Strongyloides stercoralis
publication ID |
https://doi.org/ 10.1051/parasite/2023063 |
DOI |
https://doi.org/10.5281/zenodo.12751407 |
persistent identifier |
https://treatment.plazi.org/id/0E3A6110-4A08-7444-FFCA-CD02456CA65C |
treatment provided by |
Felipe |
scientific name |
Strongyloides stercoralis |
status |
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Strongyloides stercoralis View in CoL recombinant antigens
The Strongyloides stercoralis L3NieAg.01 ( NIE) sequence (1–621 bp) deposited in the GenBank database (AF136445) was codon-optimized to be suitable for an Escherichia coli expression system and constructed into the pET22.b (+) vector (GenScript, Piscataway, NJ, USA). The recombinant NIE construct was transformed into a cloning host ( E. coli JM 109) (Novagen, Darmstadt, Germany) and an expression host ( E. coli Rosetta-gami 2 (DE3)) (Novagen). The C-terminalfused His-tagged NIE was inoculated into LB broth and induced with 1 mM IPTG and incubated at 37 ° C overnight. Bacterial cells harvested from the culture were centrifuged and then resuspended in a lysis buffer with lysozyme. The suspension was then sonicated on ice. The recombinant NIE protein was initially in insoluble form and was dissolved in 8 M urea, pH = 8 (Elago Enterprises Pty Ltd., Cherrybrook, NSW, Australia).
The solubilized NIE protein fused with 6 × His-tags at the C-terminal was purified by affinity chromatography using HisTrap™ HP 1 mL columns in the ÄKTA start protein purification system as recommended by the manufacturer (Global Life Sciences Solutions USA LLC, Marlborough, MA, USA). The purified NIE protein was examined on a 12% SDS– PAGE, and the protein concentration was measured using the Bradford Assay (Bio-Rad Laboratories, Inc., Hercules, CA, USA) with bovine serum albumin as a standard.
The Strongyloides recombinant IgG-immunoreactive (SsIR) antigen was prepared as reported previously [ 4]. The purified SsIR protein was examined on a 10% SDS– PAGE. Each recombinant antigen was stored at 4 ° C before use.
CA |
Chicago Academy of Sciences |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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