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Real-time volumetric microscopy of in-vivo dynamics and large-scale samples with SCAPE 2.0

The limited per-pixel bandwidth of most microscopy methods requires compromises between field of view, sampling density and imaging speed. This limitation constrains studies involving complex motion or fast cellular signaling, and presents a major bottleneck for high-throughput structural imaging. H...

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Detalles Bibliográficos
Autores principales: Voleti, Venkatakaushik, Patel, Kripa B., Li, Wenze, Campos, Citlali Perez, Bharadwaj, Srinidhi, Yu, Hang, Ford, Caitlin, Casper, Malte J., Yan, Richard Wenwei, Liang, Wenxuan, Wen, Chentao, Kimura, Koutarou D., Targoff, Kimara L., Hillman, Elizabeth M.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6885017/
https://www.ncbi.nlm.nih.gov/pubmed/31562489
http://dx.doi.org/10.1038/s41592-019-0579-4
Descripción
Sumario:The limited per-pixel bandwidth of most microscopy methods requires compromises between field of view, sampling density and imaging speed. This limitation constrains studies involving complex motion or fast cellular signaling, and presents a major bottleneck for high-throughput structural imaging. Here, we combine high-speed intensified camera technology with a versatile, reconfigurable and dramatically improved Swept, Confocally Aligned Planar Excitation (SCAPE) microscope design that can achieve high-resolution volumetric imaging at over 300 volumes-per-second and over 1.2 GHz pixel rates. We demonstrate near-isotropic sampling in freely moving C. elegans, and analyze real-time blood flow and calcium dynamics in the beating zebrafish heart. The same system also permits high-throughput structural imaging of mounted, intact, cleared and expanded samples. SCAPE 2.0’s significantly lower photodamage compared to point-scanning techniques is also confirmed. Our results demonstrate that SCAPE 2.0 is a powerful, yet accessible imaging platform for myriad emerging high-speed dynamic and high-throughput volumetric microscopy applications.