Characterization of storage mite allergens in human, using western blotting

1998 ◽  
Vol 95 ◽  
pp. 201
Author(s):  
S. Pennanen ◽  
L. Kulmala ◽  
J. Liesivuori
2009 ◽  
Vol 75 (5) ◽  
pp. 1345-1354 ◽  
Author(s):  
A. Rementeria ◽  
A. B. Vivanco ◽  
A. Ramirez ◽  
F. L. Hernando ◽  
J. Bikandi ◽  
...  

ABSTRACT Flagellar extracts of Salmonella enterica serovars expressing phase 2 H1 antigenic complex (H:1,2, H:1,5, H:1,6, and H:1,7) and a mutant flagellin obtained by site-directed mutagenesis of the fljB gene from serovar Typhimurium at codon 218, transforming threonine to alanine, expressed in Escherichia coli (fljB218 A ) were used to analyze the H1 antigenic complex. Cross-reactions were detected by Western blotting and dot blotting using commercial polyclonal antibodies against the different wild-type extracts and mutant FljB218A. Therefore, we produced a monoclonal antibody (MAb), 23D4, isotyped as immunoglobulin M, against H:1,2 S. enterica serovar Typhimurium flagellin. The mutant flagellin was not recognized by this MAb. When a large number of phase 1 and phase 2 flagellin antigens of different serovars were used to characterize the 23D4 MAb, only extracts of serovars Typhimurium and [4,5,12:i:−] reacted. The protein composition of phase 1 and phase 2 extracts and highly purified H:1,2 flagellin from serovar Typhimurium strain LT2 and extract of strain 286 (serovar [4,5,12:i:−]), which reacted with the MAb, was studied. Phase 2 flagellin (FljBH:1,2) was detected in phase 1 and phase 2 flagellar heat extracts of serovar Typhimurium and was the single protein identified in all spots of purified H:1,2 flagellin. FliC, FlgK, and other proteins were detected in some immunoreactive spots and in the flagellar extract of serovar [4,5,12:i:−]. Immunoelectron microscopy of complete bacteria with 23D4 showed MAb attachment at the base of flagella, although the MAb failed to recognize the filament of flagella. Nevertheless, the results obtained by the other immunological tests (enzyme-linked immunosorbent assay, Western blotting, and dot blotting) indicate a reaction against flagellins. The epitopes could also be shared by other proteins on spots where FljB is not present, such as aminopeptidase B, isocitrate lyase, InvE, EF-TuA, enolase, DnaK, and others. In conclusion, MAb 23D4 can be useful for detection and diagnostic purposes of S. enterica serovar Typhimurium and serovar [4,5,12:i:−] and could be also helpful for epitope characterization of flagellum-associated antigens.


2007 ◽  
Vol 58 (2) ◽  
pp. 177-183 ◽  
Author(s):  
Elaine Antunes de Lemos ◽  
Zila Rosa Belém ◽  
Aritânia Santos ◽  
Antônio Walter Ferreira
Keyword(s):  

1995 ◽  
pp. 317-326
Author(s):  
W. Breipohl ◽  
C. Reitz ◽  
M. H. J. Ahrend ◽  
F. H. Grus ◽  
J. Bours

Parasitology ◽  
1992 ◽  
Vol 104 (1) ◽  
pp. 1-9 ◽  
Author(s):  
U. Kawazoe ◽  
F. M. Tomley ◽  
J. A. Frazier

SUMMARYSporozoites ofEimeria tenellawere disrupted by sonication and subcellular fractions were separated by sucrose gradient ultracentrifugation. Fractions from gradients were characterized by electron microscopical appearance and their polypeptide and antigenic profiles determined by PAGE and Western blotting with antisera to sporozoites and 1st- and 2nd-generation merozoites. Fractions containing micronemes, rhoptries or membranes showed markedly different polypeptide content and antigenic reactivity. Microneme epitopes were strongly conserved between sporozoites and 2nd-generation merozoites whereas the majority of rhoptry epitopes and many membrane epitopes were sporozoite specific. The only polypeptide of sporozoites which was strongly recognized by antisera raised to 1st generation merozoites was a microneme antigen of molecular weight approximately 100 kDa.


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