|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 111, Issue 11 1567-1574, Copyright © 1998 by Company of Biologists
JOURNAL ARTICLES |
WA Linke, MR Stockmeier, M Ivemeyer, H Hosser and P Mundel
Institute of Physiology II, University of Heidelberg, Im Neuenheimer Feld 326, D-69120 Heidelberg, Germany. wolfgang.linke@urz.uni
The poly-immunoglobulin domain region of titin, located within the elastic section of this giant muscle protein, determines the extensibility of relaxed myofibrils mainly at shorter physiological lengths. To elucidate this region's contribution to titin elasticity, we measured the elastic properties of the N-terminal I-band Ig region by using immunofluorescence/immunoelectron microscopy and myofibril mechanics and tried to simulate the results with a model of entropic polymer elasticity. Rat psoas myofibrils were stained with titin-specific antibodies flanking the Ig region at the N terminus and C terminus, respectively, to record the extension behaviour of that titin segment. The segment's end-to-end length increased mainly at small stretch, reaching approximately 90% of the native contour length of the Ig region at a sarcomere length of 2.8 microm. At this extension, the average force per single titin molecule, deduced from the steady-state passive length-tension relation of myofibrils, was approximately 5 or 2.5 pN, depending on whether we assumed a number of 3 or 6 titins per half thick filament. When the force-extension curve constructed for the Ig region was simulated by the wormlike chain model, best fits were obtained for a persistence length, a measure of the chain's bending rigidity, of 21 or 42 nm (for 3 or 6 titins/half thick filament), which correctly reproduced the curve for sarcomere lengths up to 3.4 microm. Systematic deviations between data and fits above that length indicated that forces of >30 pN per titin strand may induce unfolding of Ig modules. We conclude that stretches of at least 5-6 Ig domains, perhaps coinciding with known super repeat patterns of these titin modules in the I-band, may represent the unitary lengths of the wormlike chain. The poly-Ig regions might thus act as compliant entropic springs that determine the minute levels of passive tension at low extensions of a muscle fiber.
This article has been cited by other articles:
![]() |
A. Kontrogianni-Konstantopoulos, M. A. Ackermann, A. L. Bowman, S. V. Yap, and R. J. Bloch Muscle Giants: Molecular Scaffolds in Sarcomerogenesis Physiol Rev, October 1, 2009; 89(4): 1217 - 1267. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. EINARSSON, T. HULTGREN, B. -O. LJUNG, E. RUNESSON, and J. FRIDEN Subscapularis Muscle Mechanics in Children with Obstetric Brachial Plexus Palsy J Hand Surg Eur Vol., August 1, 2008; 33(4): 507 - 512. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Bullard, T. Garcia, V. Benes, M. C. Leake, W. A. Linke, and A. F. Oberhauser The molecular elasticity of the insect flight muscle proteins projectin and kettin PNAS, March 21, 2006; 103(12): 4451 - 4456. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Udd, A. Vihola, J. Sarparanta, I. Richard, and P. Hackman Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J Neurology, February 22, 2005; 64(4): 636 - 642. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. F. Wright, J. Christodoulou, C. M. Dobson, and J. Clarke The importance of loop length in the folding of an immunoglobulin domain Protein Eng. Des. Sel., May 1, 2004; 17(5): 443 - 453. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. C. Lim, C. Zuppinger, X. Guo, G. M. Kuster, M. Helmes, H. M. Eppenberger, T. M. Suter, R. Liao, and D. B. Sawyer Anthracyclines Induce Calpain-dependent Titin Proteolysis and Necrosis in Cardiomyocytes J. Biol. Chem., February 27, 2004; 279(9): 8290 - 8299. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kontrogianni-Konstantopoulos and R. J. Bloch The Hydrophilic Domain of Small Ankyrin-1 Interacts with the Two N-terminal Immunoglobulin Domains of Titin J. Biol. Chem., January 31, 2003; 278(6): 3985 - 3991. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Minajeva, C. Neagoe, M. Kulke, and W. A Linke Titin-based contribution to shortening velocity of rabbit skeletal myofibrils J. Physiol., April 1, 2002; 540(1): 177 - 188. [Abstract] [Full Text] [PDF] |
||||
![]() |
O.-M. Mykkanen, M. Gronholm, M. Ronty, M. Lalowski, P. Salmikangas, H. Suila, and O. Carpen Characterization of Human Palladin, a Microfilament-associated Protein Mol. Biol. Cell, October 1, 2001; 12(10): 3060 - 3073. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Haravuori, A. Vihola, V. Straub, M. Auranen, I. Richard, S. Marchand, T. Voit, S. Labeit, H. Somer, L. Peltonen, et al. Secondary calpain3 deficiency in 2q-linked muscular dystrophy: Titin is the candidate gene Neurology, April 10, 2001; 56(7): 869 - 877. [Abstract] [Full Text] [PDF] |
||||
![]() |
V Person, S Kostin, K Suzuki, S Labeit, and J Schaper Antisense oligonucleotide experiments elucidate the essential role of titin in sarcomerogenesis in adult rat cardiomyocytes in long-term culture J. Cell Sci., January 11, 2000; 113(21): 3851 - 3859. [Abstract] [PDF] |
||||
![]() |
O. Cazorla, A. Freiburg, M. Helmes, T. Centner, M. McNabb, Y. Wu, K. Trombitas, S. Labeit, and H. Granzier Differential Expression of Cardiac Titin Isoforms and Modulation of Cellular Stiffness Circ. Res., January 7, 2000; 86(1): 59 - 67. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Morgan, Y. Yin, A. D. Borowsky, F. Kuo, N. Nourmand, J. I. Koontz, C. Reynolds, L. Soreng, C. A. Griffin, F. Graeme-Cook, et al. Breakpoints of the t(11;18)(q21;q21) in Mucosa-associated Lymphoid Tissue (MALT) Lymphoma Lie within or near the Previously Undescribed Gene MALT1 in Chromosome 18 Cancer Res., December 1, 1999; 59(24): 6205 - 6213. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. A. Linke, D. E. Rudy, T. Centner, M. Gautel, C. Witt, S. Labeit, and C. C. Gregorio I-Band Titin in Cardiac Muscle Is a Three-Element Molecular Spring and Is Critical for Maintaining Thin Filament Structure J. Cell Biol., August 9, 1999; 146(3): 631 - 644. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Helmes, K. Trombitas, T. Centner, M. Kellermayer, S. Labeit, W. A. Linke, and H. Granzier Mechanically Driven Contour-Length Adjustment in Rat Cardiac Titin's Unique N2B Sequence : Titin Is an Adjustable Spring Circ. Res., June 11, 1999; 84(11): 1339 - 1352. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Ohashi, D. P. Kiehart, and H. P. Erickson Dynamics and elasticity of the fibronectin matrix in living cell culture visualized by fibronectin-green fluorescent protein PNAS, March 2, 1999; 96(5): 2153 - 2158. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. A. Linke, M. Ivemeyer, P. Mundel, M. R. Stockmeier, and B. Kolmerer Nature of PEVK-titin elasticity in skeletal muscle PNAS, July 7, 1998; 95(14): 8052 - 8057. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Minajeva, C. Neagoe, M. Kulke, and W. A Linke Titin-based contribution to shortening velocity of rabbit skeletal myofibrils J. Physiol., April 1, 2002; 540(1): 177 - 188. [Abstract] [Full Text] [PDF] |
||||