Wikipedia

Picornain 3C

Picornain 3C (EC 3.4.22.28) is a protease found in picornaviruses, which cleaves peptide bonds of non-terminal sequences. Picornain 3C’s endopeptidase activity is primarily responsible for the catalytic process of selectively cleaving Gln-Gly bonds in the polyprotein of poliovirus and with substitution of Glu for Gln, and Ser or Thr for Gly in other picornaviruses. Picornain 3C are cysteine proteases related by amino acid sequence to trypsin-like serine proteases. Picornain 3C is encoded by enteroviruses, rhinoviruses, aphtoviruses and cardioviruses. These genera of picoviruses cause a wide range of infections in humans and mammals.

Picornain 3C
Ribbon diagram of picornain, PDB entry 5fx6
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EC no.3.4.22.28
CAS no.97162-88-4
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Picornavirus belongs to the family Picornaviridae. Picornavirus virions are nonenveloped and the +ssRNA nonsegmented genome is encapsulated in an icosahedral protein structure made from four capsid proteins encoded by the virus. Picornavirus viral replication typically takes place in the cytoplasm of the cell. Picornavirus +ssRNA genome then gets translated via internal ribosome entry sites (IRES) that is recognized by host cell ribosomes for cap independent translation. To compete with other mRNA transcripts, picornavirus destroys cap dependent translation in the host so host cell ribosomes will favor translation of viral transcripts. +ssRNA makes –ssRNA intermediates to make more viral +ssRNA. The genome of picornavirus is exhibited in Figure 1. As displayed, picornavirus does not have a viral 5’ cap but instead encodes for a protein Vpg. The absence of the 5’ cap is why the picornavirus genome depends on cap dependent translation for replication. The genome, however, does contain a poly-A tail on the opposite end of the Vpg protein. Both ends of the genome has UTR (untranslated regions). The picornavirus genome has three proteins (P1, P2, P3). P1 encodes for a proteins (VP1, VP2, VP3, and VP4) that make the capsid proteins. P2 and P3 proteins assist in infectivity of the picornavirus to hijack and interfere with host cell functionality. Specifically, 2B, 2C, and 3A proteins interfere with host cell function and the 3D protein encodes as the RNA polymerase. 2A and 3C act as proteinases and their function varies among the different genera of picornavirus.[1]

Figure 1- Picornavirus genome
Genus Members 3C protease activity 3C protease target
Enterovirus Poliovirus Intereferes with TATA binding protein[2] and interferes with cap dependent translation factor[3] Pyrazoles 17 and 18[4]
Coxsackievirus Activates caspase activity and interferes with cap dependent translation[5] Pyrazoles 17 and 18[6]
Rhinovirus Cleaves OCT-1 transcription[7] and interferes with cap dependent translation factor[8] Rupintrivir AG7088, Pyrazoles 17 and 18[9]
Apthovirus Foot-and-mouth disease virus Fragmentation of golgi apparatus and inhibition of microtubule regrowth (MTOC),[10] interferes with cap dependent translation factor[11] α, β-unsaturated carbonyl groups combined with peptidyl-binding elements[12]
Hepatovirus Hepatitis A Cleavage of NEMO (NF-κB)[13] hexadeoxyribonucleotides[14]

Poliovirus is a member of the family Picornaviridae. Poliovirus is transmitted through the oral-fecal route and does not always cause symptoms. A small amount of poliovirus infections cause paralysis when the virus infects the nervous system. Poliovirus infects host cells through inhibition of transcription machinery and function. Polioviruses’ protease 3C is responsible for host cell transcription shut off by cleaving the TATA-binding protein and other transcription factors at glutamine-glycine sites[15] This inhibition of transcription is caused by Protease 3C, one of Polioviruses’ 4 viral proteins encoded in its genome. Poliovirus 3C protease replication occurs in the cytoplasm, yet is able to inhibit transcription in the nucleus without any nuclear localization. Therefore, protease 3C depends on poliovirus 3CD protein for the translocation of 3C protease to carry out transcription inhibition in the nucleus. The 3CD polyprotein of poliovirus consists of the precursor of both the 3C protease (3Cpro) and the 3D RNA polymerase.[16] 3CD undergoes proteolysis, which leads to localization in the nucleus. “The 3C protein, being of unknown function, is a product of 3CD cleavage by 2Apro”.[17] Poliovirus is also involved in the cleavage of eIF4E (Eukaryotic translation initiation factor 4E). eIF4E is a protein involved in directing Eukaryotic ribosomes in cap dependent translation. The proteolytic cleavage of eIF4E disables the host from carrying out cap dependent translation.

