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红细胞中治疗性蛋白质的光控释放

Light-Controlled Release of Therapeutic Proteins from Red Blood Cells.

作者信息

Vickerman Brianna M, O'Banion Colin P, Tan Xianming, Lawrence David S

机构信息

Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States.

Division of Chemical Biology and Medicinal Chemistry, Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599, United States.

出版信息

ACS Cent Sci. 2021 Jan 27;7(1):93-103. doi: 10.1021/acscentsci.0c01151. Epub 2020 Dec 9.

Abstract

Protein therapeutics are a powerful class of drugs known for their selectivity and potency. However, the potential efficacy of these therapeutics is commonly offset by short circulatory half-lives and undesired action at otherwise healthy tissue. We describe herein a targeted protein delivery system that employs engineered red blood cells (RBCs) as carriers and light as the external trigger that promotes hemolysis and drug release. RBCs internally loaded with therapeutic proteins are readily surface modified with a dormant hemolytic peptide. The latter is activated via easily assigned wavelengths that extend into the optical window of tissue. We have demonstrated that photorelease transpires with spatiotemporal control and that the liberated proteins display the anticipated biological effects . Furthermore, we have confirmed targeted delivery of a clot-inducing enzyme in a mouse model. Finally, we anticipate that this strategy is not limited to RBC carriers but also should be applicable to nano- and microtransporters comprised of bilayer lipid membranes.

摘要

蛋白质疗法是一类强大的药物,以其选择性和效力而闻名。然而,这些疗法的潜在疗效通常会被短循环半衰期和在其他健康组织中的不良作用所抵消。我们在此描述一种靶向蛋白质递送系统,该系统采用工程化红细胞(RBC)作为载体,并利用光作为促进溶血和药物释放的外部触发因素。内部装载有治疗性蛋白质的红细胞很容易用一种休眠的溶血肽进行表面修饰。后者通过延伸到组织光学窗口的易于指定的波长被激活。我们已经证明光释放具有时空可控性,并且释放的蛋白质显示出预期的生物学效应。此外,我们已经在小鼠模型中证实了一种促凝酶的靶向递送。最后,我们预计这种策略不仅限于红细胞载体,也应该适用于由双层脂质膜组成的纳米和微转运体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b6e/7844852/60c04c259084/oc0c01151_0001.jpg

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