Conference on Structure and Function of Aminoacyl-tRNA Synthetases, October 10-15, 1998 near Strasbourg, France

氨基酰基-tRNA 合成酶的结构和功能会议,1998 年 10 月 10-15 日,法国斯特拉斯堡附近

基本信息

  • 批准号:
    9804921
  • 负责人:
  • 金额:
    $ 0.5万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Standard Grant
  • 财政年份:
    1998
  • 资助国家:
    美国
  • 起止时间:
    1998-07-01 至 1999-06-30
  • 项目状态:
    已结题

项目摘要

9804921 Musier-Forsyth This award is for partial support for a Conference on Structure and Function of Aminoacyl-tRNA Synthetases. Aminoacyl-tRNA synthetases are key enzymes in protein biosynthesis. They act as interpreters of the genetic code by relating amino acids to specific trinucleotides through the aminoacylation of their cognate tRNAs. These enzymes are divided into two entirely distinct families on the basis of the architectural organization of their catalytic cores and thus are exceptional models for the evolution of protein structure/function relationships. The synthetase field is a rapidly progressing research area. Researchers are using diverse, multidisciplinary approaches to understand structure-function relationships from a variety of perspectives, including fundamental enzymology, RNA-protein interactions, and even evolutionary biology. In a short period of time high resolution crystal structures should be available for all 20 synthetases. The proposed conference will offer a well-balanced scientific program, which will emphasize traditional topics such as synthetase structural diversity, mechanisms, editing, tRNA recognition, and tRNAs and synthetases in translation, as well as newer directions in the field such as synthetase evolution, drug design, alternate functions, and artificial aminoacylation systems. Nucleic acids are biological molecules that encode all of the information necessary for living organisms to function and survive. Ribonucleic acid (RNA) is chemically very similar to deoxyribonucleic acid (DNA), the storage molecule for the genetic code. In living cells, RNA is almost always found complexed with proteins. Unambiguous interpretation of the genetic code requires specific recognition of each of the more than 60 cellular transfer RNA (tRNA) molecules by a class of proteins known as aminoacyl-tRNA synthetases. In comparison to our knowledge of DNA-protein interactions, our understanding of RNA-protein interactions is s till quite limited. Due to the high degree of specificity between tRNAs and aminoacyl-tRNA synthetases, these molecules are excellent targets for studying the principles of protein-RNA recognition. The proposed meeting will be organized to allow a high level of participation of younger scientists, including students and postdoctorals. The meeting format will also provide an ideal framework for informal exchanges between younger scientists and more senior leaders in the field, and ensure that young scientists have the most rewarding experience possible.
9804921 Musier-Forsyth该奖项是对一次氨基酰基-tRNA合成酶结构和功能会议的部分支持。氨酰-tRNA合成酶是蛋白质生物合成的关键酶。它们作为遗传密码的解释者,通过同源tRNAs的氨基酰化将氨基酸与特定的三核苷酸联系起来。根据其催化核心的结构组织,这些酶被分为两个完全不同的家族,因此是蛋白质结构/功能关系进化的特殊模型。合成酶领域是一个发展迅速的研究领域。研究人员正在使用不同的、多学科的方法从不同的角度理解结构与功能的关系,包括基础酶学、RNA-蛋白质相互作用,甚至进化生物学。在短时间内,所有20种合成酶都应该具有高分辨率的晶体结构。拟议的会议将提供一个平衡的科学计划,其中将强调传统的主题,如合成酶结构多样性、机制、编辑、tRNA识别、tRNA和翻译中的合成酶,以及该领域的新方向,如合成酶进化、药物设计、替代功能和人工氨基酰化系统。核酸是一种生物分子,它编码了活着的有机体运作和生存所需的所有信息。核糖核酸(RNA)在化学上与脱氧核糖核酸(DNA)非常相似,脱氧核糖核酸是遗传密码的存储分子。在活细胞中,RNA几乎总是与蛋白质络合在一起。对遗传密码的明确解释需要一类被称为氨基酰-tRNA合成酶的蛋白质对60多个细胞转移RNA(TRNA)分子中的每一个进行特定识别。与我们对DNA-蛋白质相互作用的了解相比,我们对RNA-蛋白质相互作用的理解仍然是S的,直到相当有限。由于tRNAs和氨基酰tRNA合成酶之间的高度特异性,这些分子是研究蛋白质-RNA识别原理的极佳靶点。拟召开的会议将使包括学生和博士后在内的年轻科学家能够高水平地参与。会议形式还将为年轻科学家和该领域更资深的领导人之间的非正式交流提供一个理想的框架,并确保年轻科学家尽可能获得最有益的经验。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Karin Musier-Forsyth其他文献

Specific Basic and Aromatic Residues Optimize the Nucleic Acid Chaperone Activity of HIV-1 Nucleocapsid Protein
  • DOI:
    10.1016/j.bpj.2010.12.2328
  • 发表时间:
    2011-02-02
  • 期刊:
  • 影响因子:
  • 作者:
    Hao Wu;Micah McCauley;Robert Gorelick;Ioulia Rouzina;Karin Musier-Forsyth;Mark Williams
  • 通讯作者:
    Mark Williams
Mechanism of selective RNA packaging during HIV-1 particle assembly
  • DOI:
    10.1016/j.bpj.2021.11.397
  • 发表时间:
    2022-02-11
  • 期刊:
  • 影响因子:
  • 作者:
    Silver Jõemetsa;Anne X. Zhou;Raymond F. Pauszek;Arishma R. Singh;Jonathan Kitzrow;Karin Musier-Forsyth;David P. Millar
  • 通讯作者:
    David P. Millar
Replacement of a Single Aromatic Residue in HIV-1 Nucleocapsid Protein Strongly Alters its Nucleic Acid Chaperone Activity
  • DOI:
    10.1016/j.bpj.2009.12.1467
  • 发表时间:
    2010-01-01
  • 期刊:
  • 影响因子:
  • 作者:
    Hao Wu;Micah J. McCauley;Robert J. Gorelick;Ioulia Rouzina;Karin Musier-Forsyth;Mark C. Williams
  • 通讯作者:
    Mark C. Williams
Oligomerization of HIV-1 Restriction Factor APOBEC3G Transforms it from a Fast Enzyme to a Slow Nucleic Acid Binding Protein
  • DOI:
    10.1016/j.bpj.2011.11.3274
  • 发表时间:
    2012-01-31
  • 期刊:
  • 影响因子:
  • 作者:
    Kathy R. Chaurasiya;Hylkje Geertsema;Dominic F. Qualley;Tiyun Wu;Yasumasa Iwatani;Denise Chan;Amber Hertz;Judith G. Levin;Karin Musier-Forsyth;Ioulia Rouzina;Mark C. Williams
  • 通讯作者:
    Mark C. Williams
Complex Kinetics of Apobec3g Interaction with Single-Stranded Nucleic Acids
  • DOI:
    10.1016/j.bpj.2010.12.1265
  • 发表时间:
    2011-02-02
  • 期刊:
  • 影响因子:
  • 作者:
    Ioulia Rouzina;Dominic F. Qualley;Tiyun Wu;Yasumasa Iwatani;Denise S.B. Chan;Amber Hertz;Kathy Chaurasiya;Judith G. Levin;Mark C. Williams;Karin Musier-Forsyth
  • 通讯作者:
    Karin Musier-Forsyth

Karin Musier-Forsyth的其他文献

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