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血清蛋白存在下肽功能化介孔二氧化硅纳米粒子的靶向性验证

Targetability Validation of Peptide-Functionalized Mesoporous Silica Nanoparticles in the Presence of Serum Proteins.

作者信息

Paramonov Valeriy M, Gerstenberg Melanie, Sahlgren Cecilia, Lindén Mika, Rivero-Müller Adolfo

机构信息

Institute of Biomedicine, Research Centre for Integrative Physiology and Pharmacology, University of Turku, Turku, Finland.

Turku Bioscience, University of Turku and Åbo Akademi University, Turku, Finland.

出版信息

Front Chem. 2020 Nov 13;8:603616. doi: 10.3389/fchem.2020.603616. eCollection 2020.

Abstract

Demonstration of receptor-mediated targeting of nanoparticles to specific organs and/or cell types is an integral aim in many bionanomedicine development projects. However, engagement of targeted receptors with ligands on nanocarriers, which is the cornerstone of the active targeting concept, is challenging to study under biologically relevant conditions and thus often stays overlooked. In this work, we utilize an in-house established bioassay for targetability validation of mesoporous silica nanoparticles (MSNs), functionalized with high-affinity peptide ligands to somatostatin receptors via protective group chemistry, ensuring the correct orientation of the peptide's pharmacophore. We demonstrate that targeted nanoparticles, but not scrambled peptide-decorated counterparts, specifically engage the targeted receptors in living cells in culture media containing serum protein. The importance of being able to exclude false positives originating from the premature detachment of targeting peptides from the MSNs is highlighted.

摘要

在许多生物纳米医学开发项目中,证明纳米颗粒通过受体介导靶向特定器官和/或细胞类型是一个不可或缺的目标。然而,纳米载体上的配体与靶向受体的结合是主动靶向概念的基石,在生物学相关条件下进行研究具有挑战性,因此常常被忽视。在这项工作中,我们利用内部建立的生物测定法对介孔二氧化硅纳米颗粒(MSN)的靶向性进行验证,这些纳米颗粒通过保护基团化学方法用对生长抑素受体具有高亲和力的肽配体进行功能化,确保肽药效基团的正确取向。我们证明,靶向纳米颗粒而非用乱序肽修饰的对应物,在含有血清蛋白的培养基中能特异性地与活细胞中的靶向受体结合。这突出了能够排除由于靶向肽过早从MSN上脱离而产生假阳性结果的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0144/7691633/e3b80c3ac85b/fchem-08-603616-g0001.jpg

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