Coxsackievirus belongs to the Picornaviridae family and Enterovirus genus. Coxsackievirus is shed through stool and bodily fluids and is prevalent in children but can infection occur in adults. Symptoms for coxsackievirus are fever, malaise, rash and blisters. Coxsackievirus primarily infects mucosal and epithelial membranes. 3C proteinase activity in coxsackievirus causes apoptosis in host cells. Both 2A(pro) and 3C(pro) induce caspase-8-mediated by activation of caspase-3.[18] Caspase stands for cysteine-aspartic acid protease and play an essential role in the apoptotic pathway of the cell. Protease 2A and 3C also induce apoptosis via intrinsic mitochondria mediated apoptosis, which leads to the release of cytochrome C from mitochondria and activating caspase- 9 (Chau). 3C is responsible for the actions via the up-regulation of Bax and cleavage of Bid.[19] Protease 3C and 2A are also responsible for the cleavage of translation initiation eIF4GE and poly-A- binding protein, PABP. This disruption of this binding domain results in down regulation of the initiation of cap dependent translation.[20] Also, 3C and 2A are responsible for down-regulation of cyclic AMP responsive element binding protein (CREB), a cellular transcription factor.[21] CREB decreases or increases transcription of certain genes and therefore, the inhibition of CREB causes the host cell’s to lose ability of this ability to regulate transcription.[citation needed]

Rhinovirus is principal cause for the common cold. Rhinovirus, also member of picornavirus, and can be transmitted through respiratory droplets or indirectly. Rhinovirus infects the upper respiratory tract to cause common cold symptoms. Rhinovirus uses protease 3C and 3D to induce cytopathetic effects in the host cell. 3C and 3D act similarly in rhinovirus as they do in poliovirus because they are both involved in early viral infection of the host cell via host cell transcription inhibition by 3C proteolytic activity.[22] 3C and 3CD of Rhinoviruses specifically target OCT-1 transcription factor for proteolytic cleavage. This proteolytic cleavage of the OCT-1 causes the inhibition of further cellular transcription. Similar to poliovirus and coxsackievirus, Rhinovirus protease 3C is also responsible for cleaving eIF4E (Eukaryotic translation initiation factor 4E), which disables cap dependent translation in the host cell.[citation needed]

Foot and mouth disease virus (FMDV) is a part of the aphthovirus genera. Foot and mouth disease virus primarily is found in cloven-hoofed animals such as pigs and cows and causes severe fever for the first couple of days and then blisters in the foot and mouth of the animal. FMDV does not cross over or infect humans but is extremely infectious within cloven-hoofed animals. Foot and mouth disease 3C protease activity is responsible for the fragmentation of golgi apparatus and inhibition of microtubule regrowth.[23] 3C protease activity is responsible for the loss of tethering of microtubules to the microtubule organizing center (MTOC) region.[24] Both of proteolytic effects on the host cell inhibit the transport of cellular proteins to the plasma membrane. This destruction of the secretory pathway reduces expression of major histocompatibility antigens at plasma membrane therefore slowing secretion of proinflammatory cytokines.[25]

Hepatitis A 3C proteinase is a member of the cysteine proteases that are responsible for the infectivity and maturation of HAV. Hepatitis A 3C protease cleaves NEMO at the Q304 residue; NEMO is a NF-κB essential modulator responsible for activation of interferon (IFN) antiviral response.[26] Cys24Ser (C24S) is a homolog of Hepatitis 3C proteinase, is responsible for inactivating Cys172 through alkylation of the sulfur at its active site. The sulfur alkylation of Cys172 causes inactivity while the N-alkylation of His102 causes a significant rise in enzymatic activity. Modification of enzymatic activity can be controlled by solution or crystallized N-iodoacetyl-valine-phenylalanine-amide (IVF).[27] Therefore, IVF controls proteolytic inhibition through interactions with active site of enzyme.

