- Driouchi, Amine;
- Bretan, Mason;
- Davis, Brynmor;
- Heckert, Alec;
- Seeger, Markus;
- Silva, Maité;
- Forrest, William;
- Hsiung, Jessica;
- Tan, Jiongyi;
- Yang, Hongli;
- McSwiggen, David;
- Song, Linda;
- Sule, Askhay;
- Abaie, Behnam;
- Chen, Hanzhe;
- Chhun, Bryant;
- Conroy, Brianna;
- Elliott, Liam;
- Gonzalez, Eric;
- Ilkov, Fedor;
- Isaacs, Joshua;
- Labaria, George;
- Lagana, Michelle;
- Larsen, DeLaine;
- Margolin, Brian;
- Nguyen, Mai;
- Park, Eugene;
- Rine, Jeremy;
- Tang, Yangzhong;
- Vana, Martin;
- Wilkey, Andrew;
- Zhang, Zhengjian;
- Basham, Stephen;
- Ho, Jaclyn;
- Johnson, Stephanie;
- Klammer, Aaron;
- Lin, Kevin;
- Darzacq, Xavier;
- Betzig, Eric;
- Berman, Russell;
- Anderson, Daniel
An ideal tool for the study of cellular biology would enable the measure of molecular activity nondestructively within living cells. Single-molecule localization microscopy (SMLM) techniques, such as single-molecule tracking (SMT), enable in situ measurements in cells but have historically been limited by a necessary tradeoff between spatiotemporal resolution and throughput. Here we address these limitations using oblique line scan (OLS), a robust single-objective light-sheet-based illumination and detection modality that achieves nanoscale spatial resolution and sub-millisecond temporal resolution across a large field of view. We show that OLS can be used to capture protein motion up to 14 μm2 s-1 in living cells. We further extend the utility of OLS with in-solution SMT for single-molecule measurement of ligand-protein interactions and disruption of protein-protein interactions using purified proteins. We illustrate the versatility of OLS by showcasing two-color SMT, STORM and single-molecule fluorescence recovery after photobleaching. OLS paves the way for robust, high-throughput, single-molecule investigations of protein function required for basic research, drug screening and systems biology studies.