Ultrasensitive Measurement of Ca2+ Influx into Lipid Vesicles Induced by Protein Aggregates. (5th May 2017)

• Record Type: Journal Article
• Authors: Flagmeier, Patrick; De, Suman; Wirthensohn, David C.; Lee, Steven F.; Vincke, Cécile; Muyldermans, Serge; Knowles, Tuomas P. J.; Gandhi, Sonia; Dobson, Christopher M.; Klenerman, David
• Is Part Of: Angewandte Chemie. Volume 129:Number 27(2017)
• Page Start: 7858
• Page End: 7862
• Publication Date: 2017-05-05
• Subjects: Alzheimer-Krankheit -- Fluoreszenzbildgebung -- Nanobiophysik -- Neurodegeneration -- Proteinaggregation; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201700966
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: To quantify and characterize the potentially toxic protein aggregates associated with neurodegenerative diseases, a high‐throughput assay based on measuring the extent of aggregate‐induced Ca 2+ entry into individual lipid vesicles has been developed. This approach was implemented by tethering vesicles containing a Ca 2+ sensitive fluorescent dye to a passivated surface and measuring changes in the fluorescence as a result of membrane disruption using total internal reflection microscopy. Picomolar concentrations of Aβ42 oligomers could be observed to induce Ca 2+ influx, which could be inhibited by the addition of a naturally occurring chaperone and a nanobody designed to bind to the Aβ peptide. We show that the assay can be used to study aggregates from other proteins, such as α‐synuclein, and to probe the effects of complex biofluids, such as cerebrospinal fluid, and thus has wide applicability.