4D map of the tubulin code in the human neuron

人类神经元中微管蛋白代码的 4D 图

• 批准号: 10916016
• 负责人: Antonina Roll-Mecak
• 金额: $ 38.78万
• 依托单位: NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10916016
• 关键词: Antibodies; Award; Chemicals; Code; Communication; Coupled; Environment; Human; Image; Life; Maps; Mechanics; Methods; Microscope; Microscopy; Microtubule-Associated Proteins; Microtubules; Modification; Molecular; Motor; National Institute of Biomedical Imaging and Bioengineering; National Institute of Neurological Disorders and Stroke; Neurons; Polymers; Post-Translational Protein Processing; Process; Protocols documentation; Reader; Resolution; Sampling; Tubulin; alpha Tubulin; beta Tubulin; cell type; cellular imaging; imaging modality; improved; induced pluripotent stem cell; molecular imaging; nanoscale; recruit; single molecule

Life depends on the efficient and organized transport of cellular cargo on microtubules, polymers composed of alpha/beta-tubulins. No cell type is more dependent on this process than the neuron which needs to support fast, efficient communication between compartments that can be more than 1 m apart. As a result, neuronal processes are one of the densest cellular environments, with microtubules spaced as close as 20 nm that support the large continuous volume of bidirectional cellular traffic necessary for survival and optimal function. Neurons have evolved means to organize and differentiate these microtubule tracks by functionalizing tubulin with chemically diverse posttranslational modifications. An emerging paradigm is that these modifications act as a tubulin code to regulate microtubule dynamics, mechanics and recruitment of microtubule-associated proteins and microtubule-based motors. This project leverages the expertise of our groups on the tubulin code (Roll-Mecak, NINDS) and high-resolution cellular imaging (Hari Shroff, NIBIB and AIM) to generate a complete single-molecule resolution 4D map of the tubulin code and its readers in the human neuron by developing methods for expansion microscopy coupled with single molecule imaging. Since the inception of this award we succeeded in refining the expansion protocols, we validated antibodies that are compatible for expansion microscopy and developed protocols necessary for imaging these samples, which included a microscope upgrade to improve sample stability and increase camera sensitivity and resolution. The methods we develop will be broadly applicable to other structural problems that require nanoscale resolution and molecular contrast.

生命依赖于微管上细胞货物的有效和有组织的运输，微管是由α/β-微管蛋白组成的聚合物。没有一种细胞类型比神经元更依赖于这一过程，神经元需要支持隔室之间的快速、有效的通信，这些隔室之间的距离可以超过1米。因此，神经元突起是最密集的细胞环境之一，微管的间距接近20 nm，支持生存和最佳功能所需的大量连续的双向细胞流量。神经元已经进化出通过对微管蛋白进行功能化和不同的翻译后修饰来组织和区分这些微管轨迹的方法。一个新兴的范例是，这些修饰作为微管蛋白密码来调节微管的动力学、力学和微管相关蛋白和基于微管的马达的招募。该项目利用我们团队在微管蛋白密码(Roll-Mecak，NINDS)和高分辨率细胞成像(Hari Shroff，NIBIB和AIM)方面的专业知识，通过开发扩展显微镜与单分子成像相结合的方法，在人神经元中生成微管蛋白密码及其阅读器的完整单分子分辨率4D图谱。自该奖项设立以来，我们成功地完善了扩增方案，我们验证了与扩增显微镜兼容的抗体，并开发了对这些样品进行成像所需的方案，其中包括升级显微镜以改善样品的稳定性，并提高相机的灵敏度和分辨率。我们开发的方法将广泛适用于其他需要纳米级分辨率和分子对比度的结构问题。