Molecular interaction and partitioning in α-keratin using 1 H NMR spin-lattice ( T 1 ) relaxation times

Author:

Molisso Susannah1ORCID,Williams Daryl R.2ORCID,Ces Oscar1ORCID,Rowlands Lucy J.1ORCID,Marsh Jennifer M.3ORCID,Law Robert V.1ORCID

Affiliation:

1. Institute of Chemical Biology, Department of Chemistry, MSRH, Imperial College London, White City Campus, 80–92 Wood Lane, London W12 0BZ, UK

2. Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, UK

3. The Procter and Gamble Company, Mason Business Center, 8700 Mason Montgomery Road, Mason, OH 45040, USA

Abstract

The interactions between small molecules and keratins are poorly understood. In this paper, a nuclear magnetic resonance method is presented to measure changes in the 1 H T 1 relaxation times of small molecules in human hair keratin to quantify their interaction with the fibre. Two populations of small-molecule compounds were identified with distinct relaxation times, demonstrating the partitioning of the compounds into different keratin environments. The changes in relaxation time for solvent in hair compared with bulk solvent were shown to be related to the molecular weight (MW) and the partition coefficient, LogP, of the solvent investigated. Compounds with low MWs and high hydrophilicities had greater reductions in their T 1 relaxation times and therefore experienced increased interactions with the hair fibre. The relative population sizes were also calculated. This is a significant step towards modelling the behaviour of small molecules in keratinous materials and other large insoluble fibrous proteins.

Funder

Engineering and Physical Sciences Research Council

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

Reference41 articles.

1. UK Fashion and Textile Association. 2018 Industry reports & statistics. See https://www.ukft.org/business-advice/industry-reports-and-stats/ (accessed 18 March 2021).

2. National Hair & Beauty Federation. 2020 NHBF Industry research and statistics 2020. See https://www.nhbf.co.uk/about-the-nhbf/what-we-do/industry-research/ (accessed 18 March 2021).

3. Can Thiourea Dioxide Regenerate Keratin from Waste Wool?

4. Alpha-Helix Self-Assembly of Oligopeptides Originated From Beta-Sheet Keratin

5. Biocompatible, Antioxidant Nanoparticles Prepared from Natural Renewable Tea Polyphenols and Human Hair Keratins for Cell Protection and Anti-inflammation

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3