Forster resonance energy transfer and protein-induced fluorescence enhancement as synergetic multiscale molecular rulersPloetz, E., Lerner, E., Husada, F., Roelfs, M., Chung, S., Hohlbein, J., Weiss, S. & Cordes, T., 19-Sep-2016, In : Scientific Reports. 6, 18 p., 33257.
Research output: Contribution to journal › Article › Academic › peer-review
Advanced microscopy methods allow obtaining information on (dynamic) conformational changes in biomolecules via measuring a single molecular distance in the structure. It is, however, extremely challenging to capture the full depth of a three-dimensional biochemical state, binding-related structural changes or conformational cross-talk in multi-protein complexes using one-dimensional assays. In this paper we address this fundamental problem by extending the standard molecular ruler based on Forster resonance energy transfer (FRET) into a two-dimensional assay via its combination with protein-induced fluorescence enhancement (PIFE). We show that donor brightness (via PIFE) and energy transfer efficiency (via FRET) can simultaneously report on e.g., the conformational state of double stranded DNA (dsDNA) following its interaction with unlabelled proteins (BamHI, EcoRV, and T7 DNA polymerase gp5/trx). The PIFE-FRET assay uses established labelling protocols and single molecule fluorescence detection schemes (alternating-laser excitation, ALEX). Besides quantitative studies of PIFE and FRET ruler characteristics, we outline possible applications of ALEX-based PIFE-FRET for single-molecule studies with diffusing and immobilized molecules. Finally, we study transcription initiation and scrunching of E. coli RNA-polymerase with PIFE-FRET and provide direct evidence for the physical presence and vicinity of the polymerase that causes structural changes and scrunching of the transcriptional DNA bubble.
|Number of pages||18|
|Publication status||Published - 19-Sep-2016|
- ALTERNATING-LASER EXCITATION, SINGLE-STRANDED-DNA, PHOTOINDUCED ELECTRON-TRANSFER, RNA-POLYMERASE PROCEEDS, CONFORMATIONAL DYNAMICS, T7 DNA, CORRELATION SPECTROSCOPY, INTRAMOLECULAR PHOTOSTABILIZATION, ABORTIVE INITIATION, STRUCTURAL DYNAMICS