Cowpea mosaic virus

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Cowpea mosaic virus (CPMV)
Virus classification
Group: IV: (+)sense RNA Viruses
Order: Picornavirales
Family: Secoviridae
Subfamily: Comovirinae
Genus: Comovirus
Species: Cowpea mosaic virus
Synonyms

Cowpea mosaic virus, SB isolate

Structure of the Cowpea Mosaic Virus based on PDB 2BFU

Cowpea mosaic virus (CPMV) is a plant virus of the comovirus group. Infection of a susceptible cowpea leaf results in high virus yields (1-2 g/kg). Its Genome consists of 2 molecules of positive-sense RNA (RNA-1 and RNA-2) which are separately encapsidated. Both RNA1 and RNA2 have a VPg (virus genome-linked protein) at the 5'end, and polyadenylation at the 3' end. Genomic RNA1 and RNA2 are expressed by a polyprotein processing strategy. RNA1 encodes helicase, VPg, protease and RdRp. RNA2 encodes movement protein and coat protein. The virus particles are 28 nm in diameter and contain 60 copies each of a Large (L) and Small (S) coat protein. The structure is well characterised to atomic resolution, and the viral particles are thermostable.

CPMV displays a number of features that can be exploited for nanoscale biomaterial fabrication. Its genetic, biological and physical properties are well characterised, and it can be isolated readily from plants. There are many stable mutants already prepared that allow specific modification of the capsid surface. It is possible to attach a number of different chemicals to the virus surface[1][2] and to construct multilayer arrays of such nanoparticles on solid surfaces. This gives the natural or genetically engineered nanoparticles a range of properties which could be useful in nanotechnological applications such as biosensors, catalysis and nanoelectronic devices.

One example use of CPMV particles is to amplify signals in microarray based sensors. In this application, the virus particles separate the fluorescent dyes used for signaling in order to prevent the formation of non-fluorescent dimers that act as quenchers.[3] Another example is the use of CPMV as a nanoscale breadboard for molecular electronics.[4]

References[edit]

  1. ^ Q. Wang, T. Lin, L. Tang, J.E. Johnson, and M.G. Finn.Angew. Chem. Int. Ed.,41(3),459 (2002)
  2. ^ Q. Wang, T.R. Chan, R. Hilgraf, V.V. Fokin, K.B. Sharpless, and M.G. Finn. J. Am. Chem. Soc.,125,3192 (2003).
  3. ^ Fluorescent signal amplification of carbocyanine dyes using engineered viral nanoparticles. Carissa M. Soto, Amy Szuchmacher Blum, Nikolai Lebedev, Gary J. Vora, Carolyn E. Meador, Angela P. Won, Anju Chatterji, John E. Johnson, and Banahalli R. Ratna, Journal of the American Chemical Society, 128, 5184 (2006).
  4. ^ An Engineered Virus as a Scaffold for Three-Dimensional Self-Assembly on the Nanoscale. Amy Szuchmacher Blum, Carissa M. Soto, Charmaine D. Wilson, Tina L. Brower, Steven K. Pollack, Terence L. Schull, Anju Chatterji, Tianwei Lin, John E. Johnson, Christian Amsinck, Paul Franzon, Ranganathan Shashidhar and Banahalli Ratna, Small, 7, 702 (2005).

External links[edit]