<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Volkaert L</submitter><funding>Research Foundation - Flanders</funding><pagination>725</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12650577</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(11)</volume><pubmed_abstract>The phytohormone abscisic acid (ABA) plays a central role in organizing adaptive responses in plants to various abiotic stresses, helping the plant minimize the negative impact on growth and development. Rapid and direct detection of ABA is valuable for investigating plant responses to abiotic stress. In this work, we propose a novel label-free, non-competitive immunoassay for detecting and quantifying ABA easily and rapidly using a surface plasmon resonance (SPR) biosensor. The SPR sensor chip was functionalized with a commercial anti-ABA antibody, characterized for its affinity, binding kinetics, and specificity using the same platform. The direct assay demonstrated high specificity and sensitivity, with a calculated limit of detection of 1.36 ng/mL in buffer. The new immunosensor was applied to determine ABA concentrations directly in xylem sap samples from tomato plants subjected to abiotic stress (drought and high salinity) and was able to accurately reflect ABA levels corresponding to the applied stress. The results were comparable to the reference method, ultra-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS), establishing this new immunosensor as a novel detection method for rapid and reliable monitoring of ABA levels associated with abiotic stress in tomato plants.</pubmed_abstract><journal>Biosensors</journal><pubmed_title>Label-Free Rapid Quantification of Abscisic Acid in Xylem Sap Samples Using Surface Plasmon Resonance.</pubmed_title><pmcid>PMC12650577</pmcid><funding_grant_id>1S27722N</funding_grant_id><pubmed_authors>Novak O</pubmed_authors><pubmed_authors>Schols D</pubmed_authors><pubmed_authors>Lammertyn J</pubmed_authors><pubmed_authors>Van de Poel B</pubmed_authors><pubmed_authors>Volkaert L</pubmed_authors><pubmed_authors>Noppen S</pubmed_authors><pubmed_authors>Tureckova V</pubmed_authors><pubmed_authors>Spasic D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Label-Free Rapid Quantification of Abscisic Acid in Xylem Sap Samples Using Surface Plasmon Resonance.</name><description>The phytohormone abscisic acid (ABA) plays a central role in organizing adaptive responses in plants to various abiotic stresses, helping the plant minimize the negative impact on growth and development. Rapid and direct detection of ABA is valuable for investigating plant responses to abiotic stress. In this work, we propose a novel label-free, non-competitive immunoassay for detecting and quantifying ABA easily and rapidly using a surface plasmon resonance (SPR) biosensor. The SPR sensor chip was functionalized with a commercial anti-ABA antibody, characterized for its affinity, binding kinetics, and specificity using the same platform. The direct assay demonstrated high specificity and sensitivity, with a calculated limit of detection of 1.36 ng/mL in buffer. The new immunosensor was applied to determine ABA concentrations directly in xylem sap samples from tomato plants subjected to abiotic stress (drought and high salinity) and was able to accurately reflect ABA levels corresponding to the applied stress. The results were comparable to the reference method, ultra-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS), establishing this new immunosensor as a novel detection method for rapid and reliable monitoring of ABA levels associated with abiotic stress in tomato plants.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-05-19T03:16:25.386Z</modification><creation>2026-05-19T03:11:00.781Z</creation></dates><accession>S-EPMC12650577</accession><cross_references><pubmed>41294736</pubmed><doi>10.3390/bios15110725</doi></cross_references></HashMap>