Yazaki Junshi
Laboratory for Integrative Genomics, RIKEN Center for Integrative Medical Sciences (IMS), Yokohama 230-0045, Japan, 230-0045, Japan.
Bio Protoc. 2020 Sep 20;10(18):e3759. doi: 10.21769/BioProtoc.3759.
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.
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。