Abstract
We have developed a method for performing light-sheet microscopy with a single high numerical aperture lens by integrating reflective side walls into a microfluidic chip. These 45° side walls generate light-sheet illumination by reflecting a vertical light-sheet into the focal plane of the objective. Light-sheet illumination of cells loaded in the channels increases image quality in diffraction limited imaging via reduction of out-of-focus background light. Single molecule super-resolution is also improved by the decreased background resulting in better localization precision and decreased photo-bleaching, leading to more accepted localizations overall and higher quality images. Moreover, 2D and 3D single molecule super-resolution data can be acquired faster by taking advantage of the increased illumination intensities as compared to wide field, in the focused light-sheet.
| Original language | English |
|---|---|
| Pages (from-to) | 2219-36 |
| Number of pages | 18 |
| Journal | Biomedical optics express |
| Volume | 7 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 1 Jun 2016 |
| Externally published | Yes |