Jeffrey W. Bode
Principal Investigator, Professor, Eidgenössische Technische Hochschule (ETH), Zürich, Switzerland
Website:http://www.bode.ethz.ch/
E-mail:bode[at]org.chem.ethz.ch (Please replace [at] with @ when sending an email.)
Organic synthesis, carbene-catalysis, protein synthesis, bioconjugation, oligomerization
Bode is a gifted young rising star in synthetic chemistry. The work of Bode is directed towards the chemical synthesis of molecules and conjugates that are currently outside the reach of conventional synthetic methods. He is developing new chemical reactions and catalysts for making molecules of biological importance such as proteins, glycopeptides, sequence and length-controlled polymers, and covalent conjugates of these large structures. Recently, he developed a novel method for the ligation of unprotected protein segments, producing synthetic proteins very efficiently. He is also known as one of the pioneers of an entirely new branch of catalytic asymmetric synthesis, commonly known as "chiral N-heterocyclic carbene (NHC) catalysis". His catalysts will be applied in the development of molecules that selectively induce plant growth and molecules that can overcome species barrier. In addition, collaborating with the group of Ooi, he will also be involved in the development of small-molecule catalysts that can activate and transform bio-molecules in vivo.
Profile
1996 | B.S.; Trinity University, Texas, USA (Chemistry), B.A.; Trinity University, Texas, USA (Philosophy) |
1998 | Candidacy for Ph.D; California Institute of Technology, Pasadena, USA |
2001 | Dok. Nat. Sci.; ETH Zürich, Switzerland |
2001-2003 | JSPS Postdoctoral Fellow; Tokyo Institute of Technology |
2003-2007 | Assistant Professor; University of California, Santa Barbara, USA |
2007-2009 | Associate Professor; University of Pennsylvania, USA |
2009 | Full Professor; University of Pennsylvania, USA |
2010-present | Full Professor; ETH–Zürich, Switzerland |
2013-present | Visiting Professor; WPI-ITbM, Nagoya University |
Research Highlights
Selected Awards and Honors
2013 | Fellow of the Royal Society of Chemistry, UK |
2012 | ERC Starting Grant |
2011 | Elias J. Corey Award (ACS) |
2010 | Hirata Gold Medal |
2008 | Arthur C. Cope Scholar Award (ACS) |
Selected Publications
- Rohrbacher, F.; Deniau, G.; Luther, A.; Bode, J. W. Chem. Sci. 2015, 6, 4889-4896. Spontaneous Head-to-Tail Cyclization of Unprotected Linear Peptides with the KAHA Ligation. DOI: 10.1039/c5sc01774b
- Murar, C. E.; Thuaud, F.; Bode, J. W. J. Am. Chem. Soc. 2014, 136, 18140-18148. KAHA Ligations that form Aspartyl Aldehyde Residues as Synthetic Handles for Protein Modification and Purification. DOI: 10.1021/ja511231f
- Wucherpfennig, T. G.; Pattabiraman, V. R.; Limberg, F. R. P.; Ruiz-Rodríguez, J.; Bode, J. W. Angew. Chem. Int. Ed. 2014, 53, 12248-12252. Traceless Preparation of C-Terminal α-Ketoacids for Chemical Protein Synthesis by α-Ketoacid-Hydroxylamine Ligation: Synthesis of SUMO2/3. DOI: 10.1002/anie.201407014
- Huang, Y. L.; Bode, J. W. Nature Chem. 2014, 6, 877-884. Synthetic fermentation of bioactive non-ribosomal peptides without organisms, enzymes or reagents. DOI: 10.1038/nchem.2048
- Noda, H; Erős, G; Bode, J. W. J. Am. Chem. Soc. 2014, 136, 5611-5614. Rapid Ligations with Equimolar Reactants in Water with the Potassium Acyltrifluoroborate (KAT) Amide-Formation. DOI: 10.1021/ja5018442
- Members
- Yoshimura Group
- Yamaguchi Group
- Bode Group
- Crudden Group
- Frommer Group
- Itami Group
- Kamikouchi Group
- Hirota Group (collaborating with Kay)
- Kinoshita Group
- Ooi Group
- Tama Group
- Shimotohno Group (collaborating with Torii)
- Tsuchiya Group
- Yanai Group
- Laohavisit Group
- Mizuta Group
- Phung Group
- Kurihara Group
- Molecular Structure Center
- Live Imaging Center
- Chemical Library Center
- Peptide Protein Center
- Administrative Department
- Affiliated Researchers