Affiliation: | 1. Department of Internal Medicine, Section of Infectious Diseases, Yale University School of Medicine, 333 Cedar Street, New Haven, CT, 06520-8056 USA;2. Department of Cell Biology, Yale University School of Medicine, 333 Cedar Street, New Haven, CT, 06520-8002 USA;3. Department of Statistics and Data Science, Cornell University, Ithaca, NY, USA;4. Department of Cell Biology, Yale University School of Medicine, 333 Cedar Street, New Haven, CT, 06520-8002 USA Nanobiology Institute, Yale University, 850 West Campus Drive, West Haven, CT, 06516 USA |
Abstract: | The examination of the complex cell biology of the human malaria parasite Plasmodium falciparum usually relies on the time-consuming generation of transgenic parasites. Here, metabolic labeling and click chemistry are employed as a fast transfection-independent method for the microscopic examination of protein S-palmitoylation, an important post-translational modification during the asexual intraerythrocytic replication of P. falciparum. Applying various microscopy approaches such as confocal, single-molecule switching, and electron microscopy, differences in the extent of labeling within the different asexual developmental stages of P. falciparum and the host erythrocytes over time are observed. |