Abstract
One of the most popular single-molecule approaches in biological science is single-molecule fluorescence microscopy, which will be the subject of the following section of this volume. Fluorescence methods provide the sensitivity required to study biology on the single-molecule level, but they also allow access to useful measurable parameters on time and length scales relevant for the biomolecular world. Before several detailed experimental approaches will be addressed, we will first give a general overview of single-molecule fluorescence microscopy. We start with discussing the phenomenon of fluorescence in general and the history of single-molecule fluorescence microscopy. Next, we will review fluorescent probes in more detail and the equipment required to visualize them on the single-molecule level. We will end with a description of parameters measurable with such approaches, ranging from protein counting and tracking, single-molecule localization super-resolution microscopy, to distance measurements with Förster resonance energy transfer and orientation measurements with fluorescence polarization.
Original language | English |
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Title of host publication | Single Molecule Analysis |
Subtitle of host publication | Methods and Protocols |
Editors | Iddo Heller, David Dulin, Erwin J.G. Peterman |
Publisher | Humana Press Inc |
Pages | 111-132 |
Number of pages | 22 |
Edition | 3rd |
ISBN (Electronic) | 9781071633779 |
ISBN (Print) | 9781071633762, 9781071633793 |
DOIs | |
Publication status | Published - 2024 |
Publication series
Name | Methods in Molecular Biology |
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Volume | 2694 |
ISSN (Print) | 1064-3745 |
ISSN (Electronic) | 1940-6029 |
Bibliographical note
Publisher Copyright:© The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature 2024.
Funding
Thank you to the University of Jember for funding this research.
Funders | Funder number |
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Universitas Jember |
Keywords
- Confocal fluorescence
- Fluorophore
- Microscopy
- TIRF
- Wide-field epi-fluorescence