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Biology subjects

Khazen, G.

Publications and source records attributed to Khazen, G..

2 recordsLinked to original sources

Synthesis of geometrically realistic and watertight neuronal ultrastructure manifolds for in silico modeling

Understanding the intracellular dynamics of brain cells entails performing three-dimensional molecular simulations incorporating ultrastructural models that can capture cellular membrane geometries at nanometer scales. While there is an abundance of neuronal morphologies available online, e.g. from NeuroMorpho.Org, converting those fairly abstract point-and-diameter representations into geometrically realistic and simulation-ready, i.e. watertight, manifolds is challenging. Many neuronal mesh reconstruction methods have been proposed, however, their resulting meshes are either biologically unplausible or non-watertight. We present an effective and unconditionally robust method capable of generating geometrically realistic and watertight surface manifolds of spiny cortical neurons from their morphological descriptions. The robustness of our method is assessed based on a mixed dataset of cortical neurons with a wide variety of morphological classes. The implementation is seamlessly extended and applied to synthetic astrocytic morphologies that are also plausibly biological in detail. Resulting meshes are ultimately used to create volumetric meshes with tetrahedral domains to perform scalable in silico reaction-diffusion simulations for revealing cellular structure-function relationships. Availability and implementationOur method is implemented in NeuroMorphoVis, a neuroscience-specific open source Blender add-on, making it freely accessible for neuroscience researchers. Key pointsO_LIA plethora of neuronal morphologies is available in a point-and-diameter format, but there are no robust techniques capable of converting these morphologies into geometrically realistic models that can be used to conduct subcellular simulations. C_LIO_LIWe present a scalable method capable of synthesizing high fidelity watertight ultrastructural manifolds of complete neuronal models from their one-dimensional descriptions using the synaptic data obtained from the digitally reconstructed neuronal circuits of the Blue Brain Project. C_LIO_LIResulting manifold models comprise geometrically realistic somata and spine geometries, enabling accurate in silico experiments that can probe intricate structure-function relationships. C_LIO_LIOur method is extensible and can be seamlessly applied to other cellular structures such as astroglial morphologies and even large networks of cerebral vasculature. C_LI

neuroscience↗

TransINT: an interface-based prediction of membrane protein-protein interactions

Because of their considerable number and diversity, membrane proteins and their macromolecular complexes represent the functional units of cells. Their quaternary structure may be stabilized by interactions between the -helices of different proteins in the hydrophobic region of the cell membrane. Membrane proteins also represent potential pharmacological targets par excellence for various diseases. Unfortunately, their experimental 3D structure and that of their complexes with intramembrane interacting partners are scarce due to technical difficulties. To overcome this key problem, we devised PPIMem, a computational approach for the specific prediction of higher-order structures of -helical transmembrane proteins. The novel approach involves identification of the amino acid residues at the interface of complexes with a 3D structure. The identified residues compose then interaction motifs that are conveniently expressed as mathematical regular expressions. These are used for motif search in databases, and for the prediction of intramembrane protein-protein complexes. Our template interface-based approach predicted 21, 544 binary complexes between 1, 504 eukaryotic plasma membrane proteins across 39 species. We compared our predictions to experimental datasets of protein-protein interactions as a first validation method. The PPIMem online database with the annotated predicted interactions is implemented as a web server and can be accessed directly at https://transint.shinyapps.io/transint/.

bioinformatics↗