García-Vence Maria, Chantada-Vazquez Maria Del Pilar, Sosa-Fajardo Ana, Agra Rebeca, Barcia de la Iglesia Ana, Otero-Glez Alfonso, García-González Miguel, Cameselle-Teijeiro José M, Nuñez Cristina, Bravo Juan J, Bravo Susana B
Proteomic Unit, Health Research Institute of Santiago de Compostela (IDIS), University Clinical Hospital of Santiago de Compostela (CHUS), Santiago de Compostela, Spain.
Research Unit, Lucus Augusti University Hospital (HULA), Servizo Galego de Saúde (SERGAS), Lugo, Spain.
Front Med (Lausanne). 2021 May 13;8:657313. doi: 10.3389/fmed.2021.657313. eCollection 2021.
Most tissue biopsies from patients in hospital environments are formalin-fixed and paraffin-embedded (FFPE) for long-term storage. This fixation process produces a modification in the proteins called "crosslinks", which improves protein stability necessary for their conservation. Currently, these samples are mainly used in clinical practice for performing immunohistochemical analysis, since these modifications do not suppose a drawback for this technique; however, crosslinks difficult the protein extraction process. Accordingly, these modifications make the development of a good protein extraction protocol necessary. Due to the specific characteristics of each tissue, the same extraction buffers or deparaffinization protocols are not equally effective in all cases. Therefore, it is necessary to obtain a specific protocol for each tissue. The present work aims to establish a deparaffinization and protein extraction protocol from FFPE kidney samples to obtain protein enough of high quality for the subsequent proteomic analysis. Different deparaffination, protocols and protein extraction buffers will be tested in FFPE kidney samples. The optimized conditions will be applied in the identification by LC-MS/MS analysis of proteins extracted from 5, 10, and 15 glomeruli obtained through the microdissection of FFPE renal samples.
医院环境中患者的大多数组织活检样本都经过福尔马林固定和石蜡包埋(FFPE)以便长期保存。这种固定过程会使蛋白质发生一种称为“交联”的修饰,从而提高其保存所需的蛋白质稳定性。目前,这些样本主要用于临床实践中的免疫组织化学分析,因为这些修饰对该技术而言并非缺点;然而,交联会使蛋白质提取过程变得困难。因此,这些修饰使得制定一个良好的蛋白质提取方案成为必要。由于每种组织的特定特性,相同的提取缓冲液或脱石蜡方案在所有情况下并非都同样有效。所以,有必要针对每种组织制定特定的方案。本研究旨在建立一种从FFPE肾脏样本中进行脱石蜡和蛋白质提取的方案,以获得足够数量的高质量蛋白质用于后续的蛋白质组学分析。将在FFPE肾脏样本中测试不同的脱石蜡方案和蛋白质提取缓冲液。优化后的条件将应用于通过对FFPE肾脏样本进行显微切割获得的5个、10个和15个肾小球中提取的蛋白质的LC-MS/MS分析鉴定。