The single polypeptide type I restriction enzymes - minimal multifunctional molecular motors
The single polypeptide type I restriction enzymes - minimal multifunctional molecular motors
批准号:
BB/D009715/1
负责人:
Mark Dominik Szczelkun
金额:
$25.76万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2006
资助国家:
英国
项目状态:
已结题
起止时间:
2006 至 --
中文摘要
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英文摘要
To make life more straightforward, Mankind has developed machines to undertake complex tasks. But Nature got there first; life on Earth is reliant on the action of microscopic machines and motors made not from metal gears and cogs but from proteins. Miniaturised factories are working in your body right now! Take for example your genetic material, DNA. There are a great many 'molecular motor enzymes' whose task is to recognise a specific part of the DNA (a sequence made up of chemical bases called A, G, C and T) and then to convert chemical energy (in the form of a fuel compound called ATP) into mechanical events. For example, the proteins we study move along DNA many thousands of bases at a time, much like a train along a track. Once these motors reach a defined point in the DNA they stop and cut the track using an additional enzyme activity. Whilst this may seem a destructive event for the motor, it is vital to the health of the cell because these cuts are not made in the host genome but are targeted to invading viral DNA. A remarkable feature of the enzymes we wish to study is that all this complexity is contained within a single protein, a bit like a mobile phone which is also a camera, a games console and an MP3 player. How can all the multiple enzyme activities be contained in one protein unit and how are the activities coordinated so that the motor can move along DNA in a controlled fashion? This is what we intend to find out.
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DOI:
10.1093/nar/gks1209
发表时间:
2013-01
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Šišáková E, van Aelst K, Diffin FM, Szczelkun MD]
通讯作者:
Szczelkun MD
DOI:
10.1093/nar/gkp794
发表时间:
2009-11
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Smith RM, Josephsen J, Szczelkun MD]
通讯作者:
Szczelkun MD
DOI:
10.1093/nar/gkw154
发表时间:
2016-05-19
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Kulkarni M, Nirwan N, van Aelst K, Szczelkun MD, Saikrishnan K]
通讯作者:
Saikrishnan K
DNA cleavage by Type ISP Restriction-Modification enzymes is initially targeted to the 3'-5' strand.
DOI:
10.1093/nar/gks1210
发表时间:
2013-01
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[van Aelst K, Šišáková E, Szczelkun MD]
通讯作者:
Szczelkun MD
DOI:
10.1093/nar/gkp795
发表时间:
2009-11
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Smith RM, Josephsen J, Szczelkun MD]
通讯作者:
Szczelkun MD
共 7 条
Visual biochemistry of protein-nucleic acid interactions using a multi-user single-molecule optical trapping fluorescence microscope.
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批准号:BB/W019337/1
-
项目类别:Research Grant
-
资助金额:$82.59万
-
财政年份:2022
-
负责人:Mark Dominik Szczelkun
-
依托单位:
A mechanistic framework for DNA recognition and cleavage by Type V CRISPR-Cas effector nucleases
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批准号:BB/S001239/1
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项目类别:Research Grant
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资助金额:$60.99万
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财政年份:2019
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负责人:Mark Dominik Szczelkun
-
依托单位:
Understanding the pathways to R-loop formation by CRISPR/Cas immunity endonucleases
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批准号:BB/L000873/1
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项目类别:Research Grant
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资助金额:$43.23万
-
财政年份:2014
-
负责人:Mark Dominik Szczelkun
-
依托单位:
国内基金
海外基金
多肽树状物为载体的抗癌前体药物的合成和研究
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批准号:81072530
-
项目类别:面上项目
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资助金额:36.0万元
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批准年份:2010
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负责人:刘河
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依托单位: