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| Vicki Nienaber, Ph.D.: President and CSO, Founder | |||
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| Robert Meadows, Ph.D.: Co-founder | |||
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Dr. Meadows is a primary inventor of the SARbyNMR FBLD method first published in Science in 1996. The method was developed at Abbott laboratories and Dr. Meadows work contributed to two FBLD derived clinical candidates while at Abbott. He has extensive experience in cheminformatics, computational chemistry and NMR spectroscopy. Dr. Meadows built the first fragment library that is still in use at Abbott Laboratories. At Zenobia, Dr. Meadows built custom databases for storing scientific and business data. He has also served as an advisor in the design of Zenobia’s proprietary CNS library. Dr. Meadows has nearly 20 years experience in the pharmaceutical industry. |
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| Ruo Steensma, Ph.D.: Director of Medicinal Chemistry | |||
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| John Badger, Ph.D.: Director of Structural Biology | |||
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Dr. Badger has over 20 years of experience in computational crystallography, structure-based drug discovery, fragment-based lead discovery and automated structure determination. John is a pioneer in high-throughput crystallography. At SGX Pharmaceuticals, John led the development and implementation of one of the first automated structure determination pipelines. This software was used to determine over 100 novel structures, over 1000 co-crystal structures and was subsequently adapted to analyze crystallographic fragment-based screening data. Immediately prior to joining Zenobia Therapeutics, John was Director of Structural Biology at ActiveSight. He co-developed MIFit+, Rigaku's automated structure solution software suite and ran the Automatic Structure Consortium, an organization whose members included representatives from several large pharmaceutical companies. At ActiveSight, John developed algorithms to analyze fragment-screening data, designed the ActiveSight fragment library and was instrumental in performing the fragment co-crystal structure analysis for ActiveSight’s pilot lead discovery program. | ||
| Barbara Chie-Leon, M.S.: Sr. Scientist, Protein Biochemistry | |||
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Barbara Chie-Leon has over 10 years experience in the field of protein expression, purification and biochemical assay development. Barbara has been involved in several high-throughput crystallography programs such as the kinase pipeline program at SGX pharmaceuticals. While at SGX, Barbara purified nearly 60 different proteins, many of which were kinases that could not be purified by traditional purification methods. Barbara was also a member of the biochemistry group where she developed and conducted assays for lead optimization and fragment-screening by biochemical assay. Prior to joining Zenobia, Barbara was at ActiveSight. Here, she developed purification and baculovirus expression protocols for difficult proteins and successfully cloned, expressed and refolded of proteins isolated from E. coli. Barbara is known for her unique perspective and intuition in developing protocols for expression and purification of proteins that ultimately produce protein crystals. |
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| Vandana Sridhar, M.S.: Scientist, Protein Biochemistry and Crystallization | |||
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Vandana Sridhar has nearly 15 years experience in the field of protein crystallization. Vandana has worked at several prestigious institutions including Scripps Research Institute, Merck and Co., and Syrrx. While at Scripps, Vandana crystallized many difficult proteins including the first p450, 2C5 which is a membrane bound protein and oversaw the crystallization efforts of the Joint Center for Structural Genomics (JCSG). While at Syrrx, Vandana worked on several key drug discovery targets and led the kinome crystallization effort. Prior to joining Zenobia Therapeutics, Vandana was a purification and crystallization scientist at ActiveSight. During her time at ActiveSight, Vandana was widely believed to possess the Midas touch as she was able to produce diffraction quality crystals from even the most challenging targets. |
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| Cheyenne Logan, M.S.: Senior Research Associate | |||
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Cheyenne Logan was a significant team member of the Protein Structure Initiative (PSI) 1 and 2 purification group while at SGX Pharmaceuticals where she purified over 500 crystallization quality proteins which included NHRs, kinases, phosphatases, and proteases. At SGX Pharmaceuticals, she also managed, purified and characterized several targets for the Eli Lilly collaboration which included phosphorylated, lysine methylated, refolded, and secreted proteins. At the University of California, Irvine, she initiated the purification of CCR5, a transmembrane chemokine receptor utilized for HIV entry into cells. She synthesized, purified, and characterized peptides which included Byetta and Symlin while at Amylin Pharmaceuticals. Prior to joining Zenobia Therapeutics, while at ActiveSight, she cloned, expressed and purified client target protein which included kinases, tautomerases, proteases. |
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| Leslie Hernandez: Research Associate | |||
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Leslie Hernandez is a graduate of San Diego S |
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