Identification of the membrane-active regions of the severe acute respiratory syndrome coronavirus spike membrane glycoprotein using a 16/18-mer peptide scan:: Implications for the viral fusion mechanism

被引:70
作者
Guillén, J [1 ]
Pérez-Berná, AJ [1 ]
Moreno, MR [1 ]
Villalaín, J [1 ]
机构
[1] Univ Migel Hernandez, Inst Biol Mol & Celular, E-03202 Elche Alicante, Spain
关键词
D O I
10.1128/JVI.79.3.1743-1752.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have identified the membrane-active regions of the severe acute respiratory syndrome coronavirus (SARS CoV) spike glycoprotein by determining the effect on model membrane integrity of a 16/18-mer SARS CoV spike glycoprotein peptide library. By monitoring the effect of this peptide library on membrane leakage in model membranes, we have identified three regions on the SARS CoV spike glycoprotein with membrane-interacting capabilities: region 1, located immediately upstream of heptad repeat 1 (HR1) and suggested to be the fusion peptide; region 2, located between HR1 and HR2, which would be analogous to the loop domain of human immunodeficiency virus type 1; and region 3, which would correspond to the pretransmembrane region. The identification of these membrane-active regions, which are capable of modifying the biophysical properties of phospholipid membranes, supports their direct role in SARS CoV-mediated membrane fusion, as well as facilitating the future development of SARS CoV entry inhibitors.
引用
收藏
页码:1743 / 1752
页数:10
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[1]   The fusion peptide of semliki forest virus associates with sterol-rich membrane domains [J].
Ahn, A ;
Gibbons, DL ;
Kielian, M .
JOURNAL OF VIROLOGY, 2002, 76 (07) :3267-3275
[2]   HIV-1 gp41 envelope residues 650-685 exposed on native virus act as a lectin to bind epithelial cell galactosyl ceramide [J].
Alfsen, A ;
Bomsel, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (28) :25649-25659
[3]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[4]   Severe acute respiratory syndrome coroavirus (SARS-CoV) infection inhibition using spike protein heptad repeat-derived peptides [J].
Bosch, BJ ;
Martina, BEE ;
van der Zee, R ;
Lepault, J ;
Haijema, BJ ;
Versluis, C ;
Heck, AJR ;
de Groot, R ;
Osterhaus, ADME ;
Rottier, PJM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (22) :8455-8460
[5]   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
[6]  
Bottcher C, 1961, ANAL CHIM ACTA, V1061, P297
[7]   Structure and interaction with membrane model systems of a peptide derived from the major epitope region of HIV protein gp41:: Implications on viral fusion mechanism [J].
Contreras, LM ;
Aranda, FJ ;
Gavilanes, F ;
González-Ros, JM ;
Villalaín, J .
BIOCHEMISTRY, 2001, 40 (10) :3196-3207
[8]   Sphingomyelin/phosphatidylcholine/cholesterol phase diagram: Boundaries and composition of lipid rafts [J].
de Almeida, RFM ;
Fedorov, A ;
Prieto, M .
BIOPHYSICAL JOURNAL, 2003, 85 (04) :2406-2416
[9]   Cleavage inhibition of the murine coronavirus spike protein by a furin-like enzyme affects cell-cell but not virus-cell fusion [J].
de Haan, CAM ;
Stadler, K ;
Godeke, GJ ;
Bosch, BJ ;
Rottier, PJM .
JOURNAL OF VIROLOGY, 2004, 78 (11) :6048-6054
[10]   The secret life of ACE2 as a receptor for the SARS virus [J].
Dimitrov, DS .
CELL, 2003, 115 (06) :652-653