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HAV-VP1-P2A (residues 669-782)

Hepatitis A Virus Coat Protein VP1-Core Protein P2A

recombinant, E. coli

Cat. No. Amount Price (EUR) Buy / Note
PR-1114 100 μg 207,00 Add to Basket/Quote Add to Notepad

For in vitro use only!

Shipping: shipped on blue ice

Storage Conditions: store at -20 °C
avoid freeze/thaw cycles

Shelf Life: 12 months

Molecular Weight: 23.5 kDa

Purity: > 90 % (SDS-PAGE)

Form: liquid (Supplied in 10 mM Tris-HCl pH 9.6, 1.5 M urea and 50% glycerol)

Applications:
Recombinant rHAV-VP1-P2A/Mosaic Antigen may be used in ELISA and Western blots, excellent for detection of HAV with minimal specificity problems.

Description:
The protein contains the HAV Coat protein VP1 and core protein P2A immunodominant regions, amino acids 669-782. HAV core proteins are purified by proprietary chromatographic techniques.

Background: Forty-two antigenic domains were identified across the hepatitis A virus (HAV) polyprotein by using a set of 237 overlapping 20-mer synthetic peptides spanning the entire HAV polyprotein and a panel of serum samples from acutely HAVinfected patients. The term antigenic domain is used in this study to define a protein region spanned with consecutive overlapping immunoreactive peptides. Nineteen antigenic domains were found within the structural proteins, and 22 were found within the nonstructural proteins, with 1 domain spanning the junction of VP1 and P2A proteins. Five of these domains were considered immunodominant, as judged by both the breadth and the strength of their immunoreactivity. One domain is located within the VP2 protein at position 57-90 aa. A second domain, located at position 767-842 aa, contains the C-terminal part of the VP1 protein and the entire P2A protein. A third domain, located at position 1403-1456 aa, comprises the C-terminal part of the P2C protein and the N-terminal half of the P3A protein. The fourth domain, located at position 1500-1519 aa, includes almost the entire P3B, and the last domain, located at position 1719-1764 aa, contains the C-terminal region of the P3C protein and the N-terminal region of the P3D protein. It is interesting to note that four of the five most immunoreactive domains are derived from small HAV proteins and/or encompass protein cleavage sites separating different HAV proteins.

Specificity: Immunoreactive with sera of HAV-infected individuals.

Selected References:
Haro et al. (2003) Liposome entrapment and immunogenic studies of a synthetic lipophilic multiple antigenic peptide bearing VP1 and VP3 domains of the hepatitis A virus: a robust method for vaccine design. FEBS Lett. 540:133.
Costa-Mattioli et al. (2002) Molecular evolution of hepatitis A virus: a new classification based on the complete VP1 protein. J. Virol. 76:9516.
Emerson et al. (2002) Identification of VP1/2A and 2C as virulence genes of hepatitis A virus and demonstration of genetic instability of 2C. J. Virol. 76:8551.
Kang et al. (2002) A proposed vestigial translation initiation motif in VP1 of hepatitis A virus. Virus Res. 87:11.
Martin et al. (1999) Maturation of the hepatitis A virus capsid protein VP1 is not dependent on processing by the 3Cpro proteinase. J. Virol. 73:6220.
Graff et al. (1999) Hepatitis A virus capsid protein VP1 has a heterogeneous C terminus. J. Virol. 73:6015.