Precision Nanomedicine Development Based on Specific Opsonization of Human Cancer Patient-Personalized Protein Coronas

作者：Jiayu Ren, Rong Cai, Jing Wang, Muhammad Daniyal, Didar Baimanov, Ying Liu, Dongtao Yin, Yang Liu, Qing Miao, Yuliang Zhao, Chunying Chen · 发表于：Nano Letters · 年份：2019 · DOI：10.1021/acs.nanolett.9b01774 · 被引用次数：130 · 研究领域：Nanoparticle-Based Drug Delivery、Advanced biosensing and bioanalysis techniques、Bacteriophages and microbial interactions

When a nanomedicine is administrated into the human body, biomolecules in biological fluids, particularly proteins, form a layer on the surface of the nanoparticle known as a “personalized protein corona”. An understanding of the formation and behavior of the personalized protein corona not only benefits the nanotherapy treatment efficacy but also can aid in disease diagnosis. Here we used Gd@C 82 (OH) 22 nanoparticles, a nanomedicine effective against several types of cancer, as a model nanomedicine to investigate the natural protein fingerprint of the personalized protein corona formed in 10 human lung squamous cell carcinoma patients. Our analysis revealed a specific biomarker, complement component C1q, in lung cancer personalized protein coronas, abundantly bound to Gd@C 82 (OH) 22 NPs. This binding altered the secondary structure of C1q protein and led to the activation of an innate immune response, which could be exploited for cancer immune therapy. On the basis of this finding, we provide a new strategy for the development of precision nanomedicine derived from opsonization of a unique protein fingerprint within patients. This approach overcomes the common pitfall of protein corona formation and exploits the corona proteins to generate a precision nanomedicine and diagnostic tool.