玻璃海鞘匍匐枝黏附的结构基础及关键蛋白组分的界面黏附机制
批准号:
42076098
项目类别:
面上项目
资助金额:
58.0 万元
负责人:
李世国
依托单位:
学科分类:
生物海洋学与海洋生物资源
结题年份:
2024
批准年份:
2020
项目状态:
已结题
项目参与者:
李世国
中文摘要
黏附是生物污损等海洋灾害事件发生的基础。海鞘是典型的污损生物,具有强烈的致灾致害特性,严重威胁全球生态系统健康和涉海行业发展。了解海鞘黏附行为对于海洋污损生物的科学防控至关重要。前期工作表明,匍匐枝是海鞘的黏附器官且蛋白组分在其黏附过程中可能发挥重要作用。基于此,本项目拟以污损生物玻璃海鞘为研究对象,紧紧围绕海鞘黏附的结构基础及关键蛋白组分的界面黏附机制这一重要科学问题,利用显微成像、组织细胞染色等技术分析匍匐枝的外部形态、内部结构和黏附界面特征,阐明玻璃海鞘黏附的结构基础;利用质谱、蛋白组、基因敲除、显微力学等技术分析匍匐枝蛋白组成及其黏附功能,筛选关键黏附蛋白组分;进而利用定点突变、结构缺失等手段,结合室内和海上黏附测试,阐明关键蛋白组分的界面黏附机制。通过多学科交叉研究,深入解析玻璃海鞘黏附行为,全面理解海洋生物黏附特征,为海洋生物污损等灾害治理提供理论支撑,兼具科学意义和应用价值。
英文摘要
Adhesion is the presupposition of marine disaster events such as biofouling. Ascidian is a kind of typical marine adhesive organisms, which possesses obvious disaster-causing characteristics, threatening the health of global marine ecosystem and the development of aquaculture and maritime industry. In-depth analysis of adhesion behavior of ascidian is crucial for controlling marine fouling organisms. Previous studies have shown that stolon was the adhesion organ of most ascidian species and proteins may play important roles in stolon adhesion. Based on these results, this research proposal plans to take the fouling ascidian Ciona robusta as the research animal to study the adhesion structure of this species and the interface adhesion mechanisms mediated by key adhesive proteins. Various electron microscopes and cell staining methods will be used to study the morphology, ultrastructure and interface adhesion of stolon, clarifying the structure features of stolon adhesion. Mass spectrometry, proteomics and gene knockout approaches will be employed to study stolon protein compositions and their adhesion functions, identifying key adhesive proteins from this organ. The mechanisms of protein interface adhesion will also be studied by the methods of site-directed mutation, domain deletion, mechanical performance analysis and field adhesion test. Through the interdisciplinary study, this research proposal attempts to deeply clarify the adhesion behavior of C. robusta and comprehensively understand the essential characteristics of marine bioadhesion, which will provide a theoretical support for preventing marine biofouling as well as other marine ecological disasters, unitizing both scientific significance and application value.
本项目在前期研究的基础上,以代表性海洋污损生物玻璃海鞘为研究对象,利用分子生物学、生物化学、力学、材料科学和表面科学等多种技术手段,分析了该物种匍匐枝的外部形态特征、内部显微结构、黏附界面和黏着斑特征,阐明了玻璃海鞘黏附的结构基础。分析了玻璃海鞘匍匐枝、黏着斑和不同发育阶段的蛋白组成差异,从中筛选出6种与海鞘黏附密切相关的候选蛋白组分。体外重组表达并纯化了这些蛋白,而后分析了它们其在匍匐枝等不同组织器官中的功能定位,分析了重组蛋白对不同材料表面的黏附性能,从而获得了2个对玻璃海鞘水下黏附最为关键的蛋白组分;分析了这2个关键黏附蛋白的序列结构特征及其与基质材料表面之间的相互作用关系,分析了钙离子在其中的作用模式,并最终揭示了这2种蛋白的界面黏附机制和内聚作用机制。此外,开展了玻璃海鞘在不同材料表面黏附的海上现场测试,对上述得出的界面黏附机制进行了验证。这些多科学交叉研究回答了该研究领域存在的关键科学问题。研究结果有助于深入理解海洋生物黏附的共性和个性特征,为海洋生物污损等生态灾害治理提供理论支撑,也可以为环境友好型高性能水下黏附材料研发提供理论参考,兼具科学意义和实际应用价值。
TRPA1通道介导污损生物玻璃海鞘幼虫乳突黏附的分子调控机制研究
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批准号:--
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项目类别:面上项目
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资助金额:56万元
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批准年份:2022
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负责人:李世国
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依托单位:
国内基金
海外基金