Dynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy
When <i>Saccharomyces cerevisiae</i> divides, a structure composed of different septin proteins arranged according to a certain rule is formed at the cell division site. The structure undergoes multiple remodeling stages during the cell cycle, thus guiding the yeast cells to complete the...
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2021
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oai:doaj.org-article:40d22033fd9a4a9a826ab6d29d45a6a32021-11-25T18:24:38ZDynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy10.3390/microorganisms91122552076-2607https://doaj.org/article/40d22033fd9a4a9a826ab6d29d45a6a32021-10-01T00:00:00Zhttps://www.mdpi.com/2076-2607/9/11/2255https://doaj.org/toc/2076-2607When <i>Saccharomyces cerevisiae</i> divides, a structure composed of different septin proteins arranged according to a certain rule is formed at the cell division site. The structure undergoes multiple remodeling stages during the cell cycle, thus guiding the yeast cells to complete the entire division process. Although the higher-order structure of septins can be determined using electron microscopy, the septin’s dynamic processes are poorly understood because of limitations in living cell super-resolution imaging technology. Herein, we describe a high lateral resolution and temporal resolution technique, known as fast fluctuation-enhanced structured illumination microscopy (fFE-SIM), which more than doubles the SIM resolution at a frame rate of 38 Hz in living cells. This allows a highly dynamic and sparse septin structure to be observed in <i>Saccharomyces cerevisiae</i>.Longfang YaoLi ZhangLiwen ChenXingyu GongJiahui ZhongBaoju WangYiyan FeiLan MiJiong MaMDPI AGarticleCDC12septinSRRFSIMsuper-resolution microscopyliving-cell imageBiology (General)QH301-705.5ENMicroorganisms, Vol 9, Iss 2255, p 2255 (2021) |
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CDC12 septin SRRF SIM super-resolution microscopy living-cell image Biology (General) QH301-705.5 |
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CDC12 septin SRRF SIM super-resolution microscopy living-cell image Biology (General) QH301-705.5 Longfang Yao Li Zhang Liwen Chen Xingyu Gong Jiahui Zhong Baoju Wang Yiyan Fei Lan Mi Jiong Ma Dynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy |
description |
When <i>Saccharomyces cerevisiae</i> divides, a structure composed of different septin proteins arranged according to a certain rule is formed at the cell division site. The structure undergoes multiple remodeling stages during the cell cycle, thus guiding the yeast cells to complete the entire division process. Although the higher-order structure of septins can be determined using electron microscopy, the septin’s dynamic processes are poorly understood because of limitations in living cell super-resolution imaging technology. Herein, we describe a high lateral resolution and temporal resolution technique, known as fast fluctuation-enhanced structured illumination microscopy (fFE-SIM), which more than doubles the SIM resolution at a frame rate of 38 Hz in living cells. This allows a highly dynamic and sparse septin structure to be observed in <i>Saccharomyces cerevisiae</i>. |
format |
article |
author |
Longfang Yao Li Zhang Liwen Chen Xingyu Gong Jiahui Zhong Baoju Wang Yiyan Fei Lan Mi Jiong Ma |
author_facet |
Longfang Yao Li Zhang Liwen Chen Xingyu Gong Jiahui Zhong Baoju Wang Yiyan Fei Lan Mi Jiong Ma |
author_sort |
Longfang Yao |
title |
Dynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy |
title_short |
Dynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy |
title_full |
Dynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy |
title_fullStr |
Dynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy |
title_full_unstemmed |
Dynamic Structure of Yeast Septin by Fast Fluctuation-Enhanced Structured Illumination Microscopy |
title_sort |
dynamic structure of yeast septin by fast fluctuation-enhanced structured illumination microscopy |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/40d22033fd9a4a9a826ab6d29d45a6a3 |
work_keys_str_mv |
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