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2
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Nucleic Acids Res. 2020 Jan 24;48(2):e8. doi: 10.1093/nar/gkz1086.
3
Profiling Interactome Networks with the HaloTag-NAPPA In Situ Protein Array.利用HaloTag-NAPPA原位蛋白质阵列分析相互作用组网络
Curr Protoc Plant Biol. 2018 Sep;3(3):e20071. doi: 10.1002/cppb.20071. Epub 2018 Aug 14.
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Simultaneous epitope and transcriptome measurement in single cells.单细胞中表位和转录组的同步测量。
Nat Methods. 2017 Sep;14(9):865-868. doi: 10.1038/nmeth.4380. Epub 2017 Jul 31.
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Abseq: Ultrahigh-throughput single cell protein profiling with droplet microfluidic barcoding.Abseq:基于液滴微流控条码的超高通量单细胞蛋白质谱分析。
Sci Rep. 2017 Mar 14;7:44447. doi: 10.1038/srep44447.
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Mapping transcription factor interactome networks using HaloTag protein arrays.使用HaloTag蛋白阵列绘制转录因子相互作用组网络。
Proc Natl Acad Sci U S A. 2016 Jul 19;113(29):E4238-47. doi: 10.1073/pnas.1603229113. Epub 2016 Jun 29.
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Multiplex single-molecule interaction profiling of DNA-barcoded proteins.DNA条形码标记蛋白质的多重单分子相互作用分析
Nature. 2014 Nov 27;515(7528):554-7. doi: 10.1038/nature13761. Epub 2014 Sep 21.
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Tandem mass tags: a novel quantification strategy for comparative analysis of complex protein mixtures by MS/MS.串联质量标签:一种通过串联质谱对复杂蛋白质混合物进行比较分析的新型定量策略。
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涉及高亲和力捕获卤代标签的新型蛋白质-寡核苷酸偶联方法。

Novel Protein-oligonucleotide Conjugation Method Involving a High-affinity Capture HaloTag.

作者信息

Yazaki Junshi

机构信息

Laboratory for Integrative Genomics, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama 230-0045, Japan, 230-0045, Japan.

出版信息

Bio Protoc. 2020 Sep 20;10(18):e3759. doi: 10.21769/BioProtoc.3759.

DOI:10.21769/BioProtoc.3759
PMID:33659418
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7842777/
Abstract

Highly sensitive quantitative protein profiling can play a key role in the early diagnosis of diseases, such as autoimmune diseases and cancer. We developed a modified protein-oligonucleotide conjugation method termed HaloTag-mediated barcoding, for quantifying protein molecules at a higher sensitivity than conventional protein quantification methods. This novel and efficient conjugation method can be used to prepare HaloTag-barcoded proteins using a click chemistry-based labeling technique. Here, we describe the preparation of protein-DNA complexes and detection of protein-protein interactions which can be used in a HaloTag protein barcode assay to detect an antibody. The protocol includes procedures for preparing the ligand-oligonucleotide complex, plasmid DNA preparation for protein expression, and preparation of the protein-oligonucleotide complex. The described click reaction-based protocols simplify the conventional amine-ester reaction methods which require additional steps for chromatography purification.

摘要

高灵敏度定量蛋白质谱分析在疾病的早期诊断中可发挥关键作用,如自身免疫性疾病和癌症。我们开发了一种改良的蛋白质 - 寡核苷酸偶联方法,称为HaloTag介导的条形码技术,用于以比传统蛋白质定量方法更高的灵敏度定量蛋白质分子。这种新颖且高效的偶联方法可用于使用基于点击化学的标记技术制备HaloTag条形码蛋白。在此,我们描述了蛋白质 - DNA复合物的制备以及蛋白质 - 蛋白质相互作用的检测,这些可用于HaloTag蛋白质条形码分析以检测抗体。该方案包括制备配体 - 寡核苷酸复合物、用于蛋白质表达的质粒DNA制备以及蛋白质 - 寡核苷酸复合物的制备。所描述的基于点击反应的方案简化了传统的胺 - 酯反应方法,后者需要额外的色谱纯化步骤。