Jason Shear

Last updated
Jason B. Shear
Born (1967-02-28) February 28, 1967 (age 56)
Alma mater University of Texas at Austin, Stanford University
Scientific career
Fields Biomedical optics, biophotonics, nanotechnology, analytical chemistry
Institutions
Doctoral advisors Richard N. Zare, Richard H. Scheller, Watt W. Webb (postdoctoral), Thomas E. Mallouk  [ de ] (undergraduate)
Website sites.utexas.edu/shearlabs

Jason Ben Shear (born February 28, 1967) is an American chemist and expert in biomaterials and bioengineering. He is currently Professor of Chemistry at the University of Texas at Austin. [1] Shear has been considered one of the pioneers of two-photon photolithography. [2] [3] [4] [5] [6] [7] [8]

Contents

Scientific career

Shear received his BS in chemistry from UT Austin in 1989. He then moved to Stanford University to work with Richard Zare and completed his PhD in 1994. He was later an NSF Postdoctoral Fellow at Cornell University where he worked with Watt W. Webb in the laboratory that earlier developed the first two-photon excitation microscopy instrument. Shear returned to Austin to start his own independent lab at the University of Texas in 1996. [9] [10]

The Shear group has developed methods for performing solution-phase chemical separations on time frames more than 1000-fold shorter than previously accomplished, offering insights into reaction pathways of transient reaction products that are more easily characterized from their electrophoretic mobilities than from measurable spectroscopic properties. This method, based on photochemical preparation of reaction intermediates, enabled compounds to be electrophoretically probed using extremely large electric fields over distances as small as several micrometres on timescales as small as several microseconds. [11] [12]

The Shear group has also developed micro-3D-printing technologies for organizing cellular environments, a technology that allows cellular populations to be characterized under well-defined conditions and on scales in which ensemble behaviours begin to emerge. Of particular impact has been their use of these methods to probe bacterial group behaviours that underlie enhanced virulence, including quorum sensing and population-dependent antibiotic resistance. [13] [14] [15]

Shear's lab further developed novel strategies for engineering functionality into 3D printed biomaterials to provide environmentally controlled volume/shape change, chemical capabilities, and electronic properties. He has pioneered high-sensitivity multiphoton-based sensing technologies for microanalyses, developing various strategies for characterizing picoliter-sized biological samples using capillary electrophoretic analysis. Using these methods, the group has demonstrated strategies for analyzing volumes commensurate with subcellular volumes for spectrally diverse native chromophores present in attomole to zeptomole quantities. His lab was involved in foundational work developing broad-based sensor array devices for analysis of various solution-phase sample types, ranging from measurements of bodily fluids such as saliva to the determination of small-molecule components in consumables. [16] [17] [18]

Awards

Howard Hughes Fellow (1995) • Office of Naval Research Young Investigator Award (1997) • Beckman Young Investigators Award (1997) • Searle Scholars Program Award, Kinship Foundation (1998) • Alfred P. Sloan Research Fellowship (1999) • Top 100 Young Innovator citation, MIT Technology Review (1999) • Noted for a “Chemical Development of the Year” by Chemical & Engineering News (2003) • Academy of Medicine, Engineering and Science of Texas protégé (2004, 2005) • American Chemical Society Arthur F. Findeis Award in Analytical Chemistry (2005) • Texas Instruments Visiting Professor in Bioengineering, Rice University (2010–11)

Personal life

Jason's grandfather was Murray Shear, widely considered to be the Father of Chemotherapy. Jason's father David Shear was a professor of biophysics and held faculty appointments at SUNY Buffalo, the University of Georgia at Athens, and the University of Missouri at Columbia.

Related Research Articles

Microfluidics refers to a system that manipulates a small amount of fluids using small channels with sizes ten to hundreds micrometres. It is a multidisciplinary field that involves molecular analysis, molecular biology, and microelectronics. It has practical applications in the design of systems that process low volumes of fluids to achieve multiplexing, automation, and high-throughput screening. Microfluidics emerged in the beginning of the 1980s and is used in the development of inkjet printheads, DNA chips, lab-on-a-chip technology, micro-propulsion, and micro-thermal technologies.

<span class="mw-page-title-main">Electrophoresis</span> Motion of charged particles in electric field

In chemistry, electrophoresis is the motion of charged dispersed particles or dissolved charged molecules relative to a fluid under the influence of a spatially uniform electric field. As a rule, these are zwitterions. Electrophoresis of positively charged particles or molecules (cations) is sometimes called cataphoresis, while electrophoresis of negatively charged particles or molecules (anions) is sometimes called anaphoresis.

