蛋白质组
微流控
秀丽隐杆线虫
轨道轨道
样品制备
数字微流体
色谱法
化学
蛋白质组学
质谱法
计算生物学
介电泳
生物
分析化学(期刊)
纳米技术
生物化学
材料科学
物理化学
基因
电润湿
电极
作者
Max K. Steinbach,Jan Leipert,Christine Blurton,Matthias Leippe,Andreas Tholey
标识
DOI:10.1021/acs.jproteome.2c00274
摘要
Miniaturization of sample preparation, including omissible manual sample handling steps, is key for reproducible nanoproteomics, as material is often restricted to only hundreds of cells or single model organisms. Here, we demonstrate a highly sensitive digital microfluidics (DMF)-based sample preparation workflow making use of single-pot solid-phase enhanced sample preparation (SP3) in combination with high-field asymmetric-waveform ion mobility spectrometry (FAIMS), and fast and sensitive ion trap detection on an Orbitrap tribrid MS system. Compared to a manual in-tube SP3-supported sample preparation, the numbers of identified peptides and proteins were markedly increased, while lower standard deviations between replicates were observed. We repeatedly identified up to 5000 proteins from single nematodes. Moreover, label-free quantification of protein changes in single Caenorhabditis elegans treated with a heat stimulus yielded 45 differentially abundant proteins when compared to the untreated control, highlighting the potential of this technology for low-input proteomics studies. LC-MS data have been deposited to the ProteomeXchange Consortium with the data set identifier PXD033143.
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