Cost-efficient nanoscopy reveals nanoscale architecture of liver cells and platelets

Author:

Mao Hong1,Diekmann Robin2,Liang Hai Po H.3,Cogger Victoria C.34,Le Couteur David G.34,Lockwood Glen P.34,Hunt Nicholas J.34,Schüttpelz Mark5,Huser Thomas R.56,Chen Vivien M.37,McCourt Peter A.G.8

Affiliation:

1. Faculty of Health Sciences, Department of Medical Biology, University of Tromsø-The Arctic University of Norway, Hansine Hansens veg 18, Tromsø 9037, Norway, e-mail: marcomao1018@gmail.com

2. EMBL Heidelberg, Cell Biology and Biophysics Unit, 69117 Heidelberg, Germany

3. ANZAC Research Institute, Concord Repatriation General Hospital, Concord, NSW, Australia

4. The University of Sydney, Charles Perkins Centre, Nutritional Ecology and Physiology Lab, Sydney, NSW, Australia

5. Department of Physics, Bielefeld University, 33615 Bielefeld, Germany

6. Department of Internal Medicine and NSF Center for Biophotonics, University of California, Davis, Sacramento, CA 95817, USA

7. Department of Haematology, University of Sydney, Concord, NSW, Australia

8. Department of Medical Biology, University of Tromsø-The Arctic University of Norway, 9037 Tromsø, Norway

Abstract

AbstractSingle-molecule localization microscopy (SMLM) provides a powerful toolkit to specifically resolve intracellular structures on the nanometer scale, even approaching resolution classically reserved for electron microscopy (EM). Although instruments for SMLM are technically simple to implement, researchers tend to stick to commercial microscopes for SMLM implementations. Here we report the construction and use of a “custom-built” multi-color channel SMLM system to study liver sinusoidal endothelial cells (LSECs) and platelets, which costs significantly less than a commercial system. This microscope allows the introduction of highly affordable and low-maintenance SMLM hardware and methods to laboratories that, for example, lack access to core facilities housing high-end commercial microscopes for SMLM and EM. Using our custom-built microscope and freely available software from image acquisition to analysis, we image LSECs and platelets with lateral resolution down to about 50 nm. Furthermore, we use this microscope to examine the effect of drugs and toxins on cellular morphology.

Publisher

Walter de Gruyter GmbH

Subject

Electrical and Electronic Engineering,Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials,Biotechnology

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