Picornavirus 3C protease targeting

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Picornavirus 3C protease’s infectivity and proteolytic effects is what leads picornavirus to cause pathogenicity in humans and other mammals. For most of these viruses, 3C is necessary for cytopathetic effects on the host cell. So far, 3C protease inhibitors have been discovered and used to monitor effects of picornavirus. Much testing will hopefully find an effective antiviral therapy targeting 3C protease. Targeting and inhibiting 3C protease activity will hopefully reduce the infectivity of the host cell. For poliovirus, Bis-vinylic organotellurane targets 3C inhibition, which is used as antiviral therapy. Currently no anti-picornal drug targeting 3C protease is in the market yet, but inhibitors such as rupintrivir and pyrazoles show promising targeting in broad range of picornaviruses.[28]

References

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  1. ^ Acheson, Nicholas H (2011-08-30). Fundamentals of Molecular Virology,2e. John Wiley & Sons, Inc. ISBN 978-0470900598.
  2. ^ Sharma R, Raychaudhuri S, Dasgupta A (March 2004). "Nuclear entry of poliovirus protease-polymerase precursor 3CD: implications for host cell transcription shut-off". Virology. 320 (2): 195–205. doi:10.1016/j.virol.2003.10.020. PMID 15016543.
  3. ^ Etchison, D (1985). J. Virol. pp. 54, 634–638.
  4. ^ Ramajayam R, Tan KP, Liang PH (October 2011). "Recent development of 3C and 3CL protease inhibitors for anti-coronavirus and anti-picornavirus drug discovery". Biochemical Society Transactions. 39 (5): 1371–5. doi:10.1042/BST0391371. PMID 21936817.
  5. ^ Chau DH, Yuan J, Zhang H, Cheung P, Lim T, Liu Z, Sall A, Yang D (March 2007). "Coxsackievirus B3 proteases 2A and 3C induce apoptotic cell death through mitochondrial injury and cleavage of eIF4GI but not DAP5/p97/NAT1". Apoptosis. 12 (3): 513–24. doi:10.1007/s10495-006-0013-0. PMID 17195095. S2CID 7288206.
  6. ^ Ramajayam R, Tan KP, Liang PH (October 2011). "Recent development of 3C and 3CL protease inhibitors for anti-coronavirus and anti-picornavirus drug discovery". Biochemical Society Transactions. 39 (5): 1371–5. doi:10.1042/BST0391371. PMID 21936817.
  7. ^ Amineva SP, Aminev AG, Palmenberg AC, Gern JE (October 2004). "Rhinovirus 3C protease precursors 3CD and 3CD' localize to the nuclei of infected cells". The Journal of General Virology. 85 (Pt 10): 2969–79. doi:10.1099/vir.0.80164-0. PMID 15448360.
  8. ^ Etchison, D (1985). J. Virol. pp. 54, 634–638.
  9. ^ Ramajayam R, Tan KP, Liang PH (October 2011). "Recent development of 3C and 3CL protease inhibitors for anti-coronavirus and anti-picornavirus drug discovery". Biochemical Society Transactions. 39 (5): 1371–5. doi:10.1042/BST0391371. PMID 21936817.
  10. ^ Zhou Z, Mogensen MM, Powell PP, Curry S, Wileman T (November 2013). "Foot-and-mouth disease virus 3C protease induces fragmentation of the Golgi compartment and blocks intra-Golgi transport" (PDF). Journal of Virology. 87 (21): 11721–9. doi:10.1128/JVI.01355-13. PMC 3807340. PMID 23986596.
  11. ^ Etchison, D (1985). J. Virol. pp. 54, 634–638.
  12. ^ Ramajayam R, Tan KP, Liang PH (October 2011). "Recent development of 3C and 3CL protease inhibitors for anti-coronavirus and anti-picornavirus drug discovery". Biochemical Society Transactions. 39 (5): 1371–5. doi:10.1042/BST0391371. PMID 21936817.
  13. ^ Wang D, Fang L, Wei D, Zhang H, Luo R, Chen H, Li K, Xiao S (September 2014). "Hepatitis A virus 3C protease cleaves NEMO to impair induction of beta interferon". Journal of Virology. 88 (17): 10252–8. doi:10.1128/JVI.00869-14. PMC 4136334. PMID 24920812.
  14. ^ Ramajayam R, Tan KP, Liang PH (October 2011). "Recent development of 3C and 3CL protease inhibitors for anti-coronavirus and anti-picornavirus drug discovery". Biochemical Society Transactions. 39 (5): 1371–5. doi:10.1042/BST0391371. PMID 21936817.
