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Biology subjects

Schoenherr, R.

Publications and source records attributed to Schoenherr, R..

2 recordsLinked to original sources

An ultrasensitive genetically encoded voltage indicator uncovers the electrical activity of non-excitable cells

Genetically encoded voltage indicators (GEVIs) are powerful, non-invasive tools for recording action potentials in excitable cells. However, most animal cell types are non-excitable, and yet variations in the membrane potential are biologically relevant in these cells as well. Resolving such small voltage signals demands GEVIs with exceptionally high sensitivity. In this study, we applied structure-guided engineering to the GEVI ASAP3 to generate rEstus, a sensor with optimized brightness, voltage sensitivity, and voltage range. rEstus is most sensitive in the resting voltage range of non-excitable cells, exhibits a 3.6-fold improvement in fast voltage spike detection, and allows for absolute voltage calibration at the single-cell level. Using rEstus, we resolved endogenous voltage fluctuations in several non-excitable cell types and demonstrate that correlation analysis of these optically recorded fluctuations provides an easy, non-invasive, real-time readout of electrical gap-junction coupling. Our work provides greatly enhanced tools and methods for the non-invasive study of electrical signaling in excitable and non-excitable cells.

biophysics↗

InCellCryst - A streamlined approach to structure elucidation using in cellulo crystallized recombinant proteins

With the advent of serial X-ray crystallography on microfocus beamlines at free-electron laser and synchrotron facilities, the demand for protein microcrystals has significantly risen in recent years. However, by conventional methods extensive efforts are usually required to purify proteins and produce sufficiently homogeneous microcrystals. Here, we present InCellCryst, an advanced pipeline for producing homogeneous microcrystals directly within living insect cells. Our baculovirus-based cloning system enables the production of crystals from completely unmodified proteins as well as the screening of different cellular compartments to maximize chances for protein crystallization. By optimizing cloning procedures, recombinant virus production, crystallization and crystal detection, X-ray diffraction data can be collected 24 days after the start of target gene cloning. Furthermore, new strategies for serial synchrotron diffraction data collection directly from crystals within living cells abolish the need to purify the recombinant protein or the associated microcrystals.

biophysics↗