bioRxivBiophysicsPreprint
A multimodal, correlative magnetic tweezers-TIRF platform for high-throughput single-molecule interrogations
M. Sadegh FeiziD, Jelmer P. CnosseniD, Yibulayin Wubulikasimu, Salina QuackiD, Thomas BugeaiD, Andrey O. ZupnikiD, Ranjit Kumar PrajapatiiD, Asif RakibiD, Flávia S. PapiniiD, Quinte Smitskamp, Anssi M. MalineniD, David DuliniD
Abstract
Single-molecule techniques can resolve biological reactions at unmatched detail, but their low throughput and single-modality readouts have kept them out of data-intensive pipelines such as omics and drug discovery, and beyond reach of low-yield biological systems. Here we introduce a multimodal platform integrating high-throughput magnetic tweezers with ultra-wide-and flat-field objective-based total internal reflection fluorescence, enabling simultaneous force, torque, multicolor fluorescence, and temperature-dependent measurements on up to thousands of individual molecules in parallel and in real time. We demonstrate accurate single-molecule Forster resonance energy transfer (smFRET) for prism-based spectral imaging, capture temperature-dependent hairpin folding dynamics at high temporal resolution with smFRET and use correlative torque-fluorescence measurements to unravel the open-complex formation dynamics during bacterial transcription initiation. By unifying high resolution, throughput, and multimodal readout, this platform enables multidimensional dissection of complex biomolecular reactions with high statistical confidence, unlocking single-molecule biophysics for integration with drug discovery, omics, and cryo-EM workflows.
- organism: bacteria (other)
- assay: imaging
- research focus: protein folding & dynamics
- approach: experimental assay
- Citations
- 0
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