化学
移液管
蛋白质组
样品制备
基质辅助激光解吸/电离
蛋白质组学
转甲状腺素
分辨率(逻辑)
表面增强激光解吸/电离
色谱法
串联质谱法
质谱法
分析化学(期刊)
解吸
蛋白质质谱法
生物化学
基因
医学
内科学
物理化学
吸附
人工智能
有机化学
计算机科学
作者
Seonjeong Lee,Shinyeong Ju,Seok Jin Kim,Jin‐Oh Choi,Kihyun Kım,Darae Kim,Eun‐Seok Jeon,Cheolju Lee
标识
DOI:10.1021/acs.analchem.1c01722
摘要
The mass spectrometry-based analysis of protein post-translational modifications requires large amounts of sample, complicating the analysis of samples with limited amounts of proteins such as clinical biopsies. Here, we present a tip-based N-terminal analysis method, tipNrich. The entire procedure is processed in a single pipette tip to minimize sample loss, which is so highly optimized to analyze small amounts of proteins, even femtomole-scale of a single protein. With tipNrich, we investigated various single proteins purified from different organisms using a low-resolution mass spectrometer and identified several N-terminal peptides with different Nt-modifications such as ragged N-termini. Furthermore, we applied matrix-assisted laser desorption ionization time-of-flight mass spectrometry to our method for shortening the analysis time. Moreover, we showed that our method could be utilized in disease diagnosis as exemplified by the characterization of wild-type transthyretin amyloidosis patients compared to the healthy individuals based on N-terminome profiling. In summary, tipNrich will satisfy the need of identifying N-terminal peptides even with highly scarce amounts of proteins and of having faster processing time to check the quality of protein products or to characterize N-terminal proteoform-related diseases.
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