PT  - JOURNAL ARTICLE
AU  - Zehavit Shapira
AU  - Nurit Degani-Katzav
AU  - Shimon Yudovich
AU  - Asaf Grupi
AU  - Shimon Weiss
TI  - Optical Probing of Local Membrane Potential with Fluorescent Polystyrene Beads
AID  - 10.1101/2021.04.21.440831
DP  - 2021 Jan 01
TA  - bioRxiv
PG  - 2021.04.21.440831
4099  - http://biorxiv.org/content/early/2021/04/22/2021.04.21.440831.short
4100  - http://biorxiv.org/content/early/2021/04/22/2021.04.21.440831.full
AB  - Studying the electrical activity in single cells and in local circuits of excitable cells, like neurons, requires an easy to use and high throughput methodology that enables the measurement of membrane potential. Studying the electrical properties in particular sub-compartments of neurons, or in a specific type of neurons produces additional complexity. An optical voltage-imaging technique that allows high spatial and temporal resolution could be an ideal solution. However, most of the valid voltage imaging techniques are nonspecific; The ones that are more site-directed require much pre-work and specific adaptations in addition to other disadvantages. Here, a new technique for membrane voltage imaging, based on FRET between fluorescent polystyrene (FPS) beads and Dipicrylamine (DPA) is explored. Not only fluorescent intensity is demonstrated to be correlated with membrane potential, but more importantly, single particle voltage detection is demonstrated. Among other advantages, FPS beads can be synthesized with functional surface groups, and be further targeted to specific proteins via conjugation of recognition molecules. Therefore, FPS beads, in the presence of DPA, constitute single-particle detectors for membrane voltage, with a potential to be localized to specific membrane compartments. This new and accessible platform for targeted optical voltage imaging may further elucidate the mechanisms of neuronal electrical activity.Competing Interest StatementThe authors have declared no competing interest.