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通过单宁酸修饰将蛋白和肽类治疗药物靶向递送至心脏。

Targeting protein and peptide therapeutics to the heart via tannic acid modification.

机构信息

Department of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.

Predictive Model Research Center, Korea Institute of Toxicology, Daejeon, Republic of Korea.

出版信息

Nat Biomed Eng. 2018 May;2(5):304-317. doi: 10.1038/s41551-018-0227-9. Epub 2018 Apr 30.

Abstract

Systemic injection into blood vessels is the most common method of drug administration. However, targeting drugs to the heart is challenging, owing to its dynamic mechanical motions and large cardiac output. Here, we show that the modification of protein and peptide therapeutics with tannic acid-a flavonoid found in plants that adheres to extracellular matrices, elastins and collagens-improves their ability to specifically target heart tissue. Tannic-acid-modified (TANNylated) proteins do not adsorb on endothelial glycocalyx layers in blood vessels, yet they penetrate the endothelium to thermodynamically bind to myocardium extracellular matrix before being internalized by myoblasts. In a rat model of myocardial ischaemia-reperfusion injury, TANNylated basic fibroblast growth factor significantly reduced infarct size and increased cardiac function. TANNylation of systemically injected therapeutic proteins, peptides or viruses may enhance the treatment of heart diseases.

摘要

系统注射入血管是最常见的给药方法。然而,由于心脏的动态机械运动和高心输出量,将药物靶向心脏具有挑战性。在这里,我们表明,用单宁酸(一种存在于植物中的类黄酮,可附着在细胞外基质、弹性蛋白和胶原蛋白上)修饰蛋白质和肽类治疗药物,可以提高它们特异性靶向心脏组织的能力。单宁酸修饰(TANNylated)的蛋白质不会在血管内皮糖萼层上吸附,但它们可以穿透内皮,在被成肌细胞内化之前,与心肌细胞外基质热力学结合。在心肌缺血再灌注损伤的大鼠模型中,TANNylated 碱性成纤维细胞生长因子显著减少了梗死面积并增加了心脏功能。全身性注射治疗性蛋白质、肽或病毒的 TANNylation 可能会增强心脏病的治疗效果。

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