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SPATIAL ARRANGEMENT OF FUNCTIONAL SITES IN RIBOSOMES

SPATIAL ARRANGEMENT OF FUNCTIONAL SITES IN RIBOSOMES
核糖体中功能位点的空间排列
批准号:
3272029
负责人:
JAMES A LAKE
金额:
$15.4万
依托单位国家:
美国
项目类别:
财政年份:
1978
资助国家:
美国
项目状态:
已结题
起止时间:
1978-12-01 至 1986-11-30

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中文摘要
翻译
在核糖体上的三维分布的延伸和
英文摘要
The three dimensional distributions on the ribosome of elongation and initiation factors, of large and small subunit proteins, and of specific regions of RNA, will be determined. Other functional sites such as the peptidyl transferase and the exit site of the nascent polypeptide chain will also be mapped. Subunits will be reacted with antibodies directed against specific ribosomal proteins, against factors or against specific regions of RNA and observed by electron microscopy. Three dimensional sites will be mapped by comparing images of subunits (with attached antibodies) in different orientations. Our objective will be to relate the three dimensional structure of the tibosome to its function during protein synthesis. The small subunit is responsible for recongnizing the initiation site of mRNA with the participation of initiation factors and fmet-tRNA, for binding aminoacyl rRNAs, for associating with the large subunit, and for regulating the translational fidelity of messenger reading. The large subunit binds the acceptor stem of aminoacyl tRNA's entering the A site; catalyzes peptidyl transfer,and participates in elongation and translocation. By relating the three dimensional distributions of ribosomal proteins, factors and regions of RNA's with known biochemical information, we will attempt to elucidate the structural aspects of the molecular events occurring during protein synthesis. Comparative studies of ribosome structure will also be pursued in order to relate common structural features of prokaryotic, eukaryotic, and organellar ribosomes to common functions in protein synthesis.
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A PILOT STUDY FOR AN ANNELID GENOME PROJECT
A PILOT STUDY FOR AN ANNELID GENOME PROJECT
IMPROVING SEQUENCING ACCURACY WITH THERMOSTABLE PROTEINS
IMPROVING SEQUENCING ACCURACY WITH THERMOSTABLE PROTEINS
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