MRI: Acquisition of a Stimulated Emission Depletion (STED) Microscope for Nanoscopic Resolution of Biological Samples

MRI:获取受激发射损耗 (STED) 显微镜以实现生物样品的纳米级分辨率

基本信息

  • 批准号:
    0722519
  • 负责人:
  • 金额:
    $ 110万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Standard Grant
  • 财政年份:
    2007
  • 资助国家:
    美国
  • 起止时间:
    2007-08-01 至 2010-07-31
  • 项目状态:
    已结题

项目摘要

The Chemistry Department at the University of California-Los Angeles will acquire a stimulated emission depletion confocal laser scanning microscope (STED-CLSM) with this award from the Major Research Instrumentation (MRI) program. The requested microscope displays resolution down to 28 nm in the focal plane, a 10x improvement over conventional light microscopes. The instrument will be used to develop multi-color inorganic, stable, quantum rods as novel STED probes, decipher the structure of chromatin and its packaging into chromosomes in the cell, study cell signaling, viral and bacterial infection pathways, neural plasticity and many other important biological questions.STED microscopy provides an alternative to electron microscopy because it capitalizes on the well-established advantages of fluorescence microscopy (sensitivity, molecular specificity, genetically encoded probes, live cells, ease of operation). The STED concept relies on a purely physical phenomenon, stimulated emission, coupled with smart optics, to sharpen the confocal excitation spot, resulting in much more detailed, nanometer resolved images. Bridging the gap between electron and diffraction-limited light microscopy, a STED nanoscope should be a powerful tool for unraveling the relationship between structure and function in cell biology. Indeed, many outstanding problems lay in the nanometer scale, such as the organization of chromosomes, the assembly of large protein complexes and viral structures, organelle structures, as well as applications to non-biological nano-scale devices.
加州大学洛杉矶分校的化学系将获得一台受激发射耗尽共聚焦激光扫描显微镜(STED-CLSM),该显微镜来自主要研究仪器(MRI)计划。 所要求的显微镜在焦平面上显示分辨率低至28 nm,比传统光学显微镜提高了10倍。 该仪器将用于开发多色无机,稳定,量子棒作为新型STED探针,破译染色质的结构及其包装成细胞中的染色体,研究细胞信号传导,病毒和细菌感染途径,神经可塑性和许多其他重要的生物学问题。STED显微镜提供了一种替代电子显微镜,因为它充分利用了荧光显微镜的优势(灵敏度、分子特异性、基因编码探针、活细胞、操作简便)。STED概念依赖于一个纯粹的物理现象,受激发射,加上智能光学,以锐化共焦激发点,从而产生更详细的,纳米分辨率的图像。 STED纳米镜弥补了电子显微镜和衍射极限光学显微镜之间的差距,应该是解开细胞生物学中结构和功能之间关系的有力工具。 事实上,许多突出的问题在于纳米尺度,如染色体的组织,大型蛋白质复合物和病毒结构的组装,细胞器结构,以及非生物纳米尺度器件的应用。

项目成果

期刊论文数量(0)
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会议论文数量(0)
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Shimon Weiss其他文献

Single-Molecule Analysis of Transcription
  • DOI:
    10.1016/j.bpj.2008.12.1085
  • 发表时间:
    2009-02-01
  • 期刊:
  • 影响因子:
  • 作者:
    Richard Ebright;Shimon Weiss;Anirban Chakraborty;Dongye Wang;You Korlann;Achillefs Kapanidis;Emmanuel Margeat
  • 通讯作者:
    Emmanuel Margeat
High Throughput Single-Molecule Spectroscopy with Highly Parallel Excitation and Detection
  • DOI:
    10.1016/j.bpj.2009.12.3409
  • 发表时间:
    2010-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Ryan A. Colyer;Giuseppe Scalia;Fabrizio Guerrieri;Adrian Cheng;Moran Levi;Daniel Aharoni;Katsushi Arisaka;Jacques Millaud;Yoshihiko Kawai;Motohiro Suyama;Massimio Ghioni;Ivan Rech;Simone Tisa;Franco Zappa;Sergio Cova;Shimon Weiss;Xavier Michalet
  • 通讯作者:
    Xavier Michalet
Bacterial resting membrane potential: a case study with Bacillus subtilis
  • DOI:
    10.1016/j.bpj.2021.11.2017
  • 发表时间:
    2022-02-11
  • 期刊:
  • 影响因子:
  • 作者:
    Debjit Roy;Xavier Michalet;Evan W. Miller;Robert P. Gunsalus;Robert T. Clubb;Shimon Weiss
  • 通讯作者:
    Shimon Weiss
Disentangling conformational and photophysical dynamics in single-molecule FRET and PIFE experiments with multiparameter photon-by-photon hidden Markov modeling
  • DOI:
    10.1016/j.bpj.2023.11.1787
  • 发表时间:
    2024-02-08
  • 期刊:
  • 影响因子:
  • 作者:
    Paul D. Harris;Eitan Lerner;Alessandra Narducci;Christian Gebhardt;Shimon Weiss;Thorben Cordes
  • 通讯作者:
    Thorben Cordes
Daniel Chemla (1940–2008)
丹尼尔·舍梅拉(1940-2008)
  • DOI:
    10.1038/nmat2193
  • 发表时间:
    2008-06-01
  • 期刊:
  • 影响因子:
    38.500
  • 作者:
    Charles Shank;Shimon Weiss;Joseph Zyss
  • 通讯作者:
    Joseph Zyss

Shimon Weiss的其他文献

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{{ truncateString('Shimon Weiss', 18)}}的其他基金

Simultaneous characterization of near-field nanoplasmonic structure and function using super-resolved far-field optics: Solving the Inverse Problem
使用超分辨远场光学同时表征近场纳米等离子体结构和功能:解决反演问题
  • 批准号:
    1808766
  • 财政年份:
    2018
  • 资助金额:
    $ 110万
  • 项目类别:
    Standard Grant
EAGER: Methodology development for 3D atomic-scale structural dynamics movies of enzymes
EAGER:酶的 3D 原子尺度结构动力学电影的方法开发
  • 批准号:
    1842951
  • 财政年份:
    2018
  • 资助金额:
    $ 110万
  • 项目类别:
    Standard Grant
EAGER: Measuring near-field nanoplasmonics fields using super-resolved far-field optics
EAGER:使用超分辨远场光学测量近场纳米等离子体场
  • 批准号:
    1646621
  • 财政年份:
    2016
  • 资助金额:
    $ 110万
  • 项目类别:
    Standard Grant
Collaborative Research: Elucidating Pre-initiation Complex Assembly and Transcription Initiation by Pol-II Using Advanced Single Molecule and Microfluidic Methods
合作研究:利用先进的单分子和微流体方法阐明 Pol-II 的预启动复合物组装和转录启动
  • 批准号:
    1244098
  • 财政年份:
    2013
  • 资助金额:
    $ 110万
  • 项目类别:
    Continuing Grant
FIBR: How Do Proteins Fold Into Their Native and Functional Structures In-Vitro and in The Physiological Milue of The Living cell?
FIBR:蛋白质如何在体外和活细胞的生理环境中折叠成其天然和功能结构?
  • 批准号:
    0623664
  • 财政年份:
    2006
  • 资助金额:
    $ 110万
  • 项目类别:
    Continuing Grant
IDBR: Collaborative Research: Development of a Time-Resolved Photon-Counting Imager for Biology
IDBR:合作研究:开发生物学用时间分辨光子计数成像仪
  • 批准号:
    0552099
  • 财政年份:
    2006
  • 资助金额:
    $ 110万
  • 项目类别:
    Continuing Grant

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