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Selhorst, P.

Publications and source records attributed to Selhorst, P..

2 recordsLinked to original sources

SquiDBase: a community resource of raw nanopore data from microbes

Experimental data-driven research relies on raw data, which consist of unprocessed experimental outputs, whereas derived data are transformed through a number of processing steps to reveal specific insights. Such processing, however, can potentially introduce biases or information loss, compromising transparency and reproducibility. In nucleic acid sequencing, nucleotide sequences stored in the FASTQ format are widely shared, but FASTQ files are generated from platform-specific raw data outputs, which vary depending on the sequencing platform used. The raw data produced by Oxford Nanopore Technologies (ONT) sequencing devices contain valuable biological information and are also useful to improve data processing methods, which includes basecaller optimisation and modification detection. Increasing attention goes to exploring these raw signals to develop algorithms that could improve ONT device portability and enhance target enrichment efficiency through adaptive sampling. Despite these benefits, the storage and sharing of raw nanopore data remain limited due to technical constraints and the lack of appropriate, standardised and centralised infrastructure. To address this challenge, we developed SquiDBase (https://squidbase.org), a dedicated repository to collect raw microbial nanopore sequencing data. To maximise the utility of SquiDBase from its inception, we built SquiDPipe, a Nextflow pipeline for the automated removal of human or unwanted reads from raw nanopore data. Additionally, we sequenced 24 clinically relevant viruses and incorporated them into SquiDBase, significantly expanding the diversity of publicly available reference datasets. By offering a centralised, open-access raw data collection platform, SquiDBase facilitates data sharing, enhances reproducibility, and supports the development and benchmarking of novel computational tools, reinforcing open science in nanopore sequencing research.

bioinformatics↗

Mathematical Model of Mechanical Virion-Cell Interaction During Early Engulfment in HIV

Viral endocytosis involves elastic cell deformation, driven by chemical adhesion energy, and depends on physical interactions between virion and cell membrane. These interactions are not easy to quantify experimentally. Hence, this study aimed to develop a mathematical model of the interactions of HIV particles with host cells and explore the effects of mechanical and morphological parameters during full virion engulfment. The invagination force and engulfment energy were described as viscoelastic and linear-elastic functions of radius and elastic modulus of virion and cell, ligand-receptor energy density and engulfment depth. The influence of changes in the virion-cell contact geometry representing different immune cells and ultrastructural membrane features and the decrease in virion radius and shedding of gp120 proteins during maturation on invagination force and engulfment energy was investigated. A low invagination force and high ligand-receptor energy are associated with high virion entry ability. The required invagination force was the same for immune cells of different sizes but lower for a local convex geometry of the cell membrane at the virion length scale. This suggests that localized membrane features of immune cells play a role in viral entry ability. The available engulfment energy decreased during virion maturation, indicating the involvement of additional biological or biochemical changes in viral entry. The developed mathematical model offers potential for the mechanobiological assessment of the invagination of enveloped viruses towards improving the prevention and treatment of viral infections.

biophysics↗