Peng-Cheng Mei, Na An, Hua-Ming Xiao, Yao-Yu Chen, Quan-Fei Zhu, Yu-Qi Feng
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引用次数: 0
Abstract
Branched fatty acid esters of hydroxy fatty acids (FAHFAs) represent a novel class of bioactive lipids with significant physiological roles. However, their identification, particularly of low-abundance FAHFA regioisomers, remains challenging due to their high structural similarity, low natural abundance, and the limited availability of reliable FAHFA standards. In this study, we present a QSAR-based FAHFA annotation strategy that integrates a QSAR model with an ester bond position (EP) rule to determine the EPs of FAHFA regioisomers. The QSAR model quantitatively relates the retention index (RI) of FAHFAs to the EP descriptor and the GATS2m descriptor, while the EP rule establishes a quantitative relationship between the RI of FAHFA regioisomers and their EP within a given FAHFA family. By applying this QSAR-based strategy, we successfully identified a comprehensive set of 507 FAHFA regioisomers from 1207 FAHFA candidates detected across 16 food samples, achieving nearly a threefold increase in annotation coverage compared to our previous method. Overall, this strategy significantly enhances the identification capability in determining EP for FAHFA regioisomers, providing a promising analytical tool for the further exploration into these lipids.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.