Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-018-30224-z
Title: Characterization of Der f 22 - a paralogue of the major allergen Der f 2
Authors: Reginald, K
Tan, C.L
Chen, S
Yuen, L
Goh, S.Y 
Chew, F.T 
Keywords: allergen
arthropod protein
Dermatophagoides farinae antigen f 2
house dust allergen
immunoglobulin E
amino acid sequence
chemistry
classification
enzyme linked immunosorbent assay
metabolism
molecular genetics
nucleotide sequence
phylogeny
procedures
proteomics
Southern blotting
Allergens
Amino Acid Sequence
Antigens, Dermatophagoides
Arthropod Proteins
Base Sequence
Blotting, Southern
Enzyme-Linked Immunosorbent Assay
Immunoglobulin E
Molecular Sequence Data
Phylogeny
Proteomics
Issue Date: 2018
Citation: Reginald, K, Tan, C.L, Chen, S, Yuen, L, Goh, S.Y, Chew, F.T (2018). Characterization of Der f 22 - a paralogue of the major allergen Der f 2. Scientific Reports 8 (1) : 11743. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-018-30224-z
Abstract: We previously identified an expressed sequence tag clone, Der f 22, showing 41% amino acid identity to published Der f 2, and show that both genes are possible paralogues. The objective of this study was to characterize the genomic, proteomic and immunological functions Der f 22 and Der f 2. The full-length sequence of Der f 2 and Der f 22 coded for mature proteins of 129 and 135 amino acids respectively, both containing 6 cysteine residues. Phylogenetic analysis of known group 2 allergens and their homologues from our expressed sequence tag library showed that Der f 22 is a paralogue of Der f 2. Both Der f 2 and Der f 22 were single gene products with one intron. Both allergens showed specific IgE-binding to over 40% of the atopic patients, with limited of cross-reactivity. Both allergens were detected at the gut region of D. farinae by immunostaining. Der f 22 is an important allergen with significant IgE reactivity among the atopic population, and should be considered in the diagnostic panel and evaluated as future hypoallergen vaccine therapeutic target. © 2018, The Author(s).
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/175018
ISSN: 20452322
DOI: 10.1038/s41598-018-30224-z
Appears in Collections:Elements
Staff Publications

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1038_s41598-018-30224-z.pdf2.32 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.