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Backues, S. K.

Publications and source records attributed to Backues, S. K..

3 recordsLinked to original sources

Auto-AVS: A Novel Framework for Automated Autophagic Vacuole Simulation

Transmission electron microscopy (TEM) is widely used to quantify autophagic bodies in yeast, but ultra-thin sectioning provides only two-dimensional cross-sections of inherently 3D structures. Inferring the underlying size and number of autophagic bodies therefore requires assumptions about their geometry, spatial organization, and distribution within the vacuole. We introduce Auto-AVS, an open-source computational stereology framework that combines configurable 3D autophagic-vacuole simulation, optional CompuCell3D-based body deformation, virtual TEM sectioning, and statistical comparison with experimental data. We first validate the virtual sectioning pipeline against analytical stereology and an existing spherical R-based simulation. We then use Auto-AVS to examine whether explicitly modeling autophagic-body deformation alters observed section statistics and find no consistent measurable effect under the tested simulation parameters. Finally, we apply the framework to experimental wild-type and mutant TEM datasets. Auto-AVS produces body-size estimates closely consistent with conventional stereological estimates, while body-number fitting reveals substantial discrepancies between simulated and experimental distributions despite similar average count estimates. These discrepancies implicate spatial clustering and vacuole geometry as important limitations of current body-number models. Rather than replacing conventional stereology, Auto-AVS provides a computational framework for testing its underlying assumptions and determining which aspects of 3D organization affect inference from two-dimensional microscopy.

bioinformatics↗

Screening for residues in Atg11, a central organizer of selective autophagy in yeast, important for binding with Atg9

The yeast protein Atg11, whose structure is unknown, is a central organizer of autophagosome formation that recruits Atg9 during selective autophagy. Although the residues in Atg9 responsible for this interaction are known, those in Atg11 are not. In an attempt to discover the binding site of Atg9 on Atg11, we screened a number of mutants within amino acid residues 455-627 of Atg11, guided in part by an AlphaFold2-generated model of the Atg11 dimer. However, we were not able to identify specific residues essential for the interaction with Atg9, suggesting that the binding region may lie elsewhere on Atg11.

biochemistry↗

Accurate Automated Segmentation of Autophagic Bodies in Yeast Vacuoles Using Cellpose 2.0

Segmenting autophagic bodies in yeast TEM images is a key technique for measuring changes in autophagosome size and number in order to better understand autophagy. Manual segmentation of these images can be very time consuming, particularly since hundreds of images are needed for accurate measurements. Here we describe a validated Cellpose 2.0 model that can segment these images with accuracy comparable to that of human experts. This model can be used for fully automated segmentation, eliminating the need for manual body outlining, or for model-assisted segmentation, which allows human oversight but is still five times as fast as the current manual method. The model and instructions for its use are presented here for the autophagy community.

cell biology↗