Rapid purification and characterization of L-dopachrome-methyl ester tautomerase (macrophage-migration-inhibitory factor) from Trichinella spiralis, Trichuris muris and Brugia pahangi

被引:35
作者
Pennock, JL
Behnke, JM
Bickle, QD
Devaney, E
Grencis, RK
Isaac, RE
Joshua, GWP
Selkirk, ME
Zhang, YB
Meyer, DJ
机构
[1] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, Immunol Unit, London WC1E 7HT, England
[2] Univ Nottingham, Sch Biol Sci, Nottingham NG7 2RD, England
[3] Glasgow Vet Sch, Dept Vet Parasitol, Glasgow G61 1QH, Lanark, Scotland
[4] Univ Manchester, Dept Biol Sci, Manchester M13 9PT, Lancs, England
[5] Univ Leeds, Dept Biol, Leeds LS2 9JT, W Yorkshire, England
[6] Univ London Imperial Coll Sci Technol & Med, Dept Biochem, London SW7 2AY, England
基金
英国惠康基金;
关键词
D O I
10.1042/bj3350495
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
Macrophage-migration-inhibition factor (MIF) is an essential stimulator of mammalian T-lymphocyte-dependent adaptive immunity, hence MIF orthologues might be expressed by infectious organisms as an immunosubversive stratagem. Since MIF actively catalyses the tautomerization of the methyl ester of L-dopachrome (using dopachrome tautomerase), the occurrence of MIF orthologues in several parasitic helminths was investigated by assaying and characterizing such activity. Evidence of MIF orthologues (dopachrome tautomerase) was found in the soluble fraction of the nematodes Trichinella spiralis (stage 4 larvae) and Trichuris muris (adults), and the filarial nematode Brugia pahangi (adults). The MIF orthologues of Tr. muris TmMIF) and B. pahangi (BpMIF) were purified to homogeneity using phenyl-agarose chromatography, that of T. spiralis (TsMIF required a further step: cation-exchange FPLC. Retention time on reverse-phase HPLC and M-r on SDS/PAGE of the nematode MIFs were similar to those of human MIF. N-terminal sequences (19 residues) of TsMIF and TmMIF showed 47 and 36% identity, respectively, with human MIF. The N-terminal sequence of BpMIF (14 residues) was identical to that of an MIF orthologue in the genome of B. malayi (Swiss-Prot, P91850) and showed 43 % identity to either human or TsMIF. TsMIF had 10-fold higher dopachrome tautomerase activity than MIF from the other sources. The enzyme activities of TsMIF, BpMIF and TmMIF were less sensitive to inhibition by haematin (I-50 : > 15 mu M, > 15 mu M and 2.6 mu M, respectively) than that of human MIF (I-50 0.2 mu M). Significant dopachrome tautomerase or phenyl-agarose-purifiable MIF-like protein was not detected in the soluble fraction of the nematodes Heligmosomoides polygyrus and Nippostrongylus brasiliensis, the cestode Hymenolepis diminuta, or the trematodes Schistosoma mansoni, S. japonicum and S. haematobium, or the free-living nematode, Caenorhabditis elegans, which does contain an MIF-related gene.
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收藏
页码:495 / 498
页数:4
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