Department of Chemical and Biomolecular Engineering, North Carolina State University, 911 Partners Way room 2-009, Raleigh, NC 27606.
Department of Biochemistry and Biophysics, University of Rochester, Rochester, NY 14642.
J Chromatogr A. 2021 Jan 4;1635:461632. doi: 10.1016/j.chroma.2020.461632. Epub 2020 Oct 22.
Following the consolidation of therapeutic proteins in the fight against cancer, autoimmune, and neurodegenerative diseases, recent advancements in biochemistry and biotechnology have introduced a host of next-generation biotherapeutics, such as CRISPR-Cas nucleases, stem and car-T cells, and viral vectors for gene therapy. With these drugs entering the clinical pipeline, a new challenge lies ahead: how to manufacture large quantities of high-purity biotherapeutics that meet the growing demand by clinics and biotech companies worldwide. The protein ligands employed by the industry are inadequate to confront this challenge: while featuring high binding affinity and selectivity, these ligands require laborious engineering and expensive manufacturing, are prone to biochemical degradation, and pose safety concerns related to their bacterial origin. Peptides and pseudopeptides make excellent candidates to form a new cohort of ligands for the purification of next-generation biotherapeutics. Peptide-based ligands feature excellent target biorecognition, low or no toxicity and immunogenicity, and can be manufactured affordably at large scale. This work presents a comprehensive and systematic review of the literature on peptide-based ligands and their use in the affinity purification of established and upcoming biological drugs. A comparative analysis is first presented on peptide engineering principles, the development of ligands targeting different biomolecular targets, and the promises and challenges connected to the industrial implementation of peptide ligands. The reviewed literature is organized in (i) conventional (α-)peptides targeting antibodies and other therapeutic proteins, gene therapy products, and therapeutic cells; (ii) cyclic peptides and pseudo-peptides for protein purification and capture of viral and bacterial pathogens; and (iii) the forefront of peptide mimetics, such as β-/γ-peptides, peptoids, foldamers, and stimuli-responsive peptides for advanced processing of biologics.
继治疗性蛋白在癌症、自身免疫和神经退行性疾病的治疗中取得进展后,生物化学和生物技术的最新进展又带来了许多新一代的生物疗法,如 CRISPR-Cas 核酸酶、干细胞和 CAR-T 细胞,以及用于基因治疗的病毒载体。随着这些药物进入临床研发管线,一个新的挑战摆在面前:如何制造大量满足全球临床和生物技术公司不断增长需求的高纯度生物疗法。该行业使用的蛋白配体不足以应对这一挑战:虽然具有高结合亲和力和选择性,但这些配体需要艰苦的工程设计和昂贵的制造,容易发生生化降解,并且存在与细菌来源相关的安全性问题。肽和拟肽是形成新一代生物疗法纯化用配体的新候选物。基于肽的配体具有出色的靶生物识别能力、低毒性或无毒性和免疫原性,并且可以经济高效地大规模生产。本工作全面系统地综述了肽基配体及其在现有和即将推出的生物药物亲和纯化中的应用的文献。首先对肽工程原理、针对不同生物分子靶标的配体的开发以及与肽配体工业实施相关的承诺和挑战进行了比较分析。综述文献分为三部分:(i)针对抗体和其他治疗性蛋白、基因治疗产品和治疗性细胞的常规(α-)肽;(ii)用于蛋白质纯化和捕获病毒和细菌病原体的环状肽和拟肽;(iii)肽模拟物的前沿,如β-/γ-肽、肽类化合物、构象聚合物和响应性肽,用于生物制剂的高级加工。