable binding affinity values with SARS-CoV-2 MPro. The results are comparable in terms of docked poses, important amino acid participation and thermodynamic properties with the standard control drugs remdesivir, benazepril and hydroxychloroquine diphosphate. Prime MM-GBSA was employed for end-point binding energy calculation. Binding to domain I and II of MPro were mediated through the OH, SH, NH2 and non-polar side chain of amino acids. Cinnamtannin B2 and cyanin binds to MPro with many sub sites within the active site with RMSD and RMSF within 4 Å. The results computed using Prime MM-GBSA show that cinnamtannin B2 (-68.54940214 kcal/mol) and cyanin (-62.1902835 kcal/mol) have better binding affinity in comparison to hydroxychloroquine diphosphate (-54.00912412 kcal/mol) and benazepril (-53.70242369 kcal/mol). The results provide a basis for exploiting cinnamtannin B2 and cyanin as a starting point potential candidate for the development of drug against SARS-CoV-2.Communicated by Ramaswamy H. Sarma.
650    12
$a COVID-19 $7 D000086382
650    _2
$a lidé $7 D006801
650    _2
$a simulace molekulového dockingu $7 D062105
650    12
$a simulace molekulární dynamiky $7 D056004
650    _2
$a fytonutrienty $x chemie $x farmakologie $7 D064209
650    _2
$a inhibitory proteas $x chemie $7 D011480
650    _2
$a SARS-CoV-2 $7 D000086402
650    _2
$a farmakoterapie COVID-19 $7 D000093485
655    _2
$a časopisecké články $7 D016428
700    1_
$a Roy, Sudeep $u Department of Biomedical Engineering, Faculty of Electrical Engineering and Communication, Brno University of Technology, Brno, Czech Republic
700    1_
$a Ravichandran, Keerthana $u Department of Biotechnology, Mepco Schlenk Engineering College, Sivakasi, Tamil Nadu, India
700    1_
$a Mishra, Bagdevi $u Neogen Informatics, A121, Vikas Marg, New Delhi, India
700    1_
$a Gupta, Deepak K $u Neogen Informatics, A121, Vikas Marg, New Delhi, India
700    1_
$a Nagarajan, Subash $u Department of Biotechnology, Mepco Schlenk Engineering College, Sivakasi, Tamil Nadu, India
700    1_
$a Arul Selvaraj, Ruby Celsia $u Department of Biotechnology, Mepco Schlenk Engineering College, Sivakasi, Tamil Nadu, India
700    1_
$a Provaznik, Ivo $u Department of Biomedical Engineering, Faculty of Electrical Engineering and Communication, Brno University of Technology, Brno, Czech Republic
773    0_
$w MED00002554 $t Journal of biomolecular structure & dynamics $x 1538-0254 $g Roč. 40, č. 7 (2022), s. 3155-3169
856    41
$u https://pubmed.ncbi.nlm.nih.gov/33200680 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y p $z 0
990    __
$a 20220720 $b ABA008
991    __
$a 20220804135233 $b ABA008
999    __
$a ok $b bmc $g 1822546 $s 1170233
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2022 $b 40 $c 7 $d 3155-3169 $e 20201117 $i 1538-0254 $m Journal of biomolecular structure & dynamics $n J Biomol Struct Dyn $x MED00002554
LZP    __
$a Pubmed-20220720

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...