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Timing is everything: Fine-tuned molecular machines orchestrate paramyxovirus entry
- Source :
- Virology
- Publication Year :
- 2015
- Publisher :
- Elsevier BV, 2015.
-
Abstract
- The Paramyxoviridae include some of the great and ubiquitous disease-causing viruses of humans and animals. In most paramyxoviruses, two viral membrane glycoproteins, fusion protein (F) and receptor binding protein (HN, H or G) mediate a concerted process of recognition of host cell surface molecules followed by fusion of viral and cellular membranes, resulting in viral nucleocapsid entry into the cytoplasm. The interactions between the F and HN, H or G viral glycoproteins and host molecules are critical in determining host range, virulence and spread of these viruses. Recently, atomic structures, together with biochemical and biophysical studies, have provided major insights into how these two viral glycoproteins successfully interact with host receptors on cellular membranes and initiate the membrane fusion process to gain entry into cells. These studies highlight the conserved core mechanisms of paramyxovirus entry that provide the fundamental basis for rational anti-viral drug design and vaccine development.
- Subjects :
- Protein Conformation
viruses
Membrane fusion
Article
03 medical and health sciences
Viral envelope
Viral entry
Virology
Humans
Viral receptors
Paramyxovirus entry
Glycoproteins
030304 developmental biology
Atomic structure of viral glycoproteins
Host cell surface
0303 health sciences
biology
Membrane glycoproteins
030302 biochemistry & molecular biology
Viral nucleocapsid
Virus Internalization
Viral membrane
Herpesvirus glycoprotein B
Fusion protein
3. Good health
Cell biology
Viral envelope proteins
Host-Pathogen Interactions
Paramyxoviridae
biology.protein
Receptors, Virus
Capsid Proteins
Viral Fusion Proteins
Protein Binding
Subjects
Details
- ISSN :
- 00426822
- Database :
- OpenAIRE
- Journal :
- Virology
- Accession number :
- edsair.doi.dedup.....20191095209e20595690c57274f2931a
- Full Text :
- https://doi.org/10.1016/j.virol.2015.02.037