Eric Betzig
What did Eric Betzig win the Nobel Prize for?
What is near-field microscopy?
What is lattice light sheet microscopy?
What company did Eric Betzig cofound in 2019?
Where did Eric Betzig study for his bachelor’s degree?
Eric Betzig (born January 13, 1960, Ann Arbor, Michigan, U.S.) is an American physicist who won the 2014 Nobel Prize for Chemistry for using fluorescent molecules to bypass the inherent resolution limit in optical microscopy. He shared the prize with American chemist W.E. Moerner and Romanian-born German chemist Stefan Hell.
Betzig was interested in science and technology from a young age. (Even as a child, he said he wanted to win a Nobel Prize by the time he was 40.) He was an eager student and would arrive hours before classes began at Ann Arbor Pioneer High School, Michigan, to work on the computers there. He received a bachelor’s degree (1983) in physics from the California Institute of Technology in Pasadena and a master’s (1985) and a doctorate (1988) in applied and engineering physics from Cornell University in Ithaca, New York. At Cornell he worked on near-field microscopy, which uses light waves near a material’s surface to obtain images of a higher resolution than can be achieved with conventional optical microscopy, which has a resolution limit (discovered by German physicist Ernst Abbe in 1873) of about 200 nanometers (nm) for the shortest wavelengths of visible light. However, near-field microscopy has the disadvantage of being unable to look deep beneath the surface of objects such as cell membranes. Other high-resolution devices, such as electron microscopes, achieve much higher resolutions than the Abbe limit.
Betzig continued in that field at Bell Laboratories in Murray Hill, New Jersey, where he worked from 1988 to 1994. He then founded his own microscopy research and development company, NSOM Enterprises, in 1994. At that time Betzig felt that near-field microscopy had reached its limits, but in 1995 he postulated a method whereby the Abbe limit could be surpassed: If a number of point sources of light are scattered so that their positions can be resolved and those sources can be divided into classes with different optical properties, then adding the images of the different classes together would lead to an image with a resolution smaller than the Abbe limit. However, no such point sources existed. In 1996 Betzig abandoned his work on microscopy to become vice president of research and development at his father’s machine tool firm, Ann Arbor Machine Company, in Michigan; the business closed in 2009.
In 2002 Betzig founded another research and development firm, New Millennium Research, in Okemos, Michigan. In 2005 he became a group leader at the Janelia Research Campus of the Howard Hughes Medical Institute in Ashburn, Virginia. That same year Betzig learned about fluorescent proteins that could be turned on and off. He had found his point sources. In 2006 he and his collaborators attached fluorescent proteins to lysosomes and mitochondria. They activated only a few proteins, captured an image, and then activated more proteins. They repeated that process many times and combined the images to create an image with a resolution of just a few nanometers, many times better than the Abbe limit. That technique has enabled the study of active viruses and molecules in living cells.
- Awards And Honors:
- Nobel Prize (2014)
- Subjects Of Study:
- fluorescent microscope
- microscope
Shortly after winning the Nobel Prize for Chemistry in 2014, Betzig, along with his collaborators, published a paper describing a new method of microscopy: lattice light sheet microscopy, in which a specimen is illuminated by thin sheets of light. Live specimens can then be studied with minimal photobleaching, in which bright illumination causes specimens to stop fluorescing, and reduced phototoxicity, in which bright illumination damages or kills a specimen. In 2017 Betzig joined the faculty at the University of California, Berkeley. In 2019 he cofounded Eikon Therapeutics, a company that develops drugs based on observations of living cells.