Literature DB >> 24750564

Degree of polymerization of 5,6-dihydroxyindole-derived eumelanin from chemical degradation study.

Hidekazu Okuda1, Kyoji Yoshino, Kazumasa Wakamatsu, Shosuke Ito, Takayuki Sota.   

Abstract

Eumelanin is a brown-black pigment comprising 5,6-dihydroxyindole (DHI) and its 2-carboxy derivative (DHICA), but the detailed structure of eumelanin is unclear. Chemical degradation is a powerful tool for analyzing melanin. H2 O2 oxidation degradation of eumelanin affords pyrrole-2,3,5-tricarboxylic acid (PTCA) and pyrrole-2,3-dicarboxylic acid (PDCA). The ratio of PDCA to PTCA provides information about the eumelanin structure. In this article, we propose simple equations on the basis of previous experimental results on dimer yields for evaluating the yields of PTCA and PDCA from any DHI oligomers. Assuming the chemical disorder model of DHI-melanin, we solve an equation where a theoretical expression for the ratio of PDCA to PTCA is set to the corresponding experimental value to obtain a plausible Poisson distribution of DHI oligomers. The results demonstrate that the main contributors to DHI-melanin are tetramers and pentamers as shown by the mass spectrometry.
© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  5,6-dihydroxyindole; chemical disorder model; degree of polymerization; eumelanin; hydrogen peroxide oxidation

Mesh:

Substances:

Year:  2014        PMID: 24750564     DOI: 10.1111/pcmr.12254

Source DB:  PubMed          Journal:  Pigment Cell Melanoma Res        ISSN: 1755-1471            Impact factor:   4.693


  6 in total

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2.  Mimicking Melanosomes: Polydopamine Nanoparticles as Artificial Microparasols.

Authors:  Yuran Huang; Yiwen Li; Ziying Hu; Xiujun Yue; Maria T Proetto; Ying Jones; Nathan C Gianneschi
Journal:  ACS Cent Sci       Date:  2017-05-18       Impact factor: 14.553

3.  Polydopamine and eumelanin molecular structures investigated with ab initio calculations.

Authors:  Chun-Teh Chen; Francisco J Martin-Martinez; Gang Seob Jung; Markus J Buehler
Journal:  Chem Sci       Date:  2016-11-02       Impact factor: 9.825

4.  Effects of pH and Oxidants on the First Steps of Polydopamine Formation: A Thermodynamic Approach.

Authors:  Mikko Salomäki; Lauri Marttila; Henri Kivelä; Tuomo Ouvinen; Jukka Lukkari
Journal:  J Phys Chem B       Date:  2018-06-06       Impact factor: 2.991

5.  Polydopamine Nanoparticles Prepared Using Redox-Active Transition Metals.

Authors:  Mikko Salomäki; Tuomo Ouvinen; Lauri Marttila; Henri Kivelä; Jarkko Leiro; Ermei Mäkilä; Jukka Lukkari
Journal:  J Phys Chem B       Date:  2019-03-12       Impact factor: 2.991

6.  Progressive fuzzy cation-π assembly of biological catecholamines.

Authors:  Seonki Hong; Younseon Wang; Sung Young Park; Haeshin Lee
Journal:  Sci Adv       Date:  2018-09-07       Impact factor: 14.136

  6 in total

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