3.7 PRINCIPLES OF DISASSEMBLY: VIRUS PARTICLES ARE METASTABLE

 It is important to remember that all virus particles not only have to be constructed to protect the genome, but they also have to disassemble to permit the genome to enter a new target cell. This is supremely important to the virus particle as it has only the one chance to do this successfully and hence propagate its genome. The notion is developing that the particle is metastable, i.e. it can spontaneously descend to a lower energy level and, in doing so, releases its genome. Not surprisingly there are a number of fail-safe devices that tell the virus when it is safe to let go the genome. One of the simplest systems is used by enveloped animal viruses like HIV-1. This undergoes a succession of interactions between cell receptors and virus envelope protein binding sites, the passwords needed to gain entry to a high security establishment. If everything is in order, the metastable envelope protein then undergoes profound rearrangements that allow a hidden hydrophobic segment to insert into the cell membrane. This initiates fusion of the lipid bilayer of the virus with that of the cell plasma membrane, and the virus genome automatically enters the cell cytoplasm. However, if the sequence of passwords proves incorrect, the virus detaches from the cell and the process can be repeated until the correct cell is found.


Comments

Post a Comment

Popular posts from this blog

4.3 CLASSIFICATION ON THE BASIS OF VIRUS PARTICLE MORPHOLOGY

  The structural features of virus particles and the principles which underlie these structures have been described in Chapter 3. When viruses were first visualized in the electron microscope, defining classification groups on the basis of the observed particle shape or morphology was relatively simple. A key structural feature is whether or not the virus particle has a lipid envelope and this alone can be used as a designated feature, giving enveloped and nonenveloped viruses (see Section 3.4). If the virion is nonenveloped three morphological categories are defined, isometric, filamentous, and complex. Isometric viruses (see Section 3.3) appear approximately spherical but are actually icosahedrons or icosadeltahedrons. Filamentous viruses (see Section 3.2) have a simple, helical, morphology. The complex viruses are those which do not neatly fit within the other two categories. Complex shapes for virus particles may be made up of a combination of isometric and filamentous componen...
Read more

3.4 ENVELOPED (MEMBRANE-BOUND) VIRUS PARTICLES

Although they appear complex, these viruses have a conventional isometric or helical structure that is surrounded by a membrane – a 4-nm-thick lipid bilayer containing proteins. Examples include many of the larger animal viruses, but only a few plant and bacterial viruses. Traditionally these viruses were distinguished from nucleocapsid viruses by treatment with detergents or organic solvents, which disrupts the membrane and destroys infectivity. Thus they were sometimes referred to as “ether-sensitive viruses.” The envelope, which is derived from host cell membranes, is obtained by the virus budding from cell membranes, but most contain no cell proteins. How cell proteins are excluded and why retroviruses, the exception, do not exclude cell proteins from their virions are not understood (see Section 11.6). An isometric core surrounded by an isometric envelope: Sindbis virus particles Sindbis virus (a togavirus) has an icosahedral nucleocapsid that comprises a single protein, surrounde...
Read more

1.8 PROPERTIES OF VIRUSES

 With the assumption that the features of virus growth just described for particular viruses are true of all viruses, it is possible to compare and contrast the properties of viruses with those of their host cells. Whereas host cells contain both types of nucleic acid, viruses only contain one type. However, just like their host cells, viruses have their genetic information encoded in nucleic acid. Another difference is that the virus is reproduced solely from its genetic material, whereas the host cell is reproduced from the integrated sum of its components. Thus, the virus never arises directly from a pre-existing virus, whereas the cell always arises by division from a pre-existing cell. The experiments of Hershey and his collaborators showed quite clearly that the components of a virus are synthesized independently and then assembled into many virus particles. By contrast, the host cell increases its constituent parts, during which the individuality of the cell is continuously ...
Read more