Chemoproteomics enables identification of coatomer subunit zeta-1 targeted by a small molecule for enterovirus A71 inhibition

Xiaoyong Li1,2, Jin Zhang3, Yaxin Xiao1, Hao Song1, Yuexiang Li2, Wei Li2, Ruiyuan Cao2, Song Li2, Yong Qin1(), Chu Wang3(), Wu Zhong2()

PDF
MedComm ›› 2024, Vol. 5 ›› Issue (6) : e587. DOI: 10.1002/mco2.587
ORIGINAL ARTICLE

Chemoproteomics enables identification of coatomer subunit zeta-1 targeted by a small molecule for enterovirus A71 inhibition

  • Xiaoyong Li1,2, Jin Zhang3, Yaxin Xiao1, Hao Song1, Yuexiang Li2, Wei Li2, Ruiyuan Cao2, Song Li2, Yong Qin1(), Chu Wang3(), Wu Zhong2()
Author information +
History +

Abstract

Human enterovirus A71 (EV-A71) is a significant etiological agent responsible for epidemics of hand, foot, and mouth disease (HFMD) in Asia-Pacific regions. There are presently no licensed antivirals against EV-A71, and the druggable target for EV-A71 remains very limited. The phenotypic hit 10,10′-bis(trifluoromethyl) marinopyrrole A derivative, herein termed MPA-CF3, is a novel potent small-molecule inhibitor against EV-A71, but its pharmacological target(s) and antiviral mechanisms are not defined. Here, quantitative chemoproteomics deciphered the antiviral target of MAP-CF3 as host factor coatomer subunit zeta-1 (COPZ1). Mechanistically, MPA-CF3 disrupts the interaction of COPZ1 with the EV-A71 nonstructural protein 2C by destabilizing COPZ1 upon binding. The destruction of this interaction blocks the coatomer-mediated transport of 2C to endoplasmic reticulum, and ultimately inhibits EV-A71 replication. Taken together, our study disclosed that MPA-CF3 can be a structurally novel host-targeting anti-EV-A71 agent, providing a structural basis for developing the COPZ1-targeting broad-spectrum antivirals against enteroviruses. The mechanistic elucidation of MPA-CF3 against EV-A71 may offer an alternative COPZ1-involved therapeutic pathway for enterovirus infection.

Keywords

chemoproteomics / coatomer subunit zeta-1 / enterovirus A71 / marinopyrrole A derivate

Cite this article

Download citation ▾
Xiaoyong Li, Jin Zhang, Yaxin Xiao, Hao Song, Yuexiang Li, Wei Li, Ruiyuan Cao, Song Li, Yong Qin, Chu Wang, Wu Zhong. Chemoproteomics enables identification of coatomer subunit zeta-1 targeted by a small molecule for enterovirus A71 inhibition. MedComm, 2024, 5(6): e587 https://doi.org/10.1002/mco2.587

