Polymorphism of reconstituted human epidermal keratin filaments: Determination of their mass-per-length and width by scanning transmission electron microscopy (STEM)

Andreas Engel , Riva Eichner , Ueli Aebi
{"title":"Polymorphism of reconstituted human epidermal keratin filaments: Determination of their mass-per-length and width by scanning transmission electron microscopy (STEM)","authors":"Andreas Engel ,&nbsp;Riva Eichner ,&nbsp;Ueli Aebi","doi":"10.1016/S0022-5320(85)80010-1","DOIUrl":null,"url":null,"abstract":"<div><p>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.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1985-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0022-5320(85)80010-1","citationCount":"80","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of ultrastructure research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022532085800101","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 80

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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
重组人表皮角蛋白丝的多态性:扫描透射电镜(STEM)测定其单位长度和宽度
我们用扫描透射电镜(STEM)测定了未染色的冻干重组人表皮角蛋白丝的质量/长度(MPL)和宽度。从培养的人表皮细胞(CHEC)、人愈伤组织(CAL)和正常人表皮的活层(LL)和角质层(SC)中提取角蛋白重组丝。所有四种角蛋白丝类型的MPL直方图都可以通过两个或三个高斯叠加来拟合,它们各自的主峰位于17和20 kDa/nm之间。我们解释了多个MPL峰代表不同的多态形式的重组长丝。根据MPL峰位置、平均亚基分子量和46.5 nm的亚基轴向重复数计算出的每个丝截面的亚基数显示,多态变异之间的平均差异为7.5±0.9个亚基。这些数据表明,重组的人表皮角蛋白丝由2至4条8链“原纤维”组成(即由两条横向聚集的4链原丝组成),与早期观察结果一致。未染色的冻干角蛋白丝的平均宽度大于阴性染色的角蛋白丝:CHEC角蛋白丝的平均宽度为12.6 nm (9.6 nm), CAL角蛋白丝的平均宽度为12.3 nm (9.7 nm), LL角蛋白丝的平均宽度为11.6 nm (8.3 nm), SC角蛋白丝的平均宽度为11.3 nm (7.9 nm),括号内的值对应阴性染色的样品。假设MPL与细丝宽度的平方成正比,那么对于给定类型的细丝以及由不同类型的角蛋白提取物重建的细丝,MPL和宽度测量之间存在良好的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Cumulative subject index1 for volumes 86–89 The effects of zinc chloride on the RNP structures in HEp-2 cells: Accumulation of perichromatin granules Are there knobs on energy transducing membranesin situ? Quantitative analysis of development of mitochondrial ultrastructure in differentiating mouse hepatocytes during postnatal period Cell-to-cell fusion of lens fiber cellsin situ: Correlative light, scanning electron microscopic, and freeze-fracture studies
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1