Vytas A. Bankaitis　教授

Vytas A. Bankaitis             

Professor, E.L. Wehner-Welch Foundation Chair in Chemistry                

Texas A&M University, USA                

Education and Post-Graduate Training                

• Edinboro University, Edinboro, PA; BS; 1978; Biology                

• Clemson University , Clemson, SC; MS; 1980 Microbiology                

• University of North Carolina, Chapel Hill, NC; PhD; 1984; Microbiology                

• California Institute of Technology, Pasadena, CA Postdoctoral; 1986; Cell Biology                        
  

Positions and Honors                

• 1978-1980 Graduate Student, Department of Microbiology, Clemson University, Clemson, South Carolina. Advisor: Dr. Ellis L. Kline.                

• 1980-1984 Predoctoral Fellow of the Humphrey Foundation, Department of Microbiology and Immunology, The University of North Carolina School of Medicine. Advisor: Dr. Philip J. Bassford, Jr.                

• 1984-1986 Postdoctoral Fellow of the Helen Hay Whitney Foundation, Division of Biology, The California Institute of Technology, Pasadena, CA.              

• 1986-1992 Assistant Professor, Department of Microbiology, University of Illinois, Urbana, IL. Head: Dr. Charles G. Miller.                

• 1992-2001 Associate Professor then Professor, Department of Cell Biology, University of Alabama at Birmingham, Birmingham, AL. Head: Dr. Richard B. Marchase.         
  

• 2001-2011 Professor and Chair, Department of Cell & Developmental Biology, The University of North Carolina School of Medicine, Chapel Hill, NC.       

• 2012-Present E.L. Wehner-Welch Foundation Chair in Chemistry, Department of Molecular & Cellular Medicine, Texas A&M University Health Science Center, College Station, TX.                       
  

Honors                

• Recipient of an NCAA Postgraduate Fellowship - A national award presented to 6 outstanding student-athletes, 1978.                

• Recipient of the President’s Award for the outstanding student research presentation; regional meeting for the Southeastern and South Carolina branches of the American Society for Microbiology, November, 1979.                

• Recipient of a Predoctoral Fellowship of the Humphrey Foundation - awarded to outstanding incoming graduate students at the University of North Carolina, August, 1980.                

• Recipient of a Postdoctoral Fellowship of the Helen Hay Whitney Foundation, January, 1984.                

• Designated an Arnold Beckman Scholar, University of Illinois, 1986.                

• Member, Cell Biology Advisory Panel, National Science Foundation, 1988-1992.        
  

• Member CDF-2 IRG, NIH, 2001-2004.                

• Chairman CDF-2 and MMBP Initial Review Group, NIH, 2004-2006.                

• Member, Faculty of 1000, Membrane Trafficking and Sorting Section                

• Member, Editorial Advisory Board, EMBO Reports, 2012-present.                

• Vice-Chair -- Gordon Research Conferences -- Signal Transduction Within the Nucleus, 2009.                

• Chair -- Gordon Research Conferences -- Signal Transduction Within the Nucleus 2011                

• Member, Program Planning Committee, American Society for Biochemistry and Molecular Biology Annual Meeting, 2011.                

• Director, Lipid Research Division, American Society for Biochemistry and Molecular Biology, 2013               
                 

Research Interest                

Lipid-mediated Signal Transduction                

My laboratory is interested in the regulatory interfaces between novel lipid-mediated signal transduction pathways and important cellular functions. The focus of our work is the phosphatidylinositol/ phosphatidylcholine transfer proteins (PITPs), a ubiquitous but enigmatic class of proteins. Ongoing projects in the laboratory derive from a multidisciplinary approach that encompasses biochemical characterization of novel members of the metazoan PITP family, and the application of genetic, molecular and biophysical approaches to detailed structural and functional analyses of PITPs. The laboratory breaks down into two groups: a group that studies the mechanism of function of fungal and plant PITPs, and a group that generates knockout mice and analyzes the function of specific PITP isoforms in the mammal. Our collective evidence indicates that PITPs coordinate key interfaces of lipid-driven metabolic reactions and intracellular signaling pathways in both yeast and mammals. Inappropriate regulation of these interfaces compromises membrane trafficking events, growth factor receptor function, cell growth control, and regulation of key developmental pathways. Because defects in any one of these pathways define recognized mechanisms cancer-potentiating mechanisms, PITPs represent essentially unstudied regulators whose dysfunction is likely to influence the activities of cellular processes required for cellular homeostasis. Of additional interest is our recent finding that one of our PITP-deficient mouse lines potentially provides a unique model for chylomicron retention disease, hypoglycemia and brain inflammatory disease. Relevant approaches that the laboratory employs include: molecular biology, protein and lipid biochemistry, confocal and electron microscopy, mouse gene knockout technology, and classical and molecular genetics. The lab is also developing new approaches for rapidly and confidently identifying the first small molecule inhibitors directed against target PITPs of interest and other key enzymes of lipid metabolism.                

Key discoveries made by the lab include                

• The first demonstration that lipids are integral components of the strategy by which the core membrane trafficking machinery is regulated.                 

• The first identification of an in vivo function for a phospholipid-transfer protein via the determination that one of the yeast sec gene products (i.e. Sec14) is a PITP.                

• The ‘bypass Sec14’ studies that are widely credited as representing seminal advances in the membrane trafficking field on the basis of providing the first experimental evidence that lipid metabolism is intimately connected to membrane trafficking reactions.  Previous to that work, an active role for lipids was ignored in discussions of how transport vesicles bud, dock and fuse.                

• Solution of an apo-Sec14 crystal structure that provided the first description of a novel structural fold termed the Sec14-domain or, alternatively, the CRAL-TRIO domain.                

• The first demonstration that Kes1, one of the enigmatic oxysterol binding proteins, regulates TGN membrane trafficking with the Pik1 PtdIns 4-OH kinase a likely target for control.                

• The first isolation of headgroup-specific Class 1 PITP PL-binding mutants and the first analysis of what role individual PL-binding activities play in Class 1 PITP functio. 
  

• The first creation of a mammalian model for PITP nullizygosity and the demonstration that PtdIns binding is an essential functional property of a metazoan PITP.       
  

• Structural, biochemical and genetic studies that demonstrate PITPs both potentiate and determine outcomes of PtdIns kinase action, a particularly interesting and novel mode of signaling control.                

• Identification and in vivo and in vitro validation of small molecule inhibitors specifically directed against the yeast Sec14.  This effort involved assembly of a unique screening platform for indentifying SMIs directed against any PITP of the investigator’s choice.                

• Discovery that a specific ORP (Kes1) participates in a novel signaling pathway by integrating endosomal lipid metabolism with TOR signaling and nitrogen sensing.