Characterization of a monoclonal antibody (P40) against the 68 kD major allergen of Penicillium notatum
Article first published online: 27 APR 2006
Clinical & Experimental Allergy
Volume 22, Issue 4, pages 485–490, April 1992
How to Cite
SHEN, H.-D., CHOO, K.-B., CHEN, J.-H., LIN, W.-L., CHANG, Z.-N. and HAN, S.-H. (1992), Characterization of a monoclonal antibody (P40) against the 68 kD major allergen of Penicillium notatum. Clinical & Experimental Allergy, 22: 485–490. doi: 10.1111/j.1365-2222.1992.tb00151.x
- Issue published online: 27 APR 2006
- Article first published online: 27 APR 2006
- Submitted 11 June 1991; revised 1 November 1991; accepted 4 November 1991.
A monoclonal antibody (MoAb P40) against the 68 kD major allergen of penicillium notatum (P. notatum) was obtained by immunizing the mouse with a crude extract of P. notatum. Analysed by two-dimensional gel electrophoresis and immunoblotting, P40 reacted with two different isoforms of the 68 kD component of P. notatum with pIs of 5.4 and 5.5. In addition to P. notatum, P40 showed positive ELISA activity to Aspergillus fumigatus (A. fumigatus) but not to components of six other fungi including Alternaria porri, Cladosporium cladosporoides, Aureobasidium pullulans, Fusarium solani, Rhizopus arrhizus and Candida albicans. Analysed by ELISA, MoAb P40 also showed positive activity to two (P. frequentans and P. roseopurpureum) of the 10 other Penicillium species and two (A. terreus and A. flavus) of the four other Aspergillus species tested. SDS-PAGE and immunoblotting studies demonstrated P40 positive reactivity to components with MW of about 67 kD in all these Penicillium and Aspergillus species with positive ELISA activity to P40. Furthermore, immunoblotting activity of MoAb P40 to the 67 kD component of A. niger was also observed. The epitope of the 68 kD allergen of P. notatum recognized by MoAb P40 was resistant to treatment of periodate oxidation with concentration of NaIO4 up to 20 mm. This MoAb may thus be useful in the characterization and purification of the 68 kD allergen from crude extracts, and in the molecular cloning of allergen genes.