Molecular Information Theory
Molecular Information Theory
批准号:
6762011
负责人:
JACOB V MAIZEL
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
中文摘要
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英文摘要
Information theory is a powerful tool for understanding the DNA and RNA patterns that define genetic control systems. My theoretical work is divided into several levels. Level 0 is the study of genetic sequences bound by proteins or other macromolecules, briefly described below. The success of this theory suggested that other aspects of information theory should also apply to molecular biology. Level 1 theory introduces the more general concept of the molecular machine, and the concept of a machine capacity equivalent to Shannon's channel capacity. In Level 2, the Second Law of Thermodynamics is connected to the capacity theorem. This defines the limits of Maxwell's Demon and future molecular computers. The project also has three interrelated activities: theory, computer analysis and genetic engineering experiments. In level 0 I showed that binding sites on nucleic acids usually contain just about the amount of information needed for molecules to find the sites in the genome. Apparent exceptions to this "working hypothesis" have revealed many new phenomena. The first major anomaly was found at bacteriophage T7 promoters, which conserve twice as much information as the polymerase requires to locate them. The most likely explanation is that a second protein binds to the DNA. In another case, we discovered that the F incD region has a three-fold excess conservation, which implies that three proteins bind there. We are investigating both anomalies experimentally. Two graphical methods have been invented to display the structure of binding sites. A sequence logo shows the average patterns in a set of binding sites. The recently invented walker shows individual binding sites. Displaying many walkers simultaneously has become such a powerful tool for investigating genetic structure that it will undoubtedly replace consensus sequences. Walkers can be used to distinguish mutations from polymorphisms, and this has clinical applications. See http://www.lecb.ncifcrf.gov/~toms/schneider.html
for further information.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Biomolecular Recognition and Binding Mechanisms
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批准号:6753236
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:JACOB V MAIZEL
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依托单位:
Protein Structure, Stability, and Amyloid Formation
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批准号:6753234
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:JACOB V MAIZEL
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依托单位:
Structural studies on b-1,4-Galactosyltransferase family
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批准号:6762178
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:JACOB V MAIZEL
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依托单位:
Method Development--Computer Vision Based Algorithms
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批准号:6753237
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:JACOB V MAIZEL
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依托单位:
Computer Analysis of Nucleic Acid Structure
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批准号:6762009
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:JACOB V MAIZEL
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依托单位:
Oligosaccharide substrate interactions with b-1,4-Galact
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批准号:6762674
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:JACOB V MAIZEL
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依托单位:
海外基金