Super-resolution microscopy and studies of peroxisomes

被引:5
作者
Galiani, Silvia [4 ]
Eggeling, Christian [1 ,2 ,3 ,4 ,5 ]
Reglinski, Katharina [1 ,3 ,6 ]
机构
[1] Leibniz Inst Photon Technol e V, Albert Einstein Str 9, D-07745 Jena, Germany
[2] Leibniz Ctr Photon Infect Res LPI, Leibniz, Germany
[3] Friedrich Schiller Univ Jena, Inst Appl Opt & Biophys, Max Wien Pl 1, D-07743 Jena, Germany
[4] Univ Oxford, Weatherall Inst Mol Med, Human Immunol Unit, Headley Way, Oxford OX3 9DS, England
[5] Jena Ctr Soft Matter, Philosophenweg 7, D-07743 Jena, Germany
[6] Univ Clin Jena, Bachstr 18, D-07743 Jena, Germany
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
peroxisomes; STED; super-resolution microscopy; EXPANSION MICROSCOPY; FLUORESCENCE MICROSCOPY; RESOLUTION; ILLUMINATION; LIVE; NANOSCOPY; PROTEINS; CELLS; TRACKING; REVEALS;
D O I
10.1515/hsz-2022-0314
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
Fluorescence microscopy is an important tool for studying cellular structures such as organelles. Unfortunately, many details in the corresponding images are hidden due to the resolution limit of conventional lens-based far-field microscopy. An example is the study of peroxisomes, where important processes such as molecular organization during protein important can simply not be studied with conventional far-field microscopy methods. A remedy is super-resolution fluorescence microscopy, which is nowadays a well-established technique for the investigation of inner-cellular structures but has so far to a lesser extent been applied to the study of peroxisomes. To help advancing the latter, we here give an overview over the different super-resolution microscopy approaches and their potentials and challenges in cell-biological research, including labelling issues and a focus on studies on peroxisomes. Here, we also highlight experiments beyond simple imaging such as observations of diffusion dynamics of peroxisomal proteins.
引用
收藏
页码:87 / 106
页数:20
相关论文
共 123 条
[1]  
Abbe E., 1873, Arch. Mikroskopische Anat, V9, P413, DOI [10.1007/BF02956173, DOI 10.1007/BF02956173]
[2]   The 2018 correlative microscopy techniques roadmap [J].
Ando, Toshio ;
Bhamidimarri, Satya Prathyusha ;
Brending, Niklas ;
Colin-York, H. ;
Collinson, Lucy ;
De Jonge, Niels ;
de Pablo, P. J. ;
Debroye, Elke ;
Eggeling, Christian ;
Franck, Christian ;
Fritzsche, Marco ;
Gerritsen, Hans ;
Giepmans, Ben N. G. ;
Grunewald, Kay ;
Hofkens, Johan ;
Hoogenboom, Jacob P. ;
Janssen, Kris P. F. ;
Kaufman, Rainer ;
Klumpermann, Judith ;
Kurniawan, Nyoman ;
Kusch, Jana ;
Liv, Nalan ;
Parekh, Viha ;
Peckys, Diana B. ;
Rehfeldt, Florian ;
Reutens, David C. ;
Roeffaers, Maarten B. J. ;
Salditt, Tim ;
Schaap, Iwan A. T. ;
Schwarz, Ulrich S. ;
Verkade, Paul ;
Vogel, Michael W. ;
Wagner, Richard ;
Winterhalter, Mathias ;
Yuan, Haifeng ;
Zifarelli, Giovanni .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 2018, 51 (44)
[3]  
[Anonymous], 2021, Introduction to Inverse Problems in Imaging, DOI DOI 10.1201/9781003032755
[4]   SUPER-RESOLUTION APERTURE SCANNING MICROSCOPE [J].
ASH, EA ;
NICHOLLS, G .
NATURE, 1972, 237 (5357) :510-&
[5]   Biological Insight from Super-Resolution Microscopy: What We Can Learn from Localization-Based Images [J].
Baddeley, David ;
Bewersdorf, Joerg .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 87, 2018, 87 :965-989
[6]   ENHANCEMENT OF AXIAL RESOLUTION IN FLUORESCENCE MICROSCOPY BY STANDING-WAVE EXCITATION [J].
BAILEY, B ;
FARKAS, DL ;
TAYLOR, DL ;
LANNI, F .
NATURE, 1993, 366 (6450) :44-48
[7]   Nanometer resolution imaging and tracking of fluorescent molecules with minimal photon fluxes [J].
Balzarotti, Francisco ;
Eilers, Yvan ;
Gwosch, Klaus C. ;
Gynna, Arvid H. ;
Westphal, Volker ;
Stefani, Fernando D. ;
Elf, Johan ;
Hell, Stefan W. .
SCIENCE, 2017, 355 (6325) :606-612
[8]   Varying label density allows artifact-free analysis of membrane-protein nanoclusters [J].
Baumgart, Florian ;
Arnold, Andreas M. ;
Leskovar, Konrad ;
Staszek, Kaj ;
Foelser, Martin ;
Weghuber, Julian ;
Stockinger, Hannes ;
Schuetz, Gerhard J. .
NATURE METHODS, 2016, 13 (08) :661-+
[9]   3-DIMENSIONAL IMAGE-RESTORATION AND SUPERRESOLUTION IN FLUORESCENCE CONFOCAL MICROSCOPY [J].
BERTERO, M ;
BOCCACCI, P ;
BRAKENHOFF, GJ ;
MALFANTI, F ;
VANDERVOORT, HTM .
JOURNAL OF MICROSCOPY, 1990, 157 :3-20
[10]  
Betzig E., 2014, CHEM UNSERER ZEIT, V48, P425