Structure and function of SRP RNA
Structure and function of SRP RNA
批准号:
7056711
负责人:
Christian Wolfgang Zwieb
金额:
$20.42万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-01-01 至 2008-04-30
关键词:
SDS polyacrylamide gel electrophoresisbiological signal transductionconformationcrosslinkgenetic translationintermolecular interactionmatrix assisted laser desorption ionizationmolecular assembly /self assemblynucleic acid structurepolymerase chain reactionprotein protein interactionprotein signal sequenceprotein structure functionprotein transportribonucleoproteinsribosomal RNAsecretionsecretory proteinsite directed mutagenesis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
The objective of this research proposal is to advance the molecular understanding of the basic process of protein transport across biological membranes. Our particular focus is on the signal recognition particle (SRP) as it plays a central role in protein targeting and secretion. The SRP RNA is an essential component of every SRP and contains several conserved features of functional importance. The goal of our research is to understand the structural and functional role of this RNA in the human system. We will define those regions of the human SRP RNA which are involved in SRP-mediated protein secretion and SRP assembly by using a combination of site-directed mutagenesis, site-directed cross-linking, structure probing, comparative analyses, biochemical, and biophysical studies. The major topics to be investigated are: (1) Mechanisms that involve SRP RNA in SRP assembly, signal recognition, and protein translocation. Complexes will be reconstituted from recombinant components to study the formation of the SRP and translocation competence of secretory proteins. The effects of altered complexes on individual events in the SRP-cycle, such as signal peptide recognition, translation arrest, and release of the arrest, will be identified. (2) Structural and functional role of proteins SRP68 and SRP72 within the human SRP. The interactions of SRP RNA with SRP68 and SRP72 will be studied by systematic site-directed mutagenesis. RNA-protein neighborhoods will be determined by using site-directed photochemical cross-linking followed by the identification of the cross-linked nucleotides and amino acids. The data from these experiments will be viewed collectively and used to generate a three-dimensional molecular model of human SRP. (3) Biophysical characterization of the M-domain of SRP54 which binds to the SRP RNA helix 8 and the signal as well as of recombinant signal fusion protein derivatives (SFPs) manipulated to contain altered signal peptides. These studies will focus on the specific features of two critical interactions and define their dynamic relationship to SRP function.
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DOI:
10.1155/2002/729649
发表时间:
2002-03
期刊:
Archaea
影响因子:
--
作者:
[C. Zwieb;J. Eichler]
通讯作者:
C. Zwieb;J. Eichler
Swapping of functional domains using a chimeric monster deletion mutagenesis strategy.
使用嵌合怪物删除诱变策略交换功能域。
DOI:
10.2144/01314bm02
发表时间:
2001
期刊:
BioTechniques
影响因子:
2.7
作者:
[Yang,CH, Zwieb,C]
通讯作者:
Zwieb,C
Complexes with truncated RNAs from the large domain of Archaeoglobus fulgidus signal recognition particle.
与来自古生球菌信号识别颗粒大域的截短 RNA 形成的复合物。
DOI:
10.1111/j.1574-6968.2001.tb10626.x
发表时间:
2001
期刊:
FEMS microbiology letters
影响因子:
2.1
作者:
[Bhuiyan,SH, Pakhomova,ON, Hinck,AP, Zwieb,C]
通讯作者:
Zwieb,C
Sequence-specific 1H, 13C and 15N signal assignments and secondary structure of archaeoglobusfulgidus SRP19.
古生球菌 SRP19 的序列特异性 1H、13C 和 15N 信号分配和二级结构。
DOI:
10.1023/a:1011243402698
发表时间:
2001
期刊:
Journal of biomolecular NMR
影响因子:
2.7
作者:
[Pakhomova,ON, Cui,Y, Zwieb,C, Hinck,AP]
通讯作者:
Hinck,AP
Reconstitution of the signal recognition particle of the halophilic archaeon Haloferax volcanii.
嗜盐古菌 Haloferax volcanii 信号识别粒子的重建。
DOI:
10.1093/nar/gkf548
发表时间:
2002
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Tozik,Irit, Huang,Qiaojia, Zwieb,Christian, Eichler,Jerry]
通讯作者:
Eichler,Jerry
共 25 条
海外基金