Sacrificial bonds and hidden length: Unraveling molecular mesostructures in tough materials

被引:312
作者
Fantner, GE [1 ]
Oroudjev, E
Schitter, G
Golde, LS
Thurner, P
Finch, MM
Turner, P
Gutsmann, T
Morse, DE
Hansma, H
Hansma, PK
机构
[1] Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
[3] Forschungzentrum Borstel, Div Biophys, D-23845 Borstel, Germany
关键词
D O I
10.1529/biophysj.105.069344
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
Sacrificial bonds and hidden length in structural molecules and composites have been found to greatly increase the fracture toughness of biomaterials by providing a reversible, molecular-scale energy-dissipation mechanism. This mechanism relies on the energy, of order 100 eV, needed to reduce entropy and increase enthalpy as molecular segments are stretched after being released by the breaking of weak bonds, called sacrificial bonds. This energy is relatively large compared to the energy needed to break the polymer backbone, of order a few eV. In many biological cases, the breaking of sacrificial bonds has been found to be reversible, thereby additionally providing a "self-healing" property to the material. Due to the nanoscopic nature of this mechanism, single molecule force spectroscopy using an atomic force microscope has been a useful tool to investigate this mechanism. Especially when investigating natural molecular constructs, force versus distance curves quickly become very complicated. In this work we propose various types of sacrificial bonds, their combination, and how they appear in single molecule force spectroscopy measurements. We find that by close analysis of the force spectroscopy curves, additional information can be obtained about the molecules and their bonds to the native constructs.
引用
收藏
页码:1411 / 1418
页数:8
相关论文
共 38 条
[1]
Molecular nanosprings in spider capture-silk threads [J].
Becker, N ;
Oroudjev, E ;
Mutz, S ;
Cleveland, JP ;
Hansma, PK ;
Hayashi, CY ;
Makarov, DE ;
Hansma, HG .
NATURE MATERIALS, 2003, 2 (04) :278-283
[2]
Belcher AM, 1996, ABSTR PAP AM CHEM S, V212, P177
[3]
Unzipping DNA with optical tweezers: high sequence sensitivity and force flips [J].
Bockelmann, U ;
Thomen, P ;
Essevaz-Roulet, B ;
Viasnoff, V ;
Heslot, F .
BIOPHYSICAL JOURNAL, 2002, 82 (03) :1537-1553
[4]
Estimating the persistence length of a worm-like chain molecule from force-extension measurements [J].
Bouchiat, C ;
Wang, MD ;
Allemand, JF ;
Strick, T ;
Block, SM ;
Croquette, V .
BIOPHYSICAL JOURNAL, 1999, 76 (01) :409-413
[5]
BUSTAMANTE C, 1994, SCIENCE, V265, P1600
[6]
Mechanical and chemical unfolding of a single protein: A comparison [J].
Carrion-Vazquez, M ;
Oberhauser, AF ;
Fowler, SB ;
Marszalek, PE ;
Broedel, SE ;
Clarke, J ;
Fernandez, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :3694-3699
[7]
Influence of the degradation of the organic matrix on the microscopic fracture behavior of trabecular bone [J].
Fantner, GE ;
Birkedal, H ;
Kindt, JH ;
Hassenkam, T ;
Weaver, JC ;
Cutroni, JA ;
Bosma, BL ;
Bawazer, L ;
Finch, MM ;
Cidade, GAG ;
Morse, DE ;
Stucky, GD ;
Hansma, PK .
BONE, 2004, 35 (05) :1013-1022
[8]
Partial biomimetic reconstitution of avian eggshell formation [J].
Fernandez, MS ;
Passalacqua, K ;
Arias, JI ;
Arias, JL .
JOURNAL OF STRUCTURAL BIOLOGY, 2004, 148 (01) :1-10
[9]
Fisher TE, 2000, NAT STRUCT BIOL, V7, P719
[10]
The study of protein mechanics with the atomic force microscope [J].
Fisher, TE ;
Oberhauser, AF ;
Carrion-Vazquez, M ;
Marszalek, PE ;
Fernandez, JM .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (10) :379-384