Related Experiment Video
Updated: Aug 1, 2026

Detection of Post-translational Modifications on Native Intact Nucleosomes by ELISA
Published on: April 26, 2011
Label-free electronic detection of peptide post-translational modification with functional enzyme-driven assay at the
Eleonora Macchia1,2, Kim Björkström1, Amit Tewari1
1Physics and Center for Functional Materials, Faculty of Science and Engineering, Åbo Akademi University, 20500 Turku, Finland.
Abstract:
High-performance, ultra-sensitive, and universal protein post-translational modification (PTM) and protein-protein interaction (PPI) technologies are eagerly pursued in the pharmaceutical industry and bioanalytical research. Novel PTM and PPI detection methods outperform traditional assays in scope and scalability, enabling the collection of information on multiple biochemical targets. Detecting peptides and proteins at the single-molecule level is done by utilizing nanosized transducing elements and assaying solutions at very high analyte concentrations, in the nanomolar range or higher. Here, a proof of principle of a biosensing platform for single-molecule PTM detection is demonstrated. This platform is based on the single molecule with a large transistor (SiMoT) technology, encompassing a millimeter-sized electrolyte-gated organic field-effect transistor, for label-free PTM detection with a zeptomolar limit of detection. Sensitivity is improved 106- to 1012-fold compared with mass-spectrometry and luminescence-based assay methods. A functional assay for detecting enzyme-driven peptide PTMs in the zeptomolar concentration range is demonstrated using multivariate data processing, opening the way for future applications to monitor PTMs.

