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BAD-1 is an adhesin created by the dimorphic fungus Blastomyces dermatitidis, the causative agent of blastomycosis. We have determined that it has an affinity for heparin, which may explain its impact on virulence and human immune function as a number of cells related to immune function have heparin like moieties on their surfaces. This assay allows a quantification of binding between soluble BAD-1 and immobilized heparin.

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Native BAD-1 Binding to Heparin-agarose

Microbiology > Microbial biochemistry > Protein > Interaction
Author: T. Tristan Brandhorst
T. Tristan BrandhorstAffiliation: Department of Pediatrics, Division of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, USA
For correspondence: tbrandho@wisc.edu
Bio-protocol author page: a1274
Vol 4, Iss 7, 4/5/2014, 1586 views, 0 Q&A, How to cite
DOI: http://dx.doi.org/10.21769/BioProtoc.1095

[Abstract] BAD-1 is an adhesin created by the dimorphic fungus Blastomyces dermatitidis, the causative agent of blastomycosis. We have determined that it has an affinity for heparin, which may explain its impact on virulence and human immune function as a number of cells related to immune function have heparin like moieties on their surfaces. This assay allows a quantification of binding between soluble BAD-1 and immobilized heparin.

Materials and Reagents

  1. Heparin-agarose resin (Sigma-Aldrich, catalog number: H6508) (prior to use it is washed 3x in five volumes of tricine buffer to eliminate free heparin)
  2. 10 μg of BAD-1 [purified according to the method of Brandhorst et al. (2005)]
  3. 25 microliters of soluble medical-grade sodium heparin for injection (50 mg/ml) (Elkins-Sinn Inc)
  4. Tricine buffer (Sigma-Aldrich, catalog number: T0377) (see Recipes)

Equipment

  1. Accuspin micro17 microcentrifuge (Thermo Fisher Scientific)
  2. Nanodrop ND1000 spectrophotometer

Procedure

  1. 100 μl of 0.1 mg/ml BAD-1 in tricine buffer was incubated with agarose heparin resin (5 μl bed volume) for 30 min at 25 °C with occasional agitation.
  2. Resin beads were pelleted by centrifugation in an Accuspin microfuge at 7,000 x g for 1 min.
  3. Samples of the BAD-1 containing supernatant were analyzed for optical density at 280 nm in a Nanodrop ND1000 spectrophotometer. This reading was compared to a control solution of BAD-1 to which tricine buffer was added in place of heparin-agarose beads. The discrepancy in absorbance is assumed to be linear with respect to BAD-1 adhering to the heparin resin bed.
  4. Binding inhibition studies were done by repeating steps 1-3 in the presence of soluble medical grade heparin in tricine buffer. Heparin was added to the tricine binding buffer at various concentrations (0.01, 0.1 and 1 mg/ml - significant inhibition was noted at 0.1 mg/ml heparin and above.). Measurements of baseline absorbance were corrected to account for absorbance of added heparin inhibitor.

Recipes

  1. Tricine buffer
    20 mM tricine (pH 7)
    50 mM NaCl

Acknowledgments

This work was supported by funds from the United States Public Health Service (to B. S. K.), the Parker B. Francis Foundation (to T. T. B.), and the Infectious Disease Society of America (to G. M. G.). The University of Wisconsin-Madison Biophysics Instrumentation Facility, where the CD experiments were performed, was established by National Science Foundation Grant BIR9512577 and National Institutes of Health Grant RR13790.

References

  1. Brandhorst, T. T., Gauthier, G. M., Stein, R. A. and Klein, B. S. (2005). Calcium binding by the essential virulence factor BAD-1 of Blastomyces dermatitidis. J Biol Chem 280(51): 42156-42163.


How to cite this protocol: Brandhorst, T. T. (2014). Native BAD-1 Binding to Heparin-agarose. Bio-protocol 4(7): e1095. DOI: 10.21769/BioProtoc.1095; Full Text



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