Epitope analysis of the murine p53 tumour suppressor protein

被引:0
作者
Lane, DP
Stephen, CW
Midgley, CA
Sparks, A
Hupp, TR
Daniels, DA
Greaves, R
Reid, A
Vojtesek, B
Picksley, SM
机构
[1] NINEWELLS HOSP & MED SCH, DEPT PATHOL, DUNDEE DD1 9SY, SCOTLAND
[2] STANFORD UNIV, SCH MED, DEPT MICROBIOL & IMMUNOL, STANFORD, CA 94305 USA
[3] MASARYK MEM CANC INST, CR-65653 BRNO, CZECH REPUBLIC
基金
英国惠康基金;
关键词
murine p53; p53; monoclonal antibodies; epitopes;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The identification and characterisation of the p53 tumour suppressor has relied extensively on the use of immunological reagents, To facilitate further characterisation of the murine p53 protein (Mp53), and its interaction with other proteins, we have characterised the antigenic sites of Mp53 in fine detail, Using an overlapping Mp53 peptide library we report the identification by Pepscan ELISA of the epitopes of nine antibodies, We have also used this technique to determine whether corresponding epitopes were present in a human p53 (Hp53) peptide library, This comparison was extended to include polyclonal sera of mice immunized with either Mp53 or Hp53, to compare the overall range of antigenic sites, The range of antigenic sites identified by polyclonal sera is very similar, although the N-terminus of Mp53 is clearly not an immunodominant region, in contrast to the N-terminus of Hp53, However, the N-terminus of Mp53 is immunogenic in rabbits as demonstrated by the Pepscan ELISA of CM5 serum (a rabbit anti-Mp53 serum used in analysing p53 expression in mice), Since, very few new antigenic sites were identified in either Mp53 or Hp53, new approaches will have to be employed to identify novel immunological reagents against human and murine p53.
引用
收藏
页码:2461 / 2466
页数:6
相关论文
共 32 条
[1]   IMMUNOHISTOCHEMICAL ANALYSIS OF THE P53 ONCOPROTEIN ON PARAFFIN SECTIONS USING A SERIES OF NOVEL MONOCLONAL-ANTIBODIES [J].
BARTEK, J ;
BARTKOVA, J ;
LUKAS, J ;
STASKOVA, Z ;
VOJTESEK, B ;
LANE, DP .
JOURNAL OF PATHOLOGY, 1993, 169 (01) :27-34
[2]   CRYSTAL-STRUCTURE OF A P53 TUMOR-SUPPRESSOR DNA COMPLEX - UNDERSTANDING TUMORIGENIC MUTATIONS [J].
CHO, YJ ;
GORINA, S ;
JEFFREY, PD ;
PAVLETICH, NP .
SCIENCE, 1994, 265 (5170) :346-355
[3]   P53 TRANSFORMATION-RELATED PROTEIN - DETECTION BY MONOCLONAL-ANTIBODY IN MOUSE AND HUMAN-CELLS [J].
DIPPOLD, WG ;
JAY, G ;
DELEO, AB ;
KHOURY, G ;
OLD, LJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (03) :1695-1699
[4]   MIMICKING OF DISCONTINUOUS EPITOPES BY PHAGE-DISPLAYED PEPTIDES .2. SELECTION OF CLONES RECOGNIZED BY A PROTECTIVE MONOCLONAL-ANTIBODY AGAINST THE BORDETELLA-PERTUSSIS TOXIN FROM PHAGE PEPTIDE LIBRARIES [J].
FELICI, F ;
LUZZAGO, A ;
FOLGORI, A ;
CORTESE, R .
GENE, 1993, 128 (01) :21-27
[5]   ACTIVATING MUTATIONS FOR TRANSFORMATION BY P53 PRODUCE A GENE-PRODUCT THAT FORMS AN HSC70-P53 COMPLEX WITH AN ALTERED HALF-LIFE [J].
FINLAY, CA ;
HINDS, PW ;
TAN, TH ;
ELIYAHU, D ;
OREN, M ;
LEVINE, AJ .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (02) :531-539
[6]   ACTIVATING MUTATIONS IN P53 PRODUCE A COMMON CONFORMATIONAL EFFECT - A MONOCLONAL-ANTIBODY SPECIFIC FOR THE MUTANT FORM [J].
GANNON, JV ;
GREAVES, R ;
IGGO, R ;
LANE, DP .
EMBO JOURNAL, 1990, 9 (05) :1595-1602
[7]  
GREAVES R, 1988, THESIS U LONDON
[8]   MONOCLONAL-ANTIBODIES AGAINST SIMIAN VIRUS-40 T-ANTIGENS - EVIDENCE FOR DISTINCT SUBCLASSES OF LARGE T-ANTIGEN AND FOR SIMILARITIES AMONG NON-VIRAL T-ANTIGENS [J].
GURNEY, EG ;
HARRISON, RO ;
FENNO, J .
JOURNAL OF VIROLOGY, 1980, 34 (03) :752-763
[9]   MONOCLONAL-ANTIBODIES SPECIFIC FOR SIMIAN VIRUS-40 TUMOR-ANTIGENS [J].
HARLOW, E ;
CRAWFORD, LV ;
PIM, DC ;
WILLIAMSON, NM .
JOURNAL OF VIROLOGY, 1981, 39 (03) :861-869
[10]   ALLOSTERIC ACTIVATION OF LATENT P53 TETRAMERS [J].
HUPP, TR ;
LANE, DP .
CURRENT BIOLOGY, 1994, 4 (10) :865-875