Proteomic Detection and Validation of Translated Small Open Reading Frames
Q3 Biochemistry, Genetics and Molecular Biology
Alexandra Khitun, Sarah A. Slavoff
{"title":"Proteomic Detection and Validation of Translated Small Open Reading Frames","authors":"Alexandra Khitun, Sarah A. Slavoff","doi":"10.1002/cpch.77","DOIUrl":null,"url":null,"abstract":"<p>Small open reading frames (smORFs) encode previously unannotated polypeptides or short proteins that regulate translation in <i>cis</i> (eukaryotes) and/or are independently functional (prokaryotes and eukaryotes). Ongoing efforts for complete annotation and functional characterization of smORF-encoded proteins have yielded novel regulators and therapeutic targets. However, because they are excluded from protein databases, initiate at non-AUG start codons, and produce few unique tryptic peptides, unannotated small proteins cannot be detected with standard proteomic methods. Here,, we outline a procedure for mass spectrometry-based detection of translated smORFs in cultured human cells from protein extraction, digestion, and LC-MS/MS, to database preparation and data analysis. Following proteomic detection, translation from a unique smORF may be validated via siRNA-based silencing or overexpression and epitope tagging. This is necessary to unambiguously assign a peptide to a smORF within a specific transcript isoform or genomic locus. Provided that sufficient starting material is available, this workflow can be applied to any cell type/organism and adjusted to study specific (patho)physiological contexts including, but not limited to, development, stress, and disease. © 2019 by John Wiley & Sons, Inc.</p><p><b>Basic Protocol 1</b>: Protein extraction, size selection, and trypsin digestion</p><p><b>Alternate Protocol 1</b>: In-solution C8 column size selection</p><p><b>Support Protocol 1</b>: Chloroform/methanol precipitation</p><p><b>Support Protocol 2</b>: Reduction, alkylation, and in-solution protease digestion</p><p><b>Support Protocol 3</b>: Peptide de-salting</p><p><b>Basic Protocol 2</b>: Two-dimensional LC-MS/MS with ERLIC fractionation</p><p><b>Basic Protocol 3</b>: Transcriptomic database construction</p><p><b>Alternate Protocol 2</b>: Transcriptomics database generation with gffread</p><p><b>Basic Protocol 4</b>: Non-annotated peptide identification from LC-MS/MS data</p><p><b>Basic Protocol 5</b>: Validation using isotopically labeled synthetic peptide standards and siRNA</p><p><b>Basic Protocol 6</b>: Transcript validation using transient overexpression</p>","PeriodicalId":38051,"journal":{"name":"Current protocols in chemical biology","volume":"11 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpch.77","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in chemical biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpch.77","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 19
Abstract
Small open reading frames (smORFs) encode previously unannotated polypeptides or short proteins that regulate translation in cis (eukaryotes) and/or are independently functional (prokaryotes and eukaryotes). Ongoing efforts for complete annotation and functional characterization of smORF-encoded proteins have yielded novel regulators and therapeutic targets. However, because they are excluded from protein databases, initiate at non-AUG start codons, and produce few unique tryptic peptides, unannotated small proteins cannot be detected with standard proteomic methods. Here,, we outline a procedure for mass spectrometry-based detection of translated smORFs in cultured human cells from protein extraction, digestion, and LC-MS/MS, to database preparation and data analysis. Following proteomic detection, translation from a unique smORF may be validated via siRNA-based silencing or overexpression and epitope tagging. This is necessary to unambiguously assign a peptide to a smORF within a specific transcript isoform or genomic locus. Provided that sufficient starting material is available, this workflow can be applied to any cell type/organism and adjusted to study specific (patho)physiological contexts including, but not limited to, development, stress, and disease. © 2019 by John Wiley & Sons, Inc.
Basic Protocol 1: Protein extraction, size selection, and trypsin digestion
Alternate Protocol 1: In-solution C8 column size selection
Support Protocol 1: Chloroform/methanol precipitation
Support Protocol 2: Reduction, alkylation, and in-solution protease digestion
Support Protocol 3: Peptide de-salting
Basic Protocol 2: Two-dimensional LC-MS/MS with ERLIC fractionation
Basic Protocol 3: Transcriptomic database construction
Alternate Protocol 2: Transcriptomics database generation with gffread
Basic Protocol 4: Non-annotated peptide identification from LC-MS/MS data
Basic Protocol 5: Validation using isotopically labeled synthetic peptide standards and siRNA
Basic Protocol 6: Transcript validation using transient overexpression
翻译小开放阅读框的蛋白质组学检测与验证
小的开放阅读框(smorf)编码以前未注释的多肽或短蛋白,这些蛋白在顺式(真核生物)和/或独立功能(原核生物和真核生物)中调节翻译。对smorf编码蛋白的完整注释和功能表征的持续努力已经产生了新的调节因子和治疗靶点。然而,由于它们被排除在蛋白质数据库之外,在非aug启动密码子处启动,并且产生很少独特的色氨酸,因此无法用标准的蛋白质组学方法检测到未注释的小蛋白。在这里,我们概述了一种基于质谱的检测方法,从蛋白质提取、消化、LC-MS/MS到数据库准备和数据分析,在培养的人类细胞中检测翻译的smorf。在进行蛋白质组学检测后,可以通过基于sirna的沉默或过表达和表位标记来验证独特smORF的翻译。这对于明确地将肽分配到特定转录异构体或基因组位点内的smORF是必要的。只要有足够的起始材料,该工作流程可以应用于任何细胞类型/生物体,并调整以研究特定(病理)生理环境,包括但不限于发育、压力和疾病。©2019 by John Wiley &基本方案1:蛋白质提取,大小选择,胰蛋白酶消化备用方案1:溶液中C8柱大小选择支持方案1:氯仿/甲醇沉淀支持方案2:还原,烷基化,和溶液中蛋白酶消化支持方案3:肽脱盐基本方案2:二维LC-MS/MS与ERLIC分离基本方案3:转录组数据库构建备用方案2:转录组学数据库的生成与gffreadBasic协议4:从LC-MS/MS中鉴定无注释的肽。数据库协议5:使用同位素标记的合成肽标准和sirnabbasic协议6:使用瞬时过表达进行转录验证
本文章由计算机程序翻译,如有差异,请以英文原文为准。