NDC for the Optical Control of Biological Function

描述（应用摘要） 我们建议创建一个用于生物功能光学控制的NDC，以开发利用光快速打开和关闭细胞中选择蛋白质的方法。这些策略广泛适用于蛋白质类。该方法将用于非侵入性的，定量精确的，控制单个蛋白质的生物分子动力学，并用于控制蛋白质对之间的信号相互作用。这种方法可以使我们更接近生物学的核心目标之一：将特定细胞中的分子事件与器官的功能和生物体的行为直接联系起来。这些进展在药物发现、合成生物学和疾病的直接治疗方面有希望。 我们将开发三个技术平台：1）用于光学控制和化学整合到蛋白质中的模块化部件的化学和分子工具包，2）用于将光开关蛋白质安装到细胞中的病毒递送，以及3）使在体内解决这些纳米器件成为可能的光递送系统。我们将致力于解决三个工程和临床挑战：a）设计一种通用策略，用于对单个蛋白质的功能状态以及蛋白质对或蛋白质组的信号相互作用进行光学控制; B）获得对体外细胞的信号和酶活性的光学控制，以及c）调整这些方法来治疗视网膜和心脏病变。国家数据中心的成员将组成综合性的跨学科小组。我们期待三大成果。首先，化学合成、基因工程和生物学测试将有助于开发蛋白质功能的光学控制、光门的特定正交连接以及体内分子和光传递的最佳方法的基本设计。 其次，我们将在人类疾病的动物模型中使用光门控蛋白。第三，我们将在5年内制定基于细胞的药物筛选和合成细胞遥控开关的应用策略，并将评估毒性，以指导可用于临床的生物相容性设备的开发。

DESCRIPTION (application abstract) We propose to create an NDC for the Optical Control of Biological Function, to develop methods for rapidly turning select proteins in cells on and off with light. The strategies are broadly applicable across protein classes. The approach will be used for the non-invasive, quantitatively precise, control of the biomolecular dynamics of individual proteins, and for controlling signaling interactions between pairs of proteins. This approach can bring us closer to one of the central goals in biology: that of directly relating molecular events in particular cells to the function of an organ and the behavior of the organism. The developments hold promise in medicine for drug discovery, synthetic biology and the direct treatment of disease. We will develop three technology platforms: 1) chemical and molecular toolkits of modular parts for optical control and chemical integration into proteins, 2) viral delivery for installing photo-switchable proteins into cells, and 3) light delivery systems that make it possible to address these nanodvices in vivo. We will work to solve three engineering and clinical challenges: a) devise a general strategy for optical control over the functional state of individual proteins and the signaling interactions of pairs or groups of proteins; b) gain optical control over the signaling and enzymatic activity of cells in vitro, and c) adapt these approaches to treat retinal and cardiac pathologies. Members of the NDC will be organized into integrated, interdisciplinary teams. We expect three major outcomes. First, rounds of chemical synthesis, genetic engineering and biological testing will help develop the basic design for optical control of protein function, for the specific orthogonal attachment of light-gates, and for the optimal methods of molecular and light delivery in vivo. Second, we will employ light-gated proteins in animal models of human disease. Third, over 5 years we will formulate strategies for applications to cell-based drug screening and remote control switches for synthetic cells, and we will evaluate toxicity to guide the development of biocompatible devices that could be used in the clinic.