CAREER: Lipid Mass Tags Designed Via Selective Dissociation
CAREER: Lipid Mass Tags Designed Via Selective Dissociation
批准号:
2145487
负责人:
Xin Yan
金额:
$62.5万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-02-01 至 2027-01-31
中文摘要
在化学系化学测量和成像项目的支持下,Xin Yan和她在德克萨斯A M大学的团队正在努力开发使用质谱法表征不饱和脂质(脂肪酸/酯)的新方法。生物系统中脂质物质浓度的变化发生在生理过程的扰动之后,因此了解脂质的结构和浓度对于阐明它们在生理和病理过程中的作用至关重要。Yan博士和她的团队正在开发一种方法,可以在一个实验中准确定量多种不饱和脂质(包括难以检测的非极性脂质)。该综合教育计划旨在通过扩大化学教育和化学测量研究的机会来扩大科学影响,包括有趣实验的现场演示,学生参与化学开放日,并为本科生提供研究机会。通过异构体分辨率准确定量脂质混合物一直是一个长期的挑战。为了应对这一挑战,一组同量异序脂质质量标签(LMT)被设计为选择性地与脂质双键反应。通过设计和调整LMT化学,用于确定双键异构体的诊断离子在低能量碰撞诱导解离中选择性地产生。对应于来自不同样品的脂质的带电质量报告物在较高能量解离时释放,从而能够在单次运行中准确定量来自多重样品的脂质。在单次运行中将来自两个串联MS实验的信息组合使得能够定量和鉴定不饱和脂质异构体。LMT的发展将促进未来的调查脂质结构/功能的关系。教育计划的更广泛影响包括促进各级学生对化学教育和化学测量研究的兴趣并扩大其获得机会。通过现场演示传播科学旨在激励初中/高中学生在早期阶段欣赏科学。提供积极参与实验被认为是一个很好的,动手的方法,鼓励学生考虑追求职业生涯在干(科学,技术,工程和数学)相关领域。创新X计划和研究培训有望为本科生和研究生提供使用先进分析技术的机会,并为未解决的化学测量问题开发新的策略。该奖项反映了NSF的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。
英文摘要
With support from the Chemical Measurement and Imaging program in the Division of Chemistry, Xin Yan and her group at Texas A&M University are working to develop novel approaches to characterizing unsaturated lipids (fatty acids/esters) using mass spectrometry. Changes in the concentrations of lipid species in biological systems occur after perturbation by physiological processes, hence knowing the structures and concentrations of lipids is essential to elucidate their roles in physiological and pathological processes. Dr. Yan and her group are developing approaches to allow accurate quantification of multiple unsaturated lipids (including difficult-to-detect non-polar lipids) in a single experiment. The integrated educational plan seeks to amplify the scientific impact by broadening access to chemical education and chemical measurement research including live demos of fun experiments, engagement of students in chemistry open houses, and providing research opportunities for undergraduates.Accurate quantification of a lipid mixture with isomeric resolution has been a long-standing challenge. To address this challenge, a set of isobaric lipid mass tags (LMTs) is being designed to react selectively with lipid double bonds. By designing and tuning the LMT chemistry, diagnostic ions for determining double bond isomers are selectively produced in low energy collision-induced dissociation. Charged mass reporters corresponding to lipids from different samples are released upon higher energy dissociation, thereby enabling accurate quantitation of lipids from multiplexed samples in a single run. The combination of information from the two tandem MS experiments in a single run enables the quantification and identification of unsaturated lipid isomers. Development of LMTs will facilitate future investigations into lipid structure/function relationships. Broader impacts of the educational plan include promoting interest in and broadening access to chemical education and chemical measurement research for all levels of students. Disseminating science through live demos seeks to motivate middle/high school students to appreciate science at an early stage. Providing active engagement in experiments is seen as a good, hands-on approach to encouraging students to consider pursuing careers in STEM (Science, Technology, Engineering and Mathematics)-related fields. The innovation X program and research training are expected to provide undergraduate and graduate students with opportunities to work with advanced analytical technologies and develop new strategies for unsolved chemical measurement problems.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
Lipid Mass Tags via Aziridination for Probing Unsaturated Lipid Isomers and Accurate Relative Quantification**
通过氮丙啶化的脂质质量标签用于探测不饱和脂质异构体和准确的相对定量**
DOI:
10.1002/anie.202207098
发表时间:
2022
期刊:
Angewandte Chemie International Edition
影响因子:
--
作者:
[Yang, Tingyuan, Tang, Shuli, Kuo, Syuan‐Ting, Freitas, Dallas, Edwards, Madison, Wang, Hongying, Sun, Yuxiang, Yan, Xin]
通讯作者:
Yan, Xin
国内基金
海外基金
登录
查看更多内容
新肿瘤靶标 DHCR24/Lipid-Rafts 轴在急性髓系白血病中的作用和分子机制研究
-
批准号:LQ22H080007
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2021
-
负责人:吴照星
-
依托单位:
4-胺基阿拉伯糖基修饰的活性寡糖分子lipid A及衍生物的合成研究
-
批准号:22007080
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2020
-
负责人:朱玉根
-
依托单位:
CRISPR/Cas9基因编辑 PLGA/Lipid纳米可视递送系统靶向治疗骨关节炎的作用机制研究
-
批准号:2020A151501615
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2020
-
负责人:于博
-
依托单位:
CRISPR/Cas9基因编辑PLGA/Lipid纳米可视递送系统靶向治疗骨关节炎的作用机制研究
-
批准号:81974323
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:于博
-
依托单位:
超声示踪载药PLGA/Lipid复合纳泡修饰的BMSCs及其调控修复骨质疏松性骨损伤的研究
-
批准号:81871355
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2018
-
负责人:陈彦
-
依托单位:
可穿透胰腺癌双重屏障的肿瘤微环境响应型多级HSA/lipid纳米递药系统研究
-
批准号:81703010
-
项目类别:青年科学基金项目
-
资助金额:20.0万元
-
批准年份:2017
-
负责人:魏彦
-
依托单位:
革兰阴性菌中合成Kdo2-Lipid A的蛋白质反应机理研究及抑制剂筛选
-
批准号:31370731
-
项目类别:面上项目
-
资助金额:82.0万元
-
批准年份:2013
-
负责人:姚闵
-
依托单位:
以lipid A 为靶点的黄连解毒汤抗内毒素的物质基础及作用机制研究
-
批准号:81303205
-
项目类别:青年科学基金项目
-
资助金额:23.0万元
-
批准年份:2013
-
负责人:陈桂荣
-
依托单位:
lipid raft/caveolae调节PMVECs接触性抑制在肝肺综合症肺微血管扩张中的作用和机制研究
-
批准号:81270510
-
项目类别:面上项目
-
资助金额:65.0万元
-
批准年份:2012
-
负责人:鲁开智
-
依托单位:
Lipid rafts调控干燥综合征唾液腺上皮细胞凋亡信号的分子机制
-
批准号:30671948
-
项目类别:面上项目
-
资助金额:27.0万元
-
批准年份:2006
-
负责人:李萍
-
依托单位: