Home
People
Publications
Research
Meetings
News
Contact Us

We are part of:
Department of Biopharmaceutical Sciences
California Institute for Quantitative Biosciences (QB3)
Integrative Program in Quantitative Biology
Graduate Group in Biophysics
Graduate Program in Bioinformatics
Graduate Program in Chemistry and Chemical Biology (CCB)
Graduate Program in Pharmaceutical Sciences and Pharmacogenomics (PSPG)
NIH Center for Protein Folding Machinery
NIH Center on "Engineering Cellular Control: Synthetic Signaling and Motility Systems"
Synthetic Biology Engineering and Research Center (SynBERC)
We are located at:
UCSF QB3
1700 4th Street, Byers Hall
San Francisco, CA 94143-2540
(CA 94158 for courier delivery)
401 (computational lab)
409 (experimental lab)
408 B (Tanja Kortemme's office)

Internal site (password required)




Principal Investigator

 Tanja Kortemme Tanja
My main scientific interests range from the details of the physical interactions between atoms and molecules to the architecture and evolution of interaction networks in complex biological systems.

Vordiplom (BS) Chemistry,
Physical Chemistry
University of Hannover, Germany
Diplom (MSc) Biophysics Stanford University / University of Hannover
Dr.rer.nat (Ph.D.) Biochemistry EMBL Heidelberg / University of Hannover
Postdoctoral work in computational and structural biology at EMBL Heidelberg and the Howard Hughes Medical Institute, University of Washington, Seattle

Postdoctoral Researchers

 Greg Kapp Greg K.I have attended Major League Baseball games in 12 major league parks (9 currently active parks).
I am working with our computational protein design tools to build new interfaces between cell signaling proteins. Currently I am constructing and experimentally testing the redesigned specificity between small Rho-family GTPases and their exchange factors. Eventually, we would like to reintroduce these new protein-protein interactions into living cells and use them to modulate cellular behavior.

Bachelor of Science, Arts Biology, Chemistry University of Richmond
Ph.D. Biochemistry Duke University Medical Center

 Mariana Babor MarianaI enjoy travelling. A lot!
I am interested in understanding and modulating mechanisms that lead to protein cross-reactivity -- in particular those that result from protein flexibility. To address these questions, I will combine computational and experimental strategies.

Licenciatura Biology University of Buenos Aires, Argentina
Master of Science Bioinformatics Weizmann Institute of Sceince, Israel
Ph.D. Bioinformatics Weizmann Institute of Sceince, Israel

Associate Specialist

 Cristina Melero CristinaDuring my free time, I enjoy hiking, biking and other outdoors activties. I also love big white dogs, as you can see (dog not shown).
I apply a combination of computational and experimental approaches to protein-protein interactions in PDZ domain containing proteins. My work will help to elucidate the contributions of specific residues to both affinity and specificity in PDZ-ligand interactions. More generally, we hope to understand how PDZ domain containing proteins help organize multimeric complexes involved in essential cellular processes.

Bachelor of Science Physical Chemistry Complutense University, Madrid

Graduate Students

 Greg Friedland Greg F.I like to rock climb and play power ballads on guitar.
I'm working on extending our computational model of a protein from a single static structure to a dynamic ensemble of structures. To achieve this I'm using our simplified all-atom potential to develop a model for protein motions that explains NMR measurements of protein dynamics. We hope this will help us understand the types of motions proteins make in solution and what the functional consequences are of such motions.

Bachelor of Arts Computer Science and Physics Dartmouth College

 Matt Eames MattI play for keeps.
I'm investigating the molecular evolution of protein domains and networks. I'm also developing experimental techniques to probe the asymmetric evolution of genes.
Previous Work: Co-Owner - FM Mowers, VA; Driver - Red Cross, VA; Drive-Thru Cashier - Taco Bell, VA; Waiter - Luciano's, VA; Indexer - Indexing Partners, VA; Fire Fighter - National Park Service, CA; Bartender - The Yorkshire Grey, UK; Plumber/Technician - Eltron Research, CO; Chief Technical Officer - Lucid Dimensions, CO


Bachelor of Science Physics University of Virginia

 Dan Mandell DanThat's right, Billy.
My theoretical work concerns the treatment of proteins as conformational ensembles to relax the fixed-backbone assumption during protein design. Currently I am developing a procedure derived from robotic kinematics to generate multiple backbone conformations for protein interfaces to broaden the sequence space sampled during interface redesign. On the practical side, I am applying these methods for two purposes: (1) to produce "adaptor" proteins to mediate interactions between aggregation prone mutants of disease related proteins and chaperones to facilitate their folding, (2) to design highly specific cell surface-binding proteins to interfere with signaling cascades exploited during cancer metastasis and angiogenesis.

