Antiviral therapeutics directed against RNA dependent RNA polymerases from positive-sense viruses

被引:5
作者
Bhatia, Sonam [1 ]
Narayanan, Naveen [1 ]
Nagpal, Shilpi [1 ,2 ]
Nair, Deepak T. [1 ,3 ]
机构
[1] Reg Ctr Biotechnol, 3rd Milestone,Faridabad Gurgaon Expressway, Faridabad 121001, India
[2] Natl Ctr Biol Sci, GKVK Campus, GKVK Campus, Bangalore, India
[3] Reg Ctr Biotechnol, NCR Biotech Sci Cluster, 3rd Milestone,Faridabad Gurgaon Expressway,POB 3, Faridabad 121001, Haryana, India
关键词
RNA dependent RNA polymerases; +ssRNA viruses; Inhibitors; Allostery; SMALL-MOLECULE INHIBITORS; BROAD-SPECTRUM INHIBITOR; CRYSTAL-STRUCTURE; NONNUCLEOSIDE INHIBITOR; PRECLINICAL CHARACTERIZATION; SARS-COV-2; REPLICATION; HCVNS5B POLYMERASE; ERROR CATASTROPHE; STRUCTURAL BASIS; VIRAL HELICASE;
D O I
10.1016/j.mam.2021.101005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Viruses with positive-sense single stranded RNA (+ssRNA) genomes are responsible for different diseases and represent a global health problem. In addition to developing new vaccines that protect against severe illness on infection, it is imperative to identify new antiviral molecules to treat infected patients. The genome of these RNA viruses generally codes for an enzyme with RNA dependent RNA polymerase (RdRP) activity. This molecule is centrally involved in the duplication of the RNA genome. Inhibition of this enzyme by small molecules will prevent duplication of the RNA genome and thus reduce the viral titer. An overview of the different therapeutic strategies used to inhibit RdRPs from +ssRNA viruses is provided, along with an analysis of these enzymes to highlight new binding sites for inhibitors.
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页数:16
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共 187 条
[1]   Antiviral Strategies against Arthritogenic Alphaviruses [J].
Abdelnabi, Rana ;
Delang, Leen .
MICROORGANISMS, 2020, 8 (09) :1-18
[2]   Viral error catastrophe by mutagenic nucleosides [J].
Anderson, JP ;
Daifuku, R ;
Loeb, LA .
ANNUAL REVIEW OF MICROBIOLOGY, 2004, 58 :183-205
[3]   HIV resistance to zidovudine: the role of pyrophosphorolysis [J].
Arion, D ;
Parniak, MA .
DRUG RESISTANCE UPDATES, 1999, 2 (02) :91-95
[4]   Replication and packaging of Norwalk virus RNA in cultured mammalian cells [J].
Asanaka, M ;
Atmar, RL ;
Ruvolo, V ;
Crawford, SE ;
Neill, FH ;
Estes, MK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (29) :10327-10332
[5]   Enzymes and Enzyme Activity Encoded by Nonenveloped Viruses [J].
Azad, Kimi ;
Banerjee, Manidipa ;
Johnson, John E. .
ANNUAL REVIEW OF VIROLOGY, VOL 4, 2017, 4 :221-240
[6]   Antiviral drugs [J].
Balfour, HH .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (16) :1255-1268
[7]   EXPRESSION OF ANIMAL VIRUS GENOMES [J].
BALTIMORE, D .
BACTERIOLOGICAL REVIEWS, 1971, 35 (03) :235-+
[8]   Toward development of generic inhibitors against the 3C proteases of picornaviruses [J].
Banerjee, Kamalika ;
Bhat, Ruchika ;
Rao, V. U. Bhaskara ;
Nain, Anshu ;
Rallapalli, Kartik Lakshmi ;
Gangopadhyay, Sohona ;
Singh, R. P. ;
Banerjee, Manidipa ;
Jayaram, Bhyravabhotla .
FEBS JOURNAL, 2019, 286 (04) :765-787
[9]  
Barakat K, 2022, J BIOMOL STRUCT DYN, V40, P9443, DOI 10.1080/07391102.2021.1930162
[10]   T-705 (Favipiravir) Induces Lethal Mutagenesis in Influenza A H1N1 Viruses In Vitro [J].
Baranovich, Tatiana ;
Wong, Sook-San ;
Armstrong, Jianling ;
Marjuki, Henju ;
Webby, Richard J. ;
Webster, Robert G. ;
Govorkova, Elena A. .
JOURNAL OF VIROLOGY, 2013, 87 (07) :3741-3751