Receptor Recognition Mechanisms of Coronaviruses: a Decade of Structural Studies

被引:438
作者
Li, Fang [1 ]
机构
[1] Univ Minnesota Med Sch, Dept Pharmacol, Minneapolis, MN USA
关键词
RESPIRATORY-SYNDROME-CORONAVIRUS; MOUSE HEPATITIS-VIRUS; ANGIOTENSIN-CONVERTING ENZYME-2; DIPEPTIDYL PEPTIDASE 4; TRANSMISSIBLE GASTROENTERITIS VIRUS; CARCINOEMBRYONIC ANTIGEN FAMILY; INFECTIOUS-BRONCHITIS VIRUS; VIRAL MEMBRANE-FUSION; T-CELL-ACTIVATION; SPIKE PROTEIN;
D O I
10.1128/JVI.02615-14
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Receptor recognition by viruses is the first and essential step of viral infections of host cells. It is an important determinant of viral host range and cross-species infection and a primary target for antiviral intervention. Coronaviruses recognize a variety of host receptors, infect many hosts, and are health threats to humans and animals. The receptor-binding S1 subunit of coronavirus spike proteins contains two distinctive domains, the N-terminal domain (S1-NTD) and the C-terminal domain (S1-CTD), both of which can function as receptor-binding domains (RBDs). S1-NTDs and S1-CTDs from three major coronavirus genera recognize at least four protein receptors and three sugar receptors and demonstrate a complex receptor recognition pattern. For example, highly similar coronavirus S1-CTDs within the same genus can recognize different receptors, whereas very different coronavirus S1-CTDs from different genera can recognize the same receptor. Moreover, coronavirus S1-NTDs can recognize either protein or sugar receptors. Structural studies in the past decade have elucidated many of the puzzles associated with coronavirus-receptor interactions. This article reviews the latest knowledge on the receptor recognition mechanisms of coronaviruses and discusses how coronaviruses have evolved their complex receptor recognition pattern. It also summarizes important principles that govern receptor recognition by viruses in general.
引用
收藏
页码:1954 / 1964
页数:11
相关论文
共 105 条
[1]   Amino acids 270 to 510 of the severe acute respiratory syndrome coronavirus spike protein are required for interaction with receptor [J].
Babcock, GJ ;
Esshaki, DJ ;
Thomas, WD ;
Ambrosino, DM .
JOURNAL OF VIROLOGY, 2004, 78 (09) :4552-4560
[2]   Evolution of cell recognition by viruses [J].
Baranowski, E ;
Ruiz-Jarabo, CM ;
Domingo, E .
SCIENCE, 2001, 292 (5519) :1102-1105
[3]   Receptor Variation and Susceptibility to Middle East Respiratory Syndrome Coronavirus Infection [J].
Barlan, Arlene ;
Zhao, Jincun ;
Sarkar, Mayukh K. ;
Li, Kun ;
McCray, Paul B., Jr. ;
Perlman, Stanley ;
Gallagher, Tom .
JOURNAL OF VIROLOGY, 2014, 88 (09) :4953-4961
[4]  
Beauchemin N, 1999, EXP CELL RES, V252, P243
[5]   Architecture of the SARS coronavirus prefusion spike [J].
Beniac, Daniel R. ;
Andonov, Anton ;
Grudeski, Elsie ;
Booth, Tim F. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (08) :751-752
[6]   Angiotensin-converting enzyme 2 - A new cardiac regulator [J].
Boehm, M ;
Nabel, EG .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (22) :1795-1797
[7]   The coronavirus spike protein is a class I virus fusion protein: Structural and functional characterization of the fusion core complex [J].
Bosch, BJ ;
van der Zee, R ;
de Haan, CAM ;
Rottier, PJM .
JOURNAL OF VIROLOGY, 2003, 77 (16) :8801-8811
[8]   CORONAVIRUS IBV - REMOVAL OF SPIKE GLYCOPOLYPEPTIDE-S1 BY UREA ABOLISHES INFECTIVITY AND HEMAGGLUTINATION BUT NOT ATTACHMENT TO CELLS [J].
CAVANAGH, D ;
DAVIS, PJ .
JOURNAL OF GENERAL VIROLOGY, 1986, 67 :1443-1448
[9]   A nomenclature for avian coronavirus isolates and the question of species status [J].
Cavanagh, D .
AVIAN PATHOLOGY, 2001, 30 (02) :109-115
[10]   Coronavirus avian infectious bronchitis virus [J].
Cavanagh, Dave .
VETERINARY RESEARCH, 2007, 38 (02) :281-297