Charmm-gui

CHARMM-GUI is a web-based interface that prepares molecular structures and simulation inputs for computational studies of biomolecules, making complex molecular dynamics workflows more accessible. Users provide structural information, select components such as water, ions, lipids, or proteins, and configure force-field and simulation parameters; the platform then builds system coordinates, topology files, and executable input scripts through guided modules. CHARMM-GUI supports simulations with widely used engines, including CHARMM, NAMD, GROMACS, AMBER, and OpenMM. In biology, it helps researchers model membrane proteins, protein-ligand interactions, nucleic acids, and other systems while improving workflow consistency and reducing manual setup errors.

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Research

JoVE Journal - Chemistry
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A Bilingual Computational Workflow for Identifying Potential PLK1 Inhibitors in American Sign Language and English

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2026

This bilingual protocol provides a computational drug discovery workflow assessing protein-ligand interactions of Polo-Like Kinases 1 to 3 (PLK1–3) and Absorption, Distribution, Metabolism, Excretion, Toxicity, and Stability (ADMET-S) properties of database-sourced natural molecules.

Research

JoVE EoE - Neuroimaging

Live Cell Imaging of Muller Glial Nuclear Migration During Zebrafish Retinal Regeneration

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2025

Source: Lahne, M., et.al. Culture of Adult Transgenic Zebrafish Retinal Explants for Live-cell Imaging by Multiphoton Microscopy. J. Vis. Exp. (2017)This video demonstrates live-cell imaging of Muller glial nuclear migration in agarose-embedded zebrafish retinal explants following light-induced photoreceptor damage. Tumor necrosis factor-alpha (TNF-α) released by damaged photoreceptors activates Muller glial cells, triggering nuclear migration through the inner and outer nuclear layers for...

Automated Image-Guided Patch Clamp Technique for Studying Neurons in Brain Slices

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2025

In this video, brain slices are immobilized in a recording chamber, and cells of interest are located and focused on using a computer-controlled microscope. The automated image processing system then precisely positions a patch pipette to seal the cell membrane and monitor electrical signals.

Application of Automated Image-guided Patch Clamp for the Study of Neurons in Brain Slices

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Cited by 11 •

2017

This protocol describes how to conduct automatic image-guided patch-clamp experiments using a system recently developed for standard in vitro electrophysiology equipment.

Real-time Iontophoresis with Tetramethylammonium to Quantify Volume Fraction and Tortuosity of Brain Extracellular Space

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Cited by 29 •

2017

This protocol describes real-time iontophoresis, a method that measures physical parameters of the extracellular space (ECS) of living brains. The diffusion of an inert molecule released into the ECS is used to calculate the ECS volume fraction and tortuosity. It is ideal for studying acute reversible changes to brain ECS.

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