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1.
BMC Plant Biol ; 9: 24, 2009 Mar 03.
Artículo en Inglés | MEDLINE | ID: mdl-19257882

RESUMEN

BACKGROUND: Bet v 1 is an important cause of hay fever in northern Europe. Bet v 1 isoforms from the European white birch (Betula pendula) have been investigated extensively, but the allergenic potency of other birch species is unknown. The presence of Bet v 1 and closely related PR-10 genes in the genome was established by amplification and sequencing of alleles from eight birch species that represent the four subgenera within the genus Betula. Q-TOF LC-MSE was applied to identify which PR-10/Bet v 1 genes are actually expressed in pollen and to determine the relative abundances of individual isoforms in the pollen proteome. RESULTS: All examined birch species contained several PR-10 genes. In total, 134 unique sequences were recovered. Sequences were attributed to different genes or pseudogenes that were, in turn, ordered into seven subfamilies. Five subfamilies were common to all birch species. Genes of two subfamilies were expressed in pollen, while each birch species expressed a mixture of isoforms with at least four different isoforms. Isoforms that were similar to isoforms with a high IgE-reactivity (Bet v 1a = PR-10.01A01) were abundant in all species except B. lenta, while the hypoallergenic isoform Bet v 1d (= PR-10.01B01) was only found in B. pendula and its closest relatives. CONCLUSION: Q-TOF LC-MSE allows efficient screening of Bet v 1 isoforms by determining the presence and relative abundance of these isoforms in pollen. B. pendula contains a Bet v 1-mixture in which isoforms with a high and low IgE-reactivity are both abundant. With the possible exception of B. lenta, isoforms identical or very similar to those with a high IgE-reactivity were found in the pollen proteome of all examined birch species. Consequently, these species are also predicted to be allergenic with regard to Bet v 1 related allergies.


Asunto(s)
Alérgenos/genética , Antígenos de Plantas/genética , Betula/genética , Proteínas de Plantas/genética , Polen/genética , Alérgenos/inmunología , Secuencia de Aminoácidos , Antígenos de Plantas/inmunología , Betula/inmunología , Clonación Molecular , ADN de Plantas/genética , Genes de Plantas , Genómica , Inmunoglobulina E/inmunología , Datos de Secuencia Molecular , Familia de Multigenes , Filogenia , Proteínas de Plantas/inmunología , Polen/inmunología , Isoformas de Proteínas/genética , Isoformas de Proteínas/inmunología , Proteómica , Alineación de Secuencia
2.
J Chromatogr B Analyt Technol Biomed Life Sci ; 877(10): 975-82, 2009 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-19282254

RESUMEN

The detection, analysis, and quantification of individual celiac disease (CD) immune responsive gluten proteins in wheat and related cereals (barley, rye) require an adequate and reliable extraction protocol. Because different types of gluten proteins behave differently in terms of solubility, currently different extraction protocols exist. The performance of various documented gluten extraction protocols is evaluated for specificity and completeness by gel electrophoresis (SDS-PAGE), immunoblotting and RIDASCREEN Gliadin competitive ELISA. Based on these results, an optimized, two-step extraction protocol has been developed.


Asunto(s)
Antígenos de Plantas/química , Enfermedad Celíaca/inmunología , Fraccionamiento Químico/métodos , Glútenes/química , Triticum/química , Antígenos de Plantas/aislamiento & purificación , Harina/análisis , Glútenes/aislamiento & purificación , Humanos , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Triticum/inmunología
3.
J Exp Bot ; 60(4): 1273-88, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19204031

RESUMEN

During post-harvest storage, potato tubers age as they undergo an evolution of their physiological state influencing their sprouting pattern. In the present study, physiological and biochemical approaches were combined to provide new insights on potato (Solanum tuberosum L. cv. Désirée) tuber ageing. An increase in the physiological age index (PAI) value from 0.14 to 0.83 occurred during storage at 4 degrees C over 270 d. Using this reference frame, a proteomic approach was followed based on two-dimensional electrophoresis. In the experimental conditions of this study, a marked proteolysis of patatin occurred after the PAI reached a value of 0.6. In parallel, several glycolytic enzymes were up-regulated and cellular components influencing protein conformation and the response to stress were altered. The equilibrium between the 20S and 26S forms of the proteasome was modified, the 20S form that recycles oxidized proteins being up-regulated. Two proteins belonging to the cytoskeleton were also differentially expressed during ageing. As most of these changes are also observed in an oxidative stress context, an approach focused on antioxidant compounds and enzymes as well as oxidative damage on polyunsaturated fatty acids and proteins was conducted. All the changes observed during ageing seemed to allow the potato tubers to maintain their radical scavenging activity until the end of the storage period as no accumulation of oxidative damage was observed. These data are interpreted considering the impact of reactive oxygen species on the development and the behaviour of other plant systems undergoing ageing or senescence processes.


Asunto(s)
Antioxidantes/metabolismo , Tubérculos de la Planta/crecimiento & desarrollo , Tubérculos de la Planta/metabolismo , Proteoma/metabolismo , Solanum tuberosum/crecimiento & desarrollo , Solanum tuberosum/metabolismo , Ascorbato Peroxidasas , Catalasa/metabolismo , Regulación hacia Abajo , Electroforesis en Gel Bidimensional , Esterificación , Depuradores de Radicales Libres/metabolismo , Glutatión/metabolismo , Cinética , Oxilipinas/metabolismo , Peroxidasas/metabolismo , Fenoles/metabolismo , Tubérculos de la Planta/enzimología , Carbonilación Proteica , Solanum tuberosum/enzimología , Superóxido Dismutasa/metabolismo , Factores de Tiempo , Regulación hacia Arriba
4.
Proteomics ; 6(24): 6494-7, 2006 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17096317

RESUMEN

Two protein extraction procedures were tested in order to remove interfering compounds prior to 2-DE of potato tubers. These methods using SDS lysis buffer and phenol-phase extraction were compared regarding the quality of the resulting 2-D gel. While the resolution of SDS extracts on semipreparative gels seems better, both methods lead to similar extraction yields and total number of spots. The procedures are complementary regarding the Mr range of preferentially extracted proteins.


Asunto(s)
Electroforesis en Gel Bidimensional/métodos , Proteínas de Plantas/aislamiento & purificación , Proteómica/métodos , Solanum tuberosum/química , Concentración de Iones de Hidrógeno , Fenol , Proteínas de Plantas/química , Tubérculos de la Planta/química , Dodecil Sulfato de Sodio
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