材料科学
力谱学
纳米技术
纳米尺度
纳米生物技术
纳米力学
链霉亲和素
生物腐蚀
配体(生物化学)
生物物理学
原子力显微镜
纳米颗粒
化学
生物素
受体
生物
生物化学
珊瑚
生态学
作者
Samuel Kim,Marcus V. J. Cathey,Brandon C. Bounds,Zackary N. Scholl,Piotr E. Marszałek,Minkyu Kim
标识
DOI:10.1021/acsami.3c14653
摘要
Protein self-assembly plays a vital role in a myriad of biological functions and in the construction of biomaterials. Although the physical association underlying these assemblies offers high specificity, the advantage often compromises the overall durability of protein complexes. To address this challenge, we propose a novel strategy that reinforces the molecular self-assembly of protein complexes mediated by their ligand. Known for their robust noncovalent interactions with biotin, streptavidin (SAv) tetramers are examined to understand how the ligand influences the mechanical strength of protein complexes at the nanoscale and macroscale, employing atomic force microscopy-based single-molecule force spectroscopy, rheology, and bioerosion analysis. Our study reveals that biotin binding enhances the mechanical strength of individual SAv tetramers at the nanoscale. This enhancement translates into improved shear elasticity and reduced bioerosion rates when SAv tetramers are utilized as cross-linking junctions within hydrogel. This approach, which enhances the mechanical strength of protein-based materials without compromising specificity, is expected to open new avenues for advanced biotechnological applications, including self-assembled, robust biomimetic scaffolds and soft robotics.
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