» Articles » PMID: 1710287

Molecular Location of a Species-specific Epitope on the Hamster Scrapie Agent Protein

Overview
Journal J Virol
Date 1991 Jul 1
PMID 1710287
Citations 40
Authors
Affiliations
Soon will be listed here.
Abstract

Scrapie is a transmissible neurodegenerative disease of sheep and goats. An abnormal host protein, Sp33-37, is the major protein component of the scrapie agent and the only known disease- or agent-specific macromolecule. Two monoclonal antibodies (MAbs), 4H8 (immunoglobulin G2b [IgG2b]) and 6B11 (IgG1), produced by immunizing mice with the intact hamster 263K scrapie agent protein, Sp33-37Ha, were found to have species specificity similar to that reported previously for MAb 3F4 (IgG2a), which was produced by using PrP-27-30 as the immunogen (R. J. Kascsak, R. Rubenstein, P. A. Merz, M. Tonna-DeMasi, R. Fersko, R. I. Carp, H. M. Wisniewski, and H. Diringer, J. Virol. 61:3688-3693, 1987). These antibodies all bound to Sp33-37 derived from hamster but not from mouse cells. Competitive binding assays demonstrated that all three MAbs bound to the same or overlapping sites on Sp33-37Ha. The molecular location of the epitope for these antibodies was determined to within 10 residues by using an antigen competition enzyme-linked immunosorbent assay in which synthetic peptides spanning Sp33-37Ha residues 79 to 93 or 84 to 93 specifically inhibited binding of these antibodies to plates coated with purified Sp33-37Ha. A synthetic peptide with the mouse-specific sequence (83 to 92) that differed from the hamster sequence by substitution at two positions (MetHa-87----LeuMo-86 and MetHa-90----ValMo-89) did not inhibit antibody binding to Sp33-37Ha. MAb 3F4 binding to hamster Sp33-37 was eliminated by chemical modification of Sp33-37Ha with diethylpyrocarbonate or succinic anhydride and by cleavage with CNBr or trypsin. The effect of diethylpyrocarbonate on MAb 3F4 binding was not reversed by hydroxylamine treatment. MAb 3F4 binding was not affected by prolonged exposure of Sp33-37Ha to 70% formic acid or by boiling in sodium dodecyl sulfate. We conclude that the epitope for these MAbs is a linear determinant that includes Met-87, Lys-88, and Met-90 and that Met-90 is probably the major species-specific determinant.

Citing Articles

Analysis of the Glycosylation Profile of Disease-Associated Water-Soluble Prion Protein Using Lectins.

Abdel-Haq H Biomed Res Int. 2019; 2019:1053282.

PMID: 30886856 PMC: 6388326. DOI: 10.1155/2019/1053282.


Modifiers of prion protein biogenesis and recycling identified by a highly parallel endocytosis kinetics assay.

Ballmer B, Moos R, Liberali P, Pelkmans L, Hornemann S, Aguzzi A J Biol Chem. 2017; 292(20):8356-8368.

PMID: 28341739 PMC: 5437241. DOI: 10.1074/jbc.M116.773283.


Lack of prion infectivity in fixed heart tissue from patients with Creutzfeldt-Jakob disease or amyloid heart disease.

Priola S, Ward A, McCall S, Trifilo M, Choi Y, Solforosi L J Virol. 2013; 87(17):9501-10.

PMID: 23785217 PMC: 3754135. DOI: 10.1128/JVI.00692-13.


Using small molecule reagents to selectively modify epitopes based on their conformation.

Silva C Prion. 2012; 6(2):163-73.

PMID: 22436143 PMC: 3366355. DOI: 10.4161/pri.18795.


Prion uptake in the gut: identification of the first uptake and replication sites.

Kujala P, Raymond C, Romeijn M, Godsave S, van Kasteren S, Wille H PLoS Pathog. 2012; 7(12):e1002449.

PMID: 22216002 PMC: 3245311. DOI: 10.1371/journal.ppat.1002449.


References
1.
Stahl N, Baldwin M, Burlingame A, Prusiner S . Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein. Biochemistry. 1990; 29(38):8879-84. DOI: 10.1021/bi00490a001. View

2.
Bolton D, Bendheim P, Marmorstein A, Potempska A . Isolation and structural studies of the intact scrapie agent protein. Arch Biochem Biophys. 1987; 258(2):579-90. DOI: 10.1016/0003-9861(87)90380-8. View

3.
Basler K, Oesch B, Scott M, Westaway D, Walchli M, Groth D . Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene. Cell. 1986; 46(3):417-28. DOI: 10.1016/0092-8674(86)90662-8. View

4.
Gabizon R, McKinley M, Prusiner S . Purified prion proteins and scrapie infectivity copartition into liposomes. Proc Natl Acad Sci U S A. 1987; 84(12):4017-21. PMC: 305012. DOI: 10.1073/pnas.84.12.4017. View

5.
Gabizon R, McKinley M, Groth D, Prusiner S . Immunoaffinity purification and neutralization of scrapie prion infectivity. Proc Natl Acad Sci U S A. 1988; 85(18):6617-21. PMC: 282028. DOI: 10.1073/pnas.85.18.6617. View