相关实验视频
Updated: Jan 17, 2026

16:43
Visualization of Endoplasmic Reticulum Subdomains in Cultured Cells
Published on: February 18, 2014
13.6K
时间解析的光蛋白在时间和光谱领域扩展光显微镜
Zizhu Tan1, Chia-Heng Hsiung1, Jiahui Feng2
1Zhejiang Key Laboratory of Precise Synthesis of Functional Molecules, Department of Chemistry, Westlake University, 600 Dunyu Road, Hangzhou 310030, Zhejiang, China; Westlake Laboratory of Life Sciences and Biomedicine, 18 Shilongshan Road, Hangzhou 310024, Zhejiang, China.
Cell
|September 23, 2025
概括
研究人员开发了新的时间解析光蛋白 (tr-FPs),以更好地了解细胞过程. 这些tr-FP可以在活细胞中进行更详细的成像和量化,从而促进生物研究.
科学领域:
- 生物物理
- 细胞生物学
- 分子成像
背景情况:
- 光显微镜是生命科学中的关键工具.
- 常态光强度是常用的,但时间解析 (tr) 信号,特别是光寿命,较少被探索.
研究的目的:
- 开发一种具有可调节寿命的新型定时光蛋白 (tr-FPs).
- 通过控制光寿命而不改变光谱特性,实现先进的成像技术.
主要方法:
- 在可见光谱中设计和合成了具有合理控制寿命的tr-FP家族.
- 使用时光光谱解析显微镜对活细胞进行同时多蛋白成像.
- 在多重化超分辨率显微镜中应用tr-FPs.
主要成果:
- 开发了具有广泛寿命的tr-FP,覆盖了可见光谱.
- 使用时光光谱解析显微镜在活细胞中实现9种不同蛋白质的同时成像.
- 通过超分辨率显微镜和量化细胞蛋白质立体测量,同时可视化4种蛋白质.
结论:
- 引入了tr-FP作为生物研究的变革性工具集.
- 证明了tr-FPs在整合系统复杂性和定量准确性的潜力.
- 开辟了先进细胞分析和理解生物机制的新途径.
相关概念视频
Super-resolution Fluorescence Microscopy
12.2K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
12.2K
Protein Dynamics in Living Cells
2.6K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.6K
Two-Dimensional Microscopy in Microbiology
1.1K
Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...
1.1K

