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Understanding Molecular Driving Forces to Tailor Macromolecular Materials with Dual-Thermoresponsive Behavior

Understanding Molecular Driving Forces to Tailor Macromolecular Materials with Dual-Thermoresponsive Behavior
了解分子驱动力以定制具有双热响应行为的高分子材料
批准号:
1703402
负责人:
Arthi Jayaraman
金额:
$39.68万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-01 至 2021-03-31

项目摘要

项目成果

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中文摘要
翻译
热响应分子在传感器、电子、致动器、药物输送装置和组织工程基质中有着重要的应用。合成热响应聚合物,如聚n-异丙基丙烯酰胺(PNIPAAM))和生物热响应大分子,如弹性蛋白样多肽(ELPs),已经得到了广泛的研究。这些热响应聚合物的各种分子水平设计方面,例如分子组成,序列,分子量,浓度等,提供了调整其热响应行为的相变(例如较低的临界溶液温度或LCST)的方法。此外,这些热响应性聚合物与其他聚合物或衬底的共轭不仅以一种重要的方式改变了它们的LCST相变,而且由于与两种聚合物相关的双重热转变,也为操纵纳米结构的组装和拆卸提供了便利。然而,到目前为止,还缺乏一套通用的指导方针来预测这些聚合物的分子设计及其共轭物如何影响分子水平的相互作用或驱动热力学相变的物理化学性质。本研究的总体目标是捕获一类重要的热响应聚合物中控制LCST转变的分子相互作用,并利用基本的理解来设计具有两个单独可调热转变的热响应偶联物。该项目将采用elp作为模型系统,因为这些分子与其他热敏材料相比,可以对疏水性和分子量(以及由此产生的转变温度)进行精细调节。一个关键的创新是将相关肽结构域引入ELP (ELP- cxps),以便在ELP- cxp中预关联短ELP(可计算处理),将ELP lcst样转变驱动到实验可达的温度范围内。热响应型ELP块的坍塌随后驱动水溶液中预相关ELP- cxp的相分离。由于缔合块(CXP)的展开,所得到的结构也将在更高的温度下经历额外的分解转变。CXP和ELP区块的长度和组成都可以改变,以产生定制的过渡和组装/拆卸;具体的设计特点将被告知发展的计算方法。ELP- cxp缀合物的模块化设计和精确组成不仅提供了通过未报道的方法调节ELP结构域的转变温度的策略,而且还提供了操纵纳米结构的组装和拆卸的策略,这在纳米复合材料、纳米尺度模板和药物递送中有多种应用。重要的是,由于CXP结构域的存在,这些材料将能够与肽修饰的分子和纳米颗粒进一步细化,扩大了纳米技术应用中共轭物的多功能性。该研究的跨学科性质将丰富研究生和本科生的培养。建议开展外联活动,目的是征聘和留住科学和工程职业中的女性和代表性不足的少数民族研究人员。
英文摘要
1703402PI: Jayaraman, Arthi Institution: University of DelawareThermoresponsive molecules find important applications in sensors, electronics, actuators, drug delivery devices, and matrices for tissue engineering. Synthetic thermoresponsive polymers, such as poly(N-isopropyl acrylamide (PNIPAAM)), and biological thermoresponsive macromolecules, such as elastin-like polypeptides (ELPs), have been extensively studied. Various molecular-level design aspects of these thermoresponsive polymers, e.g., molecular composition, sequence, molecular weights, concentration, etc., provide ways to tune the phase transition (e.g. lower critical solution temperature or LCST) underlying their thermoresponsive behavior. Furthermore, conjugation of these thermoresponsive polymers to other polymers or substrates not only alters their LCST phase transition in a non-trivial manner but also facilitates ways to manipulate assembly and disassembly of nanostructures, by virtue of the dual thermal transitions associated with the two polymers. As of yet, however, there lacks a set of universal guidelines to predict how the molecular design of these polymers and their conjugates affect molecular-level interactions or physicochemical properties driving the thermodynamic phase transitions. The overarching goal of the proposed research is to capture the molecular interactions governing LCST transitions in an important class of thermoresponsive polymers, and to use the fundamental understanding to design thermoresponsive conjugates with two separately tunable thermal transitions. The project will employ ELPs as the model system owing to the finely tuned control of hydrophobicity and molecular weight (and consequently transition temperatures) that is possible with these molecules versus other thermoresponsive materials. A key innovation is the introduction of associating peptide domains to the ELPs (ELP-CXPs) so that pre-association of short ELPs (that are computationally tractable) in the ELP-CXP drives the ELP LCST-like transition into an