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Gockel, N.

Publications and source records attributed to Gockel, N..

2 recordsLinked to original sources

MotilA - A Python pipeline for the analysis of microglial fine process motility in 3D time-lapse multiphoton microscopy data

MotilA is a Python-based image analysis pipeline for quantifying fine process motility of microglia from 3D time-lapse two-channel fluorescence microscopy data. Developed for high-resolution multiphoton in vivo imaging datasets, MotilA enables both single-file and batch processing across multiple experimental conditions. It performs image preprocessing, segmentation, and motility quantification over time, using a pixel-based change detection strategy that yields biologically interpretable metrics such as the turnover rate (TOR) of microglial fine processes. While originally designed for microglial imaging, the pipeline can be extended to other cell types and imaging applications that require analysis of dynamic morphological changes. MotilA is openly available, platform-independent, and includes extensive documentation, tutorials, and example data to facilitate adoption by the broader scientific community. It is released under the GPL-3.0 open-source license.

neuroscience↗

PinkyCaMP a mScarlet-based calcium sensor with exceptional brightness, photostability, and multiplexing capabilities

Genetically encoded calcium (Ca2+) indicators (GECIs) are widely used for imaging neuronal activity, yet current limitations of existing red fluorescent GECIs have constrained their applicability. The inherently dim fluorescence and low signal-to-noise ratio of red-shifted GECIs have posed significant challenges. More critically, several red-fluorescent GECIs exhibit photoswitching when exposed to blue light, thereby limiting their applicability in all-optical experimental approaches. Here, we present the development of PinkyCaMP, the first mScarlet-based Ca2+ sensor that outperforms current red fluorescent sensors in brightness, photostability, signal-to-noise ratio, and compatibility with optogenetics and neurotransmitter imaging. PinkyCaMP is well-tolerated by neurons, showing no toxicity or aggregation, both in vitro and in vivo. All imaging approaches, including single-photon excitation methods such as fiber photometry, widefield imaging, miniscope imaging, as well as two-photon imaging in awake mice, are fully compatible with PinkyCaMP.

neuroscience↗