Controlling Enzyme Structure and Activity with Light Illumination

用光照控制酶的结构和活性

• 批准号: 1153699
• 负责人: C. Ted Lee, Jr.
• 金额: $ 0.33万
• 依托单位: University of Southern California
• 依托单位国家: 美国
• 项目类别: Standard Grant
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-10-01 至 2012-03-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=1153699&HistoricalAwards=false
• 关键词: Controlling; Enzyme; Structure; Activity; Light

Nanotechnology is implicit in the assembly of proteins into the thousands of active nanostructures pervasive in the human body. The utility of proteins as the building blocks of these bionanomachines derives from the fact that proteins are dynamic entities, responding to molecular interactions in unique and complex ways, often resulting in conformation changes to various non-native or associated states. These conformational transitions influence virtually every biological process. As such, knowledge of both the structure of the non-native states that form in response to various stimuli along with the dynamics of rearrangements between these states is required. This necessitates a means to rapidly induce changes in protein conformation and a method to determine the structure of non-native states (partially-folded or associated) at relatively high resolution. C. Ted Lee, Jr. of the University of Southern California plans to achieve this goal using light-responsive surfactants to induce protein unfolding or association, which will be detected with small-angle neutron scattering (SANS). Surfactants generally affect protein conformation by disrupting intramolecular or intermolecular amino acid contacts, leading to protein unfolding or the dissociation of protein aggregates, respectively. In the case of photoresponsive surfactants, however, the surfactant-amino acid associations can be switched on or off with simple light illumination. This novel method to photo-control protein conformation will be investigated on several length scales. Protein tertiary and quaternary structure will be determined with SANS through shape-reconstruction computational methods to best fit the scattering data, allowing the in vitro protein structure to be determined. SANS experiments require allocation of competitive beam time from a National Laboratory. This proposal requests funds to allow SANS data to be collected on the bioSANS instrument at Oak Ridge National Laboratory from October 14 through 17 of this year with the participation of a graduate student from the Lee Group. These experiments will allow full characterization of the photo-controlled native-to-intermediate-to-denatured or monomer-to-aggregated transitions in proteins. Broader Impacts. Allowing a graduate student to visit ORNL for three days will provide an invaluable experience. In fact, one of the previous students of the PI now currently works at NIST as a result of similar visits. Chemical Engineering education is faced with a curriculum that has become increasingly disconnected with faculty research. To close this gap, proposals such as this travel award will allow a student to work in the atmosphere in the laboratory with ultimate connectability to features of coursework.

纳米技术隐含在蛋白质组装成数千个活跃的纳米结构在人体中无处不在。蛋白质作为这些生物机器的构建块的效用源于蛋白质是动态实体的事实，以独特和复杂的方式响应分子相互作用，通常导致构象变化为各种非天然或相关状态。这些构象转变几乎影响每一个生物过程。因此，需要了解响应于各种刺激沿着形成的非原生状态的结构以及这些状态之间的重排的动态。这需要一种快速诱导蛋白质构象变化的方法和一种以相对高的分辨率确定非天然状态（部分折叠或缔合）的结构的方法。C.小泰德·李南加州大学的研究人员计划使用光响应表面活性剂来诱导蛋白质解折叠或缔合，从而实现这一目标，这将通过小角中子散射（SANS）来检测。表面活性剂通常通过破坏分子内或分子间氨基酸接触，分别导致蛋白质解折叠或蛋白质聚集体解离来影响蛋白质构象。然而，在光响应表面活性剂的情况下，表面活性剂-氨基酸缔合可以通过简单的光照来打开或关闭。这种新的方法来光控制蛋白质构象将在几个长度尺度上进行研究。蛋白质三级和四级结构将通过形状重建计算方法用SANS确定，以最佳拟合散射数据，从而确定体外蛋白质结构。SANS实验需要国家实验室分配有竞争力的射束时间。该提案要求提供资金，以便在今年10月14日至17日期间在橡树岭国家实验室的bioSANS仪器上收集SANS数据，并由李氏集团的一名研究生参与。这些实验将允许充分表征蛋白质中的光控天然到中间体到变性或单体到聚集体的转变。更广泛的影响。允许研究生访问ORNL三天将提供宝贵的经验。事实上，PI以前的学生之一现在在NIST工作，因为类似的访问。化学工程教育正面临着一个课程，已成为越来越脱离教师的研究。为了缩小这一差距，像这次旅行奖这样的提案将允许学生在实验室的气氛中工作，并最终与课程的特点相联系。