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生物工程化细菌封装蛋白纳米隔室作为靶向给药系统。

Bioengineering bacterial encapsulin nanocompartments as targeted drug delivery system.

作者信息

Van de Steen Alexander, Khalife Rana, Colant Noelle, Mustafa Khan Hasan, Deveikis Matas, Charalambous Saverio, Robinson Clare M, Dabas Rupali, Esteban Serna Sofia, Catana Diana A, Pildish Konstantin, Kalinovskiy Vladimir, Gustafsson Kenth, Frank Stefanie

机构信息

Department of Biochemical Engineering, University College London, UK.

UCL iGEM Student Team 2019, UK.

出版信息

Synth Syst Biotechnol. 2021 Sep 9;6(3):231-241. doi: 10.1016/j.synbio.2021.09.001. eCollection 2021 Sep.

Abstract

The development of Drug Delivery Systems (DDS) has led to increasingly efficient therapies for the treatment and detection of various diseases. DDS use a range of nanoscale delivery platforms produced from polymeric of inorganic materials, such as micelles, and metal and polymeric nanoparticles, but their variant chemical composition make alterations to their size, shape, or structures inherently complex. Genetically encoded protein nanocages are highly promising DDS candidates because of their modular composition, ease of recombinant production in a range of hosts, control over assembly and loading of cargo molecules and biodegradability. One example of naturally occurring nanocompartments are encapsulins, recently discovered bacterial organelles that have been shown to be reprogrammable as nanobioreactors and vaccine candidates. Here we report the design and application of a targeted DDS platform based on the encapsulin reprogrammed to display an antibody mimic protein called Designed Ankyrin repeat protein (DARPin) on the outer surface and to encapsulate a cytotoxic payload. The DARPin9.29 chosen in this study specifically binds to human epidermal growth factor receptor 2 (HER2) on breast cancer cells, as demonstrated in an cell culture model. The encapsulin-based DDS is assembled in one step by co-expressing the encapsulin-DARPin9.29 fusion protein with an engineered flavin-binding protein mini-singlet oxygen generator (MiniSOG), from a single plasmid in . Purified encapsulin-DARPin_miniSOG nanocompartments bind specifically to HER2 positive breast cancer cells and trigger apoptosis, indicating that the system is functional and specific. The DDS is modular and has the potential to form the basis of a multi-receptor targeted system by utilising the DARPin screening libraries, allowing use of new DARPins of known specificities, and through the proven flexibility of the encapsulin cargo loading mechanism, allowing selection of cargo proteins of choice.

摘要

药物递送系统(DDS)的发展使得治疗和检测各种疾病的疗法越来越高效。DDS使用一系列由无机材料聚合物制成的纳米级递送平台,如胶束、金属和聚合物纳米颗粒,但它们不同的化学成分使得其尺寸、形状或结构的改变本质上变得复杂。基因编码的蛋白质纳米笼是非常有前途的DDS候选物,因为它们具有模块化组成、易于在多种宿主中进行重组生产、能够控制货物分子的组装和装载以及具有生物可降解性。天然存在的纳米隔室的一个例子是封装蛋白,这是最近发现的细菌细胞器,已被证明可重新编程为纳米生物反应器和候选疫苗。在这里,我们报告了一种靶向DDS平台的设计和应用,该平台基于经过重新编程的封装蛋白,使其在外表面展示一种名为设计锚蛋白重复蛋白(DARPin)的抗体模拟蛋白,并封装一种细胞毒性载荷。本研究中选择的DARPin9.29特异性结合乳腺癌细胞上的人表皮生长因子受体2(HER2),这在细胞培养模型中得到了证实。基于封装蛋白的DDS通过在大肠杆菌中从单个质粒共表达封装蛋白 - DARPin9.29融合蛋白与工程化的黄素结合蛋白微型单线态氧发生器(MiniSOG)一步组装而成。纯化的封装蛋白 - DARPin_MiniSOG纳米隔室特异性结合HER2阳性乳腺癌细胞并触发细胞凋亡,表明该系统具有功能性和特异性。该DDS具有模块化,并且有潜力通过利用DARPin筛选文库形成多受体靶向系统的基础,允许使用已知特异性的新DARPins,并通过已证实的封装蛋白货物装载机制的灵活性,允许选择所需的货物蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e38d/8435816/a0e8efb62554/gr1.jpg

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