Oscillations, Waves, and Interactions - GWDG

DPI60plus – a future with biophysics 459
quantitative detail, with the aim of uncovering the physical principles underlying the
active regulation of the complex mechanical functions of cells.
References
[1] I. A. Schaap, P. J. de Pablo, and C. F. Schmidt, ‘Resolving the molecular structure
of microtubules under physiological conditions with scanning force microscopy’, Eur.
Biophys. J. 33, 462 (2004).
[2] P. J. de Pablo, I. A. Schaap, F. C. MacKintosh, and C. F. Schmidt, ‘Deformation and
collapse of microtubules on the nanometer scale’, Phys. Rev. Lett. 91, 098101 (2003).
[3] I. A. Schaap, B. Hoffmann, C. Carrasco, R. Merkel, and C. F. Schmidt, ‘Tau protein
binding forms a 1 nm thick layer along protofilaments without affecting the radial elasticity
of microtubules’, J. Struct. Biol. 158, 282 (2007).
[4] I. A. Schaap, C. Carrasco, P. J. de Pablo, F. C. MacKintosh, and C. F. Schmidt, ‘Elastic
response, buckling, and instability of microtubules under radial indentation’, Biophys.
J. 91, 1521 (2006).
[5] J. P. Michel, I. L. Ivanovska, M. M. Gibbons, W. S. Klug, C. M. Knobler, G. J. Wuite,
and C. F. Schmidt, ‘Nanoindentation studies of full and empty viral capsids and the
effects of capsid protein mutations on elasticity and strength’, Proc. Natl. Acad. Sci.
USA 103, 6184 (2006).
[6] W. S. Klug, R. F. Bruinsma, J. P. Michel, C. M. Knobler, I. L. Ivanovska, C. F. Schmidt,
and G. J. Wuite, ‘Failure of viral shells’, Phys. Rev. Lett. 97, 228101 (2006).
[7] I. L. Ivanovska, P. J. de Pablo, B. Ibarra, G. Sgalari, F. C. MacKintosh, J. L. Carrascosa,
C. F. Schmidt, and G. J. Wuite, ‘Bacteriophage capsids: tough nanoshells with complex
elastic properties’, Proc. Natl. Acad. Sci. USA 101, 7600 (2004).
[8] R. P. Goodman, I. A. Schaap, C. F. Tardin, C. M. Erben, R. M. Berry, C. F. Schmidt,
and A. J. Turberfield, ‘Rapid chiral assembly of rigid DNA building blocks for molecular
nanofabrication’, Science 310, 1661 (2005).
[9] M. J. Korneev, S. Lakämper, and C. F. Schmidt, ‘Load-dependent release limits the
processive stepping of the tetrameric Eg5 motor’, Eur. Biophys. J. 36, 675 (2007).
[10] B. H. Kwok, L. C. Kapitein, J. H. Kim, E. J. Peterman, C. F. Schmidt, and T. M.
Kapoor, ‘Allosteric inhibition of kinesin-5 modulates its processive directional motility’,
Nat. Chem. Biol. 2, 480 (2006).
[11] F. C. MacKintosh and C. F. Schmidt, ‘Microrheology’, Opin. Coll. Interf. Sci. 4, 300
(1999).
[12] C. W. Oseen, Neuere Methoden und Ergebnisse in der Hydrodynamik (Akad. Verl.-Ges.,
Leipzig, 1927).
[13] S. Lakämper and E. Meyhofer, ‘Back on track – on the role of the microtubule for
kinesin motility and cellular function’, J. Muscle Res. Cell Motil. 27, 161 (2006).
[14] S. Lakämper and E. Meyhofer, ‘The E-hook of tubulin interacts with kinesin’s head to
increase processivity and speed’, Biophys. J. 89, 3223 (2005).
[15] S. Lakämper, A. Kallipolitou, G. Woehlke, M. Schliwa, and E. Meyhofer, ‘Single fungal
kinesin motor molecules move processively along microtubules’, Biophys. J. 84, 1833
(2003).
[16] M. J. de Castro, R. M. Fondecave, L. A. Clarke, C. F. Schmidt, and R. J. Stewart, ‘Working
strokes by single molecules of the kinesin-related microtubule motor ncd’, Nat. Cell
Biol. 2, 724 (2000).
[17] M. W. Allersma, F. Gittes, M. J. de Castro, R. J. Stewart, and C. F. Schmidt, ‘Two-