Institute of Fundamental Sciences, Massey University, Palmerston North, New Zealand.
, Tewantin, QLD, Australia.
Adv Exp Med Biol. 2018;1054:57-70. doi: 10.1007/978-981-10-8195-8_6.
Although trichocyte keratins (hair, wool, quill, claw) have been studied since the 1930s it is only over the last 30 years or so that major advances have been made in our understanding of the complex structural hierarchy of the filamentous component of this important filament-matrix composite. A variety of techniques, including amino acid sequence analysis, computer modelling, X-ray fibre diffraction and protein crystallography, various forms of electron microscopy, and crosslinking methods have now combined to reveal much of the structural detail. The heterodimeric structure of the keratin molecule is clear, as are the highly-specific modes by which these molecules aggregate to form functionally viable IF. The observation that hair keratin can adopt not one but two structurally-distinct conformations, one formed in the living cells at the base of the hair follicle in a reducing environment and the second in the fully differentiated hair in dead cells in an oxidized state, was unexpected but has major implications for the mechanism of hair growth. Insights have also been made into the mechanism of the uppermost level of hair superstructure, relating to the assembly of the IF in the paracortical and orthocortical macrofibrils.
虽然毛角蛋白(毛发、羊毛、羽毛、爪)自 20 世纪 30 年代以来就一直被研究,但直到最近 30 年左右,我们才对这种重要的纤维-基质复合材料的丝状成分的复杂结构层次有了更深入的了解。现在,包括氨基酸序列分析、计算机建模、X 射线纤维衍射和蛋白质晶体学、各种形式的电子显微镜以及交联方法在内的多种技术已经结合起来,揭示了大量的结构细节。角蛋白分子的异二聚体结构是明确的,这些分子以高度特异性的方式聚集形成具有功能的 IF 也是明确的。观察到头发角蛋白可以采用两种而不是一种结构上明显不同的构象,一种在毛囊底部的活细胞中形成,处于还原环境中,另一种在完全分化的死细胞中的头发中形成,处于氧化状态,这是出乎意料的,但对毛发生长的机制有重大影响。我们还深入了解了头发超结构的最高层次的组装机制,涉及到 IF 在副皮质和正皮质大纤维中的组装。