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设计用于骨组织工程的胶原结合型骨形态发生蛋白-2。

Collagen-binding bone morphogenetic protein-2 designed for use in bone tissue engineering.

机构信息

Department of Biomaterials, Graduate School of Biomedical and Health Sciences, Hiroshima University.

Faculty of Dental Medicine, Airlangga University.

出版信息

Dent Mater J. 2024 Sep 28;43(5):718-728. doi: 10.4012/dmj.2024-138. Epub 2024 Aug 30.

Abstract

Bone tissue engineering using biodegradable porous scaffolds is a promising approach for restoring oral and maxillofacial bone defects. Recently, attempts have been made to incorporate proteins such as growth factors to create bioactive scaffolds that can engage cells to promote tissue formation. Collagen-based scaffolds containing bone morphogenetic protein-2 (BMP2) have been studied for bone formation. However, controlling the initial burst of BMP2 remains difficult. Here we designed a functional chimeric protein composed of BMP2 and a collagen-binding domain (CBD), specifically the A3 domain of von Willebrand factor, to sustain BMP2 release from collagen-based scaffolds. Based on the results of computer-based structural prediction, we prepared a chimeric protein consisting of CBD and BMP2 in this order with a peptide tag for affinity purification. The chimeric protein had a collagen-binding capacity and enhanced osteogenic differentiation of human mesenchymal stem cells. These results are consistent with insights from in silico structural prediction.

摘要

使用可生物降解多孔支架进行骨组织工程是修复口腔颌面骨缺损的一种很有前途的方法。最近,人们试图将生长因子等蛋白质掺入生物活性支架中,以激活细胞促进组织形成。含有骨形态发生蛋白 2(BMP2)的基于胶原蛋白的支架已被用于骨形成的研究。然而,控制 BMP2 的初始释放仍然很困难。在这里,我们设计了一种由 BMP2 和胶原蛋白结合域(CBD)组成的功能嵌合蛋白,特别是 von Willebrand 因子的 A3 结构域,以从基于胶原蛋白的支架中持续释放 BMP2。基于计算机结构预测的结果,我们用亲和纯化的肽标签制备了 CBD 和 BMP2 按此顺序排列的嵌合蛋白。该嵌合蛋白具有胶原蛋白结合能力,并增强了人骨髓间充质干细胞的成骨分化。这些结果与计算机结构预测的见解一致。

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