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一种新型人胶质瘤双靶点肽的发现:从模拟到作为靶向配体

Discovery of a Novel Dual Targeting Peptide for Human Glioma: From Simulation to Acting as Targeting Ligand.

作者信息

Sedghi Aminabad Negar, Saeedi Yousef, Adiban Jamal, Nemati Mahdieh, Shaterabadi Donya, Najafi Farhood, Rahbarghazi Reza, Talebi Mehdi, Zarebkohan Amir

机构信息

Department of Medical Nanotechnology, Advanced Faculty of Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Adv Pharm Bull. 2024 Jul;14(2):453-468. doi: 10.34172/apb.2024.033. Epub 2024 Mar 10.

Abstract

PURPOSE

Receptor-mediated transcytosis (RMT) is a more specific, highly efficient, and reliable approach to crossing the blood-brain-barrier (BBB) and releasing the therapeutic cargos into the brain parenchyma.

METHODS

Here, we introduced and characterized a human/mouse-specific novel leptin-derived peptide using , and experiments.

RESULTS

Based on the bioinformatics analysis and molecular dynamics (MD) simulation, a 14 amino acid peptide sequence (LDP 14) was introduced and its interaction with leptin-receptor (ObR) was analyzed in comparison with an well known leptin-derived peptide, Lep 30. MD simulation data revealed a significant stable interaction between ligand binding domains (LBD) of ObR with LDP 14. Analyses demonstrated suitable cellular uptake of LDP 14 alone and its derivatives (LDP 14-modified G4 PAMAM dendrimer and LDP 14-modified G4 PAMAM/pEGFP-N1 plasmid complexes) via ObR, energy and species dependent manner (preferred uptake by human/mouse cell lines compared to rat cell line). Importantly, our findings illustrated that the entry of LDP 14-modified dendrimers in hBCEC-D3 cells not only is not affected by protein corona (PC) formation, as the main reason for diminishing the cellular uptake, but also PC can enhance uptake rate. Finally, fluorescein labeled LDP 14-modified G4 PAMAM dendrimers efficiently accumulated in the mice brain with lower biodistribution in other organs, in our study.

CONCLUSION

LDP 14 introduced as a novel and highly efficient ligand, which can be used for drugs/genes delivery to brain tissue in different central nervous system (CNS) disorders.

摘要

目的

受体介导的转胞吞作用(RMT)是一种更具特异性、高效且可靠的穿过血脑屏障(BBB)并将治疗性货物释放到脑实质中的方法。

方法

在此,我们使用[具体实验方法]引入并表征了一种人/小鼠特异性的新型瘦素衍生肽。

结果

基于生物信息学分析和分子动力学(MD)模拟,引入了一个14个氨基酸的肽序列(LDP 14),并将其与一种知名的瘦素衍生肽Lep 30进行比较,分析其与瘦素受体(ObR)的相互作用。MD模拟数据显示ObR的配体结合域(LBD)与LDP 14之间存在显著稳定的相互作用。分析表明LDP 14单独及其衍生物(LDP 14修饰的G4 PAMAM树枝状大分子和LDP 14修饰的G4 PAMAM/pEGFP - N1质粒复合物)通过ObR以能量和物种依赖的方式(与人/小鼠细胞系相比,大鼠细胞系对其摄取偏好较低)实现了合适的细胞摄取。重要的是,我们的研究结果表明,LDP 14修饰的树枝状大分子进入hBCEC - D3细胞不仅不受蛋白质冠(PC)形成的影响(PC形成是细胞摄取减少的主要原因),而且PC还可以提高摄取率。最后,在我们的[具体实验]研究中,荧光素标记的LDP 14修饰的G4 PAMAM树枝状大分子在小鼠脑中有效积累,在其他器官中的生物分布较低。

结论

LDP 14作为一种新型高效配体被引入,可用于在不同中枢神经系统(CNS)疾病中将药物/基因递送至脑组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde6/11347739/2e9926a1e69c/apb-14-453-g001.jpg

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