Zhang L, Olsen E, Kisil F T, Hill R D, Sehon A H, Mohapatra S S
Department of Immunology, University of Manitoba, Winnipeg, Canada.
Mol Immunol. 1992 Nov;29(11):1383-9. doi: 10.1016/0161-5890(92)90175-w.
Antibody binding epitopes of a recombinant Poa p IX allergen were delineated using recombinant DNA and solid-phase peptide synthesis procedures. The full-length cDNA clone KBG60 and its four overlapping recombinant fragments, KBG60.1, KBG60.2, KBG8.3 and KBG10 which spanned the entire molecule were synthesized in E. coli with aid of the plasmid expression vector, pWR590.1. The antigenic and allergenic sites of these recombinant proteins were analyzed by ELISA using human IgE and murine IgG antibodies. It was thus demonstrated that although the epitopes were found on all the fragments tested, the majority of these were located on a C-terminal fragment, rKBG8.3. Furthermore, synthetic peptides were also employed to identify the epitopes of rKBG60 protein. The use of antisera raised against native KBG pollen extract and the recombinant KBG8.3 protein to scan a total of 56 overlapping deca-penta peptides, covering the entire rKBG60 protein, revealed that 10 positive peptides involved in the antibody-binding site(s). Taken together, the results of these studies indicate that rKBG60 protein possesses at least 10 antibody binding epitopes.
利用重组DNA和固相肽合成方法确定了重组早熟禾属p IX变应原的抗体结合表位。全长cDNA克隆KBG60及其跨越整个分子的四个重叠重组片段KBG60.1、KBG60.2、KBG8.3和KBG10,借助质粒表达载体pWR590.1在大肠杆菌中合成。使用人IgE和鼠IgG抗体通过ELISA分析这些重组蛋白的抗原和变应原位点。结果表明,虽然在所测试的所有片段上都发现了表位,但其中大多数位于C端片段rKBG8.3上。此外,还使用合成肽来鉴定rKBG60蛋白的表位。用针对天然KBG花粉提取物和重组KBG8.3蛋白产生的抗血清扫描总共56个覆盖整个rKBG60蛋白的重叠十肽至十五肽,发现10个阳性肽参与抗体结合位点。综上所述,这些研究结果表明rKBG60蛋白至少拥有10个抗体结合表位。