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研究生: 吳盈漪
Wu, Ying Yi
論文名稱: 以解離放光染料及分子轉子為基底之螢光增益探針應用於蛋白質偵測
Application of Disassembly-Emission Dye and Molecular Rotor in Fluorescence Turn-on Detection of Proteins
指導教授: 陳貴通
Tan, Kui Thong
口試委員: 黃郁棻
Huang, Yu Fen
王聖凱
Wang, Sheng Kai
學位類別: 碩士
Master
系所名稱: 理學院 - 化學系
Department of Chemistry
論文出版年: 2015
畢業學年度: 103
語文別: 中文
論文頁數: 71
中文關鍵詞: 螢光探針細胞顯影分子轉子
外文關鍵詞: fluorescence probe, cell image, molecular rotor
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  • 小分子螢光探針具有高選擇性、高靈敏度且可快速偵測等優點。因此,近年來已有許多用來偵測酶蛋白的螢光探針,藉由酶的催化反應使非螢光基團的受質結構改變造成螢光訊號的上升。然而此方法並不適用於偵測非酶蛋白,使得非酶蛋白的螢光探針在設計上仍有許多限制。在此我們設計了一種可對非酶蛋白具專一性偵測之近紅外光螢光探針,此探針是由Cy5螢光基團修飾上小分子配體而組成,其螢光增益機制是透過探針自組裝形成J型聚集而淬熄螢光。加入目標分析物後,親和性配體會和目標分析物結合使聚集後的探針回復成單體,在近紅外光波段可觀察到顯著的螢光增益。我們將此概念應用於人類碳酸酐酶之專一性檢測,並成功標記細胞表面之癌症標記物:跨模型碳酸酐酶IX,且不需多餘的清洗步驟。
    此外,我們也設計了另一個以分子轉子為基底的螢光探針,此種螢光分子在水溶液中,單鍵可自由旋轉造成非放光性的能量損失,加入目標蛋白後,藉由目標蛋白和探針結合後抑制探針的單鍵旋轉,使得螢光訊號顯著上升。我們成功將此設計應用於人類血清白蛋白之偵測上,人類血清白蛋白可做為腎臟疾病及非糖尿病患者心血管疾病的檢測指標。加入人類血清白蛋白後,此探針的螢光增益倍數高達400倍之多,且具有高選擇性和高靈敏度,我們也成功的將此探針應用於尿液中白蛋白之定量分析上。


    Currently most of the fluorogenic probes are designed for the detection of enzymes which work by converting the non-fluorescence substrate into the fluorescence product via an enzymatic reaction. On the other hand, the design of fluorogenic probes for non-enzymatic proteins remains a great challenge. Herein, we report a general strategy to create near-IR fluorogenic probes, where a small molecule ligand is conjugated to a novel γ-phenyl-substituted Cy5 fluorophore, for the selective detection of proteins through a non-enzymatic process. Detail mechanistic studies reveal that the probes self-assemble to form fluorescence-quenched J-type aggregate. In the presence of target analyte, bright fluorescence in the near-IR region is emitted through the recognition-induced disassembly of the probe aggregate. Based on this design, a fluorogenic probe for hCA II detection was constructed and was applied for the no-wash imaging of tumor cells for the detection of hypoxia-induced cancer-specific biomarker, transmembrane-type carbonic anhydrase IX.
    We have also created another fluorogenic probe which belongs to a class of fluorescent dyes called molecular rotors for the detection of human serum albumin (HSA), a key indicator for the early diagnosis of renal disease and for the cardiovascular disease in non-diabetic individuals. In aqueous buffer, molecular rotors show extremely weak fluorescence due to the unrestricted torsional rotation. In the presence of target analyte, bright fluorescence can be observed because of restricted torsional rotation. In the presence of albumin, the probe exhibits remarkable 400-fold fluorescence enhancement with high selectivity and sensitivity. The probe was successfully applied in the quantitative detection of urinary albumin.

    摘要 i Abstract ii 誌謝 iii 著作列表 iv 目錄 v 第一章 緒論 1 1-1 蛋白質 1 1-1.1酶與非酶蛋白 (Enzyme and Non-enzymatic Proteins) 1 1-1-2 蛋白質偵測方法 2 1-2 螢光增益機制 4 1-2-1 自組裝/解離 (Self-Assembly / Disassembly) 4 1-2-2 聚集放光 (Aggregation-Induced Emission, AIE) 7 1-2-3 環境黏度變化 9 1-2-4 環境極性變化 13 1-2-5螢光共振能量轉移 (Förster Resonance Energy Transfer, FRET) 16 第二章 自組裝式Cy5螢光探針 20 2-1 探針設計 20 2-1-1 設計構想 20 2-1-2 Cy5螢光探針合成 22 2-2-3 hCAII蛋白質製備 23 2-2 結果與討論 23 2-2-1 螢光探針性質測試及討論 23 2-2-2 細胞實驗 33 第三章 可偵測尿液白蛋白之螢光探針 38 3-1 人類血清白蛋白 38 3-2 探針設計 39 3-2-1 設計構想 39 3-2-2 探針合成 40 3-3 結果與討論 41 3-3-1螢光探針性質測試及討論 41 3-3-2 尿液實驗 49 第四章 結論 53 第五章 實驗部分 54 5-1 實驗藥品及儀器 54 5-2 化合物光譜資料 55 5-3 蛋白質表現與純化 58 5-3.1 配製儲備液 (Stock solution) 及緩衝溶液 (Buffer) 58 5-3.2 蛋白質表現 (Protein Expression) 60 5-3.3 蛋白質純化 (Protein Purification) 61 5-3.4 SDS-膠體電泳 (SDS-Page) 62 5-4 細胞培養及實驗 63 5-4.1 細胞培養 63 5-4.2 細胞轉染 (Transfection) 64 5-4.3 缺氧細胞培養 64 5-4.4 細胞顯影 (Cell Image) 65 5-4.5 西方點墨法 (Western Blot) 65 參考文獻 67

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