Dr. Hanein's group employs electron microscopy, electron tomography and three-dimensional image analysis.
Dr. Hanein earned her Ph.D. in Chemistry from the Weizmann Institute in Science, Rehovot, Israel in 1995.
Tomography of actin cytoskeletal networks.
Methods Enzymol. 2010;483:203-14
Molecular basis for the dual function of Eps8 on actin dynamics: bundling and capping.
Hertzog M, Milanesi F, Hazelwood L, Disanza A, Liu H, Perlade E, Malabarba MG, Pasqualato S, Maiolica A, Confalonieri S, Le Clainche C, Offenhauser N, Block J, Rottner K, Di Fiore PP, Carlier MF, Volkmann N, Hanein D, Scita G
PLoS Biol. 2010;8(6):e1000387
The structural basis of actin filament branching by the Arp2/3 complex.
Rouiller I, Xu XP, Amann KJ, Egile C, Nickell S, Nicastro D, Li R, Pollard TD, Volkmann N, Hanein D
J Cell Biol. 2008 Mar 10;180(5):887-95
The structure of the C-terminal actin-binding domain of talin.
Gingras AR, Bate N, Goult BT, Hazelwood L, Canestrelli I, Grossmann JG, Liu H, Putz NS, Roberts GC, Volkmann N, Hanein D, Barsukov IL, Critchley DR
EMBO J. 2008 Jan 23;27(2):458-69
Reconstituted NALP1 inflammasome reveals two-step mechanism of caspase-1 activation.
Faustin B, Lartigue L, Bruey JM, Luciano F, Sergienko E, Bailly-Maitre B, Volkmann N, Hanein D, Rouiller I, Reed JC
Mol Cell. 2007 Mar 9;25(5):713-24
Three-dimensional structure of vinculin bound to actin filaments.
Janssen ME, Kim E, Liu H, Fujimoto LM, Bobkov A, Volkmann N, Hanein D
Mol Cell. 2006 Jan 20;21(2):271-81
The structural basis of myosin V processive movement as revealed by electron cryomicroscopy.
Volkmann N, Liu H, Hazelwood L, Krementsova EB, Lowey S, Trybus KM, Hanein D
Mol Cell. 2005 Sep 2;19(5):595-605
Cell migration without a lamellipodium: translation of actin dynamics into cell movement mediated by tropomyosin.
Gupton SL, Anderson KL, Kole TP, Fischer RS, Ponti A, Hitchcock-DeGregori SE, Danuser G, Fowler VM, Wirtz D, Hanein D, Waterman-Storer CM
J Cell Biol. 2005 Feb 14;168(4):619-31
Myosin isoforms show unique conformations in the actin-bound state.
Volkmann N, Ouyang G, Trybus KM, DeRosier DJ, Lowey S, Hanein D
Proc Natl Acad Sci U S A. 2003 Mar 18;100(6):3227-32
Structure of Arp2/3 complex in its activated state and in actin filament branch junctions.
Volkmann N, Amann KJ, Stoilova-McPhie S, Egile C, Winter DC, Hazelwood L, Heuser JE, Li R, Pollard TD, Hanein D
Science. 2001 Sep 28;293(5539):2456-9
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Structural studies on full-length talin1 reveal a compact auto-inhibited dimer: Implications for talin activation.
Goult BT, Xu XP, Gingras AR, Swift M, Patel B, Bate N, Kopp PM, Barsukov IL, Critchley DR, Volkmann N, Hanein D
J Struct Biol. 2013 May 29;
Dorit Hanein's Research Focus
Cancer, Cardiomyopathies, Infectious Diseases, Inflammatory Bowel Disease, Pathogen Invasion, Crohn’s Disease (Colitis)
Watch Dr. Hanein describe her research
Dorit Hanein's Research Report
Electron cryo-microscopy (cryo-EM) has grown to be a powerful imaging technique applicable to almost any kind of specimen, is parsimonious in its material requirements, and allows imaging of large macromolecular assemblies close to their physiological environment. Cryo-EM provides the means to determine three-dimensional (3D) structures of pleiomorphic macromolecular assemblies in fully hydrated state, close to their native environment. Dr. Hanein’s laboratory is continuously developing and applying various cryo-EM, image analysis and bioinformatics approaches and techniques to extract high-resolution structural information of these large dynamic assemblies at the highest level of fidelity. Using a hybrid approach, Hanein and collaborators combine the generated 3D maps of the assemblies with high resolution information such as that derived from atomic resolution structures of their components, yeast two-hybrid screening, mutagenesis, biochemical and biophysical data to link structural correlates to functional outputs. The derived molecular models enable understanding of the mechanisms by which large and dynamic assemblies function and by which mutations or pathogens elicit non-regulated responses, providing benchmarks for the kinds of regulatory mechanisms associated with function in vivo.
One of the prime biological interests in Dr. Hanein’s laboratory is elucidating the molecular mechanisms underlying the assembly and regulation of the actin cytoskeleton and its associated integrin-mediated adhesions at the leading edge of motile cells. Dr. Hanein successfully applied the hybrid approaches described above to several biomedically relevant systems. Examples include studying the role of Arp2/3 complex in actin filament network assembly, the role of myosin in cell migration, the role of actin binding proteins in providing a scaffold for cell protrusions and adhesion (for example Vinculin, Talin, EPS8, Tensin, Fimbrin), and the connection of this machinery to the extracellular matrix (Integrins, Fibronectin). Other biological interests in the Hanein laboratory include pathogen invasion, the inflammatory pathway, and apoptosis.
Although high-resolution structural approaches provide critical information about individual molecules and complexes, a barrier to progress remains their structural and functional integration at the cellular level. Towards this end, the Hanein laboratory is currently developing techniques and protocols that allow imaging whole eukaryotic cell, in their fully hydrated state, and to use computational tools to correlate between the high-resolution structural information we obtained from the isolated molecules and assemblies with the in situ characterization obtained from living cells (correlative light and electron microscopy). All these projects are in close collaboration with biology, biochemistry and computational biology labs, some of them extremely long standing within the SBMRI, in the US and in the world.
About Dorit Hanein
Dorit Hanein earned her Ph.D. in Chemistry from the Weizmann Institute in Science, Rehovot, Israel in 1995. She received postdoctoral training at Boston University Medical School and Brandeis University, prior to her appointment as Assistant Professor at Sanford-Burnham Medical Research Institute in 1999. In 2000, Dr. Hanein was selected as a PEW Scholar in the Biomedical Sciences. In 2005, Dr. Hanein was promoted to an Associate Professor at Sanford-Burnham and in 2006 has been also appointed an adjunct professor at the University of California, San Diego.
Chair, Hybrid Methods 2008 Conference
Organizing Committee, Hybrid Methods 2010 Conference
2011 Sanford-Burnham Symposium: Structural Systems Biology