Literature DB >> 15132649

X-ray evidence for a "super"-secondary structure in silk fibers.

Regina Valluzzi1, Hyoung-Joon Jin.   

Abstract

X-ray studies on degummed B. mori silk fibers and on hydrogels prepared under a variety of conditions reveal moderately small angle reflections. These reflections are often highly oriented and are correlated to silk II lattice reflections. A superstructure can explain these features. Silk fibroin hydrogels were monitored as they dried to form the silk II structure. The silk II wide angle and moderately small angle patterns obtained from dried hydrogels and silk fibers are identical. The "superstructure" reflections at moderately small angle (3-7 nm) were first to appear, followed by the "intersheet" spacing, and then the remainder of the silk II wide angle scattering pattern. Thus, any superstructure hypothesized for the hydrogels (and for Silk II in fibers) must be both stable in a highly hydrated environment and must convert to silk II with little large scale diffusion. A folded structure, similar to amyloids and cross-beta-sheets but with much longer beta-strand stems, is proposed for silk II in fibers.

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Year:  2004        PMID: 15132649     DOI: 10.1021/bm0343085

Source DB:  PubMed          Journal:  Biomacromolecules        ISSN: 1525-7797            Impact factor:   6.988


  2 in total

1.  Evidence from 13C solid-state NMR spectroscopy for a lamella structure in an alanine-glycine copolypeptide: a model for the crystalline domain of Bombyx mori silk fiber.

Authors:  Tetsuo Asakura; Yasumoto Nakazawa; Erika Ohnishi; Fumika Moro
Journal:  Protein Sci       Date:  2005-10       Impact factor: 6.725

2.  Stress-induced long-range ordering in spider silk.

Authors:  Johannes A Wagner; Sandeep P Patil; Imke Greving; Marc Lämmel; Konstantinos Gkagkas; Tilo Seydel; Martin Müller; Bernd Markert; Frauke Gräter
Journal:  Sci Rep       Date:  2017-11-10       Impact factor: 4.379

  2 in total

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