| Literature DB >> 34616045 |
Song Pang1, Gleb Shtengel1, C Shan Xu2, Andreas Müller3,4,5, Alex T Ritter6, Huxley K Hoffman7,8, Shin-Ya Takemura1, Zhiyuan Lu1, H Amalia Pasolli1,9, Nirmala Iyer1, Jeeyun Chung10,11, Davis Bennett1, Aubrey V Weigel1, Melanie Freeman1,12, Schuyler B van Engelenburg7, Tobias C Walther10,11,13,14, Robert V Farese10,11, Jennifer Lippincott-Schwartz1, Ira Mellman6, Michele Solimena3,4,5,15, Harald F Hess16.
Abstract
Understanding cellular architecture is essential for understanding biology. Electron microscopy (EM) uniquely visualizes cellular structures with nanometre resolution. However, traditional methods, such as thin-section EM or EM tomography, have limitations in that they visualize only a single slice or a relatively small volume of the cell, respectively. Focused ion beam-scanning electron microscopy (FIB-SEM) has demonstrated the ability to image small volumes of cellular samples with 4-nm isotropic voxels1. Owing to advances in the precision and stability of FIB milling, together with enhanced signal detection and faster SEM scanning, we have increased the volume that can be imaged with 4-nm voxels by two orders of magnitude. Here we present a volume EM atlas at such resolution comprising ten three-dimensional datasets for whole cells and tissues, including cancer cells, immune cells, mouse pancreatic islets and Drosophila neural tissues. These open access data (via OpenOrganelle2) represent the foundation of a field of high-resolution whole-cell volume EM and subsequent analyses, and we invite researchers to explore this atlas and pose questions.Entities:
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Year: 2021 PMID: 34616045 PMCID: PMC9004664 DOI: 10.1038/s41586-021-03992-4
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962