Literature DB >> 2446004

Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins.

R J Kascsak1, R Rubenstein, P A Merz, M Tonna-DeMasi, R Fersko, R I Carp, H M Wisniewski, H Diringer.   

Abstract

Antibody response in mice to scrapie-associated fibril proteins (protease-resistant proteins [PrPs]) was generated to different epitopes depending on the source of antigen. Mice responded differently to PrPs isolated from scrapie-infected animals of homologous (mouse) versus heterologous (hamster) species. An enzyme-linked immunosorbent assay established to monitor this antibody response in mice immunized with PrPs was unable to detect such a response in scrapie-infected mice. A monoclonal antibody (MAb), 263K 3F4, derived from a mouse immunized with hamster 263K PrPs reacted with hamster but not mouse PrPs. MAb 263K 3F4 also recognized normal host protein of 33 to 35 kilodaltons in brain tissue from hamsters and humans but not from bovine, mouse, rat, sheep, or rabbit brains. This is the first demonstration of epitope differences on this host protein in different species. The defining of various epitopes on PrP through the use of MAbs will lead to a better understanding of the relationship of PrPs to their host precursor protein and to the infectious scrapie agent.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2446004      PMCID: PMC255980     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  36 in total

1.  Immunological comparison of scrapie-associated fibrils isolated from animals infected with four different scrapie strains.

Authors:  R J Kascsak; R Rubenstein; P A Merz; R I Carp; N K Robakis; H M Wisniewski; H Diringer
Journal:  J Virol       Date:  1986-09       Impact factor: 5.103

2.  Monoclonal antibodies to the cellular and scrapie prion proteins.

Authors:  R A Barry; S B Prusiner
Journal:  J Infect Dis       Date:  1986-09       Impact factor: 5.226

3.  In vitro immunization for the production of antigen-specific lymphocyte hybridomas.

Authors:  C L Reading
Journal:  Methods Enzymol       Date:  1986       Impact factor: 1.600

4.  Growth of primary plasmacytomas in the mineral oil-conditioned peritoneal environment.

Authors:  M Potter; J G Pumphrey; J L Walters
Journal:  J Natl Cancer Inst       Date:  1972-07       Impact factor: 13.506

5.  A method for producing specific antisera with small doses of immunogen.

Authors:  J Vaitukaitis; J B Robbins; E Nieschlag; G T Ross
Journal:  J Clin Endocrinol Metab       Date:  1971-12       Impact factor: 5.958

6.  Isolation of a cDNA clone encoding the leader peptide of prion protein and expression of the homologous gene in various tissues.

Authors:  N K Robakis; P R Sawh; G C Wolfe; R Rubenstein; R I Carp; M A Innis
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

7.  Human prion protein cDNA: molecular cloning, chromosomal mapping, and biological implications.

Authors:  Y C Liao; R V Lebo; G A Clawson; E A Smuckler
Journal:  Science       Date:  1986-07-18       Impact factor: 47.728

8.  Molecular cloning and complete sequence of prion protein cDNA from mouse brain infected with the scrapie agent.

Authors:  C Locht; B Chesebro; R Race; J M Keith
Journal:  Proc Natl Acad Sci U S A       Date:  1986-09       Impact factor: 11.205

9.  Antisera to scrapie-associated fibril protein and prion protein decorate scrapie-associated fibrils.

Authors:  P A Merz; R J Kascsak; R Rubenstein; R I Carp; H M Wisniewski
Journal:  J Virol       Date:  1987-01       Impact factor: 5.103

10.  The major polypeptide of scrapie-associated fibrils (SAF) has the same size, charge distribution and N-terminal protein sequence as predicted for the normal brain protein (PrP).

Authors:  J Hope; L J Morton; C F Farquhar; G Multhaup; K Beyreuther; R H Kimberlin
Journal:  EMBO J       Date:  1986-10       Impact factor: 11.598

View more
  278 in total

1.  Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state.

Authors:  M Horiuchi; B Caughey
Journal:  EMBO J       Date:  1999-06-15       Impact factor: 11.598

2.  Sulfated glycans and elevated temperature stimulate PrP(Sc)-dependent cell-free formation of protease-resistant prion protein.

Authors:  C Wong; L W Xiong; M Horiuchi; L Raymond; K Wehrly; B Chesebro; B Caughey
Journal:  EMBO J       Date:  2001-02-01       Impact factor: 11.598

3.  Immobilized prion protein undergoes spontaneous rearrangement to a conformation having features in common with the infectious form.

Authors:  E Leclerc; D Peretz; H Ball; H Sakurai; G Legname; A Serban; S B Prusiner; D R Burton; R A Williamson
Journal:  EMBO J       Date:  2001-04-02       Impact factor: 11.598

4.  Species-independent inhibition of abnormal prion protein (PrP) formation by a peptide containing a conserved PrP sequence.

Authors:  J Chabry; S A Priola; K Wehrly; J Nishio; J Hope; B Chesebro
Journal:  J Virol       Date:  1999-08       Impact factor: 5.103

5.  Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein.

Authors:  L Zulianello; K Kaneko; M Scott; S Erpel; D Han; F E Cohen; S B Prusiner
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

6.  Mimicking dominant negative inhibition of prion replication through structure-based drug design.

Authors:  V Perrier; A C Wallace; K Kaneko; J Safar; S B Prusiner; F E Cohen
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-23       Impact factor: 11.205

7.  Affinity-tagged miniprion derivatives spontaneously adopt protease-resistant conformations.

Authors:  S Supattapone; H O Nguyen; T Muramoto; F E Cohen; S J DeArmond; S B Prusiner; M Scott
Journal:  J Virol       Date:  2000-12       Impact factor: 5.103

8.  Glycosylation influences cross-species formation of protease-resistant prion protein.

Authors:  S A Priola; V A Lawson
Journal:  EMBO J       Date:  2001-12-03       Impact factor: 11.598

9.  Copper binding to the PrP isoforms: a putative marker of their conformation and function.

Authors:  Y Shaked; H Rosenmann; N Hijazi; M Halimi; R Gabizon
Journal:  J Virol       Date:  2001-09       Impact factor: 5.103

10.  Proteasomes and ubiquitin are involved in the turnover of the wild-type prion protein.

Authors:  Y Yedidia; L Horonchik; S Tzaban; A Yanai; A Taraboulos
Journal:  EMBO J       Date:  2001-10-01       Impact factor: 11.598

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.