Ariel Fernandez

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Ariel Fernandez
File:Fernandez copy2.tif
Born (1957-04-08) April 8, 1957 (age 67)
Bahía Blanca, Argentina
Residence
Citizenship
  • Argentina
  • USA
Nationality Argentinian
Fields
Institutions
Alma mater
Thesis Structural Stability of Chemical Systems at Critical Regimes (1984)
Doctoral advisor Oktay Sinanoğlu
Doctoral students
  • Jianping Chen[1]
  • Xi Zhang[2]
Known for Dehydrons
Website
http://www.profarielfernandez.com/

Ariel Fernandez (born Ariel Fernández Stigliano, April 8, 1957) is an ArgentinianAmerican physical chemist and pharmaceutical researcher.[3]

Education and early career

Fernandez received Licentiate degrees in Chemistry (1979) and Mathematics (1980) from the Universidad Nacional del Sur, Argentina.[3] He then earned a Ph.D. from Yale University in 1984 with a thesis entitled Structural Stability of Chemical Systems at Critical Regimes[4] in the lab of Oktay Sinanoğlu. His early published papers also list him as being associated with the Weizmann Institute of Science, Princeton University, and the University of California at San Diego. He was a senior researcher in the division of Nobel laureate Manfred Eigen at the Max Planck Institute for Biophysical Chemistry.[3]

Career

Fernandez has been affiliated with multiple institutions including the University of Miami, Universidad Nacional del Sur, the Max Planck Institute of Biochemistry, the University of Chicago, Osaka University, the Indiana University School of Medicine, the Morgridge Institute for Research, and National Tsing Hua University.[citation needed] Fernandez held the Karl F. Hasselmann Professorship of Bioengineering at Rice University until 2011.[5] He is a member of the National Scientific and Technical Research Council (CONICET) in Argentina.[6] Fernandez is listed as an editor for multiple journals published by OMICS Publishing Group.[7][8][9] He currently is employed at a number of self-started pharmaceutical-related companies, including ProWDSciences, AF Innovation, and Ariel Fernandez Consultancy.[3]

Fernandez developed the concept of the dehydron,[10] an adhesive structural defect in a soluble protein that promotes its own dehydration.[11] A dehydron consists of an intramolecular hydrogen bond that is "underwrapped" or incompletely shielded from attack by water in the protein's solvation shell.[12] Dehydrons cause "epistructural tension", that is, interfacial tension around the protein structure[13] and thus promote protein–protein interactions and protein–ligand associations.[14] The nonconserved nature of protein dehydrons has implications for drug discovery, as dehydrons may be targeted by highly specific drugs/ligands engineered to improve dehydron wrapping upon binding.[15] Thus, dehydrons constitute effective selectivity filters for drug design, giving rise to so-called "wrapping technology", a platform to design safer drugs.[16] This technology was first applied by Fernandez and collaborators to redesign the anticancer drug Gleevec, in order to remove its potential cardiotoxicity.[17][18] In a recent patent applying wrapping technology, dehydron-rich regions in a specific protein were targeted by Richard L. Moss and Ariel Fernandez to design drug leads to cure heart failure.[19]

Fernandez has published two books and more than 200 peer-reviewed articles.[20] Four of his articles have been questioned by journals that had earlier accepted them. Publications in BMC Genomics,[21][22] Nature,[23][24] and PLOS Genetics[25][26] have been flagged with expressions of concern, and publication of an article in Annual Review of Genetics has been withheld.[27][28] In 2006, a Proceedings of the National Academy of Sciences article was retracted as an apparent duplicate publication.[29][30] Fernandez responded saying that no evidence has been published in the scientific literature that the data in those papers are invalid.[31]

Awards

Fernandez was awarded the Camille and Henry Dreyfus Distinguished New Faculty in 1989;[3] the Camille and Henry Dreyfus Teacher-Scholar in 1991;[32] a Guggenheim fellowship in 1995;[33] and is an Elected Fellow of the American Institute for Medical and Biological Engineering (2006).[34]

Published works

Books

  • Transformative Concepts for Drug Design: Target Wrapping, by Ariel Fernández (ISBN 978-3642117916, Springer-Verlag, Berlin, Heidelberg, 2010).
  • Biomolecular Interfaces, by Ariel Fernández Stigliano (ISBN 978-3319168494, Springer-Verlag, Berlin, Heidelberg, 2015).

Articles

According to his Google Scholar profile,[35] Fernandez's highest-cited articles include:

  • A Fernández, RS Berry. 2003. Proteins with H-bond packing defects are highly interactive with lipid bilayers: Implications for amyloidogenesis. Proceedings of the National Academy of Sciences 100(5): 2391-2396.
  • A Fernández, J Kardos, LR Scott, Y Goto, RS Berry. 2003. Structural defects and the diagnosis of amyloidogenic propensity. Proceedings of the National Academy of Sciences 100(11): 6446-6451.
  • A Fernández, HA Scheraga. 2003. Insufficiently dehydrated hydrogen bonds as determinants of protein interactions. Proceedings of the National Academy of Sciences 100(1): 113-118.
  • A Fernández, R Scott. 2003. Dehydron: a structurally encoded signal for protein interaction. Biophysical Journal 85(3): 1914-1928.
  • A Fernández, A Sanguino, Z Peng, E Ozturk, J Chen, A Crespo, S Wulf, et al. 2007. An anticancer C-Kit kinase inhibitor is reengineered to make it more active and less cardiotoxic. The Journal of Clinical Investigation 117(12): 4044-4054.

References

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  4. Ariel Fernandez. Yale University Dissertation: Structural Stability of Chemical Systems at Critical Regimes (Dissipative Structures, Potential Energy Surfaces). Published/Created:1984
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  10. Fernández A, Scott R. Dehydron: a structurally encoded signal for protein interaction. Biophys J. 2003 Sep;85(3):1914-28. PMID 12944304 [1]
  11. Fernández A, Scott R. Adherence of packing defects in soluble proteins. Phys Rev Lett. 2003 91(1):018102. PMID 12906578 [2]
  12. Koppes S. for University of Chicago News Office. Discovery of new sticky force that binds proteins could lead to better drug design. 2 July 2003 [3]
  13. Fernández A. Epistructural tension promotes protein associations. Phys Rev Lett. 2012 May 4;108(18):188102. PMID 22681121 [4]
  14. Monroe D. Focus: Proteins Hook up Where Water Allows. Physics 2012 May 4; 5, 51 [5]
  15. Crunkhorn S. Anticancer drugs: Redesigning kinase inhibitors. February 2008. Nature Revs Drug Discovery 7:120-121 doi 10.1038/nrd2524 [6]
  16. Boyd J. for Rice University News and Media. Drug design: New book introduces fresh approach. 28 April 2010 [7]
  17. Demetri G. D. Structural reengineering of imatinib to decrease cardiac risk in cancer therapy.2007 Dec 3; J Clin Invest. 117(12):3650–3653. doi 10.1172/JCI34252 [8]
  18. Dunham W. Reworked Gleevec curbs heart-related complication. REUTERS December 3, 2007 [9]
  19. Wisconsin Alumni Research Foundation, Invention: Treating Heart Failure by Inhibiting Myosin Interaction with a Regulatory Myosin Binding Protein (US patent No. 9,051,387), Inventors: Richard L. Moss and Ariel Fernandez [10]
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  30. "PLOS Genetics investigating paper by Ariel Fernandez", Retraction Watch, 9 January 2015
  31. Post on profarielfernandez.com January 23, 2016.
  32. Camille Dreyfus Teacher-Scholar Awards Program Past Awards
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External links

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