Year: 2026
Type: article
Abstract: Single-molecule techniques provide exceptional resolution of biomolecular dynamics but are limited by low throughput. Here, we present a DNA barcoding strategy that enables parallel kinetic profiling of multiple protein variants in a single experiment. Each protein is covalently linked to a unique DNA barcode, decoded through transient hybridisation of fluorescent probes distinguished by colour and binding duration. Applied to a library of 16 ClpS variants, this approach revealed ~5-fold variation in dissociation kinetics and uncovered previously unrecognised bimodal binding behaviour arising from distinct structural subpopulations. By enabling scalable, multiplexed functional characterisation at the single-molecule level, this platform provides a general framework for protein engineering, directed evolution and the development of next-generation single-molecule technologies.
Source: Nature Communications
Language: English
Subfield: Biophysics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $6,990
OpenAlex ID: W7221540290
