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通过与六组氨酸-金属组装体(HmA)共组装实现抗体的高效胞内递送。

Efficient Delivery of Antibodies Intracellularly by Co-Assembly with Hexahistidine-Metal Assemblies (HmA).

机构信息

School of Ophthalmology and Optometry, Eye Hospital, School of Biomedical Engineering, Wenzhou Medical University, Wenzhou, 325035, Zhejiang Province, People's Republic of China.

Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University, Linhai, 317000, Zhejiang Province, People's Republic of China.

出版信息

Int J Nanomedicine. 2021 Nov 6;16:7449-7461. doi: 10.2147/IJN.S332279. eCollection 2021.

Abstract

PURPOSE

There has been a substantial global market for antibodies, which are based on extracellular targets. Binding intracellular targets by antibodies will bring new chances in antibody therapeutics and a huge market increase. We aim to evaluate the efficiency of a novel delivery system of His-metal assembly (HmA) in delivering intracellular antibodies and biofunctions of delivered antibodies.

METHODS

In this study, the physicochemical properties of HmA@Antibodies generated through co-assembling with antibodies and HmA were well characterized by dynamic light scatter. The cytotoxicity of HmA@Antibodies was investigated by Cell Counting Kit-8 (CCK-8). The endocytic kinetics and lysosome escape process of HmA@Antibodies were studied by flow cytometry and fluorescent staining imaging, respectively. Compared to the commercialized positive control, the intracellular delivery efficiency by HmA@Antibodies and biofunctions of delivered antibodies were evaluated by fluorescent imaging and CCK-8.

RESULTS

Various antibodies (IgG, anti-β-tubulin and anti-NPC) could co-assemble with HmA under a gentle condition, producing nano-sized (150 nm) and positively charged (+30 eV) HmA@Antibodies particles with narrow size distribution (PDI ~ 0.15). HmA displayed very low cytotoxicity to divers cells (DCs, HeLa, HCECs, and HRPE) even after 96 h for the feeding concentration ≤100 μg mL, and fast escape from endosomes. In the case of delivery IgG, the delivery efficiency into alive cells of HmA was better than a commercial protein delivery reagent (PULSin). For cases of the anti-β-tubulin and anti-NPC, HmA showed comparable delivery efficiency to their positive controls, but HmA with ability to deliver these antibodies into alive cells was still superior to positive controls delivering antibodies into dead cells through punching holes.

CONCLUSION

Our results indicate that this strategy is a feasible way to deliver various antibodies intracellularly while preserving their functions, which has great potential in various applications and treating many refractory diseases by intracellular antibody delivery.

摘要

目的

抗体在全球市场上有很大的需求,这些抗体主要针对细胞外靶点。通过抗体结合细胞内靶点将为抗体治疗带来新的机会和巨大的市场增长。本研究旨在评估新型 His-金属组装(HmA)递药系统传递细胞内抗体和递药抗体生物功能的效率。

方法

本研究通过共组装抗体和 HmA 生成 HmA@抗体,利用动态光散射对其理化性质进行了全面表征。通过细胞计数试剂盒-8(CCK-8)检测 HmA@抗体的细胞毒性。通过流式细胞术和荧光染色成像分别研究了 HmA@抗体的内吞动力学和溶酶体逃逸过程。与商业化的阳性对照相比,通过荧光成像和 CCK-8 评估了 HmA@抗体的细胞内递药效率和递药抗体的生物功能。

结果

在温和的条件下,各种抗体(IgG、抗-β-微管蛋白和抗-NPC)均可与 HmA 共组装,生成纳米级(150nm)、带正电荷(+30eV)、粒径分布窄(PDI~0.15)的 HmA@抗体颗粒。即使在喂养浓度≤100μg/ml 时,HmA 对 DCs、HeLa、HCECs 和 HRPE 等多种细胞的细胞毒性也非常低,甚至在 96 小时后仍能快速从内涵体中逃逸。在递送 IgG 的情况下,HmA 进入活细胞的递送效率优于商业蛋白递送试剂(PULSin)。对于抗-β-微管蛋白和抗-NPC 的情况,HmA 显示出与阳性对照相当的递送效率,但 HmA 具有将这些抗体递送至活细胞的能力,优于通过打孔将抗体递送至死细胞的阳性对照。

结论

我们的结果表明,该策略是一种将各种抗体递送至细胞内同时保持其功能的可行方法,在通过细胞内抗体递送来治疗各种难治性疾病方面具有很大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79b1/8579864/f0740743e2ed/IJN-16-7449-g0001.jpg

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