Cargando…
The Sequence Alteration Associated with a Mutational Hotspot in p53 Protects Cells From Lysis by Cytotoxic T Lymphocytes Specific for a Flanking Peptide Epitope
A high proportion of tumors arise due to mutation of the p53 tumor suppressor protein. A p53 hotspot mutation at amino acid position 273 from R to H, flanking a peptide epitope that spans residues 264–272, renders cells resistant to killing by human histocompatibility leukocyte antigen (HLA)-A*0201–...
Autores principales: | Theobald, Matthias, Ruppert, Thomas, Kuckelkorn, Ulrike, Hernandez, Javier, Häussler, Annett, Ferreira, Edite Antunes, Liewer, Ulrike, Biggs, Judith, Levine, Arnold J., Huber, Christoph, Koszinowski, Ulrich H., Kloetzel, Peter-M., Sherman, Linda A. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1998
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212538/ https://www.ncbi.nlm.nih.gov/pubmed/9743520 |
Ejemplares similares
-
Efficient Generation of a Hepatitis B Virus Cytotoxic T Lymphocyte Epitope Requires the Structural Features of Immunoproteasomes
por: Sijts, Alice J.A.M., et al.
Publicado: (2000) -
Inactivation of a Defined Active Site in the Mouse 20S Proteasome Complex Enhances Major Histocompatibility Complex Class I Antigen Presentation of a Murine Cytomegalovirus Protein
por: Schmidtke, Gunter, et al.
Publicado: (1998) -
Link between Organ-specific Antigen Processing by 20S Proteasomes and CD8(+) T Cell–mediated Autoimmunity
por: Kuckelkorn, Ulrike, et al.
Publicado: (2002) -
Introducing FRT-flanked p53 mice
Publicado: (2012) -
Mapping of O-GlcNAc Sites of 20 S Proteasome Subunits and Hsp90 by a Novel Biotin-Cystamine Tag
por: Overath, Thorsten, et al.
Publicado: (2012)