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微管靶向荧光探针:活癌细胞微管中超痕量微管蛋白的位点特异性检测和超分辨成像。

Microtubule-targetable fluorescent probe: site-specific detection and super-resolution imaging of ultratrace tubulin in microtubules of living cancer cells.

机构信息

†Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals; Key Laboratory of Green Chemical Media and Reactions, Ministry of Education; School of Chemistry and Chemical Engineering, Henan Normal University, 46 Jianshe Road, Muye Zone, Xinxiang, 453007, People's Republic of China.

‡Xinxiang Medical University, 601 Jinsui Road, Hongqi Zone, Xinxiang, 453000, People's Republic of China.

出版信息

Anal Chem. 2015;87(10):5216-22. doi: 10.1021/acs.analchem.5b01089. Epub 2015 May 6.

Abstract

Tubulins in microtubules have been recognized as potential targets in cancer chemotherapy for several years. However, their detection and imaging in living cells, especially following exposure to anticancer drugs, remains difficult to achieve. This difficulty is due to the very small cross section of microtubules and the very small changes in tubulin concentration involved. Photoswitchable fluorescent probes combined with the "super-resolution" fluorescence imaging technique present an exciting opportunity for site-specific detection and super-resolution imaging of specific microscopic populations, such as tubulin. In this study, a tubulin specific photoswitchable fluorescent probe (Tu-SP), that labels and detects ultratrace levels of tubulin in microtubules of living biosystems, was designed and evaluated. To realize super-resolution fluorescence imaging, the spiropyran derivative (SP), a classic photoswitch, was introduced to Tu-SP as a fluorophore. To detect ultratrace tubulin, Tu-SP employed the tubulin inhibitor, alkaloid colchicine (Tu), as a recognition unit. Tu-SP exhibited nearly nonintrinsic fluorescence before binding to tubulin, even if there were divalent metal ions and 375 nm lasers, respectively. After binding to tubulin, a dramatic increase in fluorescence was detected within milliseconds when irradiated at 375 nm, this increase is a result of the transformation of Tu-SP into a colored merocyanine (Tu-SP-1) with fluorescence. Tu-SP was successfully used for site-specific imaging of tubulin at a resolution of 20 ± 5 nm in microtubules of living cancer cells. More importantly, the probe was suitable for site-specific and quantitative detection of trace tubulin in microtubules of living biological samples.

摘要

微管中的微管蛋白已被公认为癌症化疗的潜在靶点已有数年。然而,在活细胞中检测和成像微管蛋白,尤其是在暴露于抗癌药物后,仍然难以实现。这种困难归因于微管的非常小的横截面积和涉及的微管蛋白浓度的非常小的变化。光致变色荧光探针与“超分辨率”荧光成像技术相结合,为特定微区(如微管蛋白)的特异性检测和超分辨率成像提供了令人兴奋的机会。在这项研究中,设计并评估了一种微管蛋白特异性光致变色荧光探针(Tu-SP),该探针可标记和检测活生物体系中微管内的痕量微管蛋白。为了实现超分辨率荧光成像,将螺吡喃衍生物(SP)作为荧光团引入到 Tu-SP 中,SP 是一种经典的光开关。为了检测痕量微管蛋白,Tu-SP 采用微管蛋白抑制剂生物碱秋水仙碱(Tu)作为识别单元。在与微管蛋白结合之前,Tu-SP 几乎没有固有荧光,即使存在二价金属离子和 375nm 激光也是如此。与微管蛋白结合后,在 375nm 激光照射下,在毫秒内检测到荧光的急剧增加,这是由于 Tu-SP 转化为具有荧光的有色甲川菁(Tu-SP-1)的结果。Tu-SP 成功地用于在活癌细胞的微管中以 20±5nm 的分辨率进行微管蛋白的特异性成像。更重要的是,该探针适用于活生物样品中微管内痕量微管蛋白的特异性和定量检测。

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