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Comparison of Different Buffers for Protein Extraction from Formalin-Fixed and Paraffin-Embedded Tissue Specimens

机译:从福尔马林固定和石蜡包埋的组织标本中提取蛋白质的不同缓冲液的比较

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摘要

We determined the best extraction buffer for proteomic investigation using formalin-fixation and paraffin-embedded (FFPE) specimens. A Zwittergent 3–16 based buffer, sodium dodecyl sulfate (SDS)-containing buffer with/without polyethylene glycol 20000 (PEG20000), urea-containing buffer, and FFPE-FASP protein preparation kit were compared for protein extraction from different types of rat FFPE tissues, including the heart, brain, liver, lung, and kidney. All of the samples were divided into two groups of laser microdissected (LMD) and non-LMD specimens. For both kinds of specimens, Zwittergent was the most efficient buffer for identifying peptides and proteins, was broadly applicable to different tissues without impairing the enzymatic digestion, and was well compatible with mass spectrometry analysis. As a high molecular weight carrier substance, PEG20000 improved the identification of peptides and proteins; however, such an advantage is limited to tissues containing submicrograms to micrograms of protein. Considering its low lytic strength, urea-containing buffer would not be the first alternative for protein recovery. In conclusion, Zwittergent 3–16 is an effective buffer for extracting proteins from FFPE specimens for downstream proteomics analysis.
机译:我们使用福尔马林固定和石蜡包埋(FFPE)标本确定了用于蛋白质组学研究的最佳提取缓冲液。比较了基于两性离子3–16的缓冲液,含十二烷基硫酸钠(SDS)的缓冲液(有/无聚乙二醇20000(PEG20000)),含尿素的缓冲液和FFPE-FASP蛋白制备试剂盒,用于从不同类型的大鼠FFPE中提取蛋白组织,包括心脏,大脑,肝脏,肺和肾脏。将所有样品分为激光显微切割(LMD)和非LMD样品两组。对于两种标本,两性离子试剂都是鉴定肽和蛋白质的最有效缓冲液,可广泛应用于不同组织而不会影响酶消化,并且与质谱分析兼容。作为一种高分子量的载体物质,PEG20000改善了肽和蛋白质的鉴定;但是,这种优势仅限于包含亚微克至微克蛋白质的组织。考虑到其低的裂解强度,含尿素的缓冲液将不是蛋白质回收的首选。总之,两性离子3–16是从FFPE标本中提取蛋白质以进行下游蛋白质组学分析的有效缓冲液。

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