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Physical Biosciences Division

Adam Arkin
Faculty Scientist
Assistant Professor of Bioengineering & Chemistry
University of California, Berkeley
College of Chemistry, Bioengineering Department

Department
Computational and Theoretical Biology, Synthetic Biology

Major Initiatives
Genomics:GTL (Principal Investigator)
Center for Integrated Physiome Analysis (Principle Investigator)
Systems Biology

Contact info:
Lawrence Berkeley National Laboratory
Physical Biosciences Division
One Cyclotron Road
Mailstop: Calvin Lab
Berkeley, CA 94720
USA

Location: 144 Calvin
Phone: (510) 495-2366
Fax: (510) 486-6059
Email: APArkin@lbl.gov

Web site: Arkin Lab

Research Emphasis
The Arkin Lab works on detailed modeling of genetic and biochemical networks with emphasis on developmental systems. The laboratory creates custom genetic circuitry in Saccaromyces cerivisiae and multichannel, protein and small molecule biosensors. The Arkin Lab is interested in the detailed physical analysis of the network of biochemical and genetic reactions that govern cellular development. The goal is to divine the engineering principles of the control systems that determine cell behavior and differentiation in response to internal and external signals. Because of their simplicity (relative to eukaryotic cells), and because many bacterial genome sequencing projects have recently completed, we study mostly bacterial and viral circuitry. Particular biological systems currently under study in my lab include, l-phage/Escherichia coli interactions, the role of stochastic phase-variation of type-1 pili in uropathic E. coli virulence, and analysis of the sporulation initiation and germination pathways in Bacillus subtilis. As the basis for such analyses we examine the detailed mechanisms of the underlying chemical reactions. For example, a rigorous physical analysis of the mechanisms of prokaryotic gene expression revealed that the temporal pattern of protein production from a single gene is an erratic and bursty stochastic process. Analysis of networks of such genes responsible for developmental switches demonstrated that while some architectures generate deterministic outcomes despite this noise, others exploit the noise to produce population diversity to, for example, evade attack by the immune system. In addition to theoretical analyses, the laboratory has started experimental measurements on such systems and has begun design and implementation (in yeast and E. coli) of our own custom genetic circuitry. Thus, the laboratory applies theoretical and computational analyses from dynamical systems, stochastic processes, chemical kinetics and statistical mechanics and methods from molecular biology to determine the principles of cellular signal processing and to aid in design of custom cellular circuitry that may, for example, act as sensitive biosensors.

Publications

Features
Division leads initiative to make cellulosic ethanol

Somerville awarded Balzan Prize for plant genomics

New funding awards to boost BCSB high-throughput
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