Recent advancements in structured-illumination microscopy toward live-cell imaging

被引:62
|
作者
Hirano, Yasuhiro [1 ]
Matsuda, Atsushi [1 ,2 ]
Hiraoka, Yasushi [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, 1-3 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Natl Inst Informat & Commun Technol, Adv ICT Res Inst Kobe, Nishi Ku, Kobe, Hyogo 6512492, Japan
关键词
structured-illumination microscopy; super-resolution; temporal resolution; live-cell imaging; low illumination intensity; FLUORESCENCE MICROSCOPY; PUPIL-SEGMENTATION; DIFFRACTION-LIMIT; RESOLUTION LIMIT; ADAPTIVE OPTICS; RECONSTRUCTION; DYNAMICS; IMPROVES; EMBRYOS;
D O I
10.1093/jmicro/dfv034
中图分类号
TH742 [显微镜];
学科分类号
摘要
Fluorescence microscopy allows us to observe fluorescently labeled molecules in diverse biological processes and organelle structures within living cells. However, the diffraction limit restricts its spatial resolution to about half of its wavelength, limiting the capability of biological observation at the molecular level. Structured-illumination microscopy (SIM), a type of super-resolution microscopy, doubles the spatial resolution in all three dimensions by illuminating the sample with a patterned excitation light, followed by computer reconstruction. SIM uses a relatively low illumination power compared with other methods of super-resolution microscopy and is easily available for multicolor imaging. SIM has great potential for meeting the requirements of live-cell imaging. Recent developments in diverse types of SIM have achieved higher spatial (similar to 50 nm lateral) and temporal (similar to 100 Hz) resolutions. Here, we review recent advancements in SIM and discuss its application in noninvasive live-cell imaging.
引用
收藏
页码:237 / 249
页数:13
相关论文
共 50 条
  • [21] Assessing resolution in live cell structured illumination microscopy
    Pospisil, Jakub
    Fliegel, Karel
    Klima, Milos
    PHOTONICS, DEVICES, AND SYSTEMS VII, 2017, 10603
  • [22] Signal, noise and resolution in linear and nonlinear structured-illumination microscopy
    Ingerman, E. A.
    London, R. A.
    Heintzmann, R.
    Gustafsson, M. G. L.
    JOURNAL OF MICROSCOPY, 2019, 273 (01) : 3 - 25
  • [23] Super-Resolution Photoacoustic Microscopy Using Structured-Illumination
    Amjadian, Mohammadreza
    Mostafavi, Seyed Masood
    Chen, Jiangbo
    Kavehvash, Zahra
    Zhu, Jingyi
    Wang, Lidai
    IEEE TRANSACTIONS ON MEDICAL IMAGING, 2021, 40 (09) : 2197 - 2207
  • [24] Image reconstruction for structured-illumination microscopy with low signal level
    Chu, Kaiqin
    McMillan, Paul J.
    Smith, Zachary J.
    Yin, Jie
    Atkins, Jeniffer
    Goodwin, Paul
    Wachsmann-Hogiu, Sebastian
    Lane, Stephen
    OPTICS EXPRESS, 2014, 22 (07): : 8687 - 8702
  • [25] Predictive-focus illumination for reducing photodamage in live-cell microscopy
    Schilling, Z.
    Frank, E.
    Magidson, V.
    Wason, J.
    Loncarek, J.
    Boyer, K.
    Wen, J.
    Khodjakov, A.
    JOURNAL OF MICROSCOPY, 2012, 246 (02) : 160 - 167
  • [26] Live-cell imaging of dendritic spines by STED microscopy
    Naegerl, U. Valentin
    Willig, Katrin I.
    Hein, Birka
    Hell, Stefan W.
    Bonhoeffer, Tobias
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (48) : 18982 - 18987
  • [27] Spatially-controlled illumination microscopy: For prolonged live-cell and live-tissue imaging with extended dynamic range
    Krishnaswami, Venkataraman
    Van Noorden, Cornelis J. F.
    Manders, Erik M. M.
    Hoebe, Ron A.
    QUARTERLY REVIEWS OF BIOPHYSICS, 2016, 49
  • [28] Super-resolution microscopy in live-cell imaging
    Hedde, Per Niklas
    Gayda, Susan
    Nienhaus, Karin
    Nienhaus, G. Ulrich
    EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2011, 40 : 151 - 152
  • [29] Nonlinear structured-illumination microscopy: Wide-field fluorescence imaging with theoretically unlimited resolution
    Gustafsson, MGL
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (37) : 13081 - 13086
  • [30] Self-supervised denoising for multimodal structured illumination microscopy enables long-term super-resolution live-cell imaging
    Xingye Chen
    Chang Qiao
    Tao Jiang
    Jiahao Liu
    Quan Meng
    Yunmin Zeng
    Haoyu Chen
    Hui Qiao
    Dong Li
    Jiamin Wu
    PhotoniX, 5