Self-Tensioning Aquatic Caddisfly Silk: Ca2+-Dependent Structure, Strength, and Load Cycle Hysteresis

被引:56
作者
Ashton, Nicholas N. [1 ]
Roe, Daniel R. [2 ]
Weiss, Robert B. [3 ]
Cheatham, Thomas E., III [2 ]
Stewart, Russell J. [1 ]
机构
[1] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA
关键词
MECHANICAL-PROPERTIES; SPIDER SILK; MOLECULAR-DYNAMICS; SECONDARY STRUCTURE; FIBROUS PROTEINS; SEQUENCE; TRICHOPTERA; WATER; SPECTROSCOPY; INTEGRATION;
D O I
10.1021/bm401036z
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
Caddisflies are aquatic relatives of silk-spinning terrestrial moths and butterflies. Casemaker larvae spin adhesive silk fibers for underwater construction of protective composite cases. The central region of Hesperophylax sp. H-fibroin contains a repeating pattern of three conserved subrepeats, all of which contain one or more (SX)(n) motifs with extensively phosphorylated serines. Native silk fibers were highly extensible and displayed a distinct yield point, force plateau, and load cycle hysteresis. FTIR spectroscopy of native silk showed a conformational mix of random coil, beta-sheet, and turns. Exchanging multivalent ions with Na+ EDTA disrupted fiber mechanics, shifted the secondary structure ratios from antiparallel beta-sheet toward random coil and turns, and caused the fibers to shorten, swell in diameter, and disrupted fiber birefringence. The EDTA effects were reversed by restoring Ca2+. Molecular dynamic simulations provided theoretical support for a hypothetical structure in which the (pSX)(n) motifs may assemble into two- and three-stranded, Ca2+-stabilized beta-sheets.
引用
收藏
页码:3668 / 3681
页数:14
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