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中文摘要
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描述(由申请人提供):本研究的长期目标是开发合理的方法来设计和改进穿膜的两性肽,这些肽是抗生素或细胞溶解的,或者可以将其他药物分子作为货物携带到细胞中。实现这一目标的关键知识是确定这些肽渗透膜的机制。已知这类肽具有相当大的靶特异性,这似乎源于肽与靶细胞膜脂质双分子层的相互作用,而无需蛋白质受体的干预。此外,细菌产生耐药性要困难得多,因为这需要细菌膜发生巨大变化。
英文摘要
DESCRIPTION (provided by applicant): The long-term objective of this research is the development of rational methods for the design and improvement of membrane-penetrating, amphipathic peptides that are antibiotic or cytolytic, or can carry other drug molecules as cargo into cells. Critical knowledge in reaching this objective is the determination of the mechanism of membrane penetration by these peptides. Peptides in this class are known to exhibit considerable target specificity, which appears to derive from the interaction of the peptides with the lipid bilayer of the target cell membrane without the intervention of protein receptors. Furthermore, the development of resistance by bacteria is much more difficult because it entails massive changes in the bacterial membranes. Three fundamental hypotheses relating to the mechanism of these peptides will be tested. The prediction is that specific features of the peptide sequences are necessary for peptides to penetrate cells or disrupt the membrane. Four naturally-occurring peptides were selected as the basis for new sequences that will be used to test the hypotheses. If correct, a powerful predictive program will be available to design peptides that function with a desired mechanism. Thus, the aim is to design peptides for cargo-delivery into cells or for cytolytic functions. Cargo-carrying peptides can be used to transport drugs into eukaryotic cells or antibiotics into bacterial cells. Surmounting cellular barriers, including intracellular compartments, is a major difficulty in the use of antibiotics. Furthermore, as bacteria increasingly develop resistance against conventional antibiotics, understanding the physical properties necessary for the rational design of new antibiotics that are not prone to resistance development is of the utmost importance.
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Mechanism of amphipathic and cargo-delivery peptides
Mechanisms of amphipathic and cargo delivery peptides
Mechanism of amphipathic and cargo-delivery peptides
Mechanism of Amphipathic and Cargo-Delivery Peptides
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海外基金
Segmented Filamentous Bacteria激活宿主免疫系统抑制其拮抗菌 Enterobacteriaceae维持菌群平衡及其机制研究
  • 批准号:
    81971557
  • 项目类别:
    面上项目
  • 资助金额:
    65.0万元
  • 批准年份:
    2019
  • 负责人:
    毛开睿
  • 依托单位:
电缆细菌(Cable bacteria)对水体沉积物有机污染的响应与调控机制