Literature DB >> 23612657

Imaging the invisible: resolving cellular microcompartments by superresolution microscopy techniques.

Michael Hensel1, Jürgen Klingauf, Jacob Piehler.   

Abstract

Unraveling the spatio-temporal organization of dynamic cellular microcompartments requires live cell imaging techniques capable of resolving submicroscopic structures. While the resolution of traditional far-field fluorescence imaging techniques is limited by the diffraction barrier, several fluorescence-based microscopy techniques providing sub-100 nm resolution have become available during the past decade. Here, we briefly introduce the optical principles of these techniques and compare their capabilities and limitations with respect to spatial and temporal resolution as well as live cell capabilities. Moreover, we summarize how these techniques contributed to a better understanding of plasma membrane microdomains, the dynamic nanoscale organization of neuronal synapses and the sub-compartmentation of microorganisms. Based on these applications, we highlight complementarity of these techniques and their potential to address specific challenges in the context of dynamic cellular microcompartments, as well as the perspectives to overcome current limitations of these methods.

Mesh:

Year:  2013        PMID: 23612657     DOI: 10.1515/hsz-2012-0324

Source DB:  PubMed          Journal:  Biol Chem        ISSN: 1431-6730            Impact factor:   3.915


  8 in total

1.  Dynamics and organization of cortical microtubules as revealed by superresolution structured illumination microscopy.

Authors:  George Komis; Martin Mistrik; Olga Samajová; Anna Doskočilová; Miroslav Ovečka; Peter Illés; Jiri Bartek; Jozef Samaj
Journal:  Plant Physiol       Date:  2014-03-31       Impact factor: 8.340

2.  Superresolution live imaging of plant cells using structured illumination microscopy.

Authors:  George Komis; Martin Mistrik; Olga Šamajová; Miroslav Ovečka; Jiri Bartek; Jozef Šamaj
Journal:  Nat Protoc       Date:  2015-07-23       Impact factor: 13.491

3.  Analysis of ER-mitochondria contacts using correlative fluorescence microscopy and soft X-ray tomography of mammalian cells.

Authors:  Kirstin D Elgass; Elizabeth A Smith; Mark A LeGros; Carolyn A Larabell; Michael T Ryan
Journal:  J Cell Sci       Date:  2015-06-22       Impact factor: 5.285

Review 4.  The Redox Code.

Authors:  Dean P Jones; Helmut Sies
Journal:  Antioxid Redox Signal       Date:  2015-06-01       Impact factor: 8.401

Review 5.  Interferon gamma receptor: the beginning of the journey.

Authors:  Cédric M Blouin; Christophe Lamaze
Journal:  Front Immunol       Date:  2013-09-03       Impact factor: 7.561

6.  Single molecule super-resolution imaging of proteins in living Salmonella enterica using self-labelling enzymes.

Authors:  Britta Barlag; Oliver Beutel; Dennis Janning; Frederik Czarniak; Christian P Richter; Carina Kommnick; Vera Göser; Rainer Kurre; Florian Fabiani; Marc Erhardt; Jacob Piehler; Michael Hensel
Journal:  Sci Rep       Date:  2016-08-18       Impact factor: 4.379

7.  Extracting quantitative information from single-molecule super-resolution imaging data with LAMA - LocAlization Microscopy Analyzer.

Authors:  Sebastian Malkusch; Mike Heilemann
Journal:  Sci Rep       Date:  2016-10-05       Impact factor: 4.379

8.  Optical computed tomography for spatially isotropic four-dimensional imaging of live single cells.

Authors:  Laimonas Kelbauskas; Rishabh Shetty; Bin Cao; Kuo-Chen Wang; Dean Smith; Hong Wang; Shi-Hui Chao; Sandhya Gangaraju; Brian Ashcroft; Margaret Kritzer; Honor Glenn; Roger H Johnson; Deirdre R Meldrum
Journal:  Sci Adv       Date:  2017-12-06       Impact factor: 14.136

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.