Development of an in-solution observation method using atmospheric scanning electron microscopy (ASEM)

OGURA  Toshihiko, NISHIYAMA  Hidetoshi, SUGA  Mitsuo, Chikara  SATOU

doi:10.5571/synth.8.3_116

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大気圧電子顕微鏡ASEMによる水中観察法の開発
大気圧電子顕微鏡ASEMによる水中観察法の開発 : 半導体の超薄膜技術とバイオ顕微鏡の融合研究
タイキアツデンシケンビキョウ ASEM ニヨルスイチュウカンサツホウノカイハツ : ハンドウタイノチョウハクマクギジュツトバイオケンビキョウノユウゴウケンキュウ
ー半導体の超薄膜技術とバイオ顕微鏡の融合研究ー
— Interdisciplinary research between semiconductor fabrication technology and biological electron microscopy —

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Protein complexes in cells and tissues play critical roles in various physiological functions, including embryogenesis and signal processing. To observe the dynamics of protein complexes, high resolution and high throughput electron microscopy (EM) in aqueous solution is required. However, standard EM requires the sample to be in a vacuum. With ASEM, an inverted scanning electron microscope (SEM) observes the wet sample from beneath an open dish while an optical microscope (OM) observes it from above. The disposable dish with a silicon nitride (SiN) film window can hold a few milliliters of culture medium, allowing various types of cells to be cultured in a stable environment. This system was used for the development of in situ correlative OM/SEM immuno-microscopy in liquid. We observed a dynamic string-like gathering of STIM1 on the endoplasmic reticulum in Jurkat T cells in response to Ca²⁺ store depletion. We have also observed filamentous-actin (F-actin) and tubulin in the growth cones of primary-culture neurons as well as in synapses. We monitored in-situ electrochemical reactions in electrolytes, and melting and solidification of solder using ASEM.

Journal

Synthesiology

Synthesiology 8 (3), 116-126, 2015

National Institute of Advanced Industrial Science and Technology

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