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α-氰基-5-苯基-2,4-戊二烯酸(CPPA)的合成及其在基质辅助激光解吸电离质谱法分析完整蛋白质中的基质性质。

Synthesis and Matrix Properties of α-Cyano-5-phenyl-2,4-pentadienic Acid (CPPA) for Intact Proteins Analysis by Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry.

机构信息

Agenzia delle Dogane e dei Monopoli, Ufficio delle Dogane di Bari, Corso De Tullio, 70122 Bari, Italy.

Dipartimento di Chimica, Università degli Studi di Bari Aldo Moro, Via Orabona, 70126 Bari, Italy.

出版信息

Molecules. 2020 Dec 21;25(24):6054. doi: 10.3390/molecules25246054.

DOI:10.3390/molecules25246054
PMID:33371472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7767571/
Abstract

The effectiveness of a synthesized matrix, α-cyano-5-phenyl-2,4-pentadienic acid (CPPA), for protein analysis by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) in complex samples such as foodstuff and bacterial extracts, is demonstrated. Ultraviolet (UV) absorption along with laser desorption/ionization mass spectrometry (LDI-MS) experiments were systematically conducted in positive ion mode under standard Nd:YLF laser excitation with the aim of characterizing the matrix in terms of wavelength absorption and proton affinity. Besides, the results for standard proteins revealed that CPPA significantly enhanced the protein signals, reduced the spot-to-spot variability and increased the spot homogeneity. The CPPA matrix was successful employed to investigate intact microorganisms, milk and seed extracts for protein profiling. Compared to conventional matrices such as sinapinic acid (SA), α-cyano-4-hydroxycinnamic acid (CHCA) and 4-chloro-α-cyanocinnamic acid (CClCA), CPPA exhibited better signal-to-noise (S/N) ratios and a uniform response for most examined proteins occurring in milk, hazelnut and in intact bacterial cells of . These findings not only provide a reactive proton transfer MALDI matrix with excellent reproducibility and sensitivity, but also contribute to extending the battery of useful matrices for intact protein analysis.

摘要

本文展示了一种合成基质,α-氰基-5-苯基-2,4-戊二烯酸(CPPA),在食品和细菌提取物等复杂样品中通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)进行蛋白质分析的有效性。在标准 Nd:YLF 激光激发下,以正离子模式进行了系统的紫外(UV)吸收和激光解吸/电离质谱(LDI-MS)实验,旨在根据波长吸收和质子亲和力来表征基质。此外,标准蛋白质的结果表明,CPPA 显著增强了蛋白质信号,降低了斑点间的可变性,并提高了斑点的均匀性。CPPA 基质成功用于研究完整微生物、牛奶和种子提取物中的蛋白质谱。与传统基质如 3-(4-羟基苯基)-2-丙炔酸(SA)、α-氰基-4-羟基肉桂酸(CHCA)和 4-氯-α-氰基肉桂酸(CClCA)相比,CPPA 对大多数在牛奶、榛子和完整细菌细胞中出现的蛋白质表现出更好的信噪比(S/N)比值和均匀响应。这些发现不仅提供了一种具有出色重现性和灵敏度的反应性质子转移 MALDI 基质,还有助于扩展用于完整蛋白质分析的有用基质库。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/bf6675223afe/molecules-25-06054-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/b843c859c164/molecules-25-06054-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/58d018d4f2e2/molecules-25-06054-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/ff5f8fd7f18f/molecules-25-06054-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/87d832ff0eb2/molecules-25-06054-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/36065afe47be/molecules-25-06054-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/80e1fff1c989/molecules-25-06054-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/bf6675223afe/molecules-25-06054-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/b843c859c164/molecules-25-06054-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/58d018d4f2e2/molecules-25-06054-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/ff5f8fd7f18f/molecules-25-06054-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/87d832ff0eb2/molecules-25-06054-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/36065afe47be/molecules-25-06054-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/80e1fff1c989/molecules-25-06054-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0449/7767571/bf6675223afe/molecules-25-06054-g007.jpg

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