Development of high-dose time-resolved X-ray footprinting technologies to enable detailed structural and kinetics information to be obtained for challenging biological problems

开发高剂量时间分辨 X 射线足迹技术，以获得具有挑战性的生物问题的详细结构和动力学信息

• 批准号: 10630950
• 负责人: CORIE Y RALSTON
• 金额: $ 42.45万
• 依托单位: UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB
• 依托单位国家: 美国
• 财政年份: 2018
• 资助国家: 美国
• 起止时间: 2018-01-01 至 2026-05-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10630950
• 关键词: Antibodies; Award; Binding; Biological; Biomedical Research; Blood capillaries; Cells; Collection; Communities; Complex; Country; Data; Data Collection; Development; Dose; Dose Rate; Dryness; Environment; Exclusion; Exposure to; Fingerprint; Fluorescence; Fluorescence Spectroscopy; Funding; Goals; Grant; Hybrids; Injections; Investigation; Kinetics; Light; Liquid substance; Location; Maps; Mass Spectrum Analysis; Measurement; Membrane Proteins; Methodology; Methods; Microfluidics; Molecular Conformation; Protein Dynamics; Proteins; Pump; Raman Spectrum Analysis; Research; Research Personnel; Resolution; Roentgen Rays; Sampling; Solvents; Source; Spectrum Analysis; Speed; Structure; Synchrotrons; System; Technology; Time; Tube; Water; X ray spectroscopy; beamline; biological systems; biophysical techniques; biophysical tools; chromophore; data quality; detector; experimental study; flexibility; improved; insight; instrument; instrumentation; macromolecular assembly; macromolecule; novel; protein complex; protein structure; small molecule; structural biology; success; tool

Abstract The overarching goal in this project, both in the funded award and in this renewal, is to advance the structural biology method of X-ray footprinting mass spectrometry (XFMS) in capability and accessibility such that it becomes a premiere biophysical tool for biomedical investigators around the country. XFMS is a solution state method used to map solvent accessible regions in macromolecules on a timescale of microseconds, yielding information on conformation, protein-protein dynamics, and bound water location and dynamics. It has been used to obtain useful structural information on a diverse range biological systems, from small proteins to large complexes, as well as membrane proteins, and for mapping interaction regions in antibody-target complexes. As part of the original award, we made substantial progress towards our main goal by developing a unique high-throughput and automated XFMS instrument, enabling use of the method to researchers nationwide. In this proposed renewal, we plan to build on this success to implement new capabilities in keeping with the original goal of the grant. Specifically, we plan to integrate fluorescence and Raman spectroscopies, fast mixing with jet delivery capability, and size exclusion directly inline with the XFMS instrument. The integration of these technologies into the XFMS instrument will enable even more challenging biological systems to be studied using the method. While the new specific aims are ambitious, they build naturally from our proven track record in developing complex instrumentation and the successful research team we built during the first grant period. Proof of principle for these technologies is presented, along with preliminary data, and the proposal outlines the significant technical challenges involved and how they will be overcome. The resulting technologies will be a significant gain to the biomedical research community and will be used to meet the increasing demand for access to the XFMS method.

摘要 在这个项目的总体目标，无论是在资助奖，并在此更新，是推动 X射线足迹质谱（XFMS）结构生物学方法性能和可达性 使其成为全国生物医学研究人员的首选生物物理工具。XFMS 是一种溶液状态方法，用于在时间尺度上映射大分子中的溶剂可及区域， 微秒，产生构象，蛋白质-蛋白质动力学和结合水的信息 位置和动态。它已被用来获得有用的结构信息，在不同的范围 生物系统，从小的蛋白质到大的复合物，以及膜蛋白， 绘制抗体-靶复合物中的相互作用区域。作为原始奖项的一部分，我们 通过开发一种独特的高通量和自动化的 XFMS仪器，使全国的研究人员能够使用该方法。在这次更新中，我们 计划在这一成功的基础上实施新的能力，以符合赠款的最初目标。 具体来说，我们计划整合荧光和拉曼光谱，快速混合喷射交付 能力和尺寸排阻直接与XFMS仪器串联。整合这些 XFMS仪器中的技术将使更具挑战性的生物系统成为可能。 使用该方法进行研究。虽然新的具体目标雄心勃勃，但它们自然是从我们的 在开发复杂仪器方面的良好记录和我们建立的成功研究团队 在第一个赠款期间。这些技术的原理证明，沿着 初步数据，该提案概述了所涉及的重大技术挑战，以及如何 会被克服。由此产生的技术将是生物医学研究的重大收获 社区，并将用于满足日益增长的需求访问XFMS方法。

项目成果

Heterohexamers Formed by CcmK3 and CcmK4 Increase the Complexity of Beta Carboxysome Shells.

CcmK3 和 CcmK4 形成的异六聚体增加了 Beta 羧基体壳的复杂性。

• DOI: 10.1104/pp.18.01190
• 发表时间: 2019
• 期刊: Plant physiology
• 影响因子: 7.4
• 作者: Sommer,Manuel;Sutter,Markus;Gupta,Sayan;Kirst,Henning;Turmo,Aiko;Lechno-Yossef,Sigal;Burton,RodneyL;Saechao,Christine;Sloan,NancyB;Cheng,Xiaolin;Chan,Leanne-JadeG;Petzold,ChristopherJ;Fuentes-Cabrera,Miguel;Ralston,CorieY

Multidomain architecture of estrogen receptor reveals interfacial cross-talk between its DNA-binding and ligand-binding domains.

• DOI: 10.1038/s41467-018-06034-2
• 发表时间: 2018-08-30
• 期刊: Nature communications
• 影响因子: 16.6
• 作者: Huang W;Peng Y;Kiselar J;Zhao X;Albaqami A;Mendez D;Chen Y;Chakravarthy S;Gupta S;Ralston C;Kao HY;Chance MR;Yang S
• 通讯作者: Yang S

An automated liquid jet for fluorescence dosimetry and microsecond radiolytic labeling of proteins.

• DOI: 10.1038/s42003-022-03775-1
• 发表时间: 2022-08-25
• 期刊: Communications biology
• 影响因子: 5.9

Structural analysis of a new carotenoid-binding protein: the C-terminal domain homolog of the OCP.

• DOI: 10.1038/s41598-020-72383-y
• 发表时间: 2020-09-23
• 期刊: Scientific reports
• 影响因子: 4.6
• 作者: Dominguez-Martin MA;Hammel M;Gupta S;Lechno-Yossef S;Sutter M;Rosenberg DJ;Chen Y;Petzold CJ;Ralston CY;Polívka T;Kerfeld CA
• 通讯作者: Kerfeld CA

Sneaking in SpyCatcher using cell penetrating peptides forin vivoimaging.

• DOI: 10.1088/1361-6528/acdf65
• 发表时间: 2023-08-02
• 期刊: Nanotechnology
• 影响因子: 3.5