Abstract
Super-resolution microscopy in the form of photoactivated localization microscopy (PALM) offers the possibility of counting single molecules in a cell, a cellular compartment or a molecular complex. PALM can, therefore, underpin molecular and biochemical processes with a numeric and stoichiometric understanding of the interacting players. Here, we introduce the physical principles underlying PALM and provide a step-by-step protocol of how to apply PALM to questions related to the biology and pathophysiology of P. falciparum and other malaria parasites.
Key words
- Single-molecule counting
- Photoactivated localization microscopy
- PALM
- PfEMP1
- STORM
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Acknowledgments
This work was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—Project number 240245660—SFB 1129 (M.L.) and SFB 807 (C.K. and M.H.)
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Karathanasis, C., Sanchez, C.P., Heilemann, M., Lanzer, M. (2022). Assessing Antigen Presentation on the Surface of Plasmodium falciparum-Infected Erythrocytes by Photoactivated Localization Microscopy (PALM). In: Jensen, A.T.R., Hviid, L. (eds) Malaria Immunology. Methods in Molecular Biology, vol 2470. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2189-9_34
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DOI: https://doi.org/10.1007/978-1-0716-2189-9_34
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