4.5 Article

Simultaneous Multicolor Single-Molecule Tracking with Single-Laser Excitation via Spectral Imaging

Journal

BIOPHYSICAL JOURNAL
Volume 114, Issue 2, Pages 301-310

Publisher

CELL PRESS
DOI: 10.1016/j.bpj.2017.11.013

Keywords

-

Categories

Funding

  1. Damon Runyon Cancer Research Foundation
  2. FEI company
  3. M.J. Murdock Charitable Trust
  4. Oregon Health and Science University Knight Cancer Institute
  5. NIH [U54CA163123]
  6. Office of Science, part of the U.S. Department of Energy [DE-AC02-05CH11231]
  7. Office of Biological and Environmental Research, part of the U.S. Department of Energy [DE-AC02-05CH11231]
  8. W. M. Keck Foundation
  9. Department of the Army award [W81XWH-07-1-0663]

Ask authors/readers for more resources

Single-molecule tracking (SMT) offers rich information on the dynamics of underlying biological processes, but multicolor SMT has been challenging due to spectral cross talk and a need for multiple laser excitations. Here, we describe a single-molecule spectral imaging approach for live-cell tracking of multiple fluorescent species at once using a single-laser excitation. Fluorescence signals from all the molecules in the field of view are collected using a single objective and split between positional and spectral channels. Images of the same molecule in the two channels are then combined to determine both the location and the identity of the molecule. The single-objective configuration of our approach allows for flexible sample geometry and the use of a live-cell incubation chamber required for live-cell SMT. Despite a lower photon yield, we achieve excellent spatial (20-40 nm) and spectral (10-15 nm) resolutions comparable to those obtained with dual-objective, spectrally resolved Stochastic Optical Reconstruction Microscopy. Furthermore, motions of the fluorescent molecules did not cause loss of spectral resolution owing to the dual-channel spectral calibration. We demonstrate SMT in three (and potentially more) colors using spectrally proximal fluorophores and single-laser excitation, and show that trajectories of each species can be reliably extracted with minimal cross talk.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available