References

1 D Nasri, L Bouslama, S Pillet, et al. Basic rationale, current methods and future directions for molecular typing of human enterovirus. Expert Rev Mol Diagn. 2007;7(4):419-434.
2 W Xing, Q Liao, C Viboud, et al. Hand, foot, and mouth disease in China, 2008–12: an epidemiological study. Lancet Infect Dis. 2014;14(4):308-318.
3 M Lee, T Lin, P Chiang, et al. An investigation of epidemic enterovirus 71 infection in Taiwan, 2008. Pediatr Infect Dis J. 2010;29(11):1030-1034.
4 S Liu, H Pan, P Liu, et al. Comparative epidemiology and virology of fatal and nonfatal cases of hand, foot and mouth disease in mainland China from 2008 to 2014. Rev Med Virol. 2015;25(2):115-128.
5 MH Ooi, SC Wong, Y Podin, et al. Human enterovirus 71 disease in Sarawak, Malaysia: a prospective clinical, virological, and molecular epidemiological study. Clin Infect Dis. 2007;44(5):646-656.
6 SM Wang, HY Lei, KJ Huang, et al. Pathogenesis of enterovirus 71 brainstem encephalitis in pediatric patients: roles of cytokines and cellular immune activation in patients with pulmonary edema. J Infect Dis. 2003;188(4):564-570.
7 F Zhu, W Xu, J Xia, et al. Efficacy, safety, and immunogenicity of an enterovirus 71 vaccine in China. N Engl J Med. 2014;370(9):818-828.
8 R Li, L Liu, Z Mo, et al. An inactivated enterovirus 71 vaccine in healthy children. N Engl J Med. 2014;370(9):829-837.
9 FC Zhu, FY Meng, JX Li, et al. Efficacy, safety, and immunology of an inactivated alum-adjuvant enterovirus 71 vaccine in children in China: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 2013;381(9882):2024-2032.
10 F Vincent, A Nueda, J Lee, et al. Phenotypic drug discovery: recent successes, lessons learned and new directions. Nat Rev Drug Discov. 2022;21(12):899-914.
11 Y Xiao, J Yang, L Zou, et al. Synthesis of 10,10′-bis(trifluoromethyl) marinopyrrole A derivatives and evaluation of their antiviral activities in vitro. Eur J Med Chem. 2022;238:114436.
12 S Mohammed, AJR Heck, PJ Boersema, et al. Multiplex peptide stable isotope dimethyl labeling for quantitative proteomics. Nat Protoc. 2009;4(4):484-494.
13 J Hsu, S Huang, N Chow, et al. Stable-isotope dimethyl labeling for quantitative proteomics. Anal Chem. 2003;75(24):6843-6852.
14 X Li, M Wang, A Cheng, et al. Enterovirus replication organelles and inhibitors of their formation. Front Microbiol. 2020:11.
15 M Sachse, DCI Fernández, R Tenorio, et al. The viral replication organelles within cells studied by electron microscopy. Adv Virus Res. 2019;105:1-33.
16 NY Hsu, O Ilnytska, G Belov, et al. Viral reorganization of the secretory pathway generates distinct organelles for RNA replication. Cell. 2010;141(5):799-811.
17 N Gomez-Navarro, EA Miller. COP-coated vesicles. Curr Biol. 2016;26(2):R54-R57.
18 J Wang, Z Wu, Q Jin. COPI is required for enterovirus 71 replication. PLoS One. 2012;7(5):e38035.
19 S Lunev, MFW Semmelink, JL Xian, et al. Crystal structure of truncated human coatomer protein complex subunit ζ1 (Copζ1). Acta Crystallogr F Struct Biol Commun. 2017;73(1):1-8.
20 E Kazlauskas, V Petrauskas, V Paketuryt?, et al. Standard operating procedure for fluorescent thermal shift assay (FTSA) for determination of protein-ligand binding and protein stability. Eur Biophys J. 2021;50(3-4):373-379.
21 RJ Taylor, G Tagiltsev, J Briggs. The structure of COPI vesicles and regulation of vesicle turnover. Febs Lett. 2023;597(6):819-835.
22 O Kuge, S Hara-Kuge, L Orci, et al. zeta-COP, a subunit of coatomer, is required for COP-coated vesicle assembly. J Cell Biol. 1993;123(6 Pt 2):1727-1734.
23 S Wang, K Wang, K Zhao, et al. The structure, function, and mechanisms of action of enterovirus non-structural protein 2C. Front Microbiol. 2020:11.
24 WF Tang, SY Yang, BW Wu, et al. Reticulon 3 binds the 2C protein of enterovirus 71 and is required for viral replication. J Biol Chem. 2007;282(8):5888-5898.
25 J Hong, F Liu, H Qi, et al. Changing epidemiology of hand, foot, and mouth disease in China, 2013–2019: a population-based study. Lancet Reg Health West Pac. 2022;20:100370.
26 SP Chen, YC Huang, WC Li, et al. Comparison of clinical features between coxsackievirus A2 and enterovirus 71 during the enterovirus outbreak in Taiwan, 2008: a children's hospital experience. J Microbiol Immunol Infect. 2010;43(2):99-104.
27 KY Lee. Enterovirus 71 infection and neurological complications. Korean J Pediatr. 2016;59(10):395.
28 J Wang, Y Hu, M Zheng. Enterovirus A71 antivirals: past, present, and future. Acta Pharm Sin B. 2022;12(4):1542-1566.
29 M Zhang, Y Wang, W He, et al. Design, synthesis, and evaluation of novel enterovirus 71 inhibitors as therapeutic drug leads for the treatment of human hand, foot, and mouth disease. J Med Chem. 2020;63(3):1233-1244.
