Ross W. Cheloha, Zeyang Li, Djenet Bousbaine, Andrew W. Woodham, P. Perrin, J. Volarić, H. Ploegh
{"title":"Abstract B149: Real-time analysis of cell membrane protein and virus internalization using site-specific conjugation of protease-sensitive probes","authors":"Ross W. Cheloha, Zeyang Li, Djenet Bousbaine, Andrew W. Woodham, P. Perrin, J. Volarić, H. Ploegh","doi":"10.1158/2326-6074.CRICIMTEATIAACR18-B149","DOIUrl":null,"url":null,"abstract":"Reagents that label specific subsets of cells are broadly useful for the treatment of cancer and modulation of cells of the immune system. Labeling is often achieved through the identification and characterization of proteins specifically expressed on selected cells but not others. Knowledge of cell membrane protein routing dynamics can be leveraged to efficiently deliver cytotoxic or immune stimulating payloads. The most common method for monitoring internalization relies on labeling proteins with antibodies modified with a fluorophore or other tag that can also be used to report on whether the protein of interest has been internalized. This approach requires indirect methods, such as multiple rounds of cell staining, to differentiate extracellular protein from protein that has been internalized and recycled to the cell surface. Here we report a method for the characterization of protein internalization in real time through the sortase-mediated, site-specific labeling of single domain antibodies or viral proteins with a newly developed, cathepsin-sensitive quenched-fluorophore probe. This approach allows quantitative measurement of the movement of proteins into protease-containing endosomes in real time in live cells. This method revealed variation in the rate of internalization for different cell surface receptors and allowed for kinetic characterization of influenza virus internalization. These findings help to explain the utility of certain single domain antibody-antigen conjugates for inducing humoral immune responses. The tools and methods described here should be useful for the identification of proteins expressed on target cells that are ideal for antibody-mediated drug delivery or for promotion of specific types of immune responses. Citation Format: Ross W. Cheloha, Zeyang Li, Djenet Bousbaine, Andrew Woodham, Priscillia Perrin, Jana Volaric, Hidde L. Ploegh. Real-time analysis of cell membrane protein and virus internalization using site-specific conjugation of protease-sensitive probes [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr B149.","PeriodicalId":120683,"journal":{"name":"Other Topics","volume":"23 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Other Topics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1158/2326-6074.CRICIMTEATIAACR18-B149","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Reagents that label specific subsets of cells are broadly useful for the treatment of cancer and modulation of cells of the immune system. Labeling is often achieved through the identification and characterization of proteins specifically expressed on selected cells but not others. Knowledge of cell membrane protein routing dynamics can be leveraged to efficiently deliver cytotoxic or immune stimulating payloads. The most common method for monitoring internalization relies on labeling proteins with antibodies modified with a fluorophore or other tag that can also be used to report on whether the protein of interest has been internalized. This approach requires indirect methods, such as multiple rounds of cell staining, to differentiate extracellular protein from protein that has been internalized and recycled to the cell surface. Here we report a method for the characterization of protein internalization in real time through the sortase-mediated, site-specific labeling of single domain antibodies or viral proteins with a newly developed, cathepsin-sensitive quenched-fluorophore probe. This approach allows quantitative measurement of the movement of proteins into protease-containing endosomes in real time in live cells. This method revealed variation in the rate of internalization for different cell surface receptors and allowed for kinetic characterization of influenza virus internalization. These findings help to explain the utility of certain single domain antibody-antigen conjugates for inducing humoral immune responses. The tools and methods described here should be useful for the identification of proteins expressed on target cells that are ideal for antibody-mediated drug delivery or for promotion of specific types of immune responses. Citation Format: Ross W. Cheloha, Zeyang Li, Djenet Bousbaine, Andrew Woodham, Priscillia Perrin, Jana Volaric, Hidde L. Ploegh. Real-time analysis of cell membrane protein and virus internalization using site-specific conjugation of protease-sensitive probes [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr B149.
标记特定细胞亚群的试剂广泛用于治疗癌症和调节免疫系统细胞。标记通常是通过鉴定和表征特定细胞上特异性表达的蛋白质而不是其他细胞来实现的。细胞膜蛋白路径动力学的知识可以有效地提供细胞毒性或免疫刺激有效载荷。监测内化的最常用方法依赖于用荧光基团修饰的抗体或其他标记标记蛋白质,这些标记也可用于报告感兴趣的蛋白质是否已内化。这种方法需要间接方法,如多轮细胞染色,以区分细胞外蛋白和已内化并再循环到细胞表面的蛋白。在这里,我们报告了一种通过新开发的组织蛋白酶敏感猝灭荧光探针,通过排序酶介导的单域抗体或病毒蛋白的位点特异性标记,实时表征蛋白质内化的方法。这种方法允许在活细胞中实时定量测量蛋白质进入含有蛋白酶的内体的运动。该方法揭示了不同细胞表面受体内化率的差异,并允许流感病毒内化的动力学表征。这些发现有助于解释某些单域抗体-抗原偶联物诱导体液免疫反应的效用。本文描述的工具和方法应该有助于鉴定靶细胞上表达的蛋白质,这些蛋白质对于抗体介导的药物递送或促进特定类型的免疫反应是理想的。引文格式:Ross W. Cheloha, Zeyang Li, jenet Bousbaine, Andrew Woodham, priscilla Perrin, Jana Volaric, Hidde L. Ploegh。利用蛋白酶敏感探针的位点特异性偶联实时分析细胞膜蛋白和病毒内化[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志2019;7(2增刊):摘要nr B149。