Clay Hepp, Anoop Magesh, Avinash Soundararajan, P. Pattabiraman
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Immunoprecipitation (IP) was conducted to isolate CLU HIS and all the proteins bound to it. Western blot analysis was conducted to confirmed IP worked successfully. Once it was confirmed that CLU HIS with all its binding partners was isolated successfully using IP, the media samples were sent to proteomics to determine all the specific proteins that are bound directly to CLU. \nResults:Western blot analysis confirmed that the overexpression of CLU HIS was successfully accomplished through adenovirus transfection. In addition, Western blot analysis confirmed that IP worked successfully. At the current moment, results of proteomics are still being developed, so the specific binding partners of CLU are still unknown at the time. \nConclusions and Potential Impact:Our preliminary study suggests that CLU can be overexpressed via adenovirus and analyzed via IP. Understanding this allows for the purification of the protein and its attached binding partners. Identifying these binding partners can be novel targets for improving aqueous humor outflow through trabecular meshwork to decrease IOP and decrease one’s risk for POAG.","PeriodicalId":20522,"journal":{"name":"Proceedings of IMPRS","volume":" 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Analysis of the Binding Partners of Clusterin in their Role in Increased Intraocular Pressure in Glaucoma\",\"authors\":\"Clay Hepp, Anoop Magesh, Avinash Soundararajan, P. Pattabiraman\",\"doi\":\"10.18060/27859\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background and Objective:Elevated intraocular pressure (IOP) is a risk factor for primary open-angle glaucoma (POAG). Clusterin (CLU) is a secretory chaperone protein found in trabecular meshwork tissue that is implicated with POAG risk. In this study, we aimed at understanding the role of CLU and its binding partners in IOP homeostasis and POAG pathology. \\nMethods:Normal trabecular meshwork (NTM) cell lines were used. Half of the NTM cell lines were transfected with adenovirus empty (AdMT) while the other half of the NTM cell lines were transfected with adenovirus clusterin with histidine tag (AdCLUHIS). AdCLUHIS allows for the overexpression of CLU HIS in the NTM cells. After 72 hours of transfection, the media and cell lysate were collected. As CLU is a secretory chaperone protein, the media was analyzed. Immunoprecipitation (IP) was conducted to isolate CLU HIS and all the proteins bound to it. Western blot analysis was conducted to confirmed IP worked successfully. Once it was confirmed that CLU HIS with all its binding partners was isolated successfully using IP, the media samples were sent to proteomics to determine all the specific proteins that are bound directly to CLU. \\nResults:Western blot analysis confirmed that the overexpression of CLU HIS was successfully accomplished through adenovirus transfection. In addition, Western blot analysis confirmed that IP worked successfully. At the current moment, results of proteomics are still being developed, so the specific binding partners of CLU are still unknown at the time. \\nConclusions and Potential Impact:Our preliminary study suggests that CLU can be overexpressed via adenovirus and analyzed via IP. Understanding this allows for the purification of the protein and its attached binding partners. 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引用次数: 0
摘要
背景与目的:眼压升高是原发性开角型青光眼(POAG)的一个危险因素。簇蛋白(CLU)是一种存在于小梁网组织中的分泌性伴侣蛋白,与 POAG 风险有关。本研究旨在了解 CLU 及其结合伙伴在眼压平衡和 POAG 病理中的作用。方法:使用正常小梁网(NTM)细胞系。一半的NTM细胞系转染空腺病毒(AdMT),另一半的NTM细胞系转染带有组氨酸标签的腺病毒集簇素(AdCLUHIS)。AdCLUHIS 可以在 NTM 细胞中过表达 CLU HIS。转染 72 小时后,收集培养基和细胞裂解液。由于 CLU 是一种分泌型伴侣蛋白,因此要对培养基进行分析。进行免疫沉淀(IP)以分离 CLU HIS 及其结合的所有蛋白质。进行 Western 印迹分析以确认 IP 成功发挥作用。在确认使用 IP 成功分离出 CLU HIS 及其所有结合伙伴后,培养基样本被送往蛋白质组学研究,以确定直接与 CLU 结合的所有特定蛋白质。结果:Western 印迹分析证实,通过腺病毒转染,CLU HIS 成功实现了过表达。此外,Western 印迹分析也证实了 IP 的成功。目前,蛋白质组学的研究成果仍在开发中,因此CLU的特定结合伙伴尚不清楚。结论和潜在影响:我们的初步研究表明,CLU 可以通过腺病毒过表达,并通过 IP 进行分析。了解了这一点,就可以纯化该蛋白及其附着的结合伙伴。确定这些结合伙伴可以成为改善通过小梁网流出的房水的新靶点,从而降低眼压并减少罹患 POAG 的风险。
Analysis of the Binding Partners of Clusterin in their Role in Increased Intraocular Pressure in Glaucoma
Background and Objective:Elevated intraocular pressure (IOP) is a risk factor for primary open-angle glaucoma (POAG). Clusterin (CLU) is a secretory chaperone protein found in trabecular meshwork tissue that is implicated with POAG risk. In this study, we aimed at understanding the role of CLU and its binding partners in IOP homeostasis and POAG pathology.
Methods:Normal trabecular meshwork (NTM) cell lines were used. Half of the NTM cell lines were transfected with adenovirus empty (AdMT) while the other half of the NTM cell lines were transfected with adenovirus clusterin with histidine tag (AdCLUHIS). AdCLUHIS allows for the overexpression of CLU HIS in the NTM cells. After 72 hours of transfection, the media and cell lysate were collected. As CLU is a secretory chaperone protein, the media was analyzed. Immunoprecipitation (IP) was conducted to isolate CLU HIS and all the proteins bound to it. Western blot analysis was conducted to confirmed IP worked successfully. Once it was confirmed that CLU HIS with all its binding partners was isolated successfully using IP, the media samples were sent to proteomics to determine all the specific proteins that are bound directly to CLU.
Results:Western blot analysis confirmed that the overexpression of CLU HIS was successfully accomplished through adenovirus transfection. In addition, Western blot analysis confirmed that IP worked successfully. At the current moment, results of proteomics are still being developed, so the specific binding partners of CLU are still unknown at the time.
Conclusions and Potential Impact:Our preliminary study suggests that CLU can be overexpressed via adenovirus and analyzed via IP. Understanding this allows for the purification of the protein and its attached binding partners. Identifying these binding partners can be novel targets for improving aqueous humor outflow through trabecular meshwork to decrease IOP and decrease one’s risk for POAG.