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工程化增强型表皮生长因子受体(EGFR)结合剂:西妥昔单抗人源化以改善可开发性

Engineering an Enhanced EGFR Engager: Humanization of Cetuximab for Improved Developability.

作者信息

Goulet Dennis R, Chatterjee Soumili, Lee Wai-Ping, Waight Andrew B, Zhu Yi, Mak Amanda Nga-Sze

机构信息

Protein Engineering, SystImmune, Inc., 15318 NE 95th St., Redmond, WA 98052, USA.

Process Development, SystImmune, Inc., 15318 NE 95th St., Redmond, WA 98052, USA.

出版信息

Antibodies (Basel). 2022 Jan 13;11(1):6. doi: 10.3390/antib11010006.

Abstract

The epidermal growth factor receptor (EGFR) is a receptor tyrosine kinase whose proliferative effects can contribute to the development of many types of solid tumors when overexpressed. For this reason, EGFR inhibitors such as cetuximab can play an important role in treating cancers such as colorectal cancer and head and neck cancer. Cetuximab is a chimeric monoclonal antibody containing mouse variable regions that bind to EGFR and prevent it from signaling. Although cetuximab has been used clinically since 2004 to successfully control solid tumors, advances in protein engineering have created the opportunity to address some of its shortcomings. In particular, the presence of mouse sequences could contribute to immunogenicity in the form of anti-cetuximab antibodies, and an occupied glycosylation site in FR3 can contribute to hypersensitivity reactions and product heterogeneity. Using simple framework graft or sequence-/structure-guided approaches, cetuximab was humanized onto 11 new frameworks. In addition to increasing humanness and removing the VH glycosylation site, dynamic light scattering revealed increases in stability, and bio-layer interferometry confirmed minimal changes in binding affinity, with patterns emerging across the humanization method. This work demonstrates the potential to improve the biophysical and clinical properties of first-generation protein therapeutics and highlights the advantages of computationally guided engineering.

摘要

表皮生长因子受体(EGFR)是一种受体酪氨酸激酶,当其过度表达时,其增殖作用可促进多种实体瘤的发展。因此,西妥昔单抗等EGFR抑制剂在治疗结直肠癌和头颈癌等癌症中可发挥重要作用。西妥昔单抗是一种嵌合单克隆抗体,含有与EGFR结合并阻止其信号传导的小鼠可变区。尽管西妥昔单抗自2004年以来已在临床上用于成功控制实体瘤,但蛋白质工程的进展为解决其一些缺点创造了机会。特别是,小鼠序列的存在可能以抗西妥昔单抗抗体的形式导致免疫原性,并且FR3中一个被占据的糖基化位点可能导致超敏反应和产品异质性。通过简单的框架移植或序列/结构引导方法,将西妥昔单抗人源化到11个新框架上。除了增加人源化程度和去除VH糖基化位点外,动态光散射显示稳定性增加,生物层干涉术证实结合亲和力变化最小,不同人源化方法呈现出不同模式。这项工作展示了改善第一代蛋白质治疗药物生物物理和临床特性的潜力,并突出了计算引导工程的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/965a/8788544/57b4a2ef24e2/antibodies-11-00006-g001.jpg

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