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Updated: Sep 24, 2025

Quantification of Site-specific Protein Lysine Acetylation and Succinylation Stoichiometry Using Data-independent Acquisition Mass Spectrometry
Published on: April 4, 2018
Design, synthesis and properties investigation of N α-acylation lysine based derivatives
Ting-Ting Shi1,2, Zheng Fang1, Wen-Bo Zeng1
1College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University Nanjing 211816 P. R. China guokai@nitech.edu.cn.
Abstract:
Amino acid-based compounds have attracted attention as environmentally friendly bio-based materials. Our group has recently developed a novel family of N α-acylation lysine based derivatives. We introduced long chain acyl groups at the N α position selectively by a new synthetic route that avoided the process of amino protection and deprotection. Sodium N α-octanamide lysine (C8), sodium N α-capramide lysine (C10) and sodium N α-lauramide lysine (C12) can self-assemble into vesicles spontaneously. As a result, not only do they have potential in drug delivery system but also they may be used as bio-based surfactants applied in cosmetics and other industries.
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