A major challenge in cell and organism biology is to understand how living cell physiology emerges from the biophysical properties of individual macromolecules. The morphological and physical behaviors of cells required for cell adhesion, migration and division depend on the proper spatial and temporal regulation of a vast hierarchy of multi-protein machines, called the cytoskeleton. However, while we are gaining increasing amounts of knowledge of properties of individual cytoskeletal proteins, we have very little knowledge about the self-assembly and physical properties of multi-protein assemblies that form physical structures to transmit mechanical information up to cellular length scales. For example, we do not understand how forces generated by individual molecular motors are exploited by cytoskeletal assemblies to regulate morphogenesis and force generation at the cellular level. Current understanding of the physical behavior of the cellular cytoskeleton has been limited both by the lack of experimental techniques to probe the dynamic structure and physical properties of mesoscopic cytoskeletal assemblies in living cells. I propose to establish the experimental tools to study the biophysical properties of cytoskeletal matter in living cells by integrating approaches from condensed matter physics with molecular cell biology. This work will identify the underlying physics of emergent cytoskeletal assemblies and will provide predictive analytical models to link our understanding of the biophysics of molecules to cell behaviors. Finally, this work will impact the treatment of diseases that are a result of misregulation of the physical behaviors of cells, including cancer metastasis and cardiac diseases.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
NIH Director’s Pioneer Award (NDPA) (DP1)
Project #
5DP1OD003354-03
Application #
7683827
Study Section
Special Emphasis Panel (ZGM1-NDPA-G (P2))
Program Officer
Jones, Warren
Project Start
2007-09-30
Project End
2012-07-31
Budget Start
2009-08-01
Budget End
2010-07-31
Support Year
3
Fiscal Year
2009
Total Cost
$767,500
Indirect Cost
Name
University of Chicago
Department
Physics
Type
Schools of Arts and Sciences
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Murrell, Michael; Thoresen, Todd; Gardel, Margaret (2014) Reconstitution of contractile actomyosin arrays. Methods Enzymol 540:265-82
Oakes, Patrick W; Gardel, Margaret L (2014) Stressing the limits of focal adhesion mechanosensitivity. Curr Opin Cell Biol 30:68-73
Gardel, Margaret Lise (2013) Materials science: Synthetic polymers with biological rigidity. Nature 493:618-9
Birukova, Anna A; Tian, Xinyong; Cokic, Ivan et al. (2013) Endothelial barrier disruption and recovery is controlled by substrate stiffness. Microvasc Res 87:50-7
Caswell, Thomas A; Zhang, Zexin; Gardel, Margaret L et al. (2013) Observation and characterization of the vestige of the jamming transition in a thermal three-dimensional system. Phys Rev E Stat Nonlin Soft Matter Phys 87:012303
Lenz, Martin; Thoresen, Todd; Gardel, Margaret L et al. (2012) Contractile units in disordered actomyosin bundles arise from F-actin buckling. Phys Rev Lett 108:238107
Lenz, Martin; Gardel, Margaret L; Dinner, Aaron R (2012) Requirements for contractility in disordered cytoskeletal bundles. New J Phys 14:
Aratyn-Schaus, Yvonne; Oakes, Patrick W; Gardel, Margaret L (2011) Dynamic and structural signatures of lamellar actomyosin force generation. Mol Biol Cell 22:1330-9
Norstrom, Melanie; Gardel, Margaret L (2011) Shear thickening of F-actin networks crosslinked with non-muscle myosin IIB. Soft Matter 2011:3228-3233
Maruthamuthu, Venkat; Sabass, Benedikt; Schwarz, Ulrich S et al. (2011) Cell-ECM traction force modulates endogenous tension at cell-cell contacts. Proc Natl Acad Sci U S A 108:4708-13

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