Literature DB >> 34327271

Building a Total Internal Reflection Microscope (TIRF) with Active Stabilization (Feedback SMLM).

Simao Coelho1,2,3, Jongho Baek1,2, J Justin Gooding4,5, Katharina Gaus1,2.   

Abstract

The data quality of high-resolution imaging can be markedly improved with active stabilization, which is based on feedback loops within the microscope that maintain the sample in the same location throughout the experiment. The purpose is to provide a highly accurate focus lock, therefore eliminating drift and improving localization precision. Here, we describe a step-by-step protocol for building a total internal reflection microscope combined with the feedback loops necessary for sample and detection stabilization, which we routinely use in single-molecule localization microscopy (SMLM). The performance of the final microscope with feedback loops, called feedback SMLM, has previously been described. We demonstrate how to build a replica of our system and include a list of the necessary optical components, tips, and an alignment strategy.
Copyright © 2021 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Active stabilization; Biophysics; Drift correction; Localization microscopy; Single-molecule imaging; TIRF microscopy

Year:  2021        PMID: 34327271      PMCID: PMC8292130          DOI: 10.21769/BioProtoc.4074

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  23 in total

Review 1.  Total internal reflection fluorescence microscopy in cell biology.

Authors:  D Axelrod
Journal:  Traffic       Date:  2001-11       Impact factor: 6.215

2.  Three-dimensional super-resolution imaging by stochastic optical reconstruction microscopy.

Authors:  Bo Huang; Wenqin Wang; Mark Bates; Xiaowei Zhuang
Journal:  Science       Date:  2008-01-03       Impact factor: 47.728

3.  Highly inclined thin illumination enables clear single-molecule imaging in cells.

Authors:  Makio Tokunaga; Naoko Imamoto; Kumiko Sakata-Sogawa
Journal:  Nat Methods       Date:  2008-01-06       Impact factor: 28.547

4.  Visualization of small GTPase activity with fluorescence resonance energy transfer-based biosensors.

Authors:  Kazuhiro Aoki; Michiyuki Matsuda
Journal:  Nat Protoc       Date:  2009-10-15       Impact factor: 13.491

5.  A high speed multifocal multiphoton fluorescence lifetime imaging microscope for live-cell FRET imaging.

Authors:  Simon P Poland; Nikola Krstajić; James Monypenny; Simao Coelho; David Tyndall; Richard J Walker; Viviane Devauges; Justin Richardson; Neale Dutton; Paul Barber; David Day-Uei Li; Klaus Suhling; Tony Ng; Robert K Henderson; Simon M Ameer-Beg
Journal:  Biomed Opt Express       Date:  2015-01-06       Impact factor: 3.732

6.  3D active stabilization for single-molecule imaging.

Authors:  Simao Coelho; Jongho Baek; James Walsh; J Justin Gooding; Katharina Gaus
Journal:  Nat Protoc       Date:  2020-12-02       Impact factor: 13.491

7.  3D single-molecule super-resolution microscopy with a tilted light sheet.

Authors:  Anna-Karin Gustavsson; Petar N Petrov; Maurice Y Lee; Yoav Shechtman; W E Moerner
Journal:  Nat Commun       Date:  2018-01-09       Impact factor: 14.919

8.  NicoLase-An open-source diode laser combiner, fiber launch, and sequencing controller for fluorescence microscopy.

Authors:  Philip R Nicovich; James Walsh; Till Böcking; Katharina Gaus
Journal:  PLoS One       Date:  2017-03-16       Impact factor: 3.240

9.  Ultraprecise single-molecule localization microscopy enables in situ distance measurements in intact cells.

Authors:  Simao Coelho; Jongho Baek; Matthew S Graus; James M Halstead; Philip R Nicovich; Kristen Feher; Hetvi Gandhi; J Justin Gooding; Katharina Gaus
Journal:  Sci Adv       Date:  2020-04-17       Impact factor: 14.136

10.  Adaptive optics for a time-resolved Förster resonance energy transfer (FRET) and fluorescence lifetime imaging microscopy (FLIM) in vivo.

Authors:  Simao Coelho; Simon P Poland; Viviane Devauges; Simon M Ameer-Beg
Journal:  Opt Lett       Date:  2020-05-15       Impact factor: 3.776

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