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1.
Nanoscale ; 10(29): 14245-14253, 2018 Aug 07.
Article in English | MEDLINE | ID: mdl-30010172

ABSTRACT

In situ characterization of the chemical and structural properties of black and white sheep hair was performed with a spatial resolution of 25 nm using infrared nano-spectroscopy. Comparing data sets from two types of hair allowed us to isolate the keratin FTIR fingerprint and so mark off chemical properties of the hair's melanosomes. From a polarization sensitive analysis of the nano-FTIR spectra, we showed that keratin intermediate filaments (IFs) present anisotropic molecular ordering. In stark contrast with white hair which does not contain melanosomes, in black hair, we spatially resolved single melanosomes and achieved unprecedented assignment of the vibrational modes of pheomelanin and eumelanin. The in situ experiment presented here avoids harsh chemical extractive methods used in previous studies. Our findings offer a basis for a better understanding of the keratin chemical and structural packing in different hair phenotypes as well as the involvement of melanosomes in hair color and biological functionality.


Subject(s)
Hair Color , Hair/chemistry , Melanosomes/chemistry , Spectrophotometry, Infrared , Animals , Keratins/chemistry , Melanins/chemistry , Sheep
2.
Sci Rep ; 5: 17347, 2015 Nov 30.
Article in English | MEDLINE | ID: mdl-26617337

ABSTRACT

Human hair has three main regions, the medulla, the cortex, and the cuticle. An existing model for the cortex suggests that the α-keratin- based intermediate filaments (IFs) align with the hair's axis, but are orientationally disordered in-plane. We found that there is a new region in the cortex near the cuticle's boundary in which the IFs are aligned with the hair's axis, but additionally, they are orientationally ordered in-plane due to the presence of the cuticle/hair boundary. Further into the cortex, the IF arrangement becomes disordered, eventually losing all in-plane orientation. We also find that in the cuticle, a key diffraction feature is absent, indicating the presence of the ß-keratin rather than that of the α-keratin phase. This is direct structural evidence that the cuticle contains ß-keratin sheets. This work highlights the importance of using a sub-micron x-ray beam to unravel the structures of poorly ordered, multi-phase systems.


Subject(s)
Hair/chemistry , Hair/ultrastructure , Microscopy, Electron, Scanning , Scattering, Small Angle , X-Ray Diffraction , Humans , Keratins/chemistry
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