Literature DB >> 9210481

The complete cDNA sequence and expression of the first major allergenic protein of Malassezia furfur, Mal f 1.

M Schmidt1, A Zargari, P Holt, L Lindbom, U Hellman, P Whitley, I van der Ploeg, B Härfast, A Scheynius.   

Abstract

For the first time the complete cDNA encoding a major allergen and novel protein of the yeast Malassezia furfur, Mal f 1, has been sequenced and expressed. The amino acid sequences of nine tryptic peptides of the protein were determined. Oligonucleotides were designed from these amino acid sequences. The cDNA sequence was obtained by hybridizing these primers to mRNA and enhancement by reverse-transcriptase PCR techniques. The cDNA is 1176 bp in length. It shows an open reading frame of 1050 bp coding for a protein of 38178 Da and a deduced amino acid sequence containing 350 residues. The hydropathy plot and the tryptic digest indicate that the first 22 amino acids represent a leader sequence determining a mature protein of 35 988 Da. The complete encoding cDNA was expressed as a maltose-binding protein fusion protein in Escherichia coli. The recombinant fusion protein reacted with our specific monoclonal antibody and with IgE from patients with atopic dermatitis.

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Year:  1997        PMID: 9210481     DOI: 10.1111/j.1432-1033.1997.00181.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  11 in total

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5.  Crystallization and preliminary crystallographic study of the yeast Malassezia sympodialis allergen Mala s 1.

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Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2006-01-27

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7.  Allergenic evaluation of Malassezia furfur crude extracts.

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10.  Reduction of the number of major representative allergens: from clinical testing to 3-dimensional structures.

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