Institute for Theoretical Physics Program

on
Statistical Physics and Biological Information
Institute for Theoretical Physics, Santa Barbara
dates: January 16 - June 15, 2001
Coordinators: Walter Fitch,Terence Hwa, Luca Peliti, Gary Stormo, Chao Tang


Long-term Participants

Mark Azbel

Main interests: Electron theory of metals (1955-1970, predicted cyclotron resonance, Hofstadter butterfly), DNA thermodynamics (1970-1980), mesoscopics (1980-1995, derived 2D Landauer dormula, giant conductance fluctuations, predicted 3D quantum Hall), mortality and microevolution (1995-present, phenomenological theory of survival in changing  nvironment. Concept of invariance is applied to mortality studies.  Invariance implies symmetry to specified transformations.  Symmetry yields an exact "conservation law" of the  nvariant survival, because complexity leads to invariance to an unspecified number of unquantified variables describing the population and environment. The invariant probability to survive to a given age depends on the infant mortality only. The dependence is piecewise linear, independent of population, its life history and living conditions. The intersections are simultaneous for an entire population of any age. I plan to discuss physical and biological implications of this law, which agrees with all experimental data for humans and flies, and which I argue may be universal).
 

Nicolas Buchler

My background is in biophysics, having recently finished graduate work at the University of Michigan.  The majority of my thesis was theoretical and computational approach to protein structure designability;  that is, attempting to understand the physics of why some protein structures could be easier to design or more frequent in the biological database.  My research interest and the drive behind participating in this workshop is to learn more about the interplay of evolution in biomolecular folding, structure, and function, with particular attention to genetic networks.
 

Ralf Bundschuh

With a training in theoretical condensed matter and mathematical/statistical physics I have been concentrating on problems inspired by molecular biology and bioinformatics in the last years. My main research areas have been the statistics of sequence alignment and RNA secondary structure formation. During the workshop I hope to discuss these sort of problems with a large variety of people and learn more about other areas of biology which pose interesting questions amenable to the methods of statistical physics.
 

Emily S.C. Ching

Emily S.C. Ching is trained as a theoretical physicist and her research interests are non-equilibrium nonlinear systems. In particular, she has been working on fluid turbulence. In turbulent flows, physical quantities such as velocity, pressure and temperature, display irregular fluctuations both in time and in space. The two key issues in the fundamental studies of turbulence are (i) to make sense of these complex fluctuations, and (ii) to understand the intermittent nature of turbulence and why dimensional agruments of the kind proposed by Kolmogorov are not exactly correct. Ching attempts to tackle these problems using a mixture of systematic theory, phenomenology and analyses of experiments. She has developed a formalism that characterizes the probability distribution of fluctuating quantities in terms of conditional averages. Interesting general features of the conditional averages of various turbulent quantities have been discovered in different turbulent flows.

By participating in the ITP program on statistical physics and biological information, Ching would like to learn about the state-of-the-art analyses of the large amount of biological data generated recently. Especially, she hopes to be able to make use of her experience of analyses of complex turbulent data to try to unravel biologically relevant knowledge from data such as DNA and amino-acid sequences.
 

Tom Chou

My background and training are in theoretical physical chemistry, soft condensed matter physics, and applied mathematics. Among my interests are the physical mechanisms of bioenergetics, transport, and cellular/subcellular structure. I am particularly keen on learning new mathematical ways of describing protein structure and genetic regulation.
 

Eytan Domany

My main current interest is DNA expression analysis (for details see our website and PNAS article). My other possibly relevant field of interest is protein folding.
 

Barbara Drossel

My general research fields are statistical physics of disordered systems and of system far from equilibrium. During the past few years, I began to work also on topics related to biological evolution. May main  interests in this context are
- coevolution
- networks (species networks as well as genetic networks)
- different levels of organization (spatial patterns, group formation, the role of large-scale structure)
- the evolutionary role of transpositions and other mutations which are more complicated than point mutations.

I hope to learn more about biology and about models for evolution at this workshop; I am also looking forward to meeting interesting people and having some good discussions - one or two of which hopefully lead to collaborations.
 

