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Interaction with the Receptor SLAM and Baculovirus Surface Display of Peste des petits ruminants Virus Hemagglutinin.

Authors :
Zhao, Lulu
Du, Mengtan
Liu, Xingjian
Zhang, Zhidong
Zhang, Zhifang
Meng, Xuelian
Li, Yinü
Source :
DNA & Cell Biology; Jun2020, Vol. 39 Issue 6, p992-999, 8p, 6 Diagrams
Publication Year :
2020

Abstract

Peste des petits ruminants (PPR) is an acute, highly infectious, and highly pathogenic disease, which mainly damages small ruminants such as goats and sheep. Hemagglutinin protein (H), the main antigenic protein of peste des petits ruminants virus (PPRV), has been a hot spot in the research of genetic engineering vaccine for PPRV. In this study, the silkworm baculovirus surface display technology is combined with the transmembrane structure of the silkworm baculovirus envelope protein GP64 and different characteristics of the promoters to display four kinds of fusion proteins, which contain Pph-H, Pph-HJ, Pie1-H, and Pie1-HJ. The fusion proteins displayed on baculovirus surface have been detected by western blotting, cell surface immunofluorescence, and immunogold electron microscopy. In addition, the dominant form of PPR H displayed on baculovirus surface has been determined which is fusion protein mediated by Pph containing the hemagglutinin protein and full-length GP64, Pph-H. Furthermore, by comparing the fluorescence intensity of binding of hemagglutinin protein and signaling lymphocyte activation molecules (SLAM) in Vero-SLAM cells by immunocytochemistry, Pph-H can be combined with the receptor protein of PPRV, SLAM. It provides technical support for displaying the different structure of hemagglutinin and exploring the key sites of hemagglutinin and SLAM binding. Meanwhile, it is important for exploring the pathogenesis and immune mechanism of PPRV. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10445498
Volume :
39
Issue :
6
Database :
Complementary Index
Journal :
DNA & Cell Biology
Publication Type :
Academic Journal
Accession number :
143597532
Full Text :
https://doi.org/10.1089/dna.2020.5414