Here we present a technique called single-molecule high-resolution colocalization (SHREC) of fluorescent dyes that allows the measurement of interfluorophore distances in macromolecules and macromolecular complexes with better than 10-nm resolution. By using two chromatically differing fluorescent molecules as probes, we are able to circumvent the Rayleigh criterion and measure distances much smaller than 250 nm. The probes are imaged separately and localized individually with high precision. The registration between the two imaging channels is measured by using fiduciary markers, and the centers of the two probes are mapped onto the same space. Multiple measurements can be made before the fluorophores photobleach, allowing intramolecular and intermolecular distances to be tracked through time. This technique's lower resolution limit lies at the upper resolution limit of single molecule FRET (smFRET) microscopy. The instrumentation and fluorophores used for SHREC can also be used for smFRET, allowing the two types of measurements to be made interchangeably, covering a wide range of interfluorophore distances. A dual-labeled duplex DNA molecule (30 bp) was used as a 10-nm molecular ruler to confirm the validity of the method. We also used SHREC to study the motion of myosin V. We directly observed myosin V's alternating heads while it walked hand-over-hand along an actin filament.centroid tracking ͉ dynamic conformational changes ͉ fluorescence ͉ molecular motors ͉ total internal reflection microscopy S ingle molecule fluorescence techniques are bridging the areas of structural biology and biochemistry (1). They yield structural constraints for an enzyme during its biochemical cycle. To probe close to this interface between structure and function, distances must be resolved on the order of the size of the enzyme. However, far field fluorescence microscopy is limited in its resolution by the Rayleigh criterion at Ϸ250 nm. On the other end of the size spectrum, single molecule FRET (smFRET) provides a way to estimate intramolecular distances Ͻ10 nm and has yielded insights on a range of biological molecules from the Tetrahymena ribozyme to the ribosome (2-4).Recent methods, single-molecule high-resolution imaging with photobleaching (SHRImP) and nanometer-localized multiple single-molecule (NALMS), have been developed in an attempt to bridge this ''gap'' in distance resolution. These methods are capable of measuring an intramolecular distance to high precision, but only once, because of the intrinsic destruction of one of the probes (5, 6). A time series of the intramolecular distance is not possible with these methods, removing one of the greatest potential benefits of single molecule imaging.Addressing the gap in imaging techniques suitable for studying macromolecules, we introduce a technique, single-molecule high-resolution colocalization (SHREC) of fluorescent probes, that can precisely measure intramolecular and intermolecular distances through time. By separately imaging two chromatically different fluoropho...
In long-range transport of cargo, prototypical kinesin-1 steps along a single protofilament on the microtubule, an astonishing behavior given the number of theoretically available binding sites on adjacent protofilaments. Using a laser trap assay, we analyzed the trajectories of several representatives from the kinesin-2 class on freely suspended microtubules. In stark contrast to kinesin-1, these motors display a wide range of left-handed spiraling around microtubules and thus generate torque during cargo transport. We provide direct evidence that kinesin's neck region determines the torque-generating properties. A model system based on kinesin-1 corroborates this result: disrupting the stability of the neck by inserting flexible peptide stretches resulted in pronounced left-handed spiraling. Mimicking neck stability by crosslinking significantly reduced the spiraling of the motor up to the point of protofilament tracking. Finally, we present a model that explains the physical basis of kinesin's spiraling around the microtubule.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.