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Phagocytosis of beads of different sizes: Comparison of experiment (top) and computer simulation (bottom). (Click on each picture to view movie or right-click to download.) |
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Our multiscale approach uses the tools of mechanics and high-resolution optical microscopy to deepen the understanding of how nature does things in the nanoworld and where pathogens may attack our natural defenses. On the smallest scale, we characterize isolated single-molecule interactions using custom-developed, ultrasensitive force probes. In vivo these biomolecules are often supported by soft subcellular structures like membranes or the cytoskeleton. The dynamical properties of such structures crucially affect the way in which the interacting molecules experience force. A more complete picture of biologically relevant nano-to-microscale processes, therefore, requires a sound knowledge of the mechanics of membranes and whole cells. Combining our force probes with advanced micropipette aspiration and micromanipulation allows us to study with exceptional resolution the elasticity and cohesive strength of artificial and biological membranes. Similar experimental setups are used to establish and characterize the mechanical determinants of cellular processes like leukocyte adhesion and phagocytosis and how they are affected by disease.
Automated micromanipulation and micropipette aspiration.
Custom-built force probes:
Biomembrane force probe.
Optical tweezers.
Atomic force microscope.
Kim, S.V.; Mehal, W.Z.; Dong, X.; Heinrich, V.; Pypaert, M.; Mellman, I.; Dembo, M.; Mooseker, M.S.; Wu, D.; Flavell, R.A. Modulation of cell adhesion and motility in the immune system by Myo1f. Science 2006, 314(5796), 136-139.
Herant, M.; Heinrich, V.; Dembo, M. Mechanics of neutrophil phagocytosis: experiments and quantitative models. J. Cell Sci. 2006, 119, 1903-1913.
Heinrich, V.; Leung, A.; Evans, E. Nano-to-microscale mechanical switches and fuses mediate adhesive contacts between leukocytes and the endothelium. J. Chem. Inf. Model. 2005; 45, 1482-1490. (PERSPECTIVE)
Heinrich, V.; Leung, A.; Evans, E. Nano- to microscale dynamics of P-selectin detachment from leukocyte interfaces. II. Tether flow terminated by P-selectin dissociation from PSGL-1. Biophys. J. 2005, 88, 2299-2308.
Heinrich, V.; Rawicz, W. Automated, high-resolution micropipet aspiration reveals new insight into the physical properties of fluid membranes. Langmuir 2005, 21, 1962-1971.
Herant, M.; Heinrich, V.; Dembo, M. Mechanics of neutrophil phagocytosis: behavior of the cortical tension. J. Cell Sci. 2005, 118, 1789-1797.
Evans, E.; Leung, A.; Heinrich, V.; Zhu, C. Mechanical switching and coupling between two dissociation pathways in a P-selectin adhesion bond. Proc. Natl. Acad. Sci. USA 2004, 101, 11281-11286.
Evans, E.; Heinrich, V.; Ludwig, F.; Rawicz, W. Dynamic tension spectroscopy and strength of biomembranes. Biophys. J. 2003, 85, 2342-2350.
Heinrich, V.; Bozic, B.; Svetina, S.; Zeks, B. Vesicle deformation by an axial load: from elongated shapes to tethered vesicles. Biophys. J. 1999, 76, 2056-2071.
Heinrich, V.; Sevsek, F.; Svetina, S.; Zeks, B. Large deviations of the average shapes of vesicles from equilibrium: Effects of thermal fluctuations in the presence of constraints. Phys. Rev. E 1997, 55, 1809-1818.
Heinrich, V.; Waugh, R. E. A piconewton force transducer and its application to measurement of the bending stiffness of phospholipid membranes. Ann. Biomed. Eng. 1996, 24, 595-605.
Nano-to-microscale quantitative biophysics and bioengineering. Single-molecule interactions. Biomembrane mechanics. Cell adhesion and cellular shape and motion. Design and advancement of nano-to-micromechanical core technologies: Dynamic force spectroscopy. Dynamic tension spectroscopy. Biomembrane force probe. Optical tweezers. Automated micromanipulation and micropipette aspiration.