David Lynn

David Lynn

David Lynn

Asa Griggs Candler Professor
Howard Hughes Medical Institute Professor

David G. Lynn has contributed in the general areas of molecular recognition, synthetic biology and chemical evolution, and has developed chemical and physical methods for the analysis of supramolecular self-assemblies, of signal transduction in cellular development and pathogenesis, of molecular skeletons for storing and reading information, and of the evolution of biological order.

Lynn has earned a Howard Hughes Medical Institute Professorship, the Emory Scholar-Teacher Award, a fellowship from the American Association for the Advancement of Science, and the ACS Charles H. Herty Medal.

During his tenure as Chair of the Department of Chemistry from 2006-2015, Lynn assisted in the renovation of the Atwood chemistry building. In 2018 and 2019, Lynn also served as a board member for the Atlanta Science Festival.

dlynn2@emory.edu

404-727-9348

Office Location:
Emerson E407

Website

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University, College, and School/Department
Research Focus Areas:
  • Molecular Evolution
Additional Research:
The David G. Lynn Group at Emory University works to understand the structures and forces that enable supramolecular self-assembly, how chemical information can be stored and translated into new molecular entities, and how the forces of evolution can be harnessed in new structures with new function. Some of our current research areas include the origins of prokaryotic and eukaryotic pathogenesis, template directed polymerization and dynamic combinatorial systems, amyloid diseases and protein self-assembly, and intelligent materials.

IRI Connections:

Khalid Salaita

Khalid Salaita

Khalid Salaita

Associate Professor
Samuel Candler Dobbs Professor of Chemistry
Director for Graduate Studies in the Chemistry Department
Program Faculty in the Department of Biomedical Engineering at Emory University and Georgia Institute of Technology

Khalid Salaita is the Samuel Candler Dobbs Professor of Chemistry, and Director for Graduate Studies in the Chemistry Department at Emory University in Atlanta, Georgia (USA). Khalid grew up in Jordan and moved to the US in 1997 to pursue his undergraduate studies at Old Dominion University in Norfolk, Virginia (USA). He worked under the mentorship of Prof. Nancy Xu studying the spectroscopic properties of plasmonic nanoparticles. He then obtained his Ph.D. with Prof. Chad Mirkin at Northwestern University (Evanston, IL) in 2006. 

During that time, he studied the electrochemical properties of organic adsorbates patterned onto gold films and developed massively parallel scanning probe lithography approaches. From 2006-2009, Khalid was a postdoctoral scholar with Prof. Jay T. Groves at the University of California at Berkeley (USA) where he investigated the role of receptor clustering in modulating cell signaling. In 2009, Khalid started his own lab at Emory University, where he is currently investigating the use of nucleic acids as molecular force sensors, smart drugs, and synthetic motors. 

In recognition of his independent work, Khalid has received a number of awards, most notably: the Alfred P. Sloan Research Fellowship, the Camille-Dreyfus Teacher Scholar award, the National Science Foundation Early CAREER award, the Kavli Fellowship, and Merck Future Insight Prize. Khalid is currently the director of the Center on Probes for Molecular Mechanotechnology, and an Associate Editor of SmartMat. Khalid’s program has been supported by NSF, NIH, and DARPA.

k.salaita@emory.edu

404-727-7522

Office Location:
506 Atwood

Website

Google Scholar

University, College, and School/Department
Research Focus Areas:
  • Cancer Biology
  • Molecular, Cellular and Tissue Biomechanics
Additional Research:
In 2009, Khalid started his own lab at Emory University, where he currently investigates biophysical aspects of receptor-mediated cell signaling. To achieve this goal, his group has pioneered the development of molecular force probes and nano-mechanical actuators that are integrated with living cells. These materials are used to investigate the molecular mechanisms of a number of pathways where piconewton forces are thought to be important. These pathways include the Notch-Delta pathway, T cell receptor activation and the integrin-based focal adhesion pathway.

IRI Connections: