PhD — UC Berkeley
Self-motivated, inventive biophysicist specializing in Structure-Activity Relationships, protein engineering of challenging human macromolecular enzymes, and cryo-EM. 10+ years integrating biochemistry, biophysics, and de novo protein design to drive mechanistic discovery.
"Fascinated by visualizing molecular networks at atomic resolution — and inventing the tools to do it."
Lindsey Young Goodman earned her PhD from UC Berkeley studying Structure-Activity Relationships of the Class III Phosphatidylinositol 3-Kinase Complex — a human macromolecular enzyme essential to autophagy, cancer, neurodegeneration, and heart disease — through biophysical methods, in vitro reconstitution, single-particle cryo-EM, and HDX-MS.
As a postdoctoral fellow at UC San Diego with Dr. Elizabeth Villa (HHMI), Lindsey became captivated by visualizing intact molecular networks inside cells at high spatial resolution. Recognizing a fundamental gap in available tools for molecular identification in cellular cryo-electron tomography, she invented ExoSloNano — a multi-modal nanogold labeling platform now published in Nature Methods (2026) and sold as a validated commercial product through Nanoprobes, Inc.
She has been invited to present her work at HHMI Janelia, the Biophysical Society, the University of Pennsylvania, Atlos Labs, and international Keystone Conferences, among others.
Multi-state single particle cryo-EM structure determination of macromolecular complexes. Expert in the full pipeline from sample prep to final structure.
Expression and purification of challenging human macromolecular complexes in HEK cells. Enzymatic, kinetic, and binding assays with reconstituted lipid vesicles.
Inventor of ExoSloNano — multi-modal nanogold probes for intracellular macromolecular labeling in live cells and cryo-ET datasets. Now a commercial product.
De novo protein design of small binders for phage therapy applications leveraging modern AI-based structure prediction and design tools.
Quantitative data analysis and scientific computing supporting structural biology workflows, image processing, and experimental data interpretation.
Sterile mammalian cell culture, transient transfections, molecular cloning, SDS-PAGE, and endotoxin detection supporting protein production pipelines.
* denotes equal contribution | Full publication list on Google Scholar →
Open to research collaborations, scientific consulting, and speaking invitations. Please reach out via email or connect on LinkedIn.