Literature DB >> 9468612

Intermediate filament structure: hard alpha-keratin.

L N Jones1, M Simon, N R Watts, F P Booy, A C Steven, D A Parry.   

Abstract

Structurally there are four classes of intermediate filaments (IF) with distinct but closely related axial organisations. One of these, hard alpha-keratin IF, has been studied to clarify several apparently exceptional features which include the number of molecules in the IF cross-section and the mode by which the axial organisation of its constituent molecules is stabilised. Using the dark-field mode of the STEM at the Brookhaven National Laboratory (USA) mass measurements were obtained from unstained IF isolated from hair keratin. The data thus obtained show that the number of chains in cross-section is about 30 (+/-3: standard deviation) and is very similar to the numbers determined in previous STEM experiments for the dominant filament type in other classes of IF (about 32). Furthermore, re-analysis of the low-angle equatorial X-ray diffraction pattern reveals, in contrast to earlier work, solutions that are compatible with the number of chains in cross-section indicated by the STEM data. The absence of the head-to-tail overlap between parallel molecules characteristic of most of IF may be compensated in hard alpha-keratin by a network of intermolecular disulfide bonds. It is concluded that native IF of hard alpha-keratin and desmin/vimentin--and probably many other kinds of IF as well--contain about 32 chains in cross-section, and that the axial structures of these various kinds of IF differ in small but significant ways, while generally observing the same basic modes of aggregation.

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Year:  1997        PMID: 9468612     DOI: 10.1016/s0301-4622(97)00013-6

Source DB:  PubMed          Journal:  Biophys Chem        ISSN: 0301-4622            Impact factor:   2.352


  5 in total

1.  A new deformation model of hard alpha-keratin fibers at the nanometer scale: implications for hard alpha-keratin intermediate filament mechanical properties.

Authors:  L Kreplak; A Franbourg; F Briki; F Leroy; D Dallé; J Doucet
Journal:  Biophys J       Date:  2002-04       Impact factor: 4.033

Review 2.  Structure and functions of keratin proteins in simple, stratified, keratinized and cornified epithelia.

Authors:  Hermann H Bragulla; Dominique G Homberger
Journal:  J Anat       Date:  2009-04       Impact factor: 2.610

3.  Exploring the folding pathway of green fluorescent protein through disulfide engineering.

Authors:  Derek J Pitman; Shounak Banerjee; Stephen J Macari; Christopher A Castaldi; Donna E Crone; Christopher Bystroff
Journal:  Protein Sci       Date:  2015-01-13       Impact factor: 6.725

4.  In vitro assembly and structure of trichocyte keratin intermediate filaments: a novel role for stabilization by disulfide bonding.

Authors:  H Wang; D A Parry; L N Jones; W W Idler; L N Marekov; P M Steinert
Journal:  J Cell Biol       Date:  2000-12-25       Impact factor: 10.539

Review 5.  Keratin - Based materials for biomedical applications.

Authors:  Sandleen Feroz; Nawshad Muhammad; Jithendra Ranayake; George Dias
Journal:  Bioact Mater       Date:  2020-04-16
  5 in total

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