<span class="mw-page-title-main">Zeta potential</span> Electrokinetic potential in colloidal dispersions

Zeta potential is the electrical potential at the slipping plane. This plane is the interface which separates mobile fluid from fluid that remains attached to the surface.

Micellar electrokinetic chromatography (MEKC) is a chromatography technique used in analytical chemistry. It is a modification of capillary electrophoresis (CE), extending its functionality to neutral analytes, where the samples are separated by differential partitioning between micelles and a surrounding aqueous buffer solution.

Capillary electrophoresis (CE) is a family of electrokinetic separation methods performed in submillimeter diameter capillaries and in micro- and nanofluidic channels. Very often, CE refers to capillary zone electrophoresis (CZE), but other electrophoretic techniques including capillary gel electrophoresis (CGE), capillary isoelectric focusing (CIEF), capillary isotachophoresis and micellar electrokinetic chromatography (MEKC) belong also to this class of methods. In CE methods, analytes migrate through electrolyte solutions under the influence of an electric field. Analytes can be separated according to ionic mobility and/or partitioning into an alternate phase via non-covalent interactions. Additionally, analytes may be concentrated or "focused" by means of gradients in conductivity and pH.

<span class="mw-page-title-main">Electron-capture dissociation</span>

Electron-capture dissociation (ECD) is a method of fragmenting gas-phase ions for structure elucidation of peptides and proteins in tandem mass spectrometry. It is one of the most widely used techniques for activation and dissociation of mass selected precursor ion in MS/MS. It involves the direct introduction of low-energy electrons to trapped gas-phase ions.

Electrochromatography is a chemical separation technique in analytical chemistry, biochemistry and molecular biology used to resolve and separate mostly large biomolecules such as proteins. It is a combination of size exclusion chromatography and gel electrophoresis. These separation mechanisms operate essentially in superposition along the length of a gel filtration column to which an axial electric field gradient has been added. The molecules are separated by size due to the gel filtration mechanism and by electrophoretic mobility due to the gel electrophoresis mechanism. Additionally there are secondary chromatographic solute retention mechanisms.

<span class="mw-page-title-main">Capillary electrophoresis–mass spectrometry</span>

Capillary electrophoresis–mass spectrometry (CE–MS) is an analytical chemistry technique formed by the combination of the liquid separation process of capillary electrophoresis with mass spectrometry. CE–MS combines advantages of both CE and MS to provide high separation efficiency and molecular mass information in a single analysis. It has high resolving power and sensitivity, requires minimal volume and can analyze at high speed. Ions are typically formed by electrospray ionization, but they can also be formed by matrix-assisted laser desorption/ionization or other ionization techniques. It has applications in basic research in proteomics and quantitative analysis of biomolecules as well as in clinical medicine. Since its introduction in 1987, new developments and applications have made CE-MS a powerful separation and identification technique. Use of CE–MS has increased for protein and peptides analysis and other biomolecules. However, the development of online CE–MS is not without challenges. Understanding of CE, the interface setup, ionization technique and mass detection system is important to tackle problems while coupling capillary electrophoresis to mass spectrometry.

<span class="mw-page-title-main">Affinity electrophoresis</span>

Affinity electrophoresis is a general name for many analytical methods used in biochemistry and biotechnology. Both qualitative and quantitative information may be obtained through affinity electrophoresis. Cross electrophoresis, the first affinity electrophoresis method, was created by Nakamura et al. Enzyme-substrate complexes have been detected using cross electrophoresis. The methods include the so-called electrophoretic mobility shift assay, charge shift electrophoresis and affinity capillary electrophoresis. The methods are based on changes in the electrophoretic pattern of molecules through biospecific interaction or complex formation. The interaction or binding of a molecule, charged or uncharged, will normally change the electrophoretic properties of a molecule. Membrane proteins may be identified by a shift in mobility induced by a charged detergent. Nucleic acids or nucleic acid fragments may be characterized by their affinity to other molecules. The methods have been used for estimation of binding constants, as for instance in lectin affinity electrophoresis or characterization of molecules with specific features like glycan content or ligand binding. For enzymes and other ligand-binding proteins, one-dimensional electrophoresis similar to counter electrophoresis or to "rocket immunoelectrophoresis", affinity electrophoresis may be used as an alternative quantification of the protein. Some of the methods are similar to affinity chromatography by use of immobilized ligands.

