People - Faculty - Professor: Luc Jaeger

Field(s): Biochemistry/Materials 
Email: jaeger@chem.ucsb.edu
Phone: (805) 893-3628 Fax: (805) 893-4210
Office: 4649A PSB North
Selected Publications
Go to Research Group website
Bio: Dr. Jaeger received a "Magistère" degree (M.S) in Chemistry and Biology from the University Louis Pasteur of Strasbourg in 1990, and his PhD in Structural Biochemistry and Biophysics from the same university in 1993. After postdoctoral studies at the Scripps Research Institute (La Jolla, CA), he worked as a CNRS research scientist at the "Institut de Biologie Moléculaire et Cellulaire" in Strasbourg, from 1995 to 2002. He joined the faculty at UCSB in 2002.

Current Research

Research projects in Jaeger's lab are all related to RNA tectonics, a new LEGO game for supra-molecular chemists and biochemists. It refers to the construction of artificial RNA architectures with novel properties and takes advantage of the knowledge of folding and assembly rules governing the three-dimensional shape of complex natural RNA molecules. State-of-the-art RNA tectonics combines a broad range of theoretical and experimental approaches at the interfaces of chemistry, biology, and physics.

Deciphering the logic of RNA self-assembly
We are presently undertaking a major effort to characterize self-autonomous folding and assembly properties of various RNA structural motifs found in the ribosome. This work aims (i) at characterizing RNA regions that contribute to the overall assembly of the ribosome in the absence of proteins and (ii) at defining new RNA structural and assembly principles for RNA 3D structure prediction.

Design and engineering of programmable self-assembling materials based on RNA and other nucleic acids
The incredible informative power of RNA biopolymers should allow, in theory, to direct the self-assembly of hundreds of different molecules, and to specify the precise positioning of each of these molecules within a predefined network. RNA tectonics is presently used to build programmable RNA molecules able to self-assemble into two, three and four dimensional nano-arrays. The application of self-assembling RNA and other nucleic acids to biosensors and nano-electronic devices is also investigated.

RNA structural evolution
Different complex catalytic RNA molecules (ribozymes) that share a common structural scaffold associated to different catalytic domains, have been isolated from a large library of RNA sequences by in vitro Darwinian evolution techniques (SELEX). The common structural scaffold within these ribozymes undergoes divergent evolution as a consequence of its association with different catalytic domains, offering an unprecedented way to study RNA evolution at a three-dimensional level.

Selected Research Publications
Chworos, A, Severcan, I., Koyfman, A. Y., Wienkam, P., Oroudjev, E., Hansma, H. G. & Jaeger, L. (2004). Building programmable jigsaw puzzles with RNA. Science 306, 2068-2072
Liu, B., Baudrey, S., Jaeger, L. & Bazan, G.C. (2004). Characterization of tectoRNA assembly with cationic conjugated polymers. J. Am. Chem. Soc. 126, 4076-4077.
Jaeger, L., Westhof, E. & Leontis, N.B (2001). TectoRNA: Modular assembly units for the construction of RNA nano-objects. Nucleic Acids Res. 29, 455-463.
Jaeger, L. & Leontis, N.B. (2000). Tecto-RNA: One-dimensional Self-assembly through Tertiary Interactions. Angew. Chem. Int. Ed. Engl. 39, 2521-2524; Angew. Chem. 112, 2576-2580.
Jaeger, L., Wright, M. C. & Joyce, G. F. (1999). A complex ligase ribozyme evolved in vitro from a group I ribozyme domain. Proc. Natl. Acad. Sci. USA 96, 14712-14717.
Jaeger, L. (1997). The new world of ribozymes. Current Opinion in Structural Biology, 7, 324-335.

Westhof, E. Masquida, B. & Jaeger L. (1996). RNA tectonics: towards RNA design. Folding and Design 1, 78-88.



Department of Chemistry and Biochemistry 9510
University of California
Santa Barbara CA 93106 - 9510
Department Phone: 805-893-5675
Department Fax: 805-893-4120