Exploring molecular and mechanical gradients in structural bioscaffolds

被引:157
作者
Waite, JH [1 ]
Lichtenegger, HC
Stucky, GD
Hansma, P
机构
[1] Univ Calif Santa Barbara, Dept Mol Cell & Dev Biol, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA
[4] Vienna Univ Technol, Inst Mat Sci & Testing E308, A-1040 Vienna, Austria
关键词
D O I
10.1021/bi049380h
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
Most organisms consist of a functionally adaptive assemblage of hard and soft tissues. Despite the obvious advantages reinforcing soft protoplasm with a hard scaffold, such composites can lead to tremendous mechanical stresses where the two meet. Although little is known about how nature relieves these stresses, it is generally agreed that fundamental insights about molecular adaptation at hard/soft interfaces could profoundly influence how we think about biomaterials. Based on two noncellular tissues, mussel byssus and polychaete jaws, recent studies suggest that one natural strategy to minimize interfacial stresses between adjoining stiff and soft tissue appears to be the creation of a "fuzzy" boundary, which avoids abrupt changes in mechanical properties. Instead there is a gradual mechanical change that accompanies the transcendence from stiff to soft and vice versa. In byssal threads, the biochemical medium for achieving such a gradual mechanical change involves the elegant use of collagen-based self-assembling block copolymers. There are three distinct diblock copolymer types in which one block is always collagenous, whereas the other can be either elastin-like (soft), amorphous polyglycine (intermediate), or silk-like (stiff). Gradients of these are made by an incrementally titrated expression of the three proteins in secretory cells the titration phenotype of which is linked to their location. Thus, reflecting exactly the composition of each thread, the distal cells secrete primarily the silk- and polyglycine-collagen diblocks, whereas the proximal cells secrete the elastin- and polyglycine-collagen diblocks. Those cells in between exhibit gradations of collagens with silk or elastin blocks. Spontaneous self-assembly appears to be by pH triggered metal binding by histidine (HIS)-rich sequences at both the amino and carboxy termini of the diblocks. In the polychaete jaws, HIS-rich sequences are expanded into a major block domain. Histidine predominates at over 20 mol % near the distal tip and diminishes to about 5 mol % near the proximal base. The abundance of histidine is directly correlated to transition metal content (Zn or Cu) as well as hardness determined by nanoindentation. EXAFS analyses of the jaws indicate that transition metals such as Zn are directly bound to histidine ligands and may serve as cross-linkers.
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页码:7653 / 7662
页数:10
相关论文
共 67 条
[1]   Immobilization of histidine-tagged proteins on nickel by electrochemical dip pen nanolithography [J].
Agarwal, G ;
Naik, RR ;
Stone, MO .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (24) :7408-7412
[2]  
ARNOLD FH, 1992, METAL AFFINITY PROTE
[3]   MATERIALS IN MECHANICAL DESIGN [J].
ASHBY, MF .
MRS BULLETIN, 1993, 18 (07) :43-+
[4]  
BAIRATI A, 1976, CELL TISSUE RES, V166, P219
[5]   Metal-dependent stabilization of an active HMG protein [J].
Bell, AJ ;
Xin, H ;
Taudte, S ;
Shi, ZS ;
Kallenbach, NR .
PROTEIN ENGINEERING, 2002, 15 (10) :817-825
[6]   METALS IN NEREID POLYCHAETES - THE CONTRIBUTION OF METALS IN THE JAWS TO THE TOTAL-BODY BURDEN [J].
BRYAN, GW ;
GIBBS, PE .
JOURNAL OF THE MARINE BIOLOGICAL ASSOCIATION OF THE UNITED KINGDOM, 1980, 60 (03) :641-654
[7]   ZINC - MAJOR INORGANIC COMPONENT OF NEREID POLYCHAETE JAWS [J].
BRYAN, GW ;
GIBBS, PE .
JOURNAL OF THE MARINE BIOLOGICAL ASSOCIATION OF THE UNITED KINGDOM, 1979, 59 (04) :969-973
[8]   Cross-linking in adhesive quinoproteins: Studies with model decapeptides [J].
Burzio, LA ;
Waite, JH .
BIOCHEMISTRY, 2000, 39 (36) :11147-11153
[9]   MYTILUS BYSSAL THREADS AS AN ENVIRONMENTAL MARKER FOR METALS [J].
COOMBS, TL ;
KELLER, PJ .
AQUATIC TOXICOLOGY, 1981, 1 (5-6) :291-300
[10]   Bond energies of copper ion-ligand L complexes CuL2+ determined in the gas phase by ion-ligand exchange equilibria measurements [J].
Deng, HT ;
Kebarle, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (12) :2925-2931