» Articles » PMID: 20705899

Fast Live Simultaneous Multiwavelength Four-dimensional Optical Microscopy

Abstract

Live fluorescence microscopy has the unique capability to probe dynamic processes, linking molecular components and their localization with function. A key goal of microscopy is to increase spatial and temporal resolution while simultaneously permitting identification of multiple specific components. We demonstrate a new microscope platform, OMX, that enables subsecond, multicolor four-dimensional data acquisition and also provides access to subdiffraction structured illumination imaging. Using this platform to image chromosome movement during a complete yeast cell cycle at one 3D image stack per second reveals an unexpected degree of photosensitivity of fluorophore-containing cells. To avoid perturbation of cell division, excitation levels had to be attenuated between 100 and 10,000× below the level normally used for imaging. We show that an image denoising algorithm that exploits redundancy in the image sequence over space and time allows recovery of biological information from the low light level noisy images while maintaining full cell viability with no fading.

Citing Articles

Single-shot quantitative phase microscopy: a multi-functional tool for cell analysis.

Espinosa-Momox A, Norton B, Cywinska M, Evans B, Vivero-Escoto J, Porras-Aguilar R Biomed Opt Express. 2024; 15(10):5999-6009.

PMID: 39421775 PMC: 11482191. DOI: 10.1364/BOE.533091.


In vivo organoid growth monitoring by stimulated Raman histology.

Sarri B, Chevrier V, Poizat F, Heuke S, Franchi F, De Franqueville L Npj Imaging. 2024; 2(1):18.

PMID: 38948153 PMC: 11213706. DOI: 10.1038/s44303-024-00019-1.


Observing ER Dynamics over Long Timescales Using Light Sheet Fluorescence Microscopy.

Pain C, Kriechbaumer V, Candeo A Methods Mol Biol. 2024; 2772:323-335.

PMID: 38411826 DOI: 10.1007/978-1-0716-3710-4_25.


Optogenetic control of YAP reveals a dynamic communication code for stem cell fate and proliferation.

Meyer K, Lammers N, Bugaj L, Garcia H, Weiner O Nat Commun. 2023; 14(1):6929.

PMID: 37903793 PMC: 10616176. DOI: 10.1038/s41467-023-42643-2.


Optimal sparsity allows reliable system-aware restoration of fluorescence microscopy images.

Mandracchia B, Liu W, Hua X, Forghani P, Lee S, Hou J Sci Adv. 2023; 9(35):eadg9245.

PMID: 37647399 PMC: 10468132. DOI: 10.1126/sciadv.adg9245.


References
1.
Malone C, Misner L, Le Bot N, Tsai M, Campbell J, Ahringer J . The C. elegans hook protein, ZYG-12, mediates the essential attachment between the centrosome and nucleus. Cell. 2003; 115(7):825-36. DOI: 10.1016/s0092-8674(03)00985-1. View

2.
Yokoe H, Meyer T . Spatial dynamics of GFP-tagged proteins investigated by local fluorescence enhancement. Nat Biotechnol. 1996; 14(10):1252-6. DOI: 10.1038/nbt1096-1252. View

3.
Weinert T, Hartwell L . The RAD9 gene controls the cell cycle response to DNA damage in Saccharomyces cerevisiae. Science. 1988; 241(4863):317-22. DOI: 10.1126/science.3291120. View

4.
Shaner N, Steinbach P, Tsien R . A guide to choosing fluorescent proteins. Nat Methods. 2005; 2(12):905-9. DOI: 10.1038/nmeth819. View

5.
Boulanger J, Kervrann C, Bouthemy P . Space-time adaptation for patch-based image sequence restoration. IEEE Trans Pattern Anal Mach Intell. 2007; 29(6):1096-102. DOI: 10.1109/TPAMI.2007.1064. View