Foundation of the Outstanding Toughness in Biomimetic and Natural Spider Silk

被引:42
作者
Anton, Arthur Markus [1 ]
Heidebrecht, Aniela [2 ]
Mahmood, Nasir [3 ]
Beiner, Mario [3 ,4 ]
Scheibel, Thomas [2 ,5 ,6 ,7 ,8 ,9 ]
Kremer, Friedrich [1 ]
机构
[1] Univ Leipzig, Peter Debye Inst Soft Matter Phys, Linnestr 5, D-04103 Leipzig, Germany
[2] Univ Bayreuth, Fac Engn Sci, Dept Biomat, Univ Str 30, D-95440 Bayreuth, Germany
[3] Martin Luther Univ Halle Wittenberg, Inst Chem, Heinrich Damerow Str 4, D-06120 Halle, Saale, Germany
[4] Fraunhofer Inst Microstruct Mat & Syst IMWS, Walter Hulse Str 1, D-06120 Halle, Saale, Germany
[5] Univ Bayreuth, Res Ctr Bio Macromol BIOmac, Univ Str 30, D-95440 Bayreuth, Germany
[6] Univ Bayreuth, Bayreuth Ctr Colloids & Interfaces BZKG, Univ Str 30, D-95440 Bayreuth, Germany
[7] Univ Bayreuth, Bayreuth Ctr Mol Biosci BZMB, Univ Str 30, D-95440 Bayreuth, Germany
[8] Univ Bayreuth, Bayreuth Ctr Mat Sci & Engn BayMAT, Univ Str 30, D-95440 Bayreuth, Germany
[9] Univ Bayreuth, BPI, Univ Str 30, D-95440 Bayreuth, Germany
关键词
X-RAY MICRODIFFRACTION; DRAGLINE SILK; MECHANICAL-PROPERTIES; STRUCTURAL ORGANIZATION; FTIR-SPECTROSCOPY; BLOCK-COPOLYMERS; FIBERS; ORIENTATION; PROTEINS; NANOSTRUCTURE;
D O I
10.1021/acs.biomac.7b00990
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spider dragline silk is distinguished through the highest toughness of all natural as well as artificial fiber materials. To unravel the toughness's molecular foundation and to enable manufacturing biomimetic analogues, we investigated the morphological and functional structure of recombinant fibers, which exhibit toughness similar to that of the natural template, on the molecular scale by means of vibrational spectroscopy and on the mesoscale by X-ray scattering. Whereas the former was used to identify protein secondary structures and their alignment in the natural as well as artificial silks, the latter revealed nanometer-sized crystallites on the higher structural level. Furthermore, a spectral red shift of a crystal-specific absorption band demonstrated that macroscopically applied stress is directly transferred to the molecular scale, where it is finally dissipated. Concerning this feature, both the natural as well as the biomimetic fibers are almost indistinguishable, giving rise to the toughness of both fiber materials.
引用
收藏
页码:3954 / 3962
页数:9
相关论文
共 54 条
[31]   Conformational and orientational transformation of silk proteins in the major ampullate gland of Nephila clavipes spiders [J].
Lefevre, Thierry ;
Boudreault, Simon ;
Cloutier, Conrad ;
Pezolet, Michel .
BIOMACROMOLECULES, 2008, 9 (09) :2399-2407
[32]   Protein secondary structure and orientation in silk as revealed by Raman spectromicroscopy [J].
Lefevre, Thierry ;
Rousseau, Marie-Eve ;
Pezolet, Michel .
BIOPHYSICAL JOURNAL, 2007, 92 (08) :2885-2895
[33]   Conformation Transitions of Recombinant Spidroins via Integration of Time-Resolved FTIR Spectroscopy and Molecular Dynamic Simulation [J].
Ling, Shengjie ;
Dinjaski, Nina ;
Ebrahimi, Davoud ;
Wong, Joyce Y. ;
Kaplan, David L. ;
Buehler, Markus J. .
ACS BIOMATERIALS SCIENCE & ENGINEERING, 2016, 2 (08) :1298-1308
[34]   Influence of shear processing on morphology orientation and mechanical properties of styrene butadiene triblock copolymers [J].
Mahmood, Nasir ;
Anton, Arthur Markus ;
Gupta, Gaurav ;
Babur, Tamoor ;
Knoll, Konrad ;
Thurn-Albrecht, Thomas ;
Kremer, Friedrich ;
Beiner, Mario ;
Weidisch, Roland .
POLYMER, 2014, 55 (16) :3782-3791
[35]   Molecular and Nanostructural Mechanisms of Deformation, Strength and Toughness of Spider Silk Fibrils [J].
Nova, Andrea ;
Keten, Sinan ;
Pugno, Nicola M. ;
Redaelli, Alberto ;
Buehler, Markus J. .
NANO LETTERS, 2010, 10 (07) :2626-2634
[36]   Structure-property relationships in major ampullate spider silk as deduced from polarized FTIR spectroscopy [J].
Papadopoulos, P. ;
Soelter, J. ;
Kremer, F. .
EUROPEAN PHYSICAL JOURNAL E, 2007, 24 (02) :193-199
[37]   Similarities in the Structural Organization of Major and Minor Ampullate Spider Silk [J].
Papadopoulos, Periklis ;
Ene, Roxana ;
Weidner, Immanuel ;
Kremer, Friedrich .
MACROMOLECULAR RAPID COMMUNICATIONS, 2009, 30 (9-10) :851-857
[38]   Hierarchies in the structural organization of spider silk-a quantitative model [J].
Papadopoulos, Periklis ;
Soelter, Jan ;
Kremer, Friedrich .
COLLOID AND POLYMER SCIENCE, 2009, 287 (02) :231-236
[39]   Evidence by infrared spectroscopy of the presence of two types of β-sheets in major ampullate spider silk and silkworm silk [J].
Paquet-Mercier, Francois ;
Lefevre, Thierry ;
Auger, Michele ;
Pezolet, Michel .
SOFT MATTER, 2013, 9 (01) :208-215
[40]   Relationship between microstructure and mechanical properties in spider silk fibers: identification of two regimes in the microstructural changes [J].
Plaza, Gustavo R. ;
Perez-Rigueiro, Jose ;
Riekel, Christian ;
Belen Perea, G. ;
Agullo-Rueda, Fernando ;
Burghammer, Manfred ;
Guinea, Gustavo V. ;
Elices, Manuel .
SOFT MATTER, 2012, 8 (22) :6015-6026