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mGreenLantern:一种明亮的单体荧光蛋白,具有快速表达和细胞填充特性,可用于神经元成像。

mGreenLantern: a bright monomeric fluorescent protein with rapid expression and cell filling properties for neuronal imaging.

机构信息

Helen and Robert Appel Alzheimer's Disease Research Institute, Weill Cornell Medicine, New York, NY 10021;

Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY 10021.

出版信息

Proc Natl Acad Sci U S A. 2020 Dec 1;117(48):30710-30721. doi: 10.1073/pnas.2000942117. Epub 2020 Nov 18.

Abstract

Although ubiquitous in biological studies, the enhanced green and yellow fluorescent proteins (EGFP and EYFP) were not specifically optimized for neuroscience, and their underwhelming brightness and slow expression in brain tissue limits the fidelity of dendritic spine analysis and other indispensable techniques for studying neurodevelopment and plasticity. We hypothesized that EGFP's low solubility in mammalian systems must limit the total fluorescence output of whole cells, and that improving folding efficiency could therefore translate into greater brightness of expressing neurons. By introducing rationally selected combinations of folding-enhancing mutations into GFP templates and screening for brightness and expression rate in human cells, we developed mGreenLantern, a fluorescent protein having up to sixfold greater brightness in cells than EGFP. mGreenLantern illuminates neurons in the mouse brain within 72 h, dramatically reducing lag time between viral transduction and imaging, while its high brightness improves detection of neuronal morphology using widefield, confocal, and two-photon microscopy. When virally expressed to projection neurons in vivo, mGreenLantern fluorescence developed four times faster than EYFP and highlighted long-range processes that were poorly detectable in EYFP-labeled cells. Additionally, mGreenLantern retains strong fluorescence after tissue clearing and expansion microscopy, thereby facilitating superresolution and whole-brain imaging without immunohistochemistry. mGreenLantern can directly replace EGFP/EYFP in diverse systems due to its compatibility with GFP filter sets, recognition by EGFP antibodies, and excellent performance in mouse, human, and bacterial cells. Our screening and rational engineering approach is broadly applicable and suggests that greater potential of fluorescent proteins, including biosensors, could be unlocked using a similar strategy.

摘要

虽然增强型绿色和黄色荧光蛋白(EGFP 和 EYFP)在生物研究中无处不在,但它们并没有专门针对神经科学进行优化,其亮度较低,在脑组织中的表达速度较慢,限制了树突棘分析等用于研究神经发育和可塑性的不可或缺技术的准确性。我们假设 EGFP 在哺乳动物系统中的低溶解度必须限制整个细胞的总荧光输出,因此提高折叠效率可以转化为表达神经元的更高亮度。通过在 GFP 模板中引入合理选择的折叠增强突变组合,并在人细胞中筛选亮度和表达率,我们开发了 mGreenLantern,一种在细胞中的亮度比 EGFP 高六倍的荧光蛋白。mGreenLantern 在 72 小时内照亮了小鼠大脑中的神经元,大大缩短了病毒转导和成像之间的滞后时间,而其高亮度提高了使用宽场、共聚焦和双光子显微镜检测神经元形态的能力。当体内表达到投射神经元时,mGreenLantern 的荧光比 EYFP 发展快四倍,突出了在 EYFP 标记的细胞中难以检测到的长程过程。此外,mGreenLantern 在组织清除和扩展显微镜后仍保持强荧光,从而无需免疫组织化学即可实现超分辨率和全脑成像。mGreenLantern 由于与 GFP 滤光片组兼容、被 EGFP 抗体识别以及在小鼠、人类和细菌细胞中的出色性能,可以直接替代不同系统中的 EGFP/EYFP。我们的筛选和合理的工程方法具有广泛的适用性,并表明通过类似的策略可以释放荧光蛋白(包括生物传感器)更大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec0/7720163/fc3d8947e5af/pnas.2000942117fig01.jpg

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