Part:BBa_K1621000
Glycoprotein E1 epitopes derived from Rubella Virus
This part contains the coding sequence of several epitopes derived from glycoprotein E1 of the Rubella Virus. Together with glycoproteins C and E2 it constitutes the structural proteins building the viral capsid figure 1).
Starkey et al. (1995) generated the sequence for the development of a new second generation vaccine against this virus. It covers amino acids 212 to 286 of the whole glycoprotein E1 and contains at least four epitopes that have been described before. Three epitopes located between amino acids 243 and 286 were described by Terry et al. (1988), whereas the putative neutralization domain was characterized by Mitchell et al. (1993).
New improved vaccination strategies against as well as detection methods for Rubella Virus are highly needed. Infections with this togavirus cause a rather mild disease (German measles), but become extremely dangerous if they occur in the first 12 weeks of pregnancy. A good vaccination status in the population is the first step to prevent such infections.
But as this is no guarantee for being protected, women planning to become pregnant are routinely tested for Rubella Virus infections. Therefore, a sensitive, specific and also cost efficient diagnostic tool is needed.
The part was added to the registry in standard pSB1C3 beginning with a start codon (ATG). Cloning the part into the shipping backbone was performed by Gibson Assembly.
References
Mitchell LA, Decarie D, Tingle AJ, Zrein M,Lacroix M (1993). Identification of immunoreactive regions of rubella virus E1 and E2 envelope proteins by using synthetic peptides. Virus Res. 29:33–57.
Starkey WG, Newcombe J, Corbett KM, Liu KM, Sanders PG, BEST JM (1995). Use of Rubella Virus E1 Fusion Proteins for Detection of Rubella Virus Antibodies. Journal of Clinical Microbiology, p. 270–274.
Terry GM, Ho-Terry LM, Londesborough P, Rees KR (1988). Localization of the rubella E1 epitopes. Arch. Virol. 98:189–197.
| None |