课题基金 / 基金详情

项目摘要

项目成果

PETER B. MOORE的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): The principle activity for which this application seeks support is determination of the structures of physiologically important RNAs by NMR and X-ray crystallography. The ultimate objective is a chemical understanding of the biological properties of the RNAs studied. Since RNAs play critical roles in gene expression, the knowledge sought is fundamental to our understanding of processes vital to all organisms, including humans. Two specific problems are to be investigated: the regulation of ribosomal protein synthesis in bacteria, and the pseudouridylation of ribosomal RNA transcripts in eukaryotes. In bacteria, ribosomal protein synthesis is feed-back regulated at the translational level by mechanisms that depend on interactions between specific ribosomal proteins and sequences within the mRNAs that encode them, many of which are polycistronic. The two such systems of immediate concern are the spc operon/S8 system, and L10 operon./L10 system, but time permitting, others will be investigates; e.g. the alpha operon/L4 system. The mRNA sequence critical for the regulation of each ribosomal protein operon will be determined as precisely as possible. Structures will be obtained of the complexes that form between these RNA sequences and the ribosomal proteins that bind to them. Hypotheses about the mechanism of translational repression, formulated on the basis of those structures, will then be tested biochemically. Since bacteria regulate ribosomal protein synthesis by mechanisms unlike those used by eukaryotes, it is conceivable that new ways of specifically inhibiting bacterial growth will be revealed. The second problem to be investigated is posed by the boxH/ACA snoRNP system responsible for pseudouridylating rRNA transcripts in higher organisms. The RNA components of these snRNPs are postulated to interact with sequences in rRNA transcripts in a way that has no precedent in the literature. Biochemical experiments will be done to determine whether RNA/RNA interactions of the sort hypothesized are possible, and structures will be obtained for a snoRNA, with and without an appropriate rRNA sequence bound.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1006/jmre.2001.2307
发表时间: 2001-04
期刊: Journal of magnetic resonance
影响因子: 2.2
作者: [J. J. Warren-J.;P. Moore]
通讯作者: J. J. Warren-J.;P. Moore
Measurement of H2'-C2' and H3'-C3' dipolar couplings in RNA molecules.
RNA 分子中 H2-C2 和 H3-C3 偶极耦合的测量。
DOI: 10.1023/a:1020620016891
发表时间: 2002
期刊: Journal of biomolecular NMR
影响因子: 2.7
作者: [Vallurupalli,Pramodh, Moore,PeterB]
通讯作者: Moore,PeterB
DOI: 10.1016/s0022-2836(02)01270-6
发表时间: 2003
期刊: Journal of molecular biology
影响因子: 5.6
作者: [Vallurupalli,Pramodh, Moore,PeterB]
通讯作者: Moore,PeterB
Application of dipolar coupling data to the refinement of the solution structure of the sarcin-ricin loop RNA.
应用偶极耦合数据来细化八菌素-蓖麻毒素环 RNA 的溶液结构。
DOI: 10.1023/a:1011214214552
发表时间: 2001
期刊: Journal of biomolecular NMR
影响因子: 2.7
作者: [Warren,JJ, Moore,PB]
通讯作者: Moore,PB
ANTIBIOTIC RESISTANCE MUTATIONS IN H MARISMORTUI 50S RIBOSOMAL SUBUNITS
Program in Macromolecular Structure, Motion, Control
  • 批准号:
    7529241
  • 项目类别:
  • 资助金额:
    $29.56万
  • 财政年份:
    2007
  • 负责人:
    PETER B. MOORE
  • 依托单位:
ANTIBIOTIC RESISTANCE MUTATIONS IN H MARISMORTUI 50S RIBOSOMAL SUBUNITS
CORE Program in Macromolecular Structure, Motion, Control
  • 批准号:
    7529245
  • 项目类别:
  • 资助金额:
    $43.95万
  • 财政年份:
    2007
  • 负责人:
    PETER B. MOORE
  • 依托单位:
海外基金