Abstract
AbstractHere we show that MINSTED localization, a method whereby the position of a fluorophore is identified with precisely controlled beams of a STED microscope, tracks fluorophores and hence labeled biomolecules with nanometer/millisecond spatiotemporal precision. By updating the position for each detected photon, MINSTED recognizes fluorophore steps of 16 nm within <250 μs using about 13 photons. The power of MINSTED tracking is demonstrated by resolving the stepping of the motor protein kinesin-1 walking on microtubules and switching protofilaments.
Funder
German Federal Ministry of Education and Research (BMBF)
Max Planck School of Photonics supported by the BMBF, the Max Planck and the Fraunhofer Societies
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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