3D imaging of diatoms with ion-abrasion scanning electron microscopy

被引:56
作者
Hildebrand, Mark [1 ]
Kim, Sang [2 ]
Shi, Dan [2 ]
Scott, Keana [3 ]
Subramaniam, Sriram [2 ]
机构
[1] Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA
[2] NCI, Cell Biol Lab, NIH, Bethesda, MD 20817 USA
[3] Natl Inst Stand & Technol, Gaithersburg, MD 20899 USA
关键词
Diatom; Ion-abrasion SEM; Biomineral structure formation; Biosilicification; 3D tomography; SILICA SHELL FORMATION; THALASSIOSIRA-PSEUDONANA; CELL-WALL; VALVE MORPHOGENESIS; CENTRIC DIATOM; MICROTUBULE CENTER; FINE-STRUCTURE; BIOSILICA; METABOLISM; MORPHOLOGY;
D O I
10.1016/j.jsb.2009.02.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ion-abrasion scanning electron microscopy (IASEM) takes advantage of focused ion beams to abrade thin sections from the surface of bulk specimens, coupled with SEM to image the surface of each section, enabling 3D reconstructions of subcellular architecture at similar to 30 nm resolution. Here, we report the first application of IASEM for imaging a biomineralizing organism, the marine diatom Thalassiosira pseudonana. Diatoms have highly patterned silica-based cell wall structures that are unique models for the study and application of directed nanomaterials synthesis by biological systems. Our study provides new insights into the architecture and assembly principles of both the "hard" (siliceous) and "soft" (organic) components of the cell. From 3D reconstructions of developmentally synchronized diatoms captured at different stages, we show that both micro- and nanoscale siliceous structures can be visualized at specific stages in their formation. We show that not only are structures visualized in a whole-cell context, but demonstrate that fragile, early-stage structures are visible, and that this can be combined with elemental mapping in the exposed slice. We demonstrate that the 3D architectures of silica structures, and the cellular components that mediate their creation and positioning can be visualized simultaneously, providing new opportunities to study and manipulate mineral nanostructures in a genetically tractable system. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:316 / 328
页数:13
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