TCDB is operated by the Saier Lab Bioinformatics Group

1.A.53 The Hepatitis C Virus P7 Viroporin Cation-selective Channel (HCV-P7) Family

The mechanisms and functions of viral channel proteins have been reviewed by Fischer and Hsu (2011), Fischer et al. (2012) and Hyser and Estes 2015. The P7 (HCV-P7) viroporin of hepatitis C virus is of 63aas with 2 TMSs and is derived from the HCV polyprotein. P7 forms a heptameric ion channel with selectivity for monovalent cations and H+.  Ion conduction has been demonstrated both in vivo (in cells) and in vitro (in lipid bilayers) (Clarke et al., 2006). Its ion channel activity is inhibited by amantadine and rimantadine, long alkyl chain imino-sugar derivatives, and amiloride. Another peptide derived from the HCV polyprotein, NS4A, (YP_001491554; 54aas) has also been reported to form pores (Madan et al., 2007).  The structure and function of the p7 protein has been reviewed (Atoom et al. 2014).  Retarded E2p7 precursor cleavage is essential to regulate the intracellular and secreted levels of E2 through p7-mediated modulation of the cell secretory pathway and to unmask critical novel assembly functions located at the p7 amino-terminus (Denolly et al. 2017). A broad consensus among the p7 variants indicates that distantly related HCVs preserve key features of structure and dynamics (Oestringer et al. 2019).

The two transmembrane domains of p7 are separated by a short basic loop. It forms a cation selective channel whose activity in suspended lipid bilayers. The p7 protein is essential for HCV replication, assembly, release and production of infectious progeny virions (Khaliq et al., 2011). It is required for production of infectious virus in cell culture for the related bovine viral diarrhea virus.  It can transport protons, other cations, and carboxyfluorescein (Gan et al. 2014). TMS1 in an α-helical configuration faces the lumen of the channel.  There seem to be two forms, one that transports both H+ and carboxyfluorescein, and one that transports H+ but not carboxyfluorescein (Gan et al. 2014).  Inhibitors of p7 have been identified (Mathew et al. 2015).

P7 belongs to a functional family of viral ion channels known as viroporins. These are small integral membrane proteins that homo-oligomerize to form channels that mediate cation fluxes across cellular and viral membranes. Precedent for these proteins as therapeutic targets in a clinical setting is provided by the M2 protein of influenza A virus (TC #1.A.19), which is also sensitive to amantadine and related derivatives. p7 is able to replace M2 in a functional assay. Amantadine inhibited both M2 and p7 in this assay at the same concentrations. The basic loop in the cytoplasm is critical for p7 function (Khaliq et al., 2011).

The non-structural protein p7 of Classical Swine Fever Virus (CSFV) is a small hydrophobic polypeptide with an apparent molecular mass of 6 to 7 kDa (70 aas; derived from polyprotein PolG_CSFVA (P19712), 3898 aas). The protein contains two hydrophobic stretches of amino acids interrupted by a short charged segment that is a cytosolic loop. CSFV p7 is critical for virus production and virulence (Gladue et al. 2012). Structure-function analyses in model membranes emulating the ER lipid composition confirmed that CSFV p7 is a pore-forming protein, and that pore-forming activity resides in the C-terminal transmembrane helix. Therefore, p7 is a viroporin which is clearly involved in the process of CSFV virulence in swine. The PolG_CSFVA polyprotein shows low sequence similarity with polyproteins in 1.G.3. CSFVA viroporin is homologous to viroporins from Border disease virus, Bovine diarrhea virus 1, Pronghorn antelope pestivirus and Pestivirus giraffe-1.

As noted above, the p7 peptide contains two putative transmembrane regions connected by a short hydrophilic segment. Expression of p7 protein in E. coli leads to permeabilization of bacterial cells to small molecules (Guo et al., 2013). p7 also enhances the permeability of mammalian cells, increasing the intracellular Ca2+ concentration and the permeability of cells to the translation inhibitor Hygromycin B. It forms homo-oligomers and localizes to the ER at the early stage of expression. It can be transferred to the plasma membrane at a later stage. Detergent permeabilization assays confirmed that p7 is a 2-TMS protein with its N- and C-termini exposed to the ER lumen. Deletion analysis suggested that amino acyl residues 41-63 are essential for viroporin activity of the protein (Guo et al., 2013).

GB virus B (GBV-B), a hepatotropic virus, is closely related to hepatitis C.  It infects small New World primates and replicates efficiently in primary hepatocyte cultures and is an attractive surrogate model system. Ghibaudo et al. 2004 characterized signal peptidase processing of the polyprotein segment containing the putative structural proteins. They identified the exact N termini of the mature GBV-B envelope proteins, E1 and E2, and the first nonstructural protein, NS2, by direct amino acid sequencing. These studies document the existence of a previously unrecognized 13-kDa protein (p13) located between E2 and NS2 within the polyprotein. The p13 protein sequence was compared to that of hepatitis C virus p7, a small 2 TMS membrane-spanning protein with a similar location in the polyprotein that has ion channel activity. The C-terminal half of p13 is homologous to p7, suggesting a common function, but the substantially larger size of p13, with 4 rather than 2 predicted transmembrane segments, indicates a different structural organization and/or additional functions. The identification of p13 in the GBV-B polyprotein provides support for the hypothesis that ion channel-forming proteins are essential for the life cycle of flaviviruses, possibly playing a role in virion morphogenesis and/or virus entry into cells (Ghibaudo et al. 2004).

