Journal article
Eukaryotic expression, purification and structure/function analysis of native, recombinant CRISP3 from human and mouse
M Volpert, JE Mangum, D Jamsai, R D'Sylva, MK O'Bryan, P McIntyre
Scientific Reports | Published : 2014
DOI: 10.1038/srep04217
Abstract
While the Cysteine-Rich Secretory Proteins (CRISPs) have been broadly proposed as regulators of reproduction and immunity, physiological roles have yet to be established for individual members of this family. Past efforts to investigate their functions have been limited by the difficulty of purifying correctly folded CRISPs from bacterial expression systems, which yield low quantities of correctly folded protein containing the eight disulfide bonds that define the CRISP family. Here we report the expression and purification of native, glycosylated CRISP3 from human and mouse, expressed in HEK 293 cells and isolated using ion exchange and size exclusion chromatography. Functional authenticity..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
We thank staff at the Monash Biomedical Proteomics Facility at Monash University, Australia, for support with proteomic analysis, and Monash IVF, Australia, for providing access to human seminal plasma samples. Homology modelling was carried out by Dr. Michael Kuiper, Victorian Life Science Computation Initiative (VLSCI). This work was funded by NHMRC grant 606563 to MO'B and PMc.