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Infect. Immun., Jun 1995, 2126-2132, Vol 63, No. 6
JL Lopez-Ribot, JP Martinez and WL Chaffin
Using polyclonal antibodies (PAbs) raised against the Candida albicans C3d
receptor (CR2; PAb anti-CR2) and the 58-kDa fibrinogen-binding mannoprotein
(mp58; PAb anti-mp58) as well as ligand interactions, we have studied the
relationship between these two receptors. In an indirect immunofluorescence
assay with germ tubes, greater intensity was observed on the mother
blastoconidium when PAb anti-CR2 was used, whereas greater intensity was
localized to the hyphal extension when PAb anti-mp58 or binding of soluble
fibrinogen was used. No competition or change in the fluorescence pattern
was observed in dual-labeling experiments with PAb anti-CR2 and either
fibrinogen or PAb anti-mp58. Binding competition also was not observed in
an enzyme-linked immunosorbent assay using the components present in a
beta- mercaptoethanol extract from the cell wall of germ tubes. In
immunoblots, PAb anti-CR2 recognized three different discrete bands with
apparent molecular masses of 21, 40, and 66 kDa in the beta-
mercaptoethanol extracts from the cell wall, whereas a different, single,
broader band with an apparent molecular mass of 58 kDa was detected with
PAb anti-mp58. However, when nondenaturing conditions were used to separate
the materials present in the cell wall extracts, no reactivity could be
detected on Western blots (immunoblots) with PAb anti-mp58. When PAb
anti-CR2 was used for analysis, a single band migrating in the area
corresponding to approximately 40 kDa was detected. These observations
suggest a higher molecular weight for mp58 and one or more of the
components detected with PAb anti-CR2 in their native state.
Copyright © 1995, American Society for Microbiology
Comparative study of the C3d receptor and 58-kilodalton fibrinogen- binding mannoproteins of Candida albicans
Department of Microbiology and Immunology, Texas Tech University Health Sciences Center, Lubbock 79430, USA.
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