Peptides derived from the heptad repeat region near the C-terminal of Sendai virus F protein bind the hemagglutinin-neuraminidase ectodomain

被引:12
作者
Tomasi, M
Past, C
Manfrinato, C
Dallocchio, F
Bellini, T
机构
[1] Ist Super Sanita, Lab Biol Cellulare, I-00161 Rome, Italy
[2] Univ Ferrara, Dept Biochim & Biol Mol, I-44100 Ferrara, Italy
关键词
Sendai virus; paramyxovirus; neuraminidase; membrane fusion; viral membrane protein;
D O I
10.1016/S0014-5793(03)00010-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previously, we showed that Sendai virus fusion protein (F) acts as an inhibitor of neuraminidase activity of hemagglutinin-neuraminidase (HN) protein. Here we report that synthetic peptides derived from the heptad repeat region proximal to the transmembrane domain (HR2) of Sendai virus F inhibit fusion and enhance the enzymatic activity of the HN. This occurs on the virus-bound HN and on its soluble globular head. The enhancing effect on virus-bound HN is reversible and depends on the presence of F. The data indicate that, by binding to the HN ectodomain, the HR2 peptides abolish the F inhibition of HN and disrupt the communication between the F and HN essential to promote virus-cell fusion. (C) 2003 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:56 / 60
页数:5
相关论文
共 24 条
[1]   SELECTIVE EXTRACTION OF HEMAGGLUTININ AND MATRIX PROTEIN FROM SENDAI VIRIONS BY EMPLOYING TRIFLUOPERAZINE AS A DETERGENT [J].
BAIOCCHI, M ;
PESCARMONA, M ;
BRUSCHI, ML ;
MONTECUCCO, C ;
SQUATRITI, T ;
TOMASI, M .
FEBS LETTERS, 1988, 238 (01) :171-174
[2]   SELECTIVE MODIFICATION OF SENDAI VIRUS HEMAGGLUTININ NEURAMINIDASE BY PYRIDOXAL 5'-PHOSPHATE - EVIDENCE FOR AN ALLOSTERIC MODULATION OF NEURAMINIDASE ACTIVITY [J].
BELLINI, T ;
TOMASI, M ;
DALLOCCHIO, F .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1161 (2-3) :323-327
[3]   Anomeric specificity and protein-substrate interactions support the 3D model for the hemagglutinin-neuraminidase from Sendai virus [J].
Bellini, T ;
Pasti, C ;
Manfrinato, MC ;
Tomasi, M ;
Dallocchio, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 262 (02) :401-405
[4]   HEPTAD REPEAT SEQUENCES ARE LOCATED ADJACENT TO HYDROPHOBIC REGIONS IN SEVERAL TYPES OF VIRUS FUSION GLYCOPROTEINS [J].
CHAMBERS, P ;
PRINGLE, CR ;
EASTON, AJ .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :3075-3080
[5]   Core structure of gp41 from the HIV envelope glycoprotein [J].
Chan, DC ;
Fass, D ;
Berger, JM ;
Kim, PS .
CELL, 1997, 89 (02) :263-273
[6]   The structure of the fusion glycoprotein of Newcastle disease virus suggests a novel paradigm for the molecular mechanism of membrane fusion [J].
Chen, L ;
Gorman, JJ ;
McKimm-Breschkin, J ;
Lawrence, LJ ;
Tulloch, PA ;
Smith, BJ ;
Colman, PM ;
Lawrence, MC .
STRUCTURE, 2001, 9 (03) :255-266
[7]   INHIBITION OF SENDAI VIRUS HEMAGGLUTININ-NEURAMINIDASE BY THE FUSION PROTEIN [J].
DALLOCCHIO, F ;
TOMASI, M ;
BELLINI, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 201 (02) :988-993
[8]   ACTIVATION OF THE SENDAI-VIRUS FUSION PROTEIN BY RECEPTOR-BINDING [J].
DALLOCCHIO, F ;
TOMASI, M ;
BELLINI, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 208 (01) :36-41
[9]   Structure-function study of a heptad repeat positioned near the transmembrane domain of Sendai virus fusion protein which blocks virus-cell fusion [J].
Ghosh, JK ;
Peisajovich, SG ;
Ovadia, M ;
Shai, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) :27182-27190
[10]   FLUORESCENCE METHOD FOR MEASURING THE KINETICS OF FUSION BETWEEN BIOLOGICAL-MEMBRANES [J].
HOEKSTRA, D ;
DEBOER, T ;
KLAPPE, K ;
WILSCHUT, J .
BIOCHEMISTRY, 1984, 23 (24) :5675-5681