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新型 DNA 适体靶向骨形态发生蛋白 2 用于骨再生的演变和应用。

The Evolution and Application of a Novel DNA Aptamer Targeting Bone Morphogenetic Protein 2 for Bone Regeneration.

机构信息

School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.

Advanced Biomedical Instrumentation Centre, Hong Kong Science Park, Shatin, New Territories, Hong Kong SAR, China.

出版信息

Molecules. 2024 Mar 11;29(6):1243. doi: 10.3390/molecules29061243.

Abstract

Recombinant human bone morphogenetic protein 2 (rhBMP-2) is an FDA-approved growth factor for bone regeneration and repair in medical practice. The therapeutic effects of rhBMP-2 may be enhanced through specific binding to extracellular matrix (ECM)-like scaffolds. Here, we report the selection of a novel rhBMP-2-specific DNA aptamer, functionalization of the aptamer in an ECM-like scaffold, and its application in a cellular context. A DNA aptamer BA1 was evolved and shown to have high affinity and specificity to rhBMP-2. A molecular docking model demonstrated that BA1 was probably bound to rhBMP-2 at its heparin-binding domain, as verified with experimental competitive binding assays. The BA1 aptamer was used to functionalize a type I collagen scaffold, and fraction ratios were optimized to mimic the natural ECM. Studies in the myoblast cell model C2C12 showed that the aptamer-enhanced scaffold could specifically augment the osteo-inductive function of rhBMP-2 in vitro. This aptamer-functionalized scaffold may have value in enhancing rhBMP-2-mediated bone regeneration.

摘要

重组人骨形态发生蛋白 2(rhBMP-2)是一种经 FDA 批准的生长因子,可用于医学实践中的骨再生和修复。rhBMP-2 的治疗效果可以通过与细胞外基质(ECM)样支架的特异性结合得到增强。在这里,我们报告了一种新型 rhBMP-2 特异性 DNA 适体的选择、适体在 ECM 样支架中的功能化及其在细胞环境中的应用。我们筛选出了一种 DNA 适体 BA1,其对 rhBMP-2 具有高亲和力和特异性。分子对接模型表明,BA1 可能与 rhBMP-2 的肝素结合域结合,这通过实验竞争结合测定得到了验证。BA1 适体被用于功能化 I 型胶原支架,并优化了分数比以模拟天然 ECM。在成肌细胞模型 C2C12 中的研究表明,适体增强的支架可以在体外特异性增强 rhBMP-2 的成骨诱导功能。这种适体功能化支架可能在增强 rhBMP-2 介导的骨再生方面具有价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5878/10974264/afc531d5c211/molecules-29-01243-sch001.jpg

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