| Literature DB >> 19811418 |
Zhensheng Wang1, Dingding Shao, Xiang Zhong, Cong Han, Pengfei Cai, Heng Wang.
Abstract
A homologue of mammalian macrophage migration inhibitory factor (MIF) has been identified in Plasmodium falciparum (PfMIF). This parasite-derived cytokine and its antiserum were detected in the circulation of patients with malaria. Using a monoclonal antibody, designated mAb1B9, against PfMIF, we performed biopanning using two phage display peptide libraries to screen for the main sequence of the epitope recognized by the antibody. We then expressed a series of truncated peptides in order to identify the precise sequence of the epitope. The epitope recognized by mAb1B9 is 22 amino acids long and has the following sequence: (36)LGYIMSNYDYQKNLRFGGSNEA(57). Western analysis showed that the residues (36)LG(37) and (52)G differentiated PfMIF from the rodent malaria parasite-derived MIFs, and the residues (43)Y and (48)NL(49) differentiated PfMIF from P. vivax- and P. knowlesi-derived MIFs. The precise identification of this epitope, the first identified for PfMIF, will increase the specificity of the sandwich ELISA assays used to evaluate patients with malaria. These results indicate that mAb1B9 is useful for investigating the function of PfMIF in immune responses to malaria. Both the epitope and the monoclonal antibody against it will be valuable tools in epidemiological studies concerning this P. falciparum-derived cytokine.Entities:
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Year: 2009 PMID: 19811418 DOI: 10.1080/08820130902912340
Source DB: PubMed Journal: Immunol Invest ISSN: 0882-0139 Impact factor: 3.657