The p7 viroporin of the hepatitis C virus (HCV) forms an intracellular proton-conducting transmembrane channel in virus-infected cells, shunting the pH of intracellular compartments, and thus, helping virus assembly and release. The protein sequences and drug sensitivities of p7 proteins vary between the seven major genotypes of the hepatitis C virus, but the essential channel activity is preserved. Breitinger et al. 2021 investigated the effect of several inhibitors on recombinant HCV p7 channels corresponding to genotypes 1a-b, 2a-b, 3a and 4a. They established a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT)-based cell viability assay for recombinant p7 expressed in HEK293 cells to assess channel activity. Hexamethylene amiloride (HMA) was the most potent inhibitor but possessed cytotoxic activity at higher concentrations. Rimantadine was active against p7 of all genotypes, while amantadine activity was genotype-dependent. Thus, cell viability assays can be used to assess viroporin activity and identify channel inhibitors.

The reaction catalyzed by the heptameric p7 pore is:

Cations (in) cations (out)

References associated with 1.A.53 family:

Atoom, A.M., N.G. Taylor, and R.S. Russell. (2014). The elusive function of the hepatitis C virus p7 protein. Virology 462-463: 377-387. 25001174
Breitinger, U., N.S. Farag, N.K.M. Ali, M. Ahmed, M.A. El-Azizi, and H.G. Breitinger. (2021). Cell viability assay as a tool to study activity and inhibition of hepatitis C p7 channels. J Gen Virol 102:. 33709903
Chen, W., J. Dev, J. Mezhyrova, L. Pan, A. Piai, and J.J. Chou. (2018). The Unusual Transmembrane Partition of the Hexameric Channel of the Hepatitis C Virus. Structure. [Epub: Ahead of Print] 29551287
Clarke, D., Griffin, S., Beales, L., Gelais, C.S., Burgess, S., Harris, M., and Rowlands, D. (2006). Evidence for the formation of a heptameric ion channel complex by the hepatitis C virus p7 protein in vitro. J. Biol. Chem. 281: 37057-37068. 17032656
Denolly, S., C. Mialon, T. Bourlet, F. Amirache, F. Penin, B. Lindenbach, B. Boson, and F.L. Cosset. (2017). The amino-terminus of the hepatitis C virus (HCV) p7 viroporin and its cleavage from glycoprotein E2-p7 precursor determine specific infectivity and secretion levels of HCV particle types. PLoS Pathog 13: e1006774. 29253880
Fischer, W.B. and H.J. Hsu. (2011). Viral channel forming proteins - modeling the target. Biochim. Biophys. Acta. 1808: 561-571. 20546700
Fischer, W.B., Y.T. Wang, C. Schindler, and C.P. Chen. (2012). Mechanism of function of viral channel proteins and implications for drug development. Int Rev Cell Mol Biol 294: 259-321. 22364876
Gan, S.W., W. Surya, A. Vararattanavech, and J. Torres. (2014). Two Different Conformations in Hepatitis C Virus p7 Protein Account for Proton Transport and Dye Release. PLoS One 9: e78494. 24409277
Ghibaudo, D., L. Cohen, F. Penin, and A. Martin. (2004). Characterization of GB virus B polyprotein processing reveals the existence of a novel 13-kDa protein with partial homology to hepatitis C virus p7 protein. J. Biol. Chem. 279: 24965-24975. 15060070
Gladue, D.P., E. Largo, L.G. Holinka, E. Ramirez-Medina, E.A. Vuono, K.A. Berggren, G.R. Risatti, J.L. Nieva, and M.V. Borca. (2018). Classical Swine Fever Virus p7 Protein Interacts with Host Protein CAMLG and Regulates Calcium Permeability at the Endoplasmic Reticulum. Viruses 10:. 30154321
Gladue, D.P., L.G. Holinka, E. Largo, I. Fernandez Sainz, C. Carrillo, V. O'Donnell, R. Baker-Branstetter, Z. Lu, X. Ambroggio, G.R. Risatti, J.L. Nieva, and M.V. Borca. (2012). Classical swine fever virus p7 protein is a viroporin involved in virulence in swine. J. Virol. 86: 6778-6791. 22496228
Guo, H.C., S.Q. Sun, D.H. Sun, Y.Q. Wei, J. Xu, M. Huang, X.T. Liu, Z.X. Liu, J.X. Luo, H. Yin, and D.X. Liu. (2013). Viroporin activity and membrane topology of classic swine fever virus p7 protein. Int J Biochem. Cell Biol. 45: 1186-1194. 23583663
