English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 80990/80990 (100%)
造訪人次 : 42667791      線上人數 : 2070
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋


    請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/94723


    題名: Adaptive recognition of a prokaryote-like tRNAPro by a eukaryote-like prolyl-tRNA synthetase
    作者: 拉蒂法;Latifah, Emi
    貢獻者: 生命科學系
    關鍵詞: aminoacyl-tRNA synthetase;halofuginone;identity element;protein synthesis;thermophilic bacterium;tRNA
    日期: 2024-06-21
    上傳時間: 2024-10-09 15:26:43 (UTC+8)
    出版者: 國立中央大學
    摘要: 藉由分析三個域中的Prolyl-tRNA synthetase (ProRS)可以歸納出兩種 不同的結構,真核生物/古生菌類型(E-type) ProRS和原核生物類型(P-type) ProRS,前者在C-terminal多一段domain,後者在motif 2和motif 3之間有一 段額外的domain。除此之外,不同ProRS辨識的tRNAPro也有所不同,ProRS主要 會辨識tRNAPro的anticodon和acceptor stem,雖然anticodon在所有生物中都非 常保守,acceptor stem上的序列卻不太一樣,在細菌中是G72/A73,但在真核 生物中是C72/C73,有趣的是,E. coli tRNAPro中的G72/A73是主要被辨識的序 列,但在人類tRNAPro中C72/C73並不被辨識。令人訝異的是,有數種細菌被發現 帶有E-type而非P-type的ProRS,例如嗜熱菌Thermus thermophilus,我們的 實驗結果顯示這種細菌的E-type ProRS能夠辨識G72/A73,這顯示了T. thermophilus ProRS (TtProRS)儘管在結構上類似人類的ProRS,辨識的特性 卻類似E. coli ProRS,會同時辨認anticodon上的G35/G36,和acceptor stem 上的G72/A73。然而,不同於典型P-type ProRS,TtProRS並不使用在motif 2 上非常保守的R胺基酸,而是使用同樣在motif 2中的RTR 序列,然而在典型的 E-type ProRS中RTR並不保守,這說明TtProRS從典型E-type發展出獨特的序列 及辨識機制。此外,我們也發現TtProRS相對於其他E-type ProRS對 halofuginone (一種從febrifugine衍生而來的E-type ProRS抑制劑,結構類似 於Pro-A76)耐受性較高,特性比較接近細菌類型的ProRS。這項研究顯示了一 個不可或缺且非常保守的酵素能隨著環境變化適應新的受質。;Analysis of prolyl-tRNA synthetase (ProRS) from three domains of life uncovers two separate architectures: a eukaryote/archaeon-like (E-type) ProRS, distinguished by a C-terminal extension domain, and a prokaryote-like (P-type) ProRS, distinguished by an insertion domain. Diversity also appears in tRNAPro as the substrate of ProRS. While the anticodon elements of tRNAPro are highly conserved among all organisms and important for aminoacylation, the acceptor stem elements have diverged, with G72/A73 conserved in bacteria and C72/C73 conserved in eukaryotes. In E. coli tRNAPro, G72/A73 are major determinants, whereas in humans, C72/C73 are dispensable. Paradoxically, several bacteria have been revealed to possess an E-type ProRS, with one example being Thermus thermophilus ProRS (TtProRS). This bacterial E-type ProRS has been reported to selectively charge the P- type tRNAPro with G72/A73. This investigation reveals that despite the structural similarity with human ProRS, TtProRS maintains a strong recognition towards the anticodon elements G35/G36 and the acceptor-stem elements G72/A73, similar to E. coli ProRS. However, instead of relying on the strictly conserved R residue in the motif 2 loop of P-type ProRS to recognize G72/A73, TtProRS accomplishes this using RTR, a divergent sequence found within the E-type ProRS motif 2 loop. Here we also demonstrate TtProRS′s relatively resistance to halofuginone, a synthetic inhibitor of eukaryote-type ProRS derived from febrifugine mimicking Pro-A76, a characteristic similar to that of bacterium-type ProRS. This study highlights the adaptability of a usually conserved essential enzyme to adjust to a new substrate.
    顯示於類別:[生命科學研究所 ] 博碩士論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML37檢視/開啟


    在NCUIR中所有的資料項目都受到原著作權保護.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 隱私權政策聲明