Ulrich Gerland

Previous interest:
   Mesoscopic quantum physics (weak localization and Kondo effect in quantum dots), quantum chaos, random matrix theory
Current interest:
   1. Sequence-specific mechanical properties of RNA/DNA, specifically: force-induced denaturation of RNA
   2. Protein-DNA interaction
 

Massimo Di Giulio

I am interested in all the mechanisms and molecules that are related to the origin of messenger RNA translation. In particular, as far as the origin of the genetic code is concerned, attempts have been made to falsify the proposed theories and thus identify the coevolution hypothesis as the one that best seems to capture the observations. Analysis of ß-sheets of proteins has identified the main adaptive theme that promoted the origin of genetic code organisation. I have studied the optimization level of the physicochemical properties of amino acids in the set of amino acid permutation codes that respects the biosynthetic relationships between amino acids. This analysis seems to suggest that the historical factors played a leading role in forging the genetic code organisation. Recently, I have presented evidence that the late stage of genetic code structuring took place at a high temperature. The tRNA molecule is hypothesised to have originated by means of the direct duplication of an ancient gene codifying for a hairpin structure, and a non-monophyletic origin has been suggested for this molecule. Moreover, a model has been proposed for the origin of protein synthesis which hypothesises that the interaction between two hairpin RNA structures charged with amino acids was essential to the evolution of this process. Whereas the aminoacyl-tRNA synthetases were placed, according to their class, in an evolutionary relationship with either the proteins intervening in nonribosomal synthesis of peptide antibiotics or with the family of glutamine amidotransferases. I have also presented a model for the origin of the enzyme-coenzyme complex. This model is essentially based on an intermediate formed by a tRNA-like molecule covalently linked to a polypeptide. Thus, the model attributes the majority of the catalytic role in the ribonucleoprotein world to the latter complex and, in doing this, it takes into account the birth of the key intermediary in the origin of protein synthesis, namely peptidyl-tRNA, which would have otherwise been extremely difficult to select.

Key words: Origin of life - RNA world - Origin of translation - Genetic code origin - Protein synthesis origin - tRNA origin - Last Universal Common Ancestor - Aminoacy-tRNA synthetases
 

Nigel Goldenfeld

I have worked on problems in pattern formation (e.g. snowflake growth), polymers (e.g. gelation/vulcanisation), statistical  physics (e.g. turbulence, liquid crystals, phase transition kinetics),  condensed matter physics (e.g. high temperature superconductivity) and  mathematical physics (e.g. global asymptotics, singularity formation).  During this program, I want to understand what biological  information is, what biological constraints can be used in conjunction with genome sequences to understand gene expression, and whether algorithm heuristics motivated by statistical physics can be of biological value.
 

Bailin Hao

Previous interest:
  1. 3D Ising model, see Chaos and Order in Nature, ed. by H. Haken, Springer-Verlag, 1981.
  2. Non-equilibrium statistical physics, see Physics Reports, 118 (1985)1-131.
  3. Books, see Chaos (1984, 1990), Elementary Symbolic Dynamics and Chaos in Dissipative Systems (1989), Applied Symbolic Dynamics and Chaos (1998), all published by World Sceintific

Current interest:
  1. Avoided and under-represented strings in bacterial complete genomes
  2. Prokaryote phylogeny based on complete genomes
  3. Repeated sequences in prokaryote complete genomes
 

Paul Higgs

I have a PhD on the Statistical Physics of Polymers from the University of Cambridge UK (1986-89). I held post-doc positions in France at Strasbourg (1989-90) and Saclay (1990-92). I was a Royal Society Research Fellow at the University of Sheffield (1992-95). Since 1995 I have had a tenured position in the School of Biological Sciences at the University of Manchester. I am Course Director for the MSc in Bioinformatics. I also teach evolutionary biology and genetics at undergraduate level. Details of Bioinformatics research and teaching at Manchester are available at http://bioinf.man.ac.uk.

