Fatty Acid Specificity in the DHHC Family of S-Acyltransferases: From Mechanisms to Functional Outcomes
Fatty Acid Specificity in the DHHC Family of S-Acyltransferases: From Mechanisms to Functional Outcomes
批准号:
BB/L022087/1
负责人:
Luke Chamberlain
金额:
$58.72万
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2014
资助国家:
英国
项目状态:
已结题
起止时间:
2014 至 --
中文摘要
我们体内的细胞包含一系列不同的蛋白质,它们协调和驱动特定的途径,如细胞的生长和分裂。这些蛋白质受到严格的调节模式,以确保它们能够在需要时执行特定的功能。蛋白质调节的一个重要机制是通过化学修饰,在蛋白质中加入各种不同的分子来影响它们的活性。一种受到越来越多人关注的修饰是“S-酰化”,即脂肪酸与蛋白质的结合,它由24种“二氢六氢环己烷”酶家族催化。DHHC酶的功能障碍与许多重要的疾病有关,包括糖尿病、亨廷顿病、精神分裂症、智力障碍和癌症。添加到S酰化蛋白质中的脂肪酸可以是多样化的,不同的脂肪酸很可能以不同的方式影响蛋白质。尽管如此,我们目前对添加到单个S酰化蛋白质中的脂肪酸的化学同一性以及脂肪酸同一性如何影响蛋白质功能的机制知之甚少。因此,本研究的目的是促进S这一鲜为人知的方面的重大进展-酰化。为此,我们召集了化学和生物学方面的专家,目的是使用新型化学探针来确定:(A)不同的二六六六酶是否会优先向S酰化的蛋白质添加不同类型的脂肪酸;(B)二氢六氢碳酸酯酶的哪些特性是其脂肪酸专一性的基础;以及(C)不同的脂肪酸如何影响蛋白质在细胞不同区域的定位及其在特定细胞途径中的功能。除了揭示细胞生物学中一个重要但知之甚少的方面外,这项研究还可能突出设计DHHC酶的选择性调节剂以治疗一系列临床疾病的新策略。
英文摘要
The cells in our body contain a diverse array of different proteins that coordinate and drive specific pathways, such as cell growth and division. These proteins are subjected to strict modes of regulation to ensure that they are able to perform their specific functions as and when required. One prominent mechanism of protein regulation is via chemical modification and a variety of different molecules are added to proteins that affect their activity. One modification that is receiving increasing interest is "S-acylation", the attachment of fatty acids onto proteins, which is catalysed by a family of twenty-four "DHHC" enzymes. Dysfunction of DHHC enzymes has been linked with many important disorders, including diabetes, Huntington's disease, schizophrenia, intellectual disability and cancer.The fatty acids that are added to S-acylated proteins can be diverse and it is likely that different fatty acids affect proteins in different ways. Despite this, we currently know very little about the mechanisms that specify the chemical identity of fatty acids added to individual S-acylated proteins, and how fatty acid identity impacts protein function. Therefore the aim of this research is to promote a major advance in this poorly understood aspect of S-acylation. To do this, we have brought together experts in Chemistry and Biology with the goal of using novel chemical probes to determine: (a) if different DHHC enzymes preferentially add distinct types of fatty acids onto S-acylated proteins, (b) what features of DHHC enzymes underlie their fatty acid specificity, and (c) how different fatty acids affect the localisation of proteins to different regions of the cell and their function in specific cellular pathways. In addition to shedding light on an important but poorly understood aspect of cell biology, this research may also highlight new strategies to design selective modulators of DHHC enzymes to treat a range of clinical conditions.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
DOI:
10.1242/jcs.249664
发表时间:
2020-11-05
期刊:
Journal of cell science
影响因子:
4
作者:
[Locatelli C, Lemonidis K, Salaun C, Tomkinson NCO, Chamberlain LH]
通讯作者:
Chamberlain LH
DOI:
10.1016/j.mcn.2017.07.007
发表时间:
2017-12
期刊:
Molecular and cellular neurosciences
影响因子:
--
作者:
[Salaun C, Ritchie L, Greaves J, Bushell TJ, Chamberlain LH]