experimentally accessible temperature range. The collapse of the thermoresponsive ELP block subsequently drives phase separation of the pre-associated ELP-CXPs in aqueous solution. The resulting structures will also undergo an additional disassembly transition at even higher temperatures owing to the unfolding of the associating block (CXP). Both the lengths and compositions of the CXP and ELP blocks can be altered to yield tailored transitions and assembly/disassembly; specific design features will be informed by the development of the computational methods. The modular design and precise composition of the ELP-CXP conjugates offers strategies not only to modulate the transition temperature of the ELP domain via unreported methods, but also to manipulate assembly and disassembly of nanostructures, which has multiple applications in nanocomposites, nanoscale templating, and drug delivery. Importantly, owing to the presence of the CXP domain, these materials will be competent for further elaboration with peptide-modified molecules and nanoparticles, expanding the versatility of the conjugates in nanotechnology applications. The interdisciplinary nature of the research will enrich the training of graduate and undergraduate students. Outreach activities are proposed aimed at recruitment and retention of female and underrepresented minority researchers in science and engineering careers.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1126/sciadv.abd3033
发表时间: 2020-10
期刊: Science advances
影响因子: 13.6
作者: [Qin J, Sloppy JD, Kiick KL]
通讯作者: Kiick KL
Collagen-Peptide-Based Drug Delivery Strategies
基于胶原蛋白肽的药物递送策略
DOI: 10.21300/21.4.2020.9
发表时间: 2020
期刊: Technology & Innovation
影响因子: 0.5
作者: [Jayaraman, Arthi, Price, Christopher, Sullivan, Millicent O., Kiick, Kristi L.]
通讯作者: Kiick, Kristi L.
DOI: 10.1039/d0sm01562h
发表时间: 2021-02-21
期刊: Soft matter
影响因子: 3.4
作者: [Hilderbrand AM, Taylor PA, Stanzione F, LaRue M, Guo C, Jayaraman A, Kloxin AM]
通讯作者: Kloxin AM
DOI: 10.1021/acs.jpcb.7b10916
发表时间: 2018-02-15
期刊: JOURNAL OF PHYSICAL CHEMISTRY B
影响因子: 3.3
作者: [Condon, Joshua E., Jayaraman, Arthi]
通讯作者: Jayaraman, Arthi
Development of Coarse-Grained Models and Computational Approaches for Studying Structure in Solutions of Cellulose Derivatives
  • 批准号:
    2105744
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $38.1万
  • 财政年份:
    2021
  • 负责人:
    Arthi Jayaraman
  • 依托单位:
NRT- HDR: Computing and Data Science Training for Materials Innovation, Discovery, Analytics
  • 批准号:
    2125703
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $299.9万
  • 财政年份:
    2021
  • 负责人:
    Arthi Jayaraman
  • 依托单位:
Reverse engineering methods for elucidating the molecular assembly mechanisms of thermoresponsive peptide-based conjugates: computation and experiment
  • 批准号:
    2023668
  • 项目类别:
    Standard Grant
  • 资助金额:
    $51.85万
  • 财政年份:
    2020
  • 负责人:
    Arthi Jayaraman
  • 依托单位:
DMREF/Collaborative Research: Conductive Protein Nanowires as Next Generation Polymer Nanocomposite Fillers
  • 批准号:
    1921871
  • 项目类别:
    Standard Grant
  • 资助金额:
    $31.52万
  • 财政年份:
    2019
  • 负责人:
    Arthi Jayaraman
  • 依托单位:
国内基金
海外基金
Kidney injury molecular(KIM-1)介导肾小管上皮细胞自噬在糖尿病肾病肾间质纤维化中的作用
  • 批准号:
    81300605
  • 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:
    唐琳
  • 依托单位:
Molecular Plant
Molecular Interaction Reconstruction of Rheumatoid Arthritis Therapies Using Clinical Data
Molecular Plant