30 L De Colibus, X Wang, JAB Spyrou, et al. More-powerful virus inhibitors from structure-based analysis of HEV71 capsid-binding molecules. Nat Struct Mol Biol. 2014;21(3):282-288.
31 P Li, J Yu, F Hao, et al. Discovery of potent EV71 capsid inhibitors for treatment of HFMD. Acs Med Chem Lett. 2017;8(8):841-846.
32 Q Tang, Z Xu, F Zhang, et al. Identification of a novel binding inhibitor that blocks the interaction between hSCARB2 and VP1 of enterovirus 71. Cell Insight. 2022;1(2):100016.
33 G Ma, Y Ye, D Zhang, et al. Identification and biochemical characterization of DC07090 as a novel potent small molecule inhibitor against human enterovirus 71 3C protease by structure-based virtual screening. Eur J Med Chem. 2016;124:981-991.
34 Y Hu, R Musharrafieh, M Zheng, et al. Enterovirus D68 antivirals: past, present, and future. Acs Infect Dis. 2020;6(7):1572-1586.
35 Q Tang, Z Xu, M Jin, et al. Identification of dibucaine derivatives as novel potent enterovirus 2C helicase inhibitors: in vitro, in vivo, and combination therapy study. Eur J Med Chem. 2020;202:112310.
36 E Domingo, JJ Holland. RNA virus mutations and fitness for survival. Annu Rev Microbiol. 1997;51:151-178.
37 R Sanjuán, P Domingo-Calap. Mechanisms of viral mutation. Cell Mol Life Sci. 2016;73(23):4433-4448.
38 HM van der Schaar, P Leyssen, HJ Thibaut, et al. A novel, broad-spectrum inhibitor of enterovirus replication that targets host cell factor phosphatidylinositol 4-kinase IIIβ. Antimicrob Agents Chemother. 2013;57(10):4971-4981.
39 JR Strating, L van der Linden, L Albulescu, et al. Itraconazole inhibits enterovirus replication by targeting the oxysterol-binding protein. Cell Rep. 2015;10(4):600-615.
40 R Duden. ER-to-Golgi transport: cOP I and COP II function (Review). Mol Membr Biol. 2003;20(3):197-207.
41 MC Anania, E Cetti, D Lecis, et al. Targeting COPZ1 non-oncogene addiction counteracts the viability of thyroid tumor cells. Cancer Lett. 2017;410:201-211.
42 Y Zhang, Y Kong, Y Ma, et al. Loss of COPZ1 induces NCOA4 mediated autophagy and ferroptosis in glioblastoma cell lines. Oncogene. 2021;40(8):1425-1439.
43 Y Hong, Z Xia, Y Sun, et al. A comprehensive pan-cancer analysis of the regulation and prognostic effect of coat complex subunit zeta 1. Genes-Basel. 2023;14(4):889.
44 MJ Niphakis, BF Cravatt. Enzyme inhibitor discovery by activity-based protein profiling. Annu Rev Biochem. 2014;83:341-377.
45 CY Chang, JR Li, YC Ou, et al. Enterovirus 71 infection caused neuronal cell death and cytokine expression in cultured rat neural cells. Iubmb Life. 2015;67(10):789-800.
46 Y Wang, K Dan, X Xue, et al. Curcumin assists anti-EV71 activity of IFN-α by inhibiting IFNAR1 reduction in SH-SY5Y cells. Gut Pathog. 2022;14(1).
47 D Chen, C Chen, J Tan, et al. ERK inhibition aids IFN-β promoter activation during EV71 infection by blocking CRYAB degradation in SH-SY5Y cells. Pathog Dis. 2023:81.
48 KX Wu, JJ Chu. Antiviral screen identifies EV71 inhibitors and reveals camptothecin-target, DNA topoisomerase 1 as a novel EV71 host factor. Antivir Res. 2017;143:122-133.
49 T Hao, Y Li, S Fan, et al. Design, synthesis and pharmacological evaluation of a novel mTOR-targeted anti-EV71 agent. Eur J Med Chem. 2019;175:172-186.
50 Z Li, P Hao, L Li, et al. Design and synthesis of minimalist terminal alkyne-containing diazirine photo-crosslinkers and their incorporation into kinase inhibitors for cell- and tissue-based proteome profiling. Angew Chem Int Ed Engl. 2013;52(33):8551-8556.
51 YG Li, JX Wang, GN Zhang, et al. Design, synthesis, and biological activity evaluation of a series of pleuromutilin derivatives with novel C14 side chains. Bioorg Med Chem Lett. 2020;30(7):126969.
52 F Yang, J Gao, J Che, et al. A dimethyl-labeling-based strategy for site-specifically quantitative chemical proteomics. Anal Chem. 2018;90(15):9576-9582.
53 Z Li, L Xu, D He, et al. In vivo time-related evaluation of a therapeutic neutralization monoclonal antibody against lethal enterovirus 71 infection in a mouse model. PLoS One. 2014;9(10):e109391.
54 M Shtutman, M Baig, E Levina, et al. Tumor-specific silencing of COPZ2 gene encoding coatomer protein complex subunit ζ 2 renders tumor cells dependent on its paralogous gene COPZ1. Proc Natl Acad Sci USA. 2011;108(30):12449-12454.
55 Y Li, M Liu, Y Yan, et al. Molnupiravir and its active form, EIDD-1931, show potent antiviral activity against enterovirus infections in vitro and in vivo. Viruses. 2022;14(6):1142.
56 LJ Reed, H Muench. A simple method of estimating fifty per cent endpoints. Am J Epidemiol. 1938;27(3):493-497.[CrossRef]
PDF

Accesses

Citations

Detail

Sections
Recommended

/