PREDICTION OF PROTEIN ANTIGENIC SITES IN HUMAN CORTICOTROPIN-RELEASING HORMONE PRECURSOR

被引:0
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作者
RINGAN, NS
GRAYSON, L
LOWENSTEIN, PR
LINTON, EA
LOWRY, PJ
CASTRO, MG
机构
[1] UNIV WALES COLL CARDIFF,COLL CARDIFF,DEPT PHYSIOL,CELLULAR & MOLEC NEUROBIOL LAB,POB 902,CARDIFF CF1 1SS,WALES
[2] DUNDEE INST TECHNOL,DEPT MOLEC & LIFE SCI,DUNDEE DD1 1HG,SCOTLAND
[3] UNIV DUNDEE,DEPT ANAT & PHYSIOL,DUNDEE DD1 4HN,SCOTLAND
[4] JOHN RADCLIFFE MATERN HOSP,NUFFIELD DEPT OBSTET & GYNAECOL,OXFORD OX3 9BU,ENGLAND
[5] UNIV READING,DEPT BIOCHEM & PHYSIOL,READING RG6 2AJ,BERKS,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0305-0491(93)90277-C
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
1. The primary structure of human corticotrophin-releasing hormone precursor (h pre-pro-CRH) has been analysed using a number of computer algorithms to identify the areas of highest predicted antigenicity. 2. These results were correlated with crossreactivity data obtained from studies of antibodies produced in rabbits by immunizing with h pre-proCRH, and a number of related peptides. 3. Six areas of high predicted antigenicity were identified in h pre-proCRH by the prediction routines utilized. Two of these corresponded almost exactly to the two putative cleavage sites of the prohormone, and a third lay within the C-terminal region of one of the products of post-translational processing of the prohormone, i.e. CRH(1-41). 4. Experimental crossreactivity data also indicated that a number of structural factors (e.g. Omega loops, peptide conformation) may also be involved in recognition of peptide fragments by antibodies.
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页码:521 / 529
页数:9
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