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用于流式细胞术的新型抗促红细胞生成素产生肝细胞受体B6单克隆抗体EbMab-3的研发

Development of a novel anti-erythropoietin-producing hepatocellular receptor B6 monoclonal antibody EbMab-3 for flow cytometry.

作者信息

Tanaka Tomohiro, Kaneko Yu, Yamamoto Haruto, Li Guanjie, Fujisawa Shiori, Satofuka Hiroyuki, Shinoda Keisuke, Nakamura Takuya, Kaneko Mika K, Suzuki Hiroyuki, Kato Yukinari

机构信息

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi, 980-8575, Japan.

出版信息

Biochem Biophys Rep. 2025 Feb 21;41:101960. doi: 10.1016/j.bbrep.2025.101960. eCollection 2025 Mar.

DOI:10.1016/j.bbrep.2025.101960
PMID:40065768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11891606/
Abstract

Erythropoietin-producing hepatocellular receptor B6 (EphB6) is a member of the largest Eph subfamily of receptor tyrosine kinases. EphB6 is widely expressed in various tissues and regulates cellular homeostasis by interacting with its membrane-bound ephrin ligands and other receptors. EphB6 is involved in cancer pathology despite lacking kinase activity. Developing sensitive monoclonal antibodies (mAbs) for EphB6 has been desired for treatment, diagnosis, and further analysis of EphB6. This study established a novel specific and sensitive anti-human EphB6 mAb clone EbMab-3 (mouse IgG, kappa) by the Cell-Based Immunization and Screening (CBIS) method. In flow cytometry, EbMab-3 demonstrated reactivity with EphB6-overexpressed Chinese hamster ovary-K1 cells (CHO/EphB6) and endogenously EphB6-expressing DLD-1 colorectal cancer cells. Cross-reactivity of EbMab-3 was not observed. EbMab-3 demonstrated a moderate binding affinity (dissociation constant; ) for CHO/EphB6 ( : 2.6 ± 1.0 × 10 M) and a high binding affinity for DLD-1 ( : 3.4 ± 1.3 × 10 M). EbMab-3 can detect EphB6 protein in CHO/EphB6 lysate in Western blot. EbMab-3, established by the CBIS method, could be valuable for analyzing the EphB6-associated cellular functions and has potential applications in diagnosis and treatment with specificity and high affinity for cancer cells.

摘要

促红细胞生成素产生肝细胞受体B6(EphB6)是受体酪氨酸激酶最大的Eph亚家族的成员。EphB6在各种组织中广泛表达,并通过与其膜结合的ephrin配体和其他受体相互作用来调节细胞稳态。尽管缺乏激酶活性,但EphB6仍参与癌症病理过程。开发针对EphB6的敏感单克隆抗体(mAb)一直是治疗、诊断和进一步分析EphB6所期望的。本研究通过基于细胞的免疫和筛选(CBIS)方法建立了一种新型的特异性和敏感性抗人EphB6 mAb克隆EbMab-3(小鼠IgG,κ)。在流式细胞术中,EbMab-3显示出与EphB6过表达的中国仓鼠卵巢-K1细胞(CHO/EphB6)和内源性表达EphB6的DLD-1结肠癌细胞具有反应性。未观察到EbMab-3的交叉反应性。EbMab-3对CHO/EphB6表现出中等结合亲和力(解离常数; )( :2.6±1.0×10 M),对DLD-1表现出高结合亲和力( :3.4±1.3×10 M)。在蛋白质印迹中,EbMab-3可以检测CHO/EphB6裂解物中的EphB6蛋白。通过CBIS方法建立的EbMab-3对于分析与EphB6相关的细胞功能可能具有重要价值,并且在癌细胞的诊断和治疗中具有特异性和高亲和力的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/bb0be39005db/mmcfigs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/89688d08c766/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/aa1995d41c1a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/4c33b2e4a104/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/06d04dd6a05b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/26297a8bcf12/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/bb0be39005db/mmcfigs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/89688d08c766/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/aa1995d41c1a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/4c33b2e4a104/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/06d04dd6a05b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/26297a8bcf12/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd35/11891606/bb0be39005db/mmcfigs1.jpg

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