Mpropred: A machine learning (ML) driven Web-App for bioactivity prediction of SARS-CoV-2 main protease (Mpro) antagonists

被引:4
作者
Ferdous, Nadim [1 ]
Reza, Mahjerin Nasrin [1 ]
Hossain, Mohammad Uzzal [2 ,3 ]
Mahmud, Shahin [1 ]
Napis, Suhami [4 ]
Chowdhury, Kamal [5 ]
Mohiuddin, A. K. M. [1 ]
机构
[1] Mawlana Bhashani Sci & Technol Univ, Dept Biotechnol & Genet Engn, Santosh, Tangail, Bangladesh
[2] Univ Oxford, Dept Pharmacol, Med Sci Div, Oxford, England
[3] Natl Inst Biotechnol, Bioinformat Div, Dhaka, Bangladesh
[4] Univ Putra Malaysia, Dept Mol Biol, Serdang, Selangor De, Malaysia
[5] Claflin Univ, Biol Dept, Orangeburg, SC USA
来源
PLOS ONE | 2023年 / 18卷 / 06期
关键词
COMPUTATIONAL METHODS; ANTIGENIC DRIFT; QSAR; DEFINITION; INHIBITION; EMERGENCE; COVID-19; DOCKING; TOOL;
D O I
10.1371/journal.pone.0287179
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic emerged in 2019 and still requiring treatments with fast clinical translatability. Frequent occurrence of mutations in spike glycoprotein of SARS-CoV-2 led the consideration of an alternative therapeutic target to combat the ongoing pandemic. The main protease (M-pro) is such an attractive drug target due to its importance in maturating several polyproteins during the replication process. In the present study, we used a classification structure-activity relationship (CSAR) model to find substructures that leads to to anti-M-pro activities among 758 non-redundant compounds. A set of 12 fingerprints were used to describe M-pro inhibitors, and the random forest approach was used to build prediction models from 100 distinct data splits. The data set's modelability (MODI index) was found to be robust, with a value of 0.79 above the 0.65 threshold. The accuracy (89%), sensitivity (89%), specificity (73%), and Matthews correlation coefficient (79%) used to calculate the prediction performance, was also found to be statistically robust. An extensive analysis of the top significant descriptors unveiled the significance of methyl side chains, aromatic ring and halogen groups for M-pro inhibition. Finally, the predictive model is made publicly accessible as a web-app named M(pro)pred in order to allow users to predict the bioactivity of compounds against SARS-CoV-2 M-pro. Later, CMNPD, a marine compound database was screened by our app to predict bioactivity of all the compounds and results revealed significant correlation with their binding affinity to M-pro. Molecular dynamics (MD) simulation and molecular mechanics/Poisson Boltzmann surface area (MM/PBSA) analysis showed improved properties of the complexes. Thus, the knowledge and web-app shown herein can be used to develop more effective and specific inhibitors against the SARS-CoV-2 M-pro. The web-app can be accessed from https://share.streamlit.io/nadimfrds/mpropred/Mpropred_app.py.
引用
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页数:21
相关论文
共 70 条
  • [1] Repurposing of Some Natural Product Isolates as SARS-COV-2 Main Protease Inhibitors via In Vitro Cell Free and Cell-Based Antiviral Assessments and Molecular Modeling Approaches
    Abdallah, Hossam M.
    El-Halawany, Ali M.
    Sirwi, Alaa
    El-Araby, Amr M.
    Mohamed, Gamal A.
    Ibrahim, Sabrin R. M.
    Koshak, Abdulrahman E.
    Asfour, Hani Z.
    Awan, Zuhier A.
    A. Elfaky, Mahmoud
    [J]. PHARMACEUTICALS, 2021, 14 (03)
  • [2] Gromacs: High performance molecular simulations through multi-level parallelism from laptops to supercomputers
    Abraham, Mark James
    Murtola, Teemu
    Schulz, Roland
    Páll, Szilárd
    Smith, Jeremy C.
    Hess, Berk
    Lindah, Erik
    [J]. SoftwareX, 2015, 1-2 : 19 - 25
  • [3] Mutation rate of SARS-CoV-2 and emergence of mutators during experimental evolution
    Amicone, Massimo
    Borges, Vitor
    Alves, Maria Joao
    Isidro, Joana
    Ze-Ze, Libia
    Duarte, Silvia
    Vieira, Luis
    Guiomar, Raquel
    Gomes, Joao Paulo
    Gordo, Isabel
    [J]. EVOLUTION MEDICINE AND PUBLIC HEALTH, 2022, 10 (01) : 142 - 155
  • [4] [Anonymous], PUBCHEM SUBSTR FING
  • [5] Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine
    Baden, Lindsey R.
    El Sahly, Hana M.
    Essink, Brandon
    Kotloff, Karen
    Frey, Sharon
    Novak, Rick
    Diemert, David
    Spector, Stephen A.
    Rouphael, Nadine
    Creech, C. Buddy
    McGettigan, John
    Khetan, Shishir
    Segall, Nathan
    Solis, Joel
    Brosz, Adam
    Fierro, Carlos
    Schwartz, Howard
    Neuzil, Kathleen
    Corey, Larry
    Gilbert, Peter
    Janes, Holly
    Follmann, Dean
    Marovich, Mary
    Mascola, John
    Polakowski, Laura
    Ledgerwood, Julie
    Graham, Barney S.
    Bennett, Hamilton
    Pajon, Rolando
    Knightly, Conor
    Leav, Brett
    Deng, Weiping
    Zhou, Honghong
    Han, Shu
    Ivarsson, Melanie
    Miller, Jacqueline
    Zaks, Tal
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2021, 384 (05) : 403 - 416
  • [6] Machine Learning for Molecular Modelling in Drug Design
    Ballester, Pedro J.
    [J]. BIOMOLECULES, 2019, 9 (06):
  • [7] JS']JSME: a free molecule editor in Java']JavaScript
    Bienfait, Bruno
    Ertl, Peter
    [J]. JOURNAL OF CHEMINFORMATICS, 2013, 5
  • [8] SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation
    Blewitt, Marnie E.
    Gendrel, Anne-Valerie
    Pang, Zhenyi
    Sparrow, Duncan B.
    Whitelaw, Nadia
    Craig, Jeffrey M.
    Apedaile, Anwyn
    Hilton, Douglas J.
    Dunwoodie, Sally L.
    Brockdorff, Neil
    Kay, Graham F.
    Whitelaw, Emma
    [J]. NATURE GENETICS, 2008, 40 (05) : 663 - 669
  • [9] SAR Studies and Biological Characterization of a Chromen-4-one Derivative as an Anti-Trypanosoma brucei Agent
    Borsari, Chiara
    Santarem, Nuno
    Macedo, Sara
    Dolores Jimenez-Anton, Maria
    Torrado, Juan J.
    Isabel Olias-Molero, Ana
    Corral, Maria J.
    Tait, Annalisa
    Ferrari, Stefania
    Costantino, Luca
    Luciani, Rosaria
    Ponterini, Glauco
    Gul, Sheraz
    Kuzikov, Maria
    Ellinger, Bernhard
    Behrens, Birte
    Reinshagen, Jeanette
    Maria Alunda, Jose
    Cordeiro-da-Silva, Anabela
    Costi, Maria Paola
    [J]. ACS MEDICINAL CHEMISTRY LETTERS, 2019, 10 (04): : 528 - 533
  • [10] Random forests
    Breiman, L
    [J]. MACHINE LEARNING, 2001, 45 (01) : 5 - 32