活性肽进入微米范围的细胞是其发挥功效的关键步骤之一。利用"金属离子具有控制多肽空间结构的能力"诱导活性肽形成的纳米颗粒会表现出良好的表观效应,同时基于前期研究发现带鱼酶解物中有与铁离子高亲力的活性肽，本项目进一步以带鱼活性肽为基质，提出同位素59Fe(Ⅱ)诱导带鱼活性肽自组装成"放射状结构模型" 纳米带鱼铁肽假说，从59Fe(Ⅱ)疏水核心结构设计出发，提出59Fe(Ⅱ)诱导带鱼酶解肽成放射状自组装微粒，该微粒通过纳米孔道的空间限域效应实现了带鱼肽/铁离子稳定化。同时利用γ示踪技术结合计算机模拟研究放射性59Fe(Ⅱ)标记的纳米自组装多肽在菌体内的富集及抗菌机制。围绕"金属定向诱导-纳米自组装-微粒稳定性-示踪生物活性"展开探索，验证并完善"放射状结构模型"微粒形成机理假说。通过研究深入认识纳米59Fe(Ⅱ)带鱼肽微粒的形成机理及生物学机制，为其在新功能食品领域的研发提供理论依据。

Size conversion is a pivotal step of bioactive peptide migration into the micron range of cells. Uses the principle，that metal ion having the ability to control the spatial structure of a polypeptide，induced nanoparticles from peptides will exhibit good apparent effect. Based on the research result of previous NSFC subject that hairtail hydrolysates has a kind of active peptide which has high affinity with iron ion. The project for the matrix according to the hairtail active peptide. The hypotheses are coming out that isotope 59Fe (Ⅱ) induces active peptides self-assemble into a " radial structure model ". From 59Fe (Ⅱ) hydrophobic core structure design , this paper proposes 59Fe (Ⅱ) -induced hairtail enzymatic peptides self-assemble into radially particles , the nano particles through the pore space confinement effect achieved the stabilized --peptide and iron ions. While study the antibacterial mechanisms of 59Fe (Ⅱ) -labeled nano-peptide using γ tracer techniques combined with computer simulation of radioactive. Around " metal oriented induction - nano-assembly - particulate stability - tracing biological activity ", validating and improving the formation mechanism hypothesis of" radial structure model " particle. Providing basis for its application in the field of new functional foods.