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Fluorescence lifetime DNA-PAINT for multiplexed super-resolution imaging of cells

Abstract:
Super-resolution microscopy (SRM) is a fast-developing field that encompasses fluorescence imaging techniques with the capability to resolve objects below the classical diffraction limit of optical resolution. Acknowledged with the Nobel prize in 2014, numerous SRM methods have meanwhile evolved and are being widely applied in biomedical research, all with specific strengths and shortcomings. While some techniques are capable of nanometre-scale molecular resolution, others are geared towards volumetric three-dimensional multi-colour or fast live-cell imaging. In this editorial review, we pick on the latest trends in the field. We start with a brief historical overview of both conceptual and commercial developments. Next, we highlight important parameters for imaging successfully with a particular super-resolution modality. Finally, we discuss the importance of reproducibility and quality control and the significance of open-source tools in microscopy. This article is part of the Theo Murphy meeting issue 'Super-resolution structured illumination microscopy (part 2)'
Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0002-2645-1390
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Role:
Author
ORCID:
0000-0002-6749-7555
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-6638-6298
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Role:
Author
ORCID:
0000-0003-4271-7897


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Funder identifier:
10.13039/501100001659
Grant:
EXC 2067/1–390729940


Publisher:
Nature Research
Journal:
Communications Biology More from this journal
Volume:
5
Issue:
1
Pages:
38-38
Article number:
38
Publication date:
2022-01-11
DOI:
EISSN:
2399-3642
ISSN:
2399-3642


Language:
English
Keywords:
Pubs id:
1562074
Local pid:
pubs:1562074
Source identifiers:
W4206382615
Deposit date:
2026-06-01
ARK identifier:
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