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Using Molecular Modeling to Determine Structure and Organization in Skin Lipids

Using Molecular Modeling to Determine Structure and Organization in Skin Lipids
使用分子模型确定皮肤脂质的结构和组织
批准号:
7768598
负责人:
Clare McCabe
金额:
$21.3万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-04-01 至 2013-03-31

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中文摘要
翻译
描述(申请人提供):皮肤的功能是抵抗感染、脱水和化学攻击的屏障,对健康和生存至关重要。它的屏障作用几乎完全依赖于被称为角质层(SC)的薄的外层,角质层由嵌入在高度组织化的富含脂质的环境中的死皮细胞组成。SC脂组织成有序的凝胶或晶相可以归因于其独特的组成;SC主要由神经酰胺、游离脂肪酸和胆固醇组成,与大多数生物膜不同,不存在磷脂。越来越多的证据表明,皮肤屏障受损是皮肤病甚至一些全身性疾病(如特应性皮炎患者发生哮喘和过敏性鼻炎)的主要事件,而皮肤屏障受损与SC脂类成分、组织和结构的异常不谋而合。相比之下,SC屏障的有效性是皮肤和经皮给药的中心问题。(1)了解皮肤病、屏障功能降低和有效治疗之间的关系;(2)开发新技术以降低屏障功能(更有效地输送药物)或改善屏障(防止疾病、毒性暴露和水分流失)。对SC脂质成分和组织的实验研究是关键的,但速度很慢,只能推断脂质成分和皮肤屏障功能之间的联系。因此,我们建议使用SC脂的原子化详细模型和粗粒度模型来进行分子模拟研究,以探索脂分子的分子排列及其在片层中的自组装。这项工作将是独一无二的,因为以前没有关于SC所必需的脂质系统的分子模拟研究在文献中报道。模拟(分子动力学和蒙特卡罗)将被用来分析形成的纳米级结构和驱动自组装过程的相互作用。首先,将对简单的二元和三元脂质混合物进行模拟,以探索每一类脂质在SC中的作用。这些研究的结果将从逻辑上导致对SC模型系统的模拟,该模型SC系统包含不同的游离脂肪酸、神经酰胺和胆固醇的真实水合混合物,从实验到自组装成与SC非常相似的结构。还将探讨结构对神经酰胺、游离脂肪酸和胆固醇的脂类混合物组成和比例的敏感性。此外,还将研究包括水在内的外用制剂在SC脂类中的传输及其对脂类组织的影响。在拟议研究的所有阶段,我们将把我们的结果与我们的合作者(Neubert、Bouwstra和Wertz博士)和其他人报告的合成脂质混合物的实验数据进行比较。 与公共健康相关:对皮肤最外层角质层中的脂肪组织的了解将大大增强我们对皮肤屏障和皮肤吸收过程的了解。这项工作将使基于分子的洞察脂质组织和结构的成分依赖性,这将澄清异常的脂质组成在疾病皮肤症状中的作用,帮助开发恢复屏障功能的治疗方法,并为合理设计经皮给药系统提供所需的见解。
英文摘要
DESCRIPTION (provided by applicant): The Skin's function as a barrier to infection, dehydration and chemical assault is critical to health and survival. Its barrier effectiveness rests almost entirely in the thin, outer layer, called the stratum corneum (SC), which consists of dead skin cells embedded in a highly organized lipid-rich environment. This organization of the SC lipids into ordered gel or crystalline phases can be ascribed to its unique composition; the SC is composed of mostly ceramides, free fatty acids and cholesterol, and, in contrast with most biological membranes, no phospholipids are present. There is mounting evidence that an impaired skin barrier, which is coincidental with abnormalities in composition, organization and structure of the SC lipids, is the primary event in the pathogenesis of skin disease and even some systemic diseases (e.g., occurrence of asthma and allergic rhinitis in patients with atopic dermatits). In contrast, it is the effectiveness of the SC barrier that is the central problem for dermal and transdermal drug delivery. An improved understanding of the relationship of lipid composition to lipid organization and ultimately to transport of chemicals within the SC lipids is needed: (1) to understand the relationship between skin disease, reduced barrier function and effective treatment, and (2) to develop new techniques for either reducing barrier function (to deliver drugs more effectively) or improving it (to protect against disease, toxic exposure and water loss). Experimental investigations of SC lipid composition and organization are critical but slow, and can only infer the linkage between lipid composition and skin barrier function. Therefore, we propose to perform molecular modeling studies using both atomistically detailed and coarse-grained models of the SC lipids to probe the molecular arrangement of the lipid molecules and their self-assembly into lamellae. This work will be unique since no prior molecular modeling studies on lipid systems essential to the SC have been reported in the literature. Simulations (molecular dynamics and Monte Carlo) will be performed to analyze the nano-scale structures that are formed and the interactions that drive the self-assembly process. Initially, simulations of simple binary and ternary lipid mixtures will be conducted to probe the role of each lipid class in the SC. The results from these studies will lead logically to simulations of a model SC system containing a realistic hydrated mixture of different free fatty acids, ceramides and cholesterol that are known from experiments to self-assembles into a structure that closely resembles the SC. The sensitivity of the structures to the lipid mixture composition and ratio of ceramides, free fatty acids and cholesterol will also be probed. Transport of topical agents, including water, in the SC lipids and their effect on lipid organization will also be studied. At all stages in the proposed research we will compare our results with experimental data for synthetic lipid mixtures reported by our collaborators (Drs. Neubert, Bouwstra and Wertz) and others. PUBLIC HEALTH RELEVANCE: An improved understanding of lipid organization in the stratum corneum, the outermost layer of the skin, would greatly enhance our understanding of the skin barrier and the dermal absorption process. The work proposed will allow molecular-based insight to the compositional dependence of lipid organization and structure, which would clarify the role of abnormal lipid composition in the symptoms of diseased skin, aid development of treatments for restoring barrier function, and provide insights needed for the rational design of transdermal drug delivery systems.
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Insights into skin barrier function: In silico and experimental studies of healthy and diseased stratum corneum lipid models
  • 批准号:
    9979630
  • 项目类别:
  • 资助金额:
    $30.01万
  • 财政年份:
    2018
  • 负责人:
    Clare McCabe
  • 依托单位:
Insights into skin barrier function: In silico and experimental studies of healthy and diseased stratum corneum lipid models
  • 批准号:
    9761984
  • 项目类别:
  • 资助金额:
    $30.19万
  • 财政年份:
    2018
  • 负责人:
    Clare McCabe
  • 依托单位:
Insights into skin barrier function: In silico and experimental studies of healthy and diseased stratum corneum lipid models
  • 批准号:
    10261444
  • 项目类别:
  • 资助金额:
    $29.04万
  • 财政年份:
    2018
  • 负责人:
    Clare McCabe
  • 依托单位:
MOLECULAR MODELNG OF COMPLEX BIOLOGICAL SYSTEMS
  • 批准号:
    8364285
  • 项目类别:
  • 资助金额:
    $0.11万
  • 财政年份:
    2011
  • 负责人:
    Clare McCabe
  • 依托单位:
海外基金