纳米技术
药物输送
生物相容性
生物相容性材料
计算机科学
药物发现
计算生物学
材料科学
纳米载体
分子工程
分子动力学
纳米医学
分子机器
DNA纳米技术
分子识别
化学
靶向给药
精密医学
合成生物学
药物开发
生物物理学
智能聚合物
作者
Mahboobeh Nazari,Navid Rabiee
标识
DOI:10.1002/adhm.202504112
摘要
Elastin-like polypeptides (ELPs), inspired by the natural elasticity of human elastin, are rapidly evolving as next-generation platforms for precision drug delivery. Their unique thermoresponsive behavior, genetic tunability, and biocompatibility position them at the intersection of molecular engineering and translational medicine. In this perspective, we critically examine the design strategies that shape ELP functionality, ranging from sequence-level engineering and guest residue modulation to fine-tuning of the inverse transition temperature (Tt). We highlight how these molecular design principles enable programmable self-assembly into nanostructures such as micelles and nanogels, creating versatile opportunities for both covalent and non-covalent cargo encapsulation. Beyond conventional drug delivery, ELPs are poised to transform therapeutic modalities through hyperthermia-guided targeting, multi-stimuli responsiveness, and co-delivery systems that integrate nucleic acids, siRNA, and CRISPR-based components. We also explore emerging frontiers in ELP-enabled immunotherapies, theranostic platforms, and personalized medicine, while reflecting on translational challenges, regulatory landscapes, and the growing role of artificial intelligence in accelerating ELP design. Also, we argue that ELPs are not merely biomaterials but dynamic molecular tools capable of redefining precision therapeutics, and we outline key opportunities that will shape their path toward clinical impact.
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