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

被引:55
作者
Schmidt, M
Zargari, A
Holt, P
Lindbom, L
Hellman, U
Whitley, P
VanderPloeg, I
Harfast, B
Scheynius, A
机构
[1] KAROLINSKA HOSP, DEPT LAB MED, DIV CLIN IMMUNOL, S-17176 STOCKHOLM, SWEDEN
[2] LUDWIG INST CANC RES, S-75124 UPPSALA, SWEDEN
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1997年 / 246卷 / 01期
关键词
allergy; yeast; Malassezia furfur; PCR; cDNA cloning; protein expression;
D O I
10.1111/j.1432-1033.1997.00181.x
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
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 35988 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.
引用
收藏
页码:181 / 185
页数:5
相关论文
共 26 条
  • [1] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [2] KETOCONAZOLE IN ATOPIC-DERMATITIS - THERAPEUTIC RESPONSE IS CORRELATED WITH DECREASE IN SERUM IGE
    BACK, O
    SCHEYNIUS, A
    JOHANSSON, SGO
    [J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 1995, 287 (05) : 448 - 451
  • [3] TRANSCRIPTION TERMINATION AND 3' PROCESSING - THE END IS IN SITE
    BIRNSTIEL, ML
    BUSSLINGER, M
    STRUB, K
    [J]. CELL, 1985, 41 (02) : 349 - 359
  • [4] ALLERGENS OF PITYROSPORUM-OVALE AND CANDIDA-ALBICANS .2. PHYSICOCHEMICAL CHARACTERIZATION
    DOEKES, G
    KAAL, MJH
    VANLEPERENVANDIJK, AG
    [J]. ALLERGY, 1993, 48 (06) : 401 - 408
  • [5] EGLI CM, 1994, J BIOL CHEM, V269, P27378
  • [6] FAERGEMANN J, 1983, ACTA DERM-VENEREOL, V63, P346
  • [7] SEQUENCE DIFFERENCES BETWEEN GLYCOSYLATED AND NONGLYCOSYLATED ASN-X-THR SER ACCEPTOR SITES - IMPLICATIONS FOR PROTEIN ENGINEERING
    GAVEL, Y
    VONHEIJNE, G
    [J]. PROTEIN ENGINEERING, 1990, 3 (05): : 433 - 442
  • [8] IMPROVEMENT OF AN IN-GEL DIGESTION PROCEDURE FOR THE MICROPREPARATION OF INTERNAL PROTEIN-FRAGMENTS FOR AMINO-ACID SEQUENCING
    HELLMAN, U
    WERNSTEDT, C
    GONEZ, J
    HELDIN, CH
    [J]. ANALYTICAL BIOCHEMISTRY, 1995, 224 (01) : 451 - 455
  • [9] PEPTIDE-INDUCED NONRESPONSIVENESS OF HLA-DP RESTRICTED HUMAN T-CELLS REACTIVE WITH DERMATOPHAGOIDES SPP
    HIGGINS, JA
    LAMB, JR
    MARSH, SGE
    TONKS, S
    HAYBALL, JD
    ROSENBRONSON, S
    BODMER, JG
    OHEHIR, RE
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 90 (05) : 749 - 756
  • [10] DIFFERENT CLASSES OF POLYADENYLATION SITES IN THE YEAST SACCHAROMYCES-CEREVISIAE
    IRNIGER, S
    EGLI, CM
    BRAUS, GH
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (06) : 3060 - 3069