The molecular basis of action of the toxin Microcin B17 on DNA gyrase
The molecular basis of action of the toxin Microcin B17 on DNA gyrase
批准号:
BB/J016853/1
负责人:
Anthony Maxwell
金额:
$61.29万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2012
资助国家:
英国
项目状态:
已结题
起止时间:
2012 至 --
中文摘要
我们正面临传染病危机的危险。耐多药细菌感染的综合影响,如MRSA和艰难梭菌,以及制药公司生产的新抗生素的缺乏,意味着学术实验室需要为解决这一问题做出更大的贡献。我们正在研究一种来自细菌的酶,叫做DNA回转酶,它已经成为抗生素的目标,比如环丙沙星(ciprolo沙星),这种药物在2001年美国恐慌期间用于对抗炭疽。不幸的是,由于耐药性问题,环丙沙星不再像以前那样有效,人们正在寻找替代它的抗生素。Microcin B17是一种由细菌产生的毒素,用于杀死其他细菌,它的工作方式与环丙沙星类似,但不太可能受到同样的耐药性问题的影响。我们的目标是了解Microcin B17如何工作的分子细节,以便这些信息可以用于未来设计可能取代环丙环的新抗生素。
英文摘要
We are in danger of heading for a crisis in infectious diseases. The combined effects of multi-drug-resistant bacterial infections, such as MRSA and C. difficile, and the lack of new antibiotics being produced by pharmaceutical companies, means that academic labs need to make a more significant contribution to solving this problem. We are studying an enzyme from bacteria called DNA gyrase, which is already the target for antibiotics such as Cipro (ciprofloxacin), the drug used to combat anthrax during the scare in the USA in 2001. Unfortunately, due to resistance problems, Cipro is no longer as effective as it was and the search is on for antibiotics to replace it. Microcin B17 is a toxin produced by bacteria to kill other bacteria, and it works in a manner similar to Cipro but is unlikely to be affected by the same resistance problems. We aim to understand the molecular details of how Microcin B17 works such that this information can be used in the future design of new antibiotics that can potentially replace Cipro.
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Synthesis of full length and truncated microcin B17 analogues as DNA gyrase poisons.
作为 DNA 旋转酶毒物的全长和截短的小菌素 B17 类似物的合成。
DOI:
10.1039/c3ob42516a
发表时间:
2014
期刊:
Organic & biomolecular chemistry
影响因子:
3.2
作者:
[Thompson RE]
通讯作者:
Thompson RE
DOI:
10.1016/j.cell.2018.04.037
发表时间:
2018-05-17
期刊:
Cell
影响因子:
64.5
作者:
[Iyer SS, Gensollen T, Gandhi A, Oh SF, Neves JF, Collin F, Lavin R, Serra C, Glickman J, de Silva PSA, Sartor RB, Besra G, Hauser R, Maxwell A, Llebaria A, Blumberg RS]
通讯作者:
Blumberg RS
DOI:
10.1371/journal.pone.0061459
发表时间:
2013
期刊:
PloS one
影响因子:
3.7
作者:
[Collin F, Thompson RE, Jolliffe KA, Payne RJ, Maxwell A]
通讯作者:
Maxwell A
DOI:
10.1016/j.str.2017.08.006
发表时间:
2017-10-03
期刊:
Structure (London, England : 1993)
影响因子:
--
作者:
[Ghilarov D, Serebryakova M, Stevenson CEM, Hearnshaw SJ, Volkov DS, Maxwell A, Lawson DM, Severinov K]
通讯作者:
Severinov K
Exploring novel binding pockets in DNA gyrase and DNA topoisomerase IV to address antibiotic resistance
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批准号:BB/V006983/1
-
项目类别:Research Grant
-
资助金额:$64.25万
-
财政年份:2021
-
负责人:Anthony Maxwell
-
依托单位:
Tackling tricky twists - how does DNA gyrase function inside living cells?
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项目类别:Research Grant
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资助金额:$10.07万
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财政年份:2017
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负责人:Anthony Maxwell
-
依托单位:
Understanding supercoiling-dependent DNA recognition: a combined experimental and computational approach
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财政年份:2012
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财政年份:2007
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依托单位:
TB方法在有机和生物大分子体系计算研究中的应用
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项目类别:面上项目
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