Many universities, commercial companies, and science organizations who use microscopy have outreach programs. The members of such generally love to share their enthusiasm and passion with the next generation. Content and confidence on providing such a program often comes from sharing ideas with like-minded scientists. These programs are typically delegated with the acronym STEM or STEAM: science, technology, engineering, art, and math. One of MSA's outreach programs is ProjectMICRO. Included are some STEAM ideas to share.

Fourier ptychography is an emerging computational microscopy technique that can generate gigapixel-scale images of biological samples. With only the addition of a low-cost LED array to a standard digital microscope and a reconstruction algorithm, Fourier ptychography overcomes the fundamental trade-off between a microscope's resolution and field-of-view without any moving parts. This article is the first in a three-part series that aims to introduce the fundamentals of the technology to the broader microscopy community and beyond, using intuitive explanations.

Microscopy has evolved through centuries of desire to see the unseen world. Modern technologies have pushed the limits of what's possible, inspiring the field of structural biology. Coupled with advances in biochemistry, scientists can now study the fine details of tiny intruders in the body as well as the molecular culprits of disease. Despite these monumental achievements, human health still suffers from persistent dysfunctions in biological molecules. Through cryo-electron microscopy (cryo-EM) imaging technology we can create more translatable models to uncover the atomic details of macromolecules gone awry. For instance, the tumor suppressor p53 is one of the most popular proteins in cancer research, yet there is little structural information about its complete 3D organization. The Center for Structural Oncology (CSO) at Penn State University is working to address these impactful uncertainties. Using a wealth of cryo-EM resources in the CSO, we capture dynamic snapshots of p53 assemblies while preserving their disease-related context for drug discovery and therapeutic development. With these tools in hand, the CSO is working to engineer new molecular paradigms in creating a world without cancer.

Cryo-electron tomography (cryo-ET) enables visualization of protein complexes within their native cellular environment at molecular resolution. Most cells and all tissues, however, are too thick to be imaged directly by transmission electron microscopy (TEM). Overcoming this limitation requires the production of thin biological sections called lamellae. The procedure to obtain lamellae of cells, either seeded or grown directly on electron microscopy grids, requires cryo-focused ion beam (cryo-FIB) milling to thin the samples. This method faces an additional challenge when dealing with tissues and multicellular organisms, as these samples must be high-pressure frozen, which embeds the sample in a thick layer of ice. Nonetheless, lamellae can still be prepared from such samples by extracting a small volume and transferring it to a receiver grid for lamella preparation, a process called lift-out. Here, we describe the available workflows to produce lamellae by lift-out at cryogenic conditions and recent developments in gas injection system (GIS)-free approaches to the lift-out transfer. These advances expand the applications of cryo-ET, enabling the investigation of tissues and whole organisms in situ at molecular resolution.