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A Starting Point for Fluorescence-Based Single-Molecule Measurements in Biomolecular Research

Single-molecule fluorescence techniques are ideally suited to provide information about the structure-function-dynamics relationship of a biomolecule as static and dynamic heterogeneity can be easily detected. However, what type of single-molecule fluorescence technique is suited for which kind of b...

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Autores principales: Gust, Alexander, Zander, Adrian, Gietl, Andreas, Holzmeister, Phil, Schulz, Sarah, Lalkens, Birka, Tinnefeld, Philip, Grohmann, Dina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271140/
https://www.ncbi.nlm.nih.gov/pubmed/25271426
http://dx.doi.org/10.3390/molecules191015824
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author Gust, Alexander
Zander, Adrian
Gietl, Andreas
Holzmeister, Phil
Schulz, Sarah
Lalkens, Birka
Tinnefeld, Philip
Grohmann, Dina
author_facet Gust, Alexander
Zander, Adrian
Gietl, Andreas
Holzmeister, Phil
Schulz, Sarah
Lalkens, Birka
Tinnefeld, Philip
Grohmann, Dina
author_sort Gust, Alexander
collection PubMed
description Single-molecule fluorescence techniques are ideally suited to provide information about the structure-function-dynamics relationship of a biomolecule as static and dynamic heterogeneity can be easily detected. However, what type of single-molecule fluorescence technique is suited for which kind of biological question and what are the obstacles on the way to a successful single-molecule microscopy experiment? In this review, we provide practical insights into fluorescence-based single-molecule experiments aiming for scientists who wish to take their experiments to the single-molecule level. We especially focus on fluorescence resonance energy transfer (FRET) experiments as these are a widely employed tool for the investigation of biomolecular mechanisms. We will guide the reader through the most critical steps that determine the success and quality of diffusion-based confocal and immobilization-based total internal reflection fluorescence microscopy. We discuss the specific chemical and photophysical requirements that make fluorescent dyes suitable for single-molecule fluorescence experiments. Most importantly, we review recently emerged photoprotection systems as well as passivation and immobilization strategies that enable the observation of fluorescently labeled molecules under biocompatible conditions. Moreover, we discuss how the optical single-molecule toolkit has been extended in recent years to capture the physiological complexity of a cell making it even more relevant for biological research.
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spelling pubmed-62711402018-12-27 A Starting Point for Fluorescence-Based Single-Molecule Measurements in Biomolecular Research Gust, Alexander Zander, Adrian Gietl, Andreas Holzmeister, Phil Schulz, Sarah Lalkens, Birka Tinnefeld, Philip Grohmann, Dina Molecules Review Single-molecule fluorescence techniques are ideally suited to provide information about the structure-function-dynamics relationship of a biomolecule as static and dynamic heterogeneity can be easily detected. However, what type of single-molecule fluorescence technique is suited for which kind of biological question and what are the obstacles on the way to a successful single-molecule microscopy experiment? In this review, we provide practical insights into fluorescence-based single-molecule experiments aiming for scientists who wish to take their experiments to the single-molecule level. We especially focus on fluorescence resonance energy transfer (FRET) experiments as these are a widely employed tool for the investigation of biomolecular mechanisms. We will guide the reader through the most critical steps that determine the success and quality of diffusion-based confocal and immobilization-based total internal reflection fluorescence microscopy. We discuss the specific chemical and photophysical requirements that make fluorescent dyes suitable for single-molecule fluorescence experiments. Most importantly, we review recently emerged photoprotection systems as well as passivation and immobilization strategies that enable the observation of fluorescently labeled molecules under biocompatible conditions. Moreover, we discuss how the optical single-molecule toolkit has been extended in recent years to capture the physiological complexity of a cell making it even more relevant for biological research. MDPI 2014-09-30 /pmc/articles/PMC6271140/ /pubmed/25271426 http://dx.doi.org/10.3390/molecules191015824 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Gust, Alexander
Zander, Adrian
Gietl, Andreas
Holzmeister, Phil
Schulz, Sarah
Lalkens, Birka
Tinnefeld, Philip
Grohmann, Dina
A Starting Point for Fluorescence-Based Single-Molecule Measurements in Biomolecular Research
title A Starting Point for Fluorescence-Based Single-Molecule Measurements in Biomolecular Research
title_full A Starting Point for Fluorescence-Based Single-Molecule Measurements in Biomolecular Research
title_fullStr A Starting Point for Fluorescence-Based Single-Molecule Measurements in Biomolecular Research
title_full_unstemmed A Starting Point for Fluorescence-Based Single-Molecule Measurements in Biomolecular Research
title_short A Starting Point for Fluorescence-Based Single-Molecule Measurements in Biomolecular Research
title_sort starting point for fluorescence-based single-molecule measurements in biomolecular research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271140/
https://www.ncbi.nlm.nih.gov/pubmed/25271426
http://dx.doi.org/10.3390/molecules191015824
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