Making the Electron Microscope

Summary

Biological structures exist across a vast range of scales. At one end are whole organisms, varying in size from bacteria only a few micrometers across to mammals measured in feet. These can be seen with the naked eye or with simple light microscopes, which have been in use since the mid-1600s. At the smaller end, however, are atoms, amino acids, and proteins, spanning angstroms to nanometers in size.Observing molecules at this smaller scale allows us to untangle the finer mechanisms of life: how individual neurons connect and communicate, how the ribosomal machinery translates genetic code into proteins, or how viruses like HIV invade and hijack host cells. Resolving fine structures, whether the double membrane of a chloroplast, the protein shell of a bacteriophage, or the branching architecture of a synapse, provides the bridge between atomic detail and whole-organism physiology, taking us from form to function.Neurons communicate via the release of excitatory (left) and inhibitory (right) neurotransmitters at the junction, or synapse, between two cells. This gap is roughly 20 nanometers wide. Credit: David GoodsellThe ability to explore and map such minute mechanisms eluded scientists until the invention of the electron microscope. Conceived in the 1930s, it promised theoretical resolutions on the order of angstroms, nearly a hundred times finer than the most advanced light microscope of that era. In 1931, Ernst Ruska and his advisor Max Knoll, working at the Technical University in Berlin, designed the first prototype by replacing glass lenses with electromagnetic coils to focus beams of electrons instead of light. That first instrument barely outperformed a magnifying glass in terms of resolution. But over the next century, refinements in design, sample preparation, and computation transformed the electron microscope into an indispensable tool for modern biology.By 1938, scientists used an electron microscope to take a photograph of a virus — the mouse ectromeli...