ChimeraX Demo

ChimeraX Demonstration: Analyzing Structures at the Experimental Forefront

Tom Goddard
Advisory Committee meeting
March 21, 2016

Demonstrations of ChimeraX viewing, analyzing, and modeling with "next generation" 3d data sets.

Lightsheet 3d optical microscopy. Dyche Mullins.
High-resolution (3 Angstrom) cryoEM. Paul Adams and Wah Chiu.
Models of molecular environments. Graham Johnson

These 3 demonstrations illustrate recent progress corresponding to the 3 specific aims of our proposed Technology Research and Development project (TR&D 2) on ChimeraX applications.

Lightsheet optical microscopy time series

How to quantify the lamellipodia protrusions of moving neutrophils seen in 3d optical microscopy.

Movie. Crawling through collagen filaments. Movie.

Membrane Actin Imperfect alignment Aligned Difference map
(positive orange, negative blue) Smoothed difference Mark largest connected blobs and cell center

Movie of marked protrusions, 250 frames.

Protrusion sizes and angular separation versus time. Plot of protrusion size measured as sphere radius for sphere with volume matching protrusion volume seen in smoothed difference map. Red, green and blue curves are the largest protrusions ordered by size. Angular separation of protrusions is measured (pink circles) as the average angle between cell center to protrusion center vectors.

Atomic resolution (3 Angstrom) cryoEM

Inspecting fit of individual residues in atomic resolution cryoEM maps.

Beta galactosidase cryoEM map at 2.2 Angstroms (EMDB 2984). Atomic model (PDB 5a1a)

Residue fit inspector in ChimeraX. Movie. Movie showing each residue fit.

Models of molecular environments

Viewing and building molecular models containing tens of thousands of macro-molecules. Graham Johnson's cellPACK software and ChimeraX tools build these theoretical models.

Partially revealing layers of HIV cellPACK model using drag select. Hierarchy for HIV model proteins. Building an HIV capsid lattice of protein hexamers and pentamers.