| Literature DB >> 27607692 |
Devynn M Wulstein, Kathryn E Regan, Rae M Robertson-Anderson, Ryan McGorty.
Abstract
Using light-sheet microscopy combined with digital Fourier methods we probe the dynamics of colloidal samples and DNA molecules. This combination, referred to as selective-plane illumination differential dynamic microscopy (SPIDDM), has the benefit of optical sectioning to study, with minimal photobleaching, thick samples allowing us to measure the diffusivity of colloidal particles at high volume fractions. Further, SPIDDM exploits the inherent spatially-varying thickness of Gaussian light-sheets. Where the excitation sheet is most focused, we capture high spatial frequency dynamics as the signal-to-background is high. In thicker regions, we capture the slower dynamics as diffusion out of the sheet takes longer.Year: 2016 PMID: 27607692 PMCID: PMC5946909 DOI: 10.1364/OE.24.020881
Source DB: PubMed Journal: Opt Express ISSN: 1094-4087 Impact factor: 3.894