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FIB-SEM Technology

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Research Ambition
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We aim to transcend the limitations of Focused Ion Beam Scanning Electron Microscopy (FIB-SEM) technology to enable large volume [1.0], high throughput [2.0], and artifact-free [3.0] isotropic high-resolution 3D imaging.

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Enhanced FIB-SEM 1.0: Enable large volume isotropic high resolution 3D imaging 

Isotropic high-resolution imaging of large volumes provides unprecedented opportunities to advance connectomics and cell biology research. Conventional Focused Ion Beam Scanning Electron Microscopy (FIB-SEM) offers unique benefits such as high resolution (< 10 nm in x, y, and z), minimal defects, and robust image alignment, well suited for superior tracing of neuronal processes and automated segmentation. However, its prevailing deficiencies in imaging speed and duration cap the maximum possible image volume. We developed innovative solutions to overcome these barriers and transformed FIB-SEM from a conventional lab tool lacking long term reliability to a robust imaging platform capable of years of continuous imaging without defects in the final image stack [Xu et al. 2017Xu et al. 2020aXu et al. 2020b].

These improvements have enabled the extension of the continuous imaged volume by more than four orders of magnitude from 103 µm3 to at least 107 µm3, while maintaining an isotropic sampling of 8 x 8 x 8 nm3 voxels. Moreover, by trading off imaging speed, the system can readily be operated at even higher resolutions achieving voxel sizes of 4 x 4 x 4 nm3. The expanded volumes enabled by this enhanced FIB-SEM technology 1.0 enable a vast new regime in scientific learning, where nano scale resolution coupled with meso and even macro scale volumes is critical. The largest connectome to date has been generated through this enhanced FIB-SEM platform [Xu et al. 2020c], where the superior z resolution empowers automated tracing of neuronal processes and reduces the time-consuming human proofreading effort. Higher resolution further improves the interpretation of otherwise ambiguous details. Nearly all organelles can be resolved and classified with whole cell imaging at 4 x 4 x 4 nm3 nm voxels. Additionally, by combining with super-resolution fluorescence imaging, CLEM applications unleash the full potential of intracellular organelle identification with labeling insights.

Drosophila hemibrain with 8 x 8 x 8 nmvoxels, generated by two Enhanced FIB-SEM systems through 13 hot-knife tabs. 

Enhanced FIB-SEM 2.0: Advance high throughput and large volume beyond 1.0

We are developing advance FIB milling processes to handle a block face up to 500 x 500 µm2, thus extending the imageable volume without hot-knife partitioning. Coupled with faster SEM imaging enabled by optimized staining protocol, a volume up to 500 x 500 x 1000 µm3 could be milled and imaged without the constraints and overheads of hot-knife partitioning approach. We expected more than five-folds of improvement in image acquisition alone, compared to the existing hot-knife method, and an order magnitude improvement in the entire pipeline throughput.

Enhanced FIB-SEM 3.0: Develop artifact-free 3D volume imaging

We start investigating  a 3D cryo-FIB-SEM technology that can reliably image a block of vitreously frozen cells or tissues with good contrast and without the need of heavy metal staining, dehydration, and plastic embedding. This rapid and approach will offer the potential to bypass the tedious EM sample preparation needed to be individually optimized for the large variety of tissues from different species. Most importantly, it allows the volume EM to unveil the fine details of cells and tissues in their native states.

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Progress in science depends on new techniques, new discoveries and new ideas, probably in that order.

Sydney Brenner
(1927-2019)

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