4.7 Article

Sample Preparation by Easy Extraction and Digestion (SPEED) - A Universal, Rapid, and Detergent-free Protocol for Proteomics Based on Acid Extraction

期刊

MOLECULAR & CELLULAR PROTEOMICS
卷 19, 期 1, 页码 209-222

出版社

ELSEVIER
DOI: 10.1074/mcp.TIR119.001616

关键词

proteomics; sample preparation; lysis; TFA; digestion; mass spectrometry; label-free quantification; microbiome; bacteria; pathogens; automation; protein denaturation; detergent-free; lysis; sample preparation; TFA

向作者/读者索取更多资源

Sample Preparation by Easy Extraction and Digestion (SPEED) is a universal method for peptide generation from various sources. Because of its detergent-free chemistry, SPEED offers some inherent benefits for bottom-up proteomics sample preparation, including improved quantitative reproducibility, simple applicability and enhanced proteome coverage for lysis-resistant sample types as well as very rapid sample processing. SPEED has high automatization potential and can contribute to simplify and standardize sample preparation and thus enhance reproducibility in proteomics. The main challenge of bottom-up proteomic sample preparation is to extract proteomes in a manner that enables efficient protein digestion for subsequent mass spectrometric analysis. Today's sample preparation strategies are commonly conceptualized around the removal of detergents, which are essential for extraction but strongly interfere with digestion and LC-MS. These multi-step preparations contribute to a lack of reproducibility as they are prone to losses, biases and contaminations, while being time-consuming and labor-intensive. We report a detergent-free method, named Sample Preparation by Easy Extraction and Digestion (SPEED), which consists of three mandatory steps, acidification, neutralization and digestion. SPEED is a universal method for peptide generation from various sources and is easily applicable even for lysis-resistant sample types as pure trifluoroacetic acid (TFA) is used for highly efficient protein extraction by complete sample dissolution. The protocol is highly reproducible, virtually loss-less, enables very rapid sample processing and is superior to the detergent/chaotropic agent-based methods FASP, ISD-Urea and SP3 for quantitative proteomics. SPEED holds the potential to dramatically simplify and standardize sample preparation while improving the depth of proteome coverage especially for challenging samples.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据