[Research Interests] [Representative Publications] [Lab Members] RESEARCH INTERESTSPhysical basis of the structure of biological molecules and their complexesFrom the very beginning of my scientific career, my research interests have concentrated on the physical principles of the architecture of biological macromolecules, proteins, nucleic acids and their complexes, namely the energetics of formation of their unique three-dimensional structures. These aims require experimental studies of the conformation of these molecules under various conditions and measurements of the energies involved in changes of their structures and of their association with molecular partners. The problem of molecular recognition, particularly of DNA by gene regulating proteins, attracts at the present time rapidly increasing attention. Its solution largely depends on the extent of information concerning the energetics of this process. Realization of this program has required development of a supersensitive calorimetric technique, microcalorimetry, which is now widely used in many other laboratories. Except microcalorimetry we are also using extensively various optical methods: CD, fluorescence anisotropy and florescence resonance energy transfer (FRET) to investigate the protein interaction with and changes in their structure resulted from their association. We are working with various proteins and their mutants that we construct to solve the problem of forces responsible for the protein folding and their association with the partners. In our experiments we are using also synthetic polypeptides and polynucleotides as models, particularly in studying protein interactions with their target DNAs.
REPRESENTATIVE PUBLICATIONSDragan, A.I., Hargreaves, V.V., Makeyeva, E.N., and Privalov, P.L. 2007. Mechanisms of activation of interferon regulator factor 3: the role of C-terminal domain phosphorylation in IRF-3 dimerization and DNA binding. Nucleic Acids Res. 35:3525-34. Crane-Robinson, C., Dragan, A.I., and Privalov, P.L. 2006. The extended arms of DNA-binding domains: a tale of tails. Trends Biochem Sci. 31:547-52. Dragan, A.I., Frank, L., Liu, Y., Makeyeva, E. N., Crane-Robinson, C. & Privalov, P. L 2004. Thermodynamic signature of GCN4-bZIP binding to DNA indicates the role of water in discriminating between the AP-1 and ATF/CREB sites. J. Mol. Biol . 343 , 865-878. Dragan, A.I., Liu, Y., Makeyeva, E. N., and Privalov, P.L. 2004. DNA-binding domain of GCN4 induces bending of both the ATF/CREB and AP-1 binding sites of DNA. Nucleic Acids Research , 32 , 5192-5197. Dragan, A.I., Potekhin S.A., Sivolob, A., Lu, M., and Privalov, P.L. 2004. Kinetics and thermodynamics of the unfolding/refolding of the three-stranded a -helical coiled-coil, Lpp-56. Biochemistry , 43 , 14891-14900. Dragan, A.I., Klass, J., Read, C.M Churchill, E. A., Crane-Robinson, C., and Privalov, P.L. 2003. DNA binding of a non-sequence-specific HMG-D protein is entropy driven with a substantial non-electrostatic contribution. J. Mol. Biol . 327 , 393-411. Liggins, J.R. & Privalov, P.L. 2000. Energetics of the specific binding interaction of the first three zinc fingers of the transcription factor TFIIIA with its cognate DNA sequence. Proteins: Struct. Funct. Genetics , 4 , 50-62. Lab MembersGraduate Student: |
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