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Recombinant Peptide Mimetic NanoLuc Tracer for Sensitive Immunodetection of Mycophenolic Acid

dc.contributor.authorLuque Uria, Álvaro
dc.contributor.authorPeltomaa, Riikka Johanna
dc.contributor.authorNevanen, Tarja K.
dc.contributor.authorArola, Henri O.
dc.contributor.authorIljin, Kristiina
dc.contributor.authorBenito Peña, María Elena
dc.contributor.authorMoreno Bondi, María Cruz
dc.date.accessioned2023-06-16T14:18:13Z
dc.date.available2023-06-16T14:18:13Z
dc.date.issued2021-07-14
dc.descriptionCRUE-CSIC (Acuerdos Transformativos 2021)
dc.description.abstractMycophenolic acid (MPA) is an immunosuppressant drug commonly used to prevent organ rejection in transplanted patients. MPA monitoring is of great interest due to its small therapeutic window. In this work, a phage-displayed peptide library was used to select cyclic peptides that bind to the MPA-specific recombinant antibody fragment (Fab) and mimic the behavior of MPA. After biopanning, several phage-displayed peptides were isolated and tested to confirm their epitope-mimicking nature in phagebased competitive immunoassays. After identifying the best MPA mimetic (ACEGLYAHWC with a disulfide constrained loop), several immunoassay approaches were tested, and a recombinant fusion protein containing the peptide sequence with a bioluminescent enzyme, NanoLuc, was developed. The recombinant fusion enabled its direct use as the tracer in competitive immunoassays without the need for secondary antibodies or further labeling. A bioluminescent sensor, using streptavidin-coupled magnetic beads for the immobilization of the biotinylated Fab antibody, enabled the detection of MPA with a detection limit of 0.26 ng mL−1 and an IC50 of 2.9 ± 0.5 ng mL−1 . The biosensor showed good selectivity toward MPA and was applied to the analysis of the immunosuppressive drug in clinical samples, of both healthy and MPA-treated patients, followed by validation by liquid chromatography coupled to diode array detection
dc.description.departmentDepto. de Química Analítica
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/69339
dc.identifier.doi10.1021/acs.analchem.1c02109
dc.identifier.issn0003-2700
dc.identifier.officialurlhttps://doi.org/10.1021/acs.analchem.1c02109
dc.identifier.relatedurlhttps://pubs.acs.org/doi/abs/10.1021/acs.analchem.1c02109
dc.identifier.urihttps://hdl.handle.net/20.500.14352/4596
dc.issue.number29
dc.journal.titleAnalytical Chemistry
dc.language.isoeng
dc.page.final10364
dc.page.initial10358
dc.publisherACS Publications
dc.relation.projectID(RTI2018-096410-B-C21; BES-2016- 078137)
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.keywordImmunology
dc.subject.keywordViruses
dc.subject.keywordPeptides and proteins
dc.subject.keywordAssays
dc.subject.keywordBiopolymers
dc.subject.ucmQuímica analítica (Química)
dc.subject.unesco2301 Química Analítica
dc.titleRecombinant Peptide Mimetic NanoLuc Tracer for Sensitive Immunodetection of Mycophenolic Acid
dc.typejournal article
dc.volume.number93
dspace.entity.typePublication
relation.isAuthorOfPublication548d1aba-3271-45c1-ac9b-b46279a98d60
relation.isAuthorOfPublication4f6d77c5-1abc-4cab-9a5c-eacb835fce30
relation.isAuthorOfPublicationebb3e2fd-e5d5-4a84-9ce0-c9ea12eb2a85
relation.isAuthorOfPublication8766057b-6628-4a02-a6db-20bddfaf3054
relation.isAuthorOfPublication.latestForDiscovery8766057b-6628-4a02-a6db-20bddfaf3054

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