Super-resolution microscopy: a brief history and new avenues

Author:

Prakash Kirti1ORCID,Diederich Benedict2ORCID,Heintzmann Rainer23ORCID,Schermelleh Lothar4ORCID

Affiliation:

1. Integrated Pathology Unit, Centre for Molecular Pathology, The Royal Marsden Trust and Institute of Cancer Research, Sutton SM2 5NG, UK

2. Leibniz Institute for Photonic Technology, Albert-Einstein-Strasse 9, 07745 Jena, Germany

3. Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich-Schiller-University, Helmholtzweg 4, 07743 Jena, Germany

4. Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK

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)'.

Funder

Wellcome Trust Strategic Award

European Research Council MSC ITN

Collaborative Research Center SFB

BMWi

Publisher

The Royal Society

Subject

General Physics and Astronomy,General Engineering,General Mathematics

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