Microscopy

Euan McLeod, Ph.D., works at the intersection of nanophotonics, soft materials science, and many-body systems. One of his current major research thrusts is to use optical tweezers combined with biomolecular functionalization to assemble nanostructured 3D devices out of colloidal nanoparticle building blocks. Euan also works on developing lensfree holographic microscopes that provide high resolution across an ultra-large field of view in cost-effective and compact platforms. Euan is developing new methods to improve the resolution and sensitivity of these microscopes to sense ultrafine nanoparticles like aerosols and viruses. By combining these microscopes with microfluidic chambers, he is working to develop highly multiplexed biomedical sensors. All of these areas of experimental research are supported by extensive computational and theoretical efforts. Previously in his career, Euan has published extensive research in high-speed acoustic lensing, laser-materials processing at the nanoscale, and free-surface microfluidic instabilities.

Magdalene So, PhD, is a Professor in the Immunobiology Department and Director of the Microbial Pathogenesis Program at the University of Arizona College of Medicine. Dr. So is recognized internationally for her research in the microbial pathogenesis. Her research focuses on two medically important bacterial pathogens: Neisseria gonorrhoeae, which causes over 100 million new cases of sexually transmitted infections each year worldwide, and Neisseria meiningitidis, which frequently causes meningitis epidemics in Subharan Africa. Her goal is to understand on how these two pathogens cause disease, with the aim of applying this information to developing new antibiotics for treating these infectious agents and improving current methods of vaccine development. Dr. So recently expanded her research to the commensal species in the Neisseria genus. These bacteria are normal inhabitants of the body and are closely related to the two pathogenic species; but unlike their pathogenic cousins they do not cause disease. Dr. So’s new research effort seeks to determine the differences in behavior of commensal and pathogen Neisseria. Dr. So’s research approach is multidisciplinary, involving concepts and techniques in biophysics, bioinformatics, cell biology, biochemistry and genetics. Collaborators from institutions around the world contribute to this effort. Dr. So has published over 100 peer-reviewed research papers in internationally renowned journals, and over 20 reviews and book chapters. She holds several patents as a result of her research. She is frequently invited to speak at universities and national and international meetings. She is a member of the American Academy of Microbiology, an elected body, and serves on the scientific boards of several research centers. Over the course of her career, Dr. So has trained over 44 postdoctoral fellows and graduate students. The majority of her trainees are internationally recognized researchers in their own right. Keywords: Infectious disease, microbiology

Ron Lynch received a B.S. from the University of Miami (1978) with a dual major in Chemistry (Physical) and Biology, and a Ph.D. degree from the University of Cincinnati (1984) in Physiology and Biophysics. Dr. Lynch began training in optical imaging and MR spectroscopy of cardiac metabolism while at the NIH/NHLBI under the direction of Dr. Robert Balaban from 1984-1987. In 1987, Dr. Lynch moved to a staff position in the Biomedical Imaging Group with appointment in the Physiology Department at the University of Massachusetts Medical Center where he was involved in the development of approaches for 3-dimensional imaging including deconvolution and confocal microscopy. Dr. Lynch joined the faculty of the University of Arizona in 1990 with dual appointment in the Departments of Physiology and Pharmacology, and is currently a full professor, and director of the Arizona Research Institute for Biomedical Imaging. In 2000, Dr. Lynch was a visiting scientist at the Laboratory of Functional and Molecular Imaging and the Magnetic Resonance Imaging Center with Dr. Alan Koretsky at the NIH/NINDS. Dr. Lynch is a member of the Biophysical Society, the American Physiological Society and American Diabetes Association, and regularly serves on grant review panels for the JDRF, NIH/NIDDK, and NSF. Research in the Lynch lab focuses on second messenger signaling in vascular smooth muscle cells and nutrient sensing cells (e.g., Pancreatic Beta-cells) with emphasis on alterations in signaling that occur during development of Diabetes. We are developing methods to modify and analyze beta cell mass in order to evaluate the initiation of the pre-diabetic state, and efficacy of its treatment. Analyses of subcellular protein distributions, second messenger signaling, and ligand binding is performed in our lab using state of the art microscopy and analysis approaches which is our second area of expertise. Over the past 3 decades, our lab has been involved in the development of unique microscopic imaging and spectroscopy approaches to study cell and tissue function, as well as screening assays for cell signaling and ligand binding. Keywords: Diabetes, Cancer, Optical Imaging, Targeted Contrast Agents, Metabolism, Biomedical Imaging, Drug Development

My research is focused on developing novel optical microscopy technologies and improving patient care using these technologies. My research area includes (1) low-cost smartphone in vivo microscopy, (2) high-speed comprehensive in vivo endomicroscopy, and (3) ultraminiature endomicroscopy. (1) Low-cost smartphone in vivo microscopy: I am currently leading a NIH-sponsored research project for developing smartphone confocal microscope and diagnosing Kaposi's sarcoma in Uganda with the smartphone confocal microscope. I will further advance the smartphone microscopy technology and address other applications, including diagnosis of cervical and oral cancers in low-resource settings, large-population screening of skin cancers in the US, and aiding science and medical educations. (2) High-speed comprehensive in vivo endomicroscopy: I have previously developed a high-speed confocal microscopy system and endoscopic imaging catheters and acquired largest in vivo confocal images of human organ reported. At the UA, I plan to further advance the technology by i) increasing the imaging speed by orders of magnitude and ii) incorporating fluorescence imaging modality. (3) Ultraminiature endomicroscopy: In my previous research, I have developed miniature endoscopic catheters that can visualize internal organs in vivo through a needle-sized device. At the UA, I will develop microscopic imaging catheter with a extremely small diameter and utilize it for guiding cancer diagnosis and treatment.

Ultrafast Electron Microscopy is a pivotal tool for imaging the atomic motion in real time and space. The temporal resolution, limited to a few hundreds of femtoseconds (one quadrillionth of a second) permits recording movies of only the relatively massive atomic motion. Imaging of microscopic motions outside the atomic nucleus in the real-time requires a significant enhancement in the temporal resolution. My research program aims to obtain the attosecond (one quintillionth of a second) temporal resolution in electron microscopy and establish the “Attomicroscopy” —the fastest camera ever known—which takes the field of ultrafast imaging to the next level. Attomicroscopy provides a real-time access to all microscopic motions outside the atomic core and radically change our insight into the workings of the microcosm. We will use the Attomicroscopy to image the electron motion in biochemical molecules such as amino acids, DNA, protein…. etc. Attosecond imaging and controlling of the electron motion at the atomic scale will open exciting new ground and prospects in multiple fields of basic science, biological applications, and information technology.