  15. ^ Sharma R, Raychaudhuri S, Dasgupta A (March 2004). "Nuclear entry of poliovirus protease-polymerase precursor 3CD: implications for host cell transcription shut-off". Virology. 320 (2): 195–205. doi:10.1016/j.virol.2003.10.020. PMID 15016543.
  16. ^ Tian W, Cui Z, Zhang Z, Wei H, Zhang X (January 2011). "Poliovirus 2A(pro) induces the nucleic translocation of poliovirus 3CD and 3C' proteins". Acta Biochimica et Biophysica Sinica. 43 (1): 38–44. doi:10.1093/abbs/gmq112. PMID 21173057.
  17. ^ Tian W, Cui Z, Zhang Z, Wei H, Zhang X (January 2011). "Poliovirus 2A(pro) induces the nucleic translocation of poliovirus 3CD and 3C' proteins". Acta Biochimica et Biophysica Sinica. 43 (1): 38–44. doi:10.1093/abbs/gmq112. PMID 21173057.
  18. ^ Chau DH, Yuan J, Zhang H, Cheung P, Lim T, Liu Z, Sall A, Yang D (March 2007). "Coxsackievirus B3 proteases 2A and 3C induce apoptotic cell death through mitochondrial injury and cleavage of eIF4GI but not DAP5/p97/NAT1". Apoptosis. 12 (3): 513–24. doi:10.1007/s10495-006-0013-0. PMID 17195095. S2CID 7288206.
  19. ^ Chau DH, Yuan J, Zhang H, Cheung P, Lim T, Liu Z, Sall A, Yang D (March 2007). "Coxsackievirus B3 proteases 2A and 3C induce apoptotic cell death through mitochondrial injury and cleavage of eIF4GI but not DAP5/p97/NAT1". Apoptosis. 12 (3): 513–24. doi:10.1007/s10495-006-0013-0. PMID 17195095. S2CID 7288206.
  20. ^ Etchison, D (1985). J. Virol. pp. 54, 634–638.
  21. ^ Chau DH, Yuan J, Zhang H, Cheung P, Lim T, Liu Z, Sall A, Yang D (March 2007). "Coxsackievirus B3 proteases 2A and 3C induce apoptotic cell death through mitochondrial injury and cleavage of eIF4GI but not DAP5/p97/NAT1". Apoptosis. 12 (3): 513–24. doi:10.1007/s10495-006-0013-0. PMID 17195095. S2CID 7288206.
  22. ^ Amineva SP, Aminev AG, Palmenberg AC, Gern JE (October 2004). "Rhinovirus 3C protease precursors 3CD and 3CD' localize to the nuclei of infected cells". The Journal of General Virology. 85 (Pt 10): 2969–79. doi:10.1099/vir.0.80164-0. PMID 15448360.
  23. ^ Zhou, Zhigang (2013). "Foot-and-Mouth Disease Virus 3C Protease Induces Fragmentation of the Golgi Compartment and Blocks Intra-Golgi Transport". Journal of Virology. 87 (21): 11721–9. doi:10.1128/JVI.01355-13. PMC 3807340. PMID 23986596.
  24. ^ Armer H, Moffat K, Wileman T, Belsham GJ, Jackson T, Duprex WP, Ryan M, Monaghan P (November 2008). "Foot-and-mouth disease virus, but not bovine enterovirus, targets the host cell cytoskeleton via the nonstructural protein 3Cpro". Journal of Virology. 82 (21): 10556–66. doi:10.1128/JVI.00907-08. PMC 2573224. PMID 18753210.
  25. ^ Zhou Z, Mogensen MM, Powell PP, Curry S, Wileman T (November 2013). "Foot-and-mouth disease virus 3C protease induces fragmentation of the Golgi compartment and blocks intra-Golgi transport". Journal of Virology. 87 (21): 11721–9. doi:10.1128/JVI.01355-13. PMC 3807340. PMID 23986596.
  26. ^ Wang D, Fang L, Wei D, Zhang H, Luo R, Chen H, Li K, Xiao S (September 2014). "Hepatitis A virus 3C protease cleaves NEMO to impair induction of beta interferon". Journal of Virology. 88 (17): 10252–8. doi:10.1128/JVI.00869-14. PMC 4136334. PMID 24920812.
  27. ^ Yin J, Bergmann EM, Cherney MM, Lall MS, Jain RP, Vederas JC, James MN (December 2005). "Dual modes of modification of hepatitis A virus 3C protease by a serine-derived beta-lactone: selective crystallization and formation of a functional catalytic triad in the active site". Journal of Molecular Biology. 354 (4): 854–71. doi:10.1016/j.jmb.2005.09.074. PMC 7118759. PMID 16288920.
  28. ^ Ramajayam R, Tan KP, Liang PH (October 2011). "Recent development of 3C and 3CL protease inhibitors for anti-coronavirus and anti-picornavirus drug discovery". Biochemical Society Transactions. 39 (5): 1371–5. doi:10.1042/BST0391371. PMID 21936817.
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