Bachelor of Science Symbolic Systems Stanford University
Master of Science Artificial Intelligence University of Edinburgh, UK

 Elisabeth Humphris ElisabethI heart proteins.
I am working on extending our lab's current computational methods for the prediction and design of protein-protein interactions by developing a "multi-state" design algorithm, which would allow multiple selective pressures to simultaneously be present during the computational optimization process. This project would model the integration of various selective pressures on cellular signaling proteins which have evolved a specific amino acid sequence for both maximizing desired properties (such as fold stability and correct binding of desired signaling molecules) while simultaneously minimizing undesirable properties (such as unwanted cross-talk with incorrect binding partners). If successful, "multi-state" design methodologies should give us 1) an improved understanding of a per-residue contribution to binding specificity and 2) improvement in our ability to experimentally engineering "designer" proteins with altered binding properties. Once developed in relation to protein-protein specificity, the "multi-state" design methodology proposed here could easily be extended to determine the optimal amino acid sequence for proteins which could adopt several structural conformations or perform several functions.

Bachelor of Arts Natural Sciences (Biology/Mathematics) New College of Florida

 Rich Oberdorf RichI am but a man, hanging off the edge of an enormous protein.
I'm interested in developing mathematical models to describe various aspects of cell signaling. My work is specifically geared toward understanding the roles of scaffolding proteins and the formation of assemblies of proteins in signal transduction. Towards this goal, I am building models to relate assembly formation by the scaffolding protein INAD and kinetics of TRP channel gating during photoresponse in Drosophila photoreceptor cells. Ultimately, we hope to see modeling insights borne out in an experimental system.

Bachelor of Science Physics and Mathematics Brandeis University

 Colin Smith ColinMy other scientific interest is studying self-induced hypothermia while swimming in San Francisco Bay.
My research centers around the functionally relevant loop motions of proteins in their native state. I am developing and evaluating models which capture and efficiently sample those motions in all-atom simulations. Using Monte Carlo and other techniques, I am interested in improving our ability to accurately predict the free energies of transitions on the microsecond time scale. Towards that end, I aim to develop model systems for experimentally testing and refining our techniques for prediction/design of directed flexibility. Longer term, I want to engineer a local allosteric switch into a protein which is not currently allosterically regulated.

Bachelor of Arts Biology and Computer Science New York University

 Ryan Ritterson Ryan I would start a company that would build a hydrogen infrastructure so we can move our economy off petroleum.
I am principally interested in the computational reengineering and redesign of biological objects to both answer difficult scientific questions as well as solve interesting problems in both biological systems and larger abiotic contexts. Currently, I am seeking ways to pry out new knowledge about the relationship between cadherin- mediated adhesion and cell to cell signaling, with the hope of both learning more about how the two processes are interrelated and perhaps discovering novel ways of controlling them.

Bachelor of Science Computational Engineering Science UC Berkeley

Current Rotation Students

Elaine Kirshke, Biophysics
Charles Kehoe, BMI
Noah Ollikainen, BMI

Past Rotation Students

Jaline Gerardin, Biophysics, Fall, 2007
Alvin Tamsir, Tetrad, Spring, 2007
Sheel Dandekar, Biophysics, Spring 2006
Reid Williams, Biophysics, Fall 2006
Dan Gray, CCB, Fall 2006
Michael Hicks, PSPG, Winter 2005
Chris McClendon, Biophysics, Fall 2005
Ian Harwood, Biophysics, Spring 2005
Kareen Riviere, PSPG, Winter 2005
Mike Keiser, BMI, Fall 2004