免疫原性
体内
蛋白质工程
细胞通透性
小分子
计算生物学
变性(裂变材料)
化学
蛋白质稳定性
纳米技术
体外
生物物理学
生物化学
医学
生物
材料科学
生物技术
免疫系统
免疫学
酶
核化学
作者
Sasha B. Ebrahimi,Devleena Samanta
标识
DOI:10.1038/s41467-023-38039-x
摘要
Protein-based therapeutics have led to new paradigms in disease treatment. Projected to be half of the top ten selling drugs in 2023, proteins have emerged as rivaling and, in some cases, superior alternatives to historically used small molecule-based medicines. This review chronicles both well-established and emerging design strategies that have enabled this paradigm shift by transforming protein-based structures that are often prone to denaturation, degradation, and aggregation in vitro and in vivo into highly effective therapeutics. In particular, we discuss strategies for creating structures with increased affinity and targetability, enhanced in vivo stability and pharmacokinetics, improved cell permeability, and reduced amounts of undesired immunogenicity.
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