Polymorphism of reconstituted human epidermal keratin filaments: determination of their mass-per-length and width by scanning transmission electron microscopy (STEM)
- PMID: 2416949
- DOI: 10.1016/s0022-5320(85)80010-1
Polymorphism of reconstituted human epidermal keratin filaments: determination of their mass-per-length and width by scanning transmission electron microscopy (STEM)
Abstract
We have determined the mass-per-length (MPL) and the width of unstained freeze-dried reconstituted human epidermal keratin filaments by scanning transmission electron microscopy (STEM). Filaments were reassembled from keratins extracted from four different sources: cultured human epidermal cells (CHEC), human callus (CAL), and the living layers (LL) and stratum corneum (SC) of normal human epidermis. MPL histograms of all four keratin filament types could be fitted by a superposition of two or three Gaussians, with their respective major peaks located between 17 and 20 kDa/nm. We interpreted the multiple MPL peaks to represent different polymorphic forms of the reconstituted filaments. The number of subunits per filament cross section calculated from MPL peak positions, average subunit molecular weight, and an axial repeat of the subunits within the filament of 46.5 nm revealed an average difference between polymorphic variants of 7.5 +/- 0.9 subunits. These data suggest that reconstituted human epidermal keratin filaments are made of two to four 8-stranded "protofibrils" (i.e., made of two laterally aggregated 4-stranded protofilaments), in agreement with earlier observations. The average widths of unstained freeze-dried keratin filaments were larger than those of negatively stained filaments: 12.6 nm (9.6 nm) for CHEC, 12.3 nm (9.7 nm) for CAL, 11.6 nm (8.3 nm) for LL, and 11.3 nm (7.9 nm) for SC keratin filaments, with the values in brackets corresponding to negatively stained samples. Assuming the MPL to be proportional to the square of the filament width, there is a good correlation between the MPL and width measurements both for filaments within a given type as well as among those reconstituted from different types of keratin extracts.
Similar articles
-
Structural features of epidermal keratin filaments reassembled in vitro.J Invest Dermatol. 1983 Jul;81(1 Suppl):86s-90s. doi: 10.1111/1523-1747.ep12540757. J Invest Dermatol. 1983. PMID: 6190964
-
The role of keratin subfamilies and keratin pairs in the formation of human epidermal intermediate filaments.J Cell Biol. 1986 May;102(5):1767-77. doi: 10.1083/jcb.102.5.1767. J Cell Biol. 1986. PMID: 2422179 Free PMC article.
-
The fibrillar substructure of keratin filaments unraveled.J Cell Biol. 1983 Oct;97(4):1131-43. doi: 10.1083/jcb.97.4.1131. J Cell Biol. 1983. PMID: 6194161 Free PMC article.
-
Human epidermal keratin filaments: studies on their structure and assembly.Ann N Y Acad Sci. 1985;455:381-402. doi: 10.1111/j.1749-6632.1985.tb50424.x. Ann N Y Acad Sci. 1985. PMID: 2417522 Review. No abstract available.
-
Developmental expression of human epidermal keratins and filaggrin.Curr Top Dev Biol. 1987;22:127-51. doi: 10.1016/s0070-2153(08)60101-5. Curr Top Dev Biol. 1987. PMID: 2443308 Review. No abstract available.
Cited by
-
A multimethod approach for analyzing FapC fibrillation and determining mass per length.Biophys J. 2021 Jun 1;120(11):2262-2275. doi: 10.1016/j.bpj.2021.03.031. Epub 2021 Apr 1. Biophys J. 2021. PMID: 33812849 Free PMC article.
-
The focal adhesion scaffold protein Hic-5 regulates vimentin organization in fibroblasts.Mol Biol Cell. 2019 Dec 1;30(25):3037-3056. doi: 10.1091/mbc.E19-08-0442. Epub 2019 Oct 23. Mol Biol Cell. 2019. PMID: 31644368 Free PMC article.
-
A potential role for the COOH-terminal domain in the lateral packing of type III intermediate filaments.J Cell Biol. 1991 Aug;114(4):773-86. doi: 10.1083/jcb.114.4.773. J Cell Biol. 1991. PMID: 1714461 Free PMC article.
-
"Panta rhei": Perpetual cycling of the keratin cytoskeleton.Bioarchitecture. 2011 Jan;1(1):39-44. doi: 10.4161/bioa.1.1.14815. Bioarchitecture. 2011. PMID: 21866261 Free PMC article.
-
Genetic mutations in the K1 and K10 genes of patients with epidermolytic hyperkeratosis. Correlation between location and disease severity.J Clin Invest. 1994 Apr;93(4):1533-42. doi: 10.1172/JCI117132. J Clin Invest. 1994. PMID: 7512983 Free PMC article.