Major mountain cedar allergen, Jun a 1, contains conformational as well as linear IgE epitopes

Shikha Varshney, Randall M. Goldblum, Christopher Kearney, Masanao Watanabe, Terumi Midoro-Horiuti

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

We have previously identified four linear IgE epitopes on Jun a 1, the dominant allergen in mountain cedar pollen and mapped these to the surfaces of a molecular model and to the crystal structure of this glycoprotein. The aim of the present study was to determine if Jun a 1 also displays conformational IgE epitopes. Jun a 1 was denatured by heating at 75 °C for 1 h, exposure to 6 M guanidine or by reductive alkylation in the presence and absence of guanidine. The effects of these manipulations on the binding to IgE from patients with mountain cedar hypersensitivity was evaluated by an ImmunoCAP inhibition assay, using Jun a 1-specific caps. Treatment-associated changes in the 3D-structure were assessed by dynamic light scattering and CD spectroscopy. IgE binding to native Jun a 1 was inhibited 92 ± 9% by soluble native protein and 92 ± 9% by reduced and alkylated Jun a 1. However, the capacity of Jun a 1 to inhibit the binding of IgE antibodies was significantly diminished upon denaturation by heat, guanidine alone, or reduction and alkylation in guanidine, compared to native Jun a 1. Reductive alkylation treatment under denaturing conditions also increased the Stoke's radius, suggesting that the protein was partially unfolded. Analysis of the circular dichroism (CD) spectra suggested that heating and treatment with guanidine caused a loss of α-helical structure. Guanidine also caused an increase in random coil structure. Thus, at least a portion of the anti-Jun a 1 IgE antibodies produced by allergic humans recognize conformational epitopes and it is likely that some of these epitopes reside in α-helical structures of Jun a 1.

Original languageEnglish (US)
Pages (from-to)2781-2785
Number of pages5
JournalMolecular Immunology
Volume44
Issue number10
DOIs
StatePublished - Apr 2007

Fingerprint

Guanidine
Allergens
Immunoglobulin E
Epitopes
Alkylation
Circular Dichroism
Heating
Molecular Models
Antibodies
Pollen
Spectrum Analysis
Glycoproteins
Hypersensitivity
Proteins
Therapeutics
Hot Temperature

Keywords

  • Allergen structure
  • Cedar pollen hypersensitivity
  • Conformational epitopes
  • Cry j 1
  • IgE epitope
  • Jun a 1
  • Juniperus ashei
  • Mountain cedar
  • Protein denaturation

ASJC Scopus subject areas

  • Molecular Biology
  • Immunology

Cite this

Major mountain cedar allergen, Jun a 1, contains conformational as well as linear IgE epitopes. / Varshney, Shikha; Goldblum, Randall M.; Kearney, Christopher; Watanabe, Masanao; Midoro-Horiuti, Terumi.

In: Molecular Immunology, Vol. 44, No. 10, 04.2007, p. 2781-2785.

Research output: Contribution to journalArticle

Varshney, Shikha ; Goldblum, Randall M. ; Kearney, Christopher ; Watanabe, Masanao ; Midoro-Horiuti, Terumi. / Major mountain cedar allergen, Jun a 1, contains conformational as well as linear IgE epitopes. In: Molecular Immunology. 2007 ; Vol. 44, No. 10. pp. 2781-2785.
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abstract = "We have previously identified four linear IgE epitopes on Jun a 1, the dominant allergen in mountain cedar pollen and mapped these to the surfaces of a molecular model and to the crystal structure of this glycoprotein. The aim of the present study was to determine if Jun a 1 also displays conformational IgE epitopes. Jun a 1 was denatured by heating at 75 °C for 1 h, exposure to 6 M guanidine or by reductive alkylation in the presence and absence of guanidine. The effects of these manipulations on the binding to IgE from patients with mountain cedar hypersensitivity was evaluated by an ImmunoCAP inhibition assay, using Jun a 1-specific caps. Treatment-associated changes in the 3D-structure were assessed by dynamic light scattering and CD spectroscopy. IgE binding to native Jun a 1 was inhibited 92 ± 9{\%} by soluble native protein and 92 ± 9{\%} by reduced and alkylated Jun a 1. However, the capacity of Jun a 1 to inhibit the binding of IgE antibodies was significantly diminished upon denaturation by heat, guanidine alone, or reduction and alkylation in guanidine, compared to native Jun a 1. Reductive alkylation treatment under denaturing conditions also increased the Stoke's radius, suggesting that the protein was partially unfolded. Analysis of the circular dichroism (CD) spectra suggested that heating and treatment with guanidine caused a loss of α-helical structure. Guanidine also caused an increase in random coil structure. Thus, at least a portion of the anti-Jun a 1 IgE antibodies produced by allergic humans recognize conformational epitopes and it is likely that some of these epitopes reside in α-helical structures of Jun a 1.",
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