A Recombinant Isoform of the Ole E 7 Olive Pollen Allergen Assembled by De Novo Mass Spectrometry Retains the Allergenic Ability of the Natural Allergen
Overview
Authors
Affiliations
Significance: Olive pollen is an important cause of allergy. The non-specific lipid binding protein Ole e 7 is a major allergen with a high incidence and a phenotype associated to severe clinical symptoms. Despite its relevance, its cloning and recombinant expression has been unable by classical techniques. Here, we have inferred the primary amino acid sequence of Ole e 7 by mass-spectrometry. We separated Ole e 7 isolated from pollen by 2DE. After in-gel digestion with trypsin and a direct analysis by nLC-MS/MS in an LTQ-Orbitrap Velos, we got the complete de novo sequenced peptides repertoire that allowed the assembling of the primary sequence of Ole e 7. After its protein expression, purification to homogeneity, and structural and immunological characterization using sera from olive pollen allergic patients and cell-based assays, we observed that the recombinant allergen retained the antigenic and allergenic properties of the natural allergen. Collectively, we show that the recombinant protein assembled by proteomics would be suitable for a better in vitro diagnosis of olive pollen allergic patients.
Alvarez P, Aguado R, Molina J, Trujillo-Aguilera A, Villalba M, Diaz-Perales A Nutrients. 2024; 16(17).
PMID: 39275185 PMC: 11396898. DOI: 10.3390/nu16172869.
Lipid Transfer Proteins (LTPs)-Structure, Diversity and Roles beyond Antimicrobial Activity.
Costa Amador V, Dos Santos-Silva C, Vilela L, Oliveira-Lima M, Rego M, Roldan-Filho R Antibiotics (Basel). 2021; 10(11).
PMID: 34827219 PMC: 8615156. DOI: 10.3390/antibiotics10111281.
Pascal M, Moreno C, Davila I, Tabar A, Bartra J, Labrador M Clin Transl Allergy. 2021; 11(7):e12052.
PMID: 34582103 PMC: 9082998. DOI: 10.1002/clt2.12052.