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与非天然氨基酸结合的抗体。

Antibody conjugates with unnatural amino acids.

作者信息

Hallam Trevor J, Wold Erik, Wahl Alan, Smider Vaughn V

机构信息

†Sutro Biopharma, 310 Utah Avenue, Suite 150, South San Francisco, California 94080, United States.

‡The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States.

出版信息

Mol Pharm. 2015 Jun 1;12(6):1848-62. doi: 10.1021/acs.molpharmaceut.5b00082. Epub 2015 May 21.

Abstract

Antibody conjugates are important in many areas of medicine and biological research, and antibody-drug conjugates (ADCs) are becoming an important next generation class of therapeutics for cancer treatment. Early conjugation technologies relied upon random conjugation to multiple amino acid side chains, resulting in heterogeneous mixtures of labeled antibody. Recent studies, however, strongly support the notion that site-specific conjugation produces a homogeneous population of antibody conjugates with improved pharmacologic properties over randomly coupled molecules. Genetically incorporated unnatural amino acids (uAAs) allow unique orthogonal coupling strategies compared to those used for the 20 naturally occurring amino acids. Thus, uAAs provide a novel paradigm for creation of next generation ADCs. Additionally, uAA-based site-specific conjugation could also empower creation of additional multifunctional conjugates important as biopharmaceuticals, diagnostics, or reagents.

摘要

抗体偶联物在医学和生物学研究的许多领域都很重要,而抗体药物偶联物(ADC)正成为癌症治疗中一类重要的下一代治疗药物。早期的偶联技术依赖于与多个氨基酸侧链的随机偶联,导致标记抗体的混合物不均一。然而,最近的研究有力地支持了这样一种观点,即位点特异性偶联产生的抗体偶联物群体均一,其药理学性质优于随机偶联的分子。与用于20种天然存在的氨基酸的偶联策略相比,基因掺入的非天然氨基酸(uAA)允许独特的正交偶联策略。因此,uAA为下一代ADC的创建提供了一种新的范例。此外,基于uAA的位点特异性偶联还可以促进创建作为生物制药、诊断试剂或试剂很重要的其他多功能偶联物。

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