I am currently working in the following areas.
1. RNA structure and evolution. Selection for thermodynamically stable secondary structures in molecules such as ribosomal RNA and transfer RNA has effects on the properties of the sequences and their rates of evolutionary change.
2. Phylogenetic methods. We are developing methods for construction of phylogenetic trees from molecular sequences using maximum likelihood and Markov chain Monte Carlo methods. We are particularly interested in applications to RNA phylogenies.
3. We are developing a relational database for comparative genome analysis. This will allow systematic study of genome evolution (gene duplications, losses and rearrangements), comparison of codon usage between organisms and between genes, and comparison of rates of evolution of different genes.
4. Together with A McKane and B Drossel, also at this ITP meeting, I have been working on the Webworld model of the evolution of multi-species communities. The model generates foodweb structures for sets of many interacting species and considers the the short term population dynamics (predator-prey equations) and the long term evolutionary dynamics (speciations and extinctions).

I will be at ITP from April-June. I look forward to starting new research collaborations. If anyone has any suggestions for work we can do together, please e-mail me before then: Paul.Higgs@man.ac.uk.
 

Joachim Krug

My general background is in nonequilibrium statistical physics. In the past, I have worked mostly on nonequilibrium phenomena at surfaces, such as growth and electromigration. Recently I have moved away from generic models, such as the celebrated Kardar-Parisi-Zhang theory, towards the microscopic kinetic  processes occurring at real crystal surfaces, e.g. in- and interlayer diffusion and two-dimensional nucleation. A second field of recent activity is driven single-file transport in lattice gases and cellular automata, with applications to traffic flow.

I also have a long standing but largely dilettante interest in biological evolution, which has so far resulted in some preliminary work on quasispecies dynamics. I come to Santa Barbara to learn about current developments in molecular biology, notably in protein folding and related areas, in the hope of picking up some interesting kinetic or statistical problems that I might work on in the future.
 

Hoong-Chein Paul Lee

WHO am I. b. HK 1941. BSc Nat'l Taiwan U 1963. PhD McGill 1969. Chalk River Labs. Ontario Canada 1969-1993.  Chair, Nat'l Chung Hsing U 1993-1995.  Professor, Phys Dept, Nat'l Central U 1995-present; joint appointment at Life Sci. Dept 2000-present.

WHAT I do. Prior to 1996: nucl phys, many-body, part. phys, quantum field theory, quantum group/algebra and exactly solvable models. 1996-97, complexity.  From 1997 on: computational biology/bioinformatics. In particular:
Biosequences    - http://www.phy.ncu.edu.tw/hclee/SURE/reprints/hao00.pdf
Protein folding - http://www.phy.ncu.edu.tw/hclee/SURE/reprints/hcl00a.pdf
                - http://www.phy.ncu.edu.tw/hclee/SURE/reprints/hcl00b.pdf
                - http://www.phy.ncu.edu.tw/hclee/preprints/hpg.pdf
DNA uptake system in human pathogens  - http://www.phy.ncu.edu.tw/hclee/preprints/uss1.pdf
mol. evolution  - http://www.phy.ncu.edu.tw/hclee/preprints/oligo1.pdf

E-mail: hclee@phy.ncu.edu.tw

Peter Lenz

My background is in theoretical condensed matter physics. Till now, my research has focused on issues related to the morphology of soft matter systems such as the shape of droplets on patterned substrates or shape instabilities of highly charged helium bubbles. I'm interested in applying methods and techniques of soft matter physics to biological systems.
 

David Lubensky

I am a 6th year graduate student in the physics department at Harvard and a Graduate Fellow at the ITP.  My training is in theoretical soft condensed matter physics (e.g. polymers and colloids) and statistical physics; while at Harvard I have worked with David Nelson on several biologically inspired problems.  In collaboration with an experimental biophysics, I have looked at the dynamics of polymers threaded through narrow pores.  Under the influence of an electric field, single-stranded polynucleotides can be driven through biological pores; we sought to understand what determines their distribution of passage times.  More recently, I have been interested in single molecule micromanipulation experiments (in which, for example, beads are attached to a polymer and used to pull on it), especially in the presence of quenched randomness. In particular, we have obtained results on the mechanical denaturantion of DNA with a random based sequence.
 

