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首页> 外文期刊>Biomedical Optics Express >Fast monitoring of in-vivo conformational changes in myosin using single scan polarization-SHG microscopy
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Fast monitoring of in-vivo conformational changes in myosin using single scan polarization-SHG microscopy

机译:使用单扫描偏振-SHG显微镜快速监测肌球蛋白的体内构象变化

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摘要

Fast imaging of molecular changes under high-resolution and label-free conditions are essential for understanding in-vivo processes, however, current techniques are not able to monitor such changes in real time. Polarization sensitive second harmonic generation (PSHG) imaging is a minimally invasive optical microscopy technique capable of quantifying molecular conformational changes occurring below the diffraction limit. Up to now, such information is generally retrieved by exciting the sample with different linear polarizations. This procedure requires the sample to remain static during measurements (from a few second to minutes), preventing the use of PSHG microscopy from studying moving samples or molecular dynamics in living organisms. Here we demonstrate an imaging method that is one order of magnitude faster than conventional PSHG. Based on circular polarization excitation and instantaneous polarimetry analysis of the second harmonic signal generated in the tissue, the method is able to instantaneously obtain molecular information within a pixel dwell time. As a consequence, a single scan is only required to retrieve all the information. This allowed us to perform PSHG imaging in moving C. elegans, monitoring myosin’s dynamics during the muscular contraction and relaxation. Since the method provides images of the molecular state, an unprecedented global understanding of the muscles dynamics is possible by correlating changes in different regions of the sample.
机译:在高分辨率和无标记条件下快速成像的分子变化对于了解体内过程至关重要,但是,当前的技术无法实时监控此类变化。偏振敏感二次谐波生成(PSHG)成像是一种微创光学显微镜技术,能够量化发生在衍射极限以下的分子构象变化。到目前为止,通常通过激发具有不同线性极化的样品来检索此类信息。此过程要求样品在测量过程中(从几秒钟到几分钟)保持静态,从而防止使用PSHG显微镜研究活生物体中的移动样品或分子动力学。在这里,我们演示了一种比传统PSHG快一个数量级的成像方法。基于圆极化激发和组织中产生的二次谐波信号的瞬时极化分析,该方法能够在像素停留时间内瞬时获得分子信息。结果,只需要一次扫描即可检索所有信息。这使我们能够在移动的秀丽隐杆线虫中执行PSHG成像,从而监测肌肉收缩和松弛过程中肌球蛋白的动态。由于该方法提供了分子状态的图像,因此可以通过关联样品不同区域的变化来对肌肉动力学进行前所未有的全面了解。

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