Bennike Tue Bjerg, Kastaniegaard Kenneth, Padurariu Simona, Gaihede Michael, Birkelund Svend, Andersen Vibeke, Stensballe Allan
Research Unit for Molecular Diagnostic and Clinical Research, Hospital of Southern Jutland, Aabenraa, Denmark; Department of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Department of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Data Brief. 2016 Feb 6;6:942-7. doi: 10.1016/j.dib.2016.01.061. eCollection 2016 Mar.
Large repositories of well characterized RNAlater preserved samples and formalin-fixed, paraffin-embedded samples have been generated worldwide. However, the impact on the proteome of the preservation methods remain poorly described. Therefore, we analyzed the impact on the proteome of preserving samples in RNAlater, and by formalin-fixation, paraffin-embedding on human soft tissue, using directly frozen samples as a control ("Comparing the proteome of snap frozen, RNAlater preserved, and formalin-fixed paraffin-embedded human tissue samples" [1]). We here report the data from the analysis. The comparative analysis was performed on 24 colon mucosa biopsies, extracted from the sigmoideum of two gastroenterologically healthy participants for the purpose of this study. A set of biopsies were additionally stored for 30 min at room temperature prior to formalin-fixation. The samples were analyzed by high throughput gel free quantitative proteomics. The MS proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PRIDE: PXD002029.
全球已建立了大量经过充分表征的经RNA Later保存的样本以及福尔马林固定、石蜡包埋的样本库。然而,保存方法对蛋白质组的影响仍鲜有描述。因此,我们分析了将样本保存在RNA Later中以及通过福尔马林固定、石蜡包埋对人体软组织蛋白质组的影响,并将直接冷冻的样本作为对照(“比较速冻、经RNA Later保存和福尔马林固定石蜡包埋的人体组织样本的蛋白质组”[1])。我们在此报告分析数据。本研究从两名胃肠健康参与者的乙状结肠提取了24份结肠黏膜活检样本进行比较分析。一组活检样本在福尔马林固定前还在室温下额外保存了30分钟。通过高通量无凝胶定量蛋白质组学对样本进行分析。质谱蛋白质组学数据已通过PRIDE合作伙伴存储库存入蛋白质组交换联盟,数据集标识符为PRIDE:PXD002029。