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用于核仁形态稳定成像和核仁应激产生剂筛选的 RNA 缓冲荧光探针。

Rna Buffering Fluorogenic Probe for Nucleolar Morphology Stable Imaging And Nucleolar Stress-Generating Agents Screening.

机构信息

CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, 116023, China.

University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Adv Sci (Weinh). 2024 Apr;11(15):e2309743. doi: 10.1002/advs.202309743. Epub 2024 Feb 7.

DOI:10.1002/advs.202309743
PMID:38326089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11022735/
Abstract

In the realm of cell research, membraneless organelles have become a subject of increasing interest. However, their ever-changing and amorphous morphological characteristics have long presented a formidable challenge when it comes to studying their structure and function. In this paper, a fluorescent probe Nu-AN is reported, which exhibits the remarkable capability to selectively bind to and visualize the nucleolus morphology, the largest membraneless organelle within the nucleus. Nu-AN demonstrates a significant enhancement in fluorescence upon its selective binding to nucleolar RNA, due to the inhibited twisted intramolecular charge-transfer (TICT) and reduced hydrogen bonding with water. What sets Nu-AN apart is its neutral charge and weak interaction with nucleolus RNA, enabling it to label the nucleolus selectively and reversibly. This not only reduces interference but also permits the replacement of photobleached probes with fresh ones outside the nucleolus, thereby preserving imaging photostability. By closely monitoring morphology-specific changes in the nucleolus with this buffering fluorogenic probe, screenings for agents are conducted that induce nucleolar stress within living cells.

摘要

在细胞研究领域,无膜细胞器已成为研究热点。然而,由于其形态不断变化且无定形,研究其结构和功能一直具有挑战性。本文报道了一种荧光探针 Nu-AN,它具有选择性结合和可视化核仁形态的显著能力,核仁是细胞核内最大的无膜细胞器。Nu-AN 选择性结合核仁 RNA 时荧光显著增强,这是由于扭曲的分子内电荷转移(TICT)受到抑制和与水的氢键减少。Nu-AN 的独特之处在于其中性电荷和与核仁 RNA 的弱相互作用,使其能够选择性和可逆地标记核仁。这不仅减少了干扰,还允许在核仁外更换光漂白探针,从而保持成像的光稳定性。通过使用这种缓冲荧光探针密切监测核仁的形态特异性变化,可以对活细胞内诱导核仁应激的试剂进行筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/4fa28c63a6a0/ADVS-11-2309743-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/192cf1aadec8/ADVS-11-2309743-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/8b1a1ea50f36/ADVS-11-2309743-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/1ef2891070d7/ADVS-11-2309743-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/0f99165c42f6/ADVS-11-2309743-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/4fa28c63a6a0/ADVS-11-2309743-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/192cf1aadec8/ADVS-11-2309743-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/8b1a1ea50f36/ADVS-11-2309743-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/1ef2891070d7/ADVS-11-2309743-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/0f99165c42f6/ADVS-11-2309743-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06c/11022735/4fa28c63a6a0/ADVS-11-2309743-g001.jpg

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