Herrmann Harald, Aebi Ueli
Functional Architecture of the Cell (B065), German Cancer Research Center (DKFZ), D-69120 Heidelberg, Germany, and Institute of Neuropathology, University Hospital Erlangen, D-91054 Erlangen, Germany.
Biozentrum, University of Basel, CH-4056 Basel, Switzerland.
Cold Spring Harb Perspect Biol. 2016 Nov 1;8(11):a018242. doi: 10.1101/cshperspect.a018242.
Proteins of the intermediate filament (IF) supergene family are ubiquitous structural components that comprise, in a cell type-specific manner, the cytoskeleton proper in animal tissues. All IF proteins show a distinctly organized, extended α-helical conformation prone to form two-stranded coiled coils, which are the basic building blocks of these highly flexible, stress-resistant cytoskeletal filaments. IF proteins are highly charged, thus representing versatile polyampholytes with multiple functions. Taking vimentin, keratins, and the nuclear lamins as our prime examples, we present an overview of their molecular and structural parameters. These, in turn, document the ability of IF proteins to form distinct, highly diverse supramolecular assemblies and biomaterials found, for example, at the inner nuclear membrane, throughout the cytoplasm, and in highly complex extracellular appendages, such as hair and nails, of vertebrate organisms. Ultimately, our aim is to set the stage for a more rational understanding of the immediate effects that missense mutations in IF genes have on cellular functions and for their far-reaching impact on the development of the numerous IF diseases caused by them.
中间丝(IF)超基因家族的蛋白质是普遍存在的结构成分,它们以细胞类型特异性的方式构成动物组织中的细胞骨架本身。所有IF蛋白都呈现出明显有组织的、延伸的α-螺旋构象,易于形成双链卷曲螺旋,这些是这些高度灵活、抗应力的细胞骨架细丝的基本构建块。IF蛋白带电量很高,因此是具有多种功能的通用聚两性电解质。以波形蛋白、角蛋白和核纤层蛋白为例,我们概述了它们的分子和结构参数。这些反过来又证明了IF蛋白能够形成不同的、高度多样的超分子组装体和生物材料,例如在脊椎动物的内核膜、整个细胞质以及毛发和指甲等高度复杂的细胞外附属物中发现的那些。最终,我们的目标是为更合理地理解IF基因中的错义突变对细胞功能的直接影响以及它们对由其引起的众多IF疾病发展的深远影响奠定基础。