Cryo-EM

Cryogenic electron microscopy showed for the first time that large RNA complexes can assemble without the help of proteins. 

Researchers found a protein that's essential for an enterovirus to enter human cells. That could help the search for vaccines and treatments. 

The microelectronics that power daily life and speed discoveries in science and technology are the focus of a bold new vision to make them more energy efficient and able to operate in extreme environments.

Disabling those hinges could be a good strategy for designing vaccines and treatments against a broad range of coronavirus infections.

Peter Dahlberg has combined two complex imaging techniques into one. The 2021 Panofsky Fellow adds cryo-ET and biosensors to fluorescence microscopy to give context to high-resolution images of individual proteins in cells.

New SLAC-Stanford Battery Center bridges the gaps between discovering, manufacturing and deploying innovative energy storage solutions. 

Cryogenic electron microscopy (cryo-EM) is a revolutionary tool for studying the molecular architecture of protein, viruses, cells and the specialized molecular machines within cells. This video explains how cryo-EM works, from preparing samples for study to capturing atomic imagery and...

Presented by Peter  D. Dahlberg. Viewing cellular machinery at the nanoscale. 

Public lecture presented by Peter  D. Dahlberg

Researchers used cryo-EM (left) to discover how a chamber in human cells (right) directs protein folding.