Alison Axtman

Research Associate Professor at University of North Carolina at Chapel Hill
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Contact Information
us****@****om
(386) 825-5501
Location
US
Languages
  • English -
  • Spanish -

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Bio

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Experience

    • United States
    • Higher Education
    • 700 & Above Employee
    • Research Associate Professor
      • Apr 2021 - Present

    • Research Assistant Professor
      • Jun 2015 - Apr 2021

      Principal Investigator, Medicinal Chemistry for the SGC-UNC, a center within the UNC Eshelman School of Pharmacy that functions as an open discovery network for protein kinases and a hub of the Structural Genomics Consortium (www.thesgc.org), an international public-private partnership that supports the discovery of new medicines through open access research.

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Investigator
      • Mar 2014 - Jun 2015

      Chemical Biology group Chemical Biology group

    • United States
    • Higher Education
    • 700 & Above Employee
    • Postdoctoral Scholar
      • Apr 2011 - Feb 2014

      • Developed high-throughput mixed lymphocyte response, immune-mediated cytotoxicity and lymphocyte activation assays in-house. • Confirmed that non-toxic, bryostatin-like PKC activators stimulate the immune system, leading to cancer cell death. • Forged new partnerships and managed multi-institutional collaborations with 2 U.S. universities as well as 4 Stanford University labs. • Proposed and efficiently synthesized novel diacylglycerol analogues that display PKC affinity on par with complex natural product leads. • Generated major advancements toward solving the biologically relevant membrane-associated, ligand-bound form of PKC with the Cegelski lab, treating resistant cancers using siRNA with the Teng lab, and exploring PKC-induced neuronal growth with the Cui lab.

    • United States
    • Higher Education
    • 700 & Above Employee
    • ACS Organic Chemistry and NIH Graduate Fellow
      • Aug 2006 - Mar 2011

      • Designed, prepared and evaluated novel modulators of the Hsp90 C-terminus that elicit anti-cancer and neuroprotective activities. • Conceived efficient syntheses of potential cancer chemotherapeutics that outperform clinically used agents in vitro and in vivo. • Managed multi-institutional collaborations with the NIH and 2 U.S. universities to facilitate advanced biological testing of leads. • Guided a subgroup of postdoctoral fellows and graduate students as a collaborative team working toward the design and preparation of novobiocin-inspired libraries.

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Research Assistant
      • Jun 2008 - Aug 2008

      • Established role of phosphorylation in Hsp90 regulation through making mutants of yeast Hsp90 and expressing human Hsp90 in E. coli. • Identified three novel classes of C-terminal Hsp90 modulators and explored protein isoform selectivity in yeast. • Extended collaboration through synthesis of an inhibitor of Hsp90 phosphorylation targeting Wee1 for use in vivo. • Established role of phosphorylation in Hsp90 regulation through making mutants of yeast Hsp90 and expressing human Hsp90 in E. coli. • Identified three novel classes of C-terminal Hsp90 modulators and explored protein isoform selectivity in yeast. • Extended collaboration through synthesis of an inhibitor of Hsp90 phosphorylation targeting Wee1 for use in vivo.

    • United States
    • Higher Education
    • 700 & Above Employee
    • Independent Undergraduate Researcher
      • Jun 2005 - May 2006

      • Prepared non-natural nucleotides that terminate chain elongation when DNA is damaged as potential anti-cancer chemotherapeutics. • Prepared non-natural nucleotides that terminate chain elongation when DNA is damaged as potential anti-cancer chemotherapeutics.

    • United States
    • Higher Education
    • 700 & Above Employee
    • Independent Undergraduate Researcher
      • Aug 2003 - May 2004

      • Synthesized organophosphorus compounds for development of new catalytic reactions and construction of novel materials. • Synthesized organophosphorus compounds for development of new catalytic reactions and construction of novel materials.

Education

  • University of Kansas
    Doctor of Philosophy (Ph.D.), Medicinal Chemistry
    2006 - 2011
  • University of Kansas
    Master of Science (M.Sc.), Medicinal Chemistry
    2006 - 2009
  • Case Western Reserve University
    Bachelor of Science (B.S.), Chemistry
    2002 - 2006
  • Case Western Reserve University
    Bachelor of Arts (B.A.), Spanish Language and Literature
    2002 - 2006

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