通讯作者:
Chamberlain LH
DOI:
10.1016/j.saa.2018.01.064
发表时间:
2018-05-15
期刊:
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
影响因子:
--
作者:
[Jamieson LE, Greaves J, McLellan JA, Munro KR, Tomkinson NCO, Chamberlain LH, Faulds K, Graham D]
通讯作者:
Graham D
DOI:
10.1038/s41598-017-00036-8
发表时间:
2017-01-31
期刊:
Scientific reports
影响因子:
4.6
作者:
[Diez-Ardanuy C, Greaves J, Munro KR, Tomkinson NC, Chamberlain LH]
通讯作者:
Chamberlain LH
DOI:
10.1016/j.jbc.2022.102754
发表时间:
2023-01
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
[Butler L, Locatelli C, Allagioti D, Lousa I, Lemonidis K, Tomkinson NCO, Salaun C, Chamberlain LH]
通讯作者:
Chamberlain LH
共 8 条
S-Acylation of transmembrane proteins in the early secretory pathway
-
批准号:BB/X001504/1
-
项目类别:Research Grant
-
资助金额:$56.2万
-
财政年份:2023
-
负责人:Luke Chamberlain
-
依托单位:
Analysis of the substrate network and neurodevelopmental functions of the intellectual disability enzyme, zDHHC9
-
批准号:MR/S011080/1
-
项目类别:Research Grant
-
资助金额:$60.16万
-
财政年份:2019
-
负责人:Luke Chamberlain
-
依托单位:
ANALYSIS OF ZDHHC17 INTERACTION NETWORKS AND PROTEIN INTERACTIONS LINKED TO NEURODEGENERATION
-
批准号:MR/R011842/1
-
项目类别:Research Grant
-
资助金额:$51.7万
-
财政年份:2018
-
负责人:Luke Chamberlain
-
依托单位:
Molecular dissection of DHHC protein targeting and its importance for post-synaptic palmitoylation dynamics
-
批准号:BB/J006432/1
-
项目类别:Research Grant
-
资助金额:$49.63万
-
财政年份:2012
-
负责人:Luke Chamberlain
-
依托单位:
Palmitoylation of Exocytic Proteins: Role in Membrane Compartmentalization, Intracellular Trafficking, and Function
-
批准号:G0601597/2
-
项目类别:Fellowship
-
资助金额:$72.88万
-
财政年份:2011
-
负责人:Luke Chamberlain
-
依托单位:
Palmitoylation of Exocytic Proteins: Role in Membrane Compartmentalization, Intracellular Trafficking, and Function
-
批准号:G0601597/1
-
项目类别:Fellowship
-
资助金额:$208.13万
-
财政年份:2007
-
负责人:Luke Chamberlain
-
依托单位:
国内基金
海外基金
登录
查看更多内容
棕榈酸Palmitic acid通过靶向JAK-STAT通路促进致病性Th17细胞分化在儿童性系统性红斑狼疮中的作用及机制研究
-
批准号:2026JJ81716
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:唐金玲
-
依托单位:
基于F/IGF1R/PKC ζ 通路研究夏枯草中
Mesonolic acid B抑制RSV感染性肺炎的
作用机制
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2025
-
负责人:唐维
-
依托单位:
Quinic acid通过抑制肠道菌群代谢产物脱氧胆酸调节巨噬细胞M1向M2极化改善动脉粥样硬化的机制研究
-
批准号:2025JJ80556
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:吴鹏翠
-
依托单位:
巨噬细胞来源代谢物suberic acid抑制蜕膜早衰防治早产的作用机制研究
-
批准号:--
-
项目类别:青年科学基金项目
-
资助金额:--
-
批准年份:2024
-
负责人:梅又文
-
依托单位:
色氨酸代谢产物Kynurenic Acid在脓毒症肠损伤中的诊断价值及其机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:5.0万元
-
批准年份:2024
-
负责人:陈慧
-
依托单位:
石榴皮活性成分Ellagic acid调控脂肪酸代谢重编程抑制NASH相关肝癌发生的作用机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2022
-
负责人:
-
依托单位:
具有抗耐药甲氧西林金黄色葡萄球菌活性天然产物quiannulatic acid的分子作用机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:55万元
-
批准年份:2022
-
负责人:韩晓乐
-
依托单位:
丹参红花药对活性组分 Salvianolic acid B-Hydrosafflow yellow A 调控Piezo1-YAP/TAZ-JNK 调节动脉粥样硬化炎症反应机制的研究
-
批准号:LQ22H290004
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2021
-
负责人:张春晓
-
依托单位:
DPA(docosapentaenoic acid, 22:5n-3)对溃疡性结肠炎小鼠肠道菌群影响及特异性菌群筛选的研究
-
批准号:LQ22C200008
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2021
-
负责人:郑振霄
-
依托单位:
木霉菌抗真菌物质Harzianic Acid的合成机制及其应用研究
-
批准号:32072674
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:张建
-
依托单位: