研究生: |
林彥甫 Yen-Fu Lin |
---|---|
論文名稱: |
胃幽門螺旋桿菌26695結構基因體-HP0404蛋白質結構與功能的探討 Structural genomics of H. pylori 26695-Solution structural and functional studies of protein HP0404 from Helicobacter pylori |
指導教授: |
程家維
Jya-Wei Cheng |
口試委員: | |
學位類別: |
碩士 Master |
系所名稱: |
生命科學暨醫學院 - 生物科技研究所 Biotechnology |
論文出版年: | 2005 |
畢業學年度: | 93 |
語文別: | 中文 |
論文頁數: | 127 |
中文關鍵詞: | 幽門螺旋桿菌 、蛋白質激酶C抑制劑 、超高速離心機 、旋光儀 、螢光儀 、感應偶合電漿質譜儀 、核磁共振 |
外文關鍵詞: | Helicobacter pylori, protein kinase C inhibitor, Analytical ultracentrifuge, Circular Dichroism, Fluorescence Spectrometer, ICP-MS, NMR |
相關次數: | 點閱:2 下載:0 |
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近幾年來,由於結構基因體學蓬勃發展,基因序列資訊結合了最新的分子與結構生物學,使得大家對結構基因有更深一層的認識與探討。幽門螺旋桿菌(Helicobacter pylori, HP)是一個格蘭氏陰性菌、成長慢、具有鞭毛及螺旋外狀的細菌,它會引起很嚴重的胃潰瘍與十二指腸的疾病,幾乎全世界有一半的人口均受此菌感染。由於目前科學家們對於幽門螺旋桿菌的基因體序列所產生之蛋白質了解甚少,因此,我們選擇了幽門螺旋桿菌作為整個結構基因體計畫的主角。
這篇論文主要是研究幽門螺旋桿菌基因體中的一個蛋白質-HP0404,利用胺基酸序列比對的結果,推測其生物活性可能為PKC的抑制劑。藉由旋光儀偵測HP0404的二級結構和蛋白質穩定性,顯示HP0404是一個熱穩定性蛋白。另外在生物活性研究方面,使用螢光儀偵測蛋白質與金屬離子的鍵結能力,並且以ICP-MS將蛋白質內的金屬離子作定量分析,印證了HP0404對Zn2+具有專一性的鍵結作用。此外,利用非放射性PKC活性偵測實驗,測試出HP0404的確具有抑制PKC活性的功能。蛋白質結構方面,以NMR技術分析HP0404和HP0404 C14A的蛋白質結構之差異性。不但如此,X-Ray技術的應用也在嘗試研究中,以點晶方式將HP0404蛋白質培養成晶體,目的就是希望藉由不同方式研究HP0404蛋白質的分子結構。
In recent years, the structural genomics has been studied and developed thoroughly. Genomic sequencing information has combined the latest molecular and structural biology; hence scientists are able to move one step further in the structural genomics. Helicobacter pylori is a Gram-negative, microaerophilic, and slow-growing bacterium with flagellum and spiral appearance. It causes serious gastric ulcer and duodenum-associated diseases, and almost half population of the world has been infected by this bacterium. Since scientists have little understanding in the proteins produced by Helicobacter pylori genomics so far, we have chosen this bacterium as the major subject of the structural genomic project.
The aim of this thesis is to investigate a protein called HP0404 from Hlicobacter pylori genomics. The results from amino acid sequence alignment inferred that its biological activity might be inhibition of PKC. The secondary structure and stability of the protein were determined by circular dichroism, and it revealed that HP0404 is a heat stable protein. In addition, fluorescence spectrometer was used to detect the binding ability between the protein and metal ions, and the quantitative analysis of the metal ions within the protein was performed by ICP-MS, thus it is shown that HP0404 has specific binding with Zn2+. Furthermore, the non- radioactive method was applied to demonstrate that HP0404 could effectively suppress the PKC activity. The difference between the protein structures of HP0404 and HP0404 C14A was examined by NMR. Moreover, we attempted to use X-ray technology to study the protein structure of HP0404. The hanging-drop method was applied to crystallize HP0404, and the structure would be determined by X-ray. The purpose was to study the molecular structure of HP0404 in a different way.
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