Suppr超能文献

量子点与工程化光伏蛋白可调共轭物中的自组装和能量收集机制。

Mechanisms of Self-Assembly and Energy Harvesting in Tuneable Conjugates of Quantum Dots and Engineered Photovoltaic Proteins.

机构信息

School of Biochemistry Biomedical Sciences Building, University of Bristol, University Walk, Bristol, BS8 1TD, UK.

Wolfson Bioimaging Facility, Biomedical Sciences Building, University of Bristol, University Walk, Bristol, BS8 1TD, UK.

出版信息

Small. 2019 Jan;15(4):e1804267. doi: 10.1002/smll.201804267. Epub 2018 Dec 20.

Abstract

Photoreaction centers facilitate the solar energy transduction at the heart of photosynthesis and there is increasing interest in their incorporation into biohybrid devices for solar energy conversion, sensing, and other applications. In this work, the self-assembly of conjugates between engineered bacterial reaction centers (RCs) and quantum dots (QDs) that act as a synthetic light harvesting system is described. The interface between protein and QD is provided by a polyhistidine tag that confers a tight and specific binding and defines the geometry of the interaction. Protein engineering that changes the pigment composition of the RC is used to identify Förster resonance energy transfer as the mechanism through which QDs can drive RC photochemistry with a high energy transfer efficiency. A thermodynamic explanation of RC/QD conjugation based on a multiple/independent binding model is provided. It is also demonstrated that the presence of multiple binding sites affects energy coupling not only between RCs and QDs but also among the bound RCs themselves, effects which likely stem from restricted RC dynamics at the QD surface in denser conjugates. These findings are readily transferrable to many other conjugate systems between proteins or combinations of proteins and other nanomaterials.

摘要

光反应中心促进光合作用核心的太阳能转化,人们对将其纳入生物混合设备以进行太阳能转换、传感和其他应用越来越感兴趣。在这项工作中,描述了工程细菌反应中心 (RC) 和量子点 (QD) 之间的缀合物的自组装,这些缀合物充当合成光收集系统。蛋白质和 QD 之间的界面由多组氨酸标签提供,该标签赋予紧密和特异性结合,并定义了相互作用的几何形状。蛋白质工程改变了 RC 的色素组成,以确定Förster 共振能量转移是 QD 可以以高能量转移效率驱动 RC 光化学的机制。基于多/独立结合模型,提供了对 RC/QD 缀合的热力学解释。还表明,多个结合位点的存在不仅影响 RC 和 QD 之间的能量偶联,而且影响结合的 RC 本身之间的能量偶联,这些影响可能源于在更密集的缀合物中 QD 表面上受限的 RC 动力学。这些发现很容易转移到许多其他蛋白质或蛋白质与其他纳米材料之间的缀合系统。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验