Enzo Marinari

I mainly work on disordered systems: the protoptypes in the field are spin glasses, that are materials that are maybe not so interesting in themselves, but have the merit of having started a quantitative study of disordered systems. Numerical simulations are a technique of choice for studying this kind of materials, but the very complex free energy landscape of these systems makes the task very difficult to accomplish. Because of that I have been using and trying to improve Optimized Monte Carlo methods, that are also very needed when studying, for example, protein folding.

The most relevant physics question connected to this issues is about if realistic, finite dimensional spin glass like systems behave like the analytic solution of the mean field theory or not.

A different activity we just started recently is based on explicitely finding T=0 ground states of disordered systems. In this way one avoids the slowing down of the numerical simulations. I have recently been doing work on the connection among the T=0 results and the T>0 landscape.

I have also recently worked analyzing the dynamical behavior of these very complex systems: I have tried to determine, for example, the scaling laws governing the (potentially different) time scales of the process.
 

Alan McKane

My early research was mainly in the application of field theory ideas to statistical mechanics, for instance renormalization group methods and the use of instantons to describe rare fluctuations and the asymptotic nature of perturbation expansions. Later my interests turned to non-equilibrium statistical mechanics, and I have recently used similar techniques to investigate topics such as stochastic ratchets, state selection and the coarse-graining of partial differential equations.

My background in non-equilibrium systems naturally led me to develop an interest in the modelling of ecological systems. Recent work includes: a model of food web dynamics which describes processes on both ecological and evolutionary time scales, a model of a species-rich ecological community which makes predictions about the species abundance distribution
and other generic features of ecosystems, and the use of a continuous form of the Lotka-Volterra competition equations to investigate character displacement and competitive speciation.

I'd like to meet people at the workshop with different backgrounds and approaches to ecological modelling, and to come away with a better understanding and appreciation of other modelling philosophies.
 
 

Jerome K. Percus

Background- primarily statistical physics

Directions of interest: Equilibrium and dynamics of single chain macromolecules, unconfined and confined, Effect of evolutionary models on current distribution and associations of biomolecules Tracking information flow through hierarchy of levels between molecular and organism populations

Reason for participation: to get better intuitive grasp of characteristics and dynamics of molecularly based complex biosystems

accompanied by:  Ora E. Percus

Background- combinatorics, probability, and statistics

Directions of interest: Combinatorial and applied probability problems arising in molecular biology

Reason for participation: to get helpful biologicak background
 

Ramakrishna Ramaswamy

In the past few years I have been interested in the analysis of DNA sequences to detect short- or long-ranged correlations.  Coding regions of the DNA in all organisms have a universal short-range correlation: there is a marked 3-base periodicity. This periodicity is most easily detected via the Fourier transform and shows up as a sharp peak in the power spectrum. We use this feature in a in-silico gene detection technique, GeneScan, which is an ab inito or non consensus method for locating genes. My current research focuses on the uses of different correlation-function based methods in order to identify biologically significant features (genes, repeats, etc.) on genomic DNA.
 

Sorin Solomon
 

Ed Trifonov

Originally physicist (electronics). 30 years doing biology, but with physical mind setting. Currently mostly involved with genomic sequence codes, protein structure and reconstruction of the earliest stages of evolution. Contributions to: Origin and evolution of the triplet code, Stages of protein evolution, Loop structure of proteins, Molecular theory of fast adaptation (tuning function of tandem repeats), Multiple overlapping codes, Chromatin code, DNA shape code (sequence-dependent DNA curvature and writhe), Translation framing code, Genome units, combinatorial fusion theory of genome evolution, Linguistic complexity.
Would like to take home updates on: complexity, chirality, prebiotic chemistry, pattern recognition, signal processing, time series.
Hobbies: story teller, drinking parties, bird watching, mushrooms, quiet music.
Experiences: Leningrad siege, Gulag, Siberia, Dissident and Jewish movement in Russia, 24 years in Israel.



 
 


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