| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Biophys J, February 2001, p. 852-863, Vol. 80, No. 2


§ and
*Department of Biophysics, Pécs University Medical School,
Pécs, H-7624 Hungary;
Department of Veterinary
Comparative Anatomy, Pharmacology, and Physiology, Washington
State University, Pullman, Washington 99164, and Departments of
Physics and §Molecular and Cell Biology,
University of California, Berkeley, California 94720 USA
Relaxed striated muscle cells exhibit mechanical fatigue
when exposed to repeated stretch and release cycles. To understand the
molecular basis of such mechanical fatigue, single molecules of the
giant filamentous protein titin, which is the main determinant of
sarcomeric elasticity, were repetitively stretched and released while
their force response was characterized with optical tweezers. During
repeated stretch-release cycles titin becomes mechanically worn out in
a process we call molecular fatigue. The process is characterized by a
progressive shift of the stretch-force curve toward increasing
end-to-end lengths, indicating that repeated mechanical cycles increase
titin's effective contour length. Molecular fatigue occurs only in a
restricted force range (0-25 pN) during the initial part of the
stretch half-cycle, whereas the rest of the force response is repeated
from one mechanical cycle to the other. Protein-folding models fail to
explain molecular fatigue on the basis of an incomplete refolding of
titin's globular domains. Rather, the process apparently derives from
the formation of labile nonspecific bonds cross-linking various sites
along a pre-unfolded titin segment. Because titin's molecular fatigue
occurs in a physiologically relevant force range, the process may play
an important role in dynamically adjusting muscle's response to the
recent history of mechanical perturbations.
Biophys J, February 2001, p. 852-863, Vol. 80, No. 2
© 2001 by the Biophysical Society 0006-3495/01/02/852/12 $2.00
This article has been cited by other articles:
![]() |
S. Guo, C. Ray, A. Kirkpatrick, N. Lad, and B. B. Akhremitchev Effects of Multiple-Bond Ruptures on Kinetic Parameters Extracted from Force Spectroscopy Measurements: Revisiting Biotin-Streptavidin Interactions Biophys. J., October 15, 2008; 95(8): 3964 - 3976. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. Z. Kellermayer, P. Bianco, Z. Martonfalvi, A. Nagy, A. Kengyel, D. Szatmari, T. Huber, M. Linari, M. Caremani, and V. Lombardi Muscle Thixotropy: More than Just Cross-Bridges? Response to Comment by Campbell and Lakie Biophys. J., January 1, 2008; 94(1): 329 - 330. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. H. Lee, J. Hsin, O. Mayans, and K. Schulten Secondary and Tertiary Structure Elasticity of Titin Z1Z2 and a Titin Chain Model Biophys. J., September 1, 2007; 93(5): 1719 - 1735. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Nagy, L. Grama, T. Huber, P. Bianco, K. Trombitas, H. L. Granzier, and M. S. Z. Kellermayer Hierarchical Extensibility in the PEVK Domain of Skeletal-Muscle Titin Biophys. J., July 1, 2005; 89(1): 329 - 336. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Speich, L. Borgsmiller, C. Call, R. Mohr, and P. H. Ratz ROK-induced cross-link formation stiffens passive muscle: reversible strain-induced stress softening in rabbit detrusor Am J Physiol Cell Physiol, July 1, 2005; 289(1): C12 - C21. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. Z. Kellermayer, L. Grama, A. Karsai, A. Nagy, A. Kahn, Z. L. Datki, and B. Penke Reversible Mechanical Unzipping of Amyloid {beta}-Fibrils J. Biol. Chem., March 4, 2005; 280(9): 8464 - 8470. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. S. Kirton, A. J. Taberner, P. M. F. Nielsen, A. A. Young, and D. S. Loiselle Strain softening behaviour in nonviable rat right-ventricular trabeculae, in the presence and the absence of butanedione monoxime Exp Physiol, September 1, 2004; 89(5): 593 - 604. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. Leake, D. Wilson, M. Gautel, and R. M. Simmons The Elasticity of Single Titin Molecules Using a Two-Bead Optical Tweezers Assay Biophys. J., August 1, 2004; 87(2): 1112 - 1135. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. L. Granzier and S. Labeit The Giant Protein Titin: A Major Player in Myocardial Mechanics, Signaling, and Disease Circ. Res., February 20, 2004; 94(3): 284 - 295. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Trombitas, Y. Wu, M. McNabb, M. Greaser, M. S. Z. Kellermayer, S. Labeit, and H. Granzier Molecular Basis of Passive Stress Relaxation in Human Soleus Fibers: Assessment of the Role of Immunoglobulin-Like Domain Unfolding Biophys. J., November 1, 2003; 85(5): 3142 - 3153. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Grama, B. Somogyi, and M. S. Z. Kellermayer Global configuration of single titin molecules observed through chain-associated rhodamine dimers PNAS, November 15, 2001; (2001) 191494098. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Grama, B. Somogyi, and M. S. Z. Kellermayer Global configuration of single titin molecules observed through chain-associated rhodamine dimers PNAS, December 4, 2001; 98(25): 14362 - 14367. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |