Identification of polcalcin as a novel allergen of Amaranthus retroflexus pollen.
Adolescent
Adult
Allergens
/ immunology
Amaranthus
/ immunology
Antigens, Plant
/ immunology
Calcium-Binding Proteins
/ immunology
Cloning, Molecular
Cross Reactions
Escherichia coli
/ genetics
Female
Gene Expression
Humans
Immunoglobulin E
/ metabolism
Male
Plant Extracts
Pollen
/ immunology
Recombinant Proteins
/ isolation & purification
Rhinitis, Allergic, Seasonal
/ immunology
Skin Tests
Young Adult
Allergen characterization
Amaranthus retroflexus
Cloning
Polcalcin
Journal
Allergologia et immunopathologia
ISSN: 1578-1267
Titre abrégé: Allergol Immunopathol (Madr)
Pays: Singapore
ID NLM: 0370073
Informations de publication
Date de publication:
Historique:
received:
09
08
2018
revised:
13
12
2018
accepted:
29
12
2018
pubmed:
17
2
2019
medline:
14
1
2020
entrez:
17
2
2019
Statut:
ppublish
Résumé
Amaranthus retroflexus (Redroot Pigweed) is one of the main sources of allergenic pollens in temperate areas. Polcalcin is a well-known panallergen involved in cross-reactivity between different plants. The aim of this study was the molecular cloning and expression of polcalcin, as well as evaluating its IgE-reactivity with A. retroflexus sensitive patients' sera. Allergenic extract was prepared from A. retroflexus pollen and the IgE-reactivity profile was determined by ELISA and immunoblotting using sera from twenty A. retroflexus sensitive patients. Polcalcin-coding sequence was amplified by conventional PCR method and the product was inserted into pET-21b(+) vector. The recombinant protein was expressed in E. coli BL21 and purified by metal affinity chromatography. The IgE-binding capability of the recombinant protein was analyzed by ELISA and immunoblotting assays, and compared with crude extract. Of 20 skin prick test positive patients, 17 patients were positive in IgE-specific ELISA. Western blotting confirmed that approximately 53% of ELISA positive patients reacted with 10kDa protein in crude extract. The A. retroflexus polcalcin gene, encoding to 80 amino acid residues was cloned and expressed as a soluble protein and designated as Ama r 3. The recombinant polcalcin showed rather identical IgE-reactivity in ELISA and western blotting with 10kDa protein in crude extract. These results were confirmed by inhibition methods, too. The recombinant form of A. retroflexus polcalcin (Ama r 3) could be easily produced in E. coli in a soluble form and shows rather similar IgE-reactivity with its natural counterpart.
Identifiants
pubmed: 30770138
pii: S0301-0546(19)30005-9
doi: 10.1016/j.aller.2018.12.006
pii:
doi:
Substances chimiques
Allergens
0
Antigens, Plant
0
Calcium-Binding Proteins
0
Plant Extracts
0
Recombinant Proteins
0
Immunoglobulin E
37341-29-0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
357-364Informations de copyright
Copyright © 2019 SEICAP. Published by Elsevier España, S.L.U. All rights reserved.