Liao Renjie, Mondal Manas, Nazaroff Christopher D, Mastroeni Diego, Coleman Paul D, Labaer Joshua, Guo Jia
Biodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, AZ, United States.
Division of Pulmonary Medicine, Department of Biochemistry and Molecular Biology, Mayo Clinic Arizona, Scottsdale, AZ, United States.
Front Cell Dev Biol. 2021 Jan 8;8:614624. doi: 10.3389/fcell.2020.614624. eCollection 2020.
The ability to comprehensively profile proteins in intact tissues is crucial for our understanding of health and disease. However, the existing methods suffer from low sensitivity and limited sample throughput. To address these issues, here we present a highly sensitive and multiplexed protein analysis approach using cleavable fluorescent tyramide and off-the-shelf antibodies. Compared with the current methods, this approach enhances the detection sensitivity and reduces the imaging time by 1-2 orders of magnitude, and can potentially detect hundreds of proteins in intact tissues at the optical resolution. Applying this approach, we studied protein expression heterogeneity in a population of genetically identical cells, and performed protein expression correlation analysis to identify co-regulated proteins. We also profiled >6,000 neurons in a human formalin-fixed paraffin-embedded (FFPE) hippocampus tissue. By partitioning these neurons into varied cell clusters based on their multiplexed protein expression profiles, we observed different sub-regions of the hippocampus consist of neurons from distinct clusters.
在完整组织中对蛋白质进行全面分析的能力对于我们理解健康与疾病至关重要。然而,现有方法存在灵敏度低和样本通量有限的问题。为了解决这些问题,我们在此展示一种使用可裂解荧光酪胺和现成抗体的高灵敏度和多重蛋白质分析方法。与当前方法相比,该方法提高了检测灵敏度,并将成像时间减少了1 - 2个数量级,并且有可能在光学分辨率下检测完整组织中的数百种蛋白质。应用此方法,我们研究了基因相同细胞群体中的蛋白质表达异质性,并进行了蛋白质表达相关性分析以鉴定共同调控的蛋白质。我们还对人类福尔马林固定石蜡包埋(FFPE)海马组织中的6000多个神经元进行了分析。通过根据其多重蛋白质表达谱将这些神经元划分为不同的细胞簇,我们观察到海马体的不同亚区域由来自不同簇的神经元组成。