Edward S. Yeung is a Chinese-American chemist who studies spectroscopy and chromatography. Yeung is a Distinguished Professor Emeritus at Iowa State University. He was elected as a Fellow of the American Association for the Advancement of Science. He was a founding co-editor of the Annual Review of Analytical Chemistry from 2008 to 2014 and has served on the editorial committees of a number of other journals.

David M. Goodall is a British chemist. He is Emeritus Professor of chemistry affiliated with the University of York (UK). Throughout his career he has made a considerable impact on the field of analytical chemistry.

<span class="mw-page-title-main">Milos Novotny</span> American chemist (born 1942)

Milos Vratislav Novotny is an American chemist, currently the Distinguished Professor Emeritus and Director of the Novotny Glycoscience Laboratory and the Institute for Pheromone Research at Indiana University, and also a published author. Milos Novotny received his Bachelor of Science from the University of Brno, Czechoslovakia in 1962. In 1965, Novotny received his Ph.D. at the University of Brno. Novotny also holds honorary doctorates from Uppsala University, Masaryk University and Charles University, and he has been a major figure in analytical separation methods. Novotny was recognized for the development of PAGE Polyacrylamide Gel-filled Capillaries for Capillary Electrophoresis in 1993. In his years of work dedicated to analytical chemistry he has earned a reputation for being especially innovative in the field and has contributed a great deal to several analytical separation methods. Most notably, Milos has worked a great deal with microcolumn separation techniques of liquid chromatography, supercritical fluid chromatography, and capillary electrophoresis. Additionally, he is highly acclaimed for his research in proteomics and glycoanalysis and for identifying the first mammalian pheromones.

Jennifer S. Brodbelt is an American chemist known for her research using mass spectrometry to characterize organic compounds, especially biopolymers and proteins.

<span class="mw-page-title-main">Nancy Allbritton</span> American biologist

Nancy Allbritton is a Professor of Bioengineering and the Frank & Julie Jungers Dean of the College of Engineering at the University of Washington. She was previously a Kenan Professor and Chair in the Joint Department of Biomedical Engineering at the University of North Carolina at Chapel Hill and North Carolina State University.

Jonathan V Sweedler is an American chemist specializing in bioanalytical chemistry, neurochemistry and cell to cell biology and behavior. He is the James R. Eiszner Family Endowed Chair in Chemistry at the University of Illinois at Urbana-Champaign. Additionally, he holds a faculty appointment in the Beckman Institute. He is also an Elected Fellow to the American Chemical Society, for which he is also the society's Editor in Chief for the journal Analytical Chemistry.

Microfluidics refers to the flow of fluid in channels or networks with at least one dimension on the micron scale. In open microfluidics, also referred to as open surface microfluidics or open-space microfluidics, at least one boundary confining the fluid flow of a system is removed, exposing the fluid to air or another interface such as a second fluid.

Peter Nemes is a Hungarian-American chemist, who is active in the fields of bioanalytical chemistry, mass spectrometry, cell/developmental biology, neuroscience, and biochemistry.

Pier Giorgio Righetti is a professor emeritus of chemistry. He worked primarily at the University of Milano (1971-1995) and at the Department of Chemistry of the Politecnico di Milano in Milan, Italy (2005-2011). He has served as the President of the Società Italiana di Proteomica.

Robert Travis Kennedy is an American chemist specializing in bioanalytical chemistry including liquid chromatography, capillary electrophoresis, and microfluidics. He is currently the Hobart H. Willard Distinguished University Professor of Chemistry and the chair of the department of chemistry at the University of Michigan. He holds joint appointments with the Department of Pharmacology and Department Macromolecular Science and Engineering. Kennedy is an Associate Editor of Analytical Chemistry and ACS Measurement Science AU.

Alexandra Ros is a German analytical chemist who is a professor in both the School of Molecular Sciences and Center for Applied Structural Discovery at The Biodesign Institute, Arizona State University. Her research considers microfluidic platforms and their use in analysis. She was awarded the 2020 Advancing Electrokinetic Science AES Electrophoresis Society Mid-Career Achievement Award.