Hyser, J.M. and M.K. Estes. (2015). Pathophysiological Consequences of Calcium-Conducting Viroporins. Annu Rev Virol 2: 473-496. 26958925
Khaliq, S., S. Jahan, and S. Hassan. (2011). Hepatitis C virus p7: molecular function and importance in hepatitis C virus life cycle and potential antiviral target. Liver Int 31: 606-617. 21457434
Largo, E., C. Verdiá-Báguena, V.M. Aguilella, J.L. Nieva, and A. Alcaraz. (2016). Ion channel activity of the CSFV p7 viroporin in surrogates of the ER lipid bilayer. Biochim. Biophys. Acta. 1858: 30-37. 26464198
Largo, E., D.P. Gladue, J. Torralba, V.M. Aguilella, A. Alcaraz, M.V. Borca, and J.L. Nieva. (2018). Mutation-induced changes of transmembrane pore size revealed by combined ion-channel conductance and single vesicle permeabilization analyses. Biochim. Biophys. Acta. 1860: 1015-1021. [Epub: Ahead of Print] 29317201
Lin, Z., W. Liang, K. Kang, H. Li, Z. Cao, and Y. Zhang. (2014). Classical swine fever virus and p7 protein induce secretion of IL-1β in macrophages. J Gen Virol 95: 2693-2699. 25146005
Luik, P., C. Chew, J. Aittoniemi, J. Chang, P. Wentworth, Jr, R.A. Dwek, P.C. Biggin, C. Vénien-Bryan, and N. Zitzmann. (2009). The 3-dimensional structure of a hepatitis C virus p7 ion channel by electron microscopy. Proc. Natl. Acad. Sci. USA 106: 12712-12716. 19590017
Madan, V. and R. Bartenschlager. (2015). Structural and Functional Properties of the Hepatitis C Virus p7 Viroporin. Viruses 7: 4461-4481. 26258788
Madan, V., S. Sánchez-Martínez, N. Vedovato, G. Rispoli, L. Carrasco, and J.L. Nieva. (2007). Plasma membrane-porating domain in poliovirus 2B protein. A short peptide mimics viroporin activity. J. Mol. Biol. 374: 951-964. 17963782
Mathew, S., K. Fatima, M.Q. Fatmi, G. Archunan, M. Ilyas, N. Begum, E. Azhar, G. Damanhouri, and I. Qadri. (2015). Computational Docking Study of p7 Ion Channel from HCV Genotype 3 and Genotype 4 and Its Interaction with Natural Compounds. PLoS One 10: e0126510. 26030803
Montserret, R., N. Saint, C. Vanbelle, A.G. Salvay, J.P. Simorre, C. Ebel, N. Sapay, J.G. Renisio, A. Böckmann, E. Steinmann, T. Pietschmann, J. Dubuisson, C. Chipot, and F. Penin. (2010). NMR structure and ion channel activity of the p7 protein from hepatitis C virus. J. Biol. Chem. 285: 31446-31461. 20667830
Oestringer, B.P., J.H. Bolivar, J.K. Claridge, L. Almanea, C. Chipot, F. Dehez, N. Holzmann, J.R. Schnell, and N. Zitzmann. (2019). Hepatitis C virus sequence divergence preserves p7 viroporin structural and dynamic features. Sci Rep 9: 8383. 31182749
Popescu, C.I., N. Callens, D. Trinel, P. Roingeard, D. Moradpour, V. Descamps, G. Duverlie, F. Penin, L. Héliot, Y. Rouillé, and J. Dubuisson. (2011). NS2 protein of hepatitis C virus interacts with structural and non-structural proteins towards virus assembly. PLoS Pathog 7: e1001278. 21347350
Scull, M.A., W.M. Schneider, B.R. Flatley, R. Hayden, C. Fung, C.T. Jones, M. van de Belt, F. Penin, and C.M. Rice. (2015). The N-terminal Helical Region of the Hepatitis C Virus p7 Ion Channel Protein Is Critical for Infectious Virus Production. PLoS Pathog 11: e1005297. 26588073
Walter, S., A. Bollenbach, J. Doerrbecker, S. Pfaender, R.J. Brown, G. Vieyres, C. Scott, R. Foster, A. Kumar, N. Zitzmann, S. Griffin, F. Penin, T. Pietschmann, and E. Steinmann. (2016). Ion-channel function and cross-species determinants in viral assembly of nonprimate hepacivirus p7. J. Virol. [Epub: Ahead of Print] 26962224
Wang YT., Schilling R., Fink RH. and Fischer WB. (2014). Ion-dynamics in hepatitis C virus p7 helical transmembrane domains--a molecular dynamics simulation study. Biophys Chem. 192:33-40. 24997299
Ying, B., S. Pang, J. Yang, Y. Zhong, and J. Wang. (2018). Computational Study of HCV p7 Channel: Insight into a New Strategy for HCV Inhibitor Design. Interdiscip Sci. [Epub: Ahead of Print] 30194627
You, D.G., H.R. Lee, W.K. Kim, H.J. Kim, G.Y. Lee, and Y.D. Yoo. (2017). Hepatitis C virus p7 induces mitochondrial depolarization of isolated liver mitochondria. Mol Med Rep 16: 9533-9538. 29039530