The multi-domain non-structural protein 3 (Nsp3) is the largest protein encoded by the coronavirus (CoV) genome, with an average molecular mass of about 200 kD. Nsp3 is an essential component of the replication/transcription complex. It comprises various domains, the organization of which differs between CoV genera, due to duplication or absence of some domains. However, eight domains of Nsp3 exist in all known CoVs: the ubiquitin-like domain 1 (Ubl1), the Glu-rich acidic domain (also called “hypervariable region”), a macrodomain (also named “X domain”), the ubiquitin-like domain 2 (Ubl2), the papain-like protease 2 (PL2 pro ), the Nsp3 ectodomain (3Ecto, also called “zinc-finger domain”), as well as the domains Y1 and CoV-Y of unknown functions. In addition, the two transmembrane regions, TM1 and TM2, exist in all CoVs. The three-dimensional structures of domains in the N-terminal two thirds of Nsp3 have been investigated by X-ray crystallography and/or nuclear magnetic resonance (NMR) spectroscopy since the outbreaks of Severe Acute Respiratory Syndrome coronavirus (SARS-CoV) in 2003 as well as Middle-East Respiratory Syndrome coronavirus (MERS-CoV) in 2012. In this review, the structures and functions of these domains of Nsp3 are discussed in depth. Highlights • Nonstructural protein 3 (∼200 kD) is a multifunctional protein comprising up to 16 different domains and regions. • Nsp3 binds to viral RNA, nucleocapsid protein, as well as other viral proteins, and participates in polyprotein processing. • The papain-like protease of Nsp3 is an established target for new antivirals. • Through its de-ADP-ribosylating, de-ubiquitinating, and de-ISGylating activities, Nsp3 counteracts host innate immunity. • Structural data are available for the N-terminal two thirds of Nsp3, but domains in the remainder are poorly characterized.
【저자키워드】 structural biology, Innate immunity, Papain-like protease, N, nucleocapsid, HCoV, human coronavirus, MHV, mouse hepatitis virus, IFN, interferon, SARS, Severe acute respiratory syndrome, NSP, non-structural protein, UTR, untranslated region, NTD, N-terminal domain, CoV, coronavirus, TNF, Tumor Necrosis Factor, ORF, open reading frame, IBV, infectious bronchitis virus, Mpro, main protease, macrodomain, ER, endoplasmic reticulum, NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells, PARP, poly(ADP-ribose) polymerase, MERS, middle-East respiratory syndrome, ubiquitin-like domain, TGEV, transmissible gastroenteritis virus, HEV, hepatitis E virus, TM, transmembrane, IRF, Interferon regulatory factor, CHIKV, Chikungunya virus, TRS, transcriptional regulatory sequence, IL-6, interleukin 6, 3CLpro, 3C-Like protease, PLpro, Papain-like protease, DMV, double-membrane vesicle, RTC, replication/transcription complex, Nucleic-acid binding domain, 3Ecto, Nsp3 ectodomain, ADPr, ADP-ribose, ADRP, ADP-ribose-1″-phosphate phosphatase, ARTD, ADP-ribosyltransferases diphtheria toxin-like, βSM, betacoronavirus-specific marker, CM, convoluted membrane, DPUP, Domain Preceding Ubl2 and PL2pro, DUB, deubiquitinating, GST, glutathione S-transferase, hISG15, human interferon-stimulated gene 15, HKU, Hong Kong University, HVR, hypervariable region, mISG15, mouse interferon-stimulated gene 15, Mac, macrodomain, MARylation, mono-ADP-ribosylation, MDM2, mouse double minute 2 homolog, MKRN, makorin ring finger protein, NAB, nucleic-acid binding domain, PABP, poly(A)-binding protein, PARylation, poly-ADP-ribosylation, RCHY1, RING finger and CHY zinc-finger domain-containing protein 1, RID, Ras-interacting domain, R.M.S.D., root-mean-square deviation, SUD, SARS-unique domain, Ubl, ubiquitin-like, Ub, ubiquitin, USP, ubiquitin-specific protease, VEEV, Venezuelan equine encephalitis virus,