Back to Search Start Over

In-plate recapturing of a dual-tagged recombinant Fasciola antigen (FhLAP) by a monoclonal antibody (US9) prevents non-specific binding in ELISA

Authors :
Marta González-Warleta
Victoria Martínez-Sernández
Mercedes Mezo
F. Romarís
Ana Hernández-González
M.J. Perteguer
Teresa Gárate
Florencio M. Ubeira
Esperanza Paniagua
Ricardo A. Orbegozo-Medina
Ministerio de Economía y Competitividad (España)
Ministerio de Economía, Industria y Competitividad (España)
Gobierno de Galicia
Source :
PLOS ONE, PLoS ONE, Vol 14, Iss 2, p e0211035 (2019), Repisalud, Instituto de Salud Carlos III (ISCIII), PLoS ONE
Publication Year :
2019
Publisher :
Public Library of Science (PLoS), 2019.

Abstract

Recombinant proteins expressed in E. coli are frequently purified by immobilized metal affinity chromatography (IMAC). By means of this technique, tagged proteins containing a polyhistidine sequence can be obtained up to 95% pure in a single step, but some host proteins also bind with great affinity to metal ions and contaminate the sample. A way to overcome this problem is to include a second tag that is recognized by a preexistent monoclonal antibody (mAb) in the gene encoding the target protein, allowing further purification. With this strategy, the recombinant protein can be directly used as target in capture ELISA using plates sensitized with the corresponding mAb. As a proof of concept, in this study we engineered a Trichinella-derived tag (MTFSVPIS, recognized by mAb US9) into a His-tagged recombinant Fasciola antigen (rFhLAP) to make a new chimeric recombinant protein (rUS9-FhLAP), and tested its specificity in capture and indirect ELISAs with sera from sheep and cattle. FhLAP was selected since it was previously reported to be immunogenic in ruminants and is expressed in soluble form in E. coli, which anticipates a higher contamination by host proteins than proteins expressed in inclusion bodies. Our results showed that a large number of sera from non-infected ruminants (mainly cattle) reacted in indirect ELISA with rUS9-FhLAP after single-step purification by IMAC, but that this reactivity disappeared testing the same antigen in capture ELISA with mAb US9. These results demonstrate that the 6XHis and US9 tags can be combined when double purification of recombinant proteins is required. This work was supported by: Ministerio de Economía y Competitividad (Spain) [grant number AGL2011-30563-C03 and AGL2014-57125R], Ministerio de Economía, Industria y Competitividad (INIA, Spain) [grants numbers RTA2017-00010-C02-01 and RTA2017-00010-C02-02] and the Consellería de Cultura, Educación e Ordenación Universitaria (Xunta de Galicia, Spain) [grant number ED431B 2017/18]. RAOM holds a predoctoral fellowship from the Spanish Ministerio de Economía y Competitividad (Programa de Formación de Personal Investigador). VMS is supported by a contract under the grant ED431B 2017/18. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Sí

Details

ISSN :
19326203 and 20113056
Volume :
14
Issue :
2
Database :
OpenAIRE
Journal :
PLOS ONE
Accession number :
edsair.doi.dedup.....54b7f95c381b07127c3de3d78c52efed
Full Text :
https://doi.org/10.1371/journal.pone.0211035