References

  1. "The Shear Research Group at UT Austin". The University of Texas at Austin. Retrieved August 18, 2021.
  2. "3D-printed structures reveal bacterial chit-chat". The Conversation. 7 October 2013. Retrieved August 18, 2021.
  3. "'Honey, I Shrunk the Cell Culture': Scientists Use Shrink Ray for Biomedical Research". The University of Texas at Austin. 23 October 2018. Retrieved August 18, 2021.
  4. "Arthur F. Findeis Award for Achievements by an Analytical Scientist". The American Chemical Society. 4 April 2019. Retrieved August 19, 2021.
  5. "Jason Shear, Beckman Fellow". Beckman Foundation. Retrieved August 19, 2021.
  6. "Jason Shear - Tech Titans by Tech Review". MIT Technology Review. Retrieved August 19, 2021.
  7. "New Sloan Laureates". Alfred P. Sloan Foundation. Retrieved August 19, 2021.
  8. "Texas Professor creates a novel shrink ray". KXAN features. 12 November 2018. Retrieved August 19, 2021.
  9. Shear, Jason. "NSF Postdoctoral Fellowship". National Science Foundation Grants. Retrieved August 18, 2021.
  10. "Searle Scholar Shear". The Searle Scholars Program. Retrieved August 18, 2021.
  11. Plenert, M. L.; Shear, J. B. (2003). "Microsecond electrophoresis". Proceedings of the National Academy of Sciences. 100 (7): 3853–3857. Bibcode:2003PNAS..100.3853P. doi: 10.1073/pnas.0637211100 . PMC   153011 . PMID   12629208.
  12. Ritschdorff, Eric T.; Plenert, Matthew L.; Shear, Jason B. (2009). "Microsecond Analysis of Transient Molecules Using Bi-Directional Capillary Electrophoresis". Analytical Chemistry. 81 (21): 8790–8796. doi:10.1021/ac901283y. PMC   3169189 . PMID   19874052.
  13. Connell, Jodi L.; Wessel, Aimee K.; Parsek, Matthew R.; Ellington, Andrew D.; Whiteley, Marvin; Shear, Jason B. (2010). "Probing Prokaryotic Social Behaviors with Bacterial "Lobster Traps"". mBio. 1 (4). doi:10.1128/mBio.00202-10. PMC   2975351 . PMID   21060734.
  14. Connell, J. L.; Ritschdorff, E. T.; Whiteley, M.; Shear, J. B. (2013). "3D printing of microscopic bacterial communities". Proceedings of the National Academy of Sciences. 110 (46): 18380–18385. Bibcode:2013PNAS..11018380C. doi: 10.1073/pnas.1309729110 . PMC   3832025 . PMID   24101503.
  15. Spivey, Eric C.; Xhemalce, Blerta; Shear, Jason B.; Finkelstein, Ilya J. (2014). "3D-Printed Microfluidic Microdissector for High-Throughput Studies of Cellular Aging". Analytical Chemistry. 86 (15): 7406–7412. doi:10.1021/ac500893a. PMC   4636036 . PMID   24992972.
  16. Kaehr, Bryan; Shear, Jason B. (2008). "Multiphoton fabrication of chemically responsive protein hydrogels for microactuation". Proceedings of the National Academy of Sciences. 105 (26): 8850–8854. Bibcode:2008PNAS..105.8850K. doi: 10.1073/pnas.0709571105 . PMC   2449329 . PMID   18579775.
  17. Gostkowski, Michael L.; McDoniel, J. Bridget; Wei, Jing; Curey, Theodore E.; Shear, Jason B. (1998). "Characterizing Spectrally Diverse Biological Chromophores Using Capillary Electrophoresis with Multiphoton-Excited Fluorescence". Journal of the American Chemical Society. 120: 18–22. doi:10.1021/ja9727427.
  18. Goodey, Adrian; Lavigne, John J.; Savoy, Steve M.; Rodriguez, Marc D.; Curey, Theodore; Tsao, Andrew; Simmons, Glen; Wright, John; Yoo, Seung-Jin; Sohn, Youngsoo; Anslyn, Eric V.; Shear, Jason B.; Neikirk, Dean P.; McDevitt, John T. (2001). "Development of Multianalyte Sensor Arrays Composed of Chemically Derivatized Polymeric Microspheres Localized in Micromachined Cavities". Journal of the American Chemical Society. 123 (11): 2559–2570. doi:10.1021/ja003341l. PMID   11456925.