Cornwell Susannah Emily, Okocha Sarah Ogechukwu, Ferrari Enrico
Department of Life Sciences, University of Lincoln, Lincolnshire, Lincoln LN6 7TS, UK.
Nanomaterials (Basel). 2023 Nov 4;13(21):2901. doi: 10.3390/nano13212901.
When nanoparticles are introduced into the bloodstream, plasma proteins accumulate at their surface, forming a protein corona. This corona affects the properties of intravenously administered nanomedicines. The firmly bound layer of plasma proteins in direct contact with the nanomaterial is called the "hard corona". There is also a "soft corona" of loosely associated proteins. While the hard corona has been extensively studied, the soft corona is less understood due to its inaccessibility to analytical techniques. Our study used dynamic light scattering to determine the dissociation constant and thickness of the protein corona formed in solutions of silica or gold nanoparticles mixed with serum albumin, transferrin or prothrombin. Multivariate analysis showed that the nanoparticle material had a greater impact on binding properties than the protein type. Serum albumin had a distinct binding pattern compared to the other proteins tested. This pilot study provides a blueprint for future investigations into the complexity of the soft protein corona, which is key to developing nanomedicines.
当纳米颗粒被引入血液中时,血浆蛋白会在其表面聚集,形成蛋白质冠层。这种冠层会影响静脉注射纳米药物的性质。与纳米材料直接接触的紧密结合的血浆蛋白层被称为“硬冠层”。还存在由松散结合的蛋白质组成的“软冠层”。虽然硬冠层已得到广泛研究,但由于分析技术难以触及,软冠层的情况则了解较少。我们的研究使用动态光散射来确定在与血清白蛋白、转铁蛋白或凝血酶原混合的二氧化硅或金纳米颗粒溶液中形成的蛋白质冠层的解离常数和厚度。多变量分析表明,纳米颗粒材料对结合特性的影响比蛋白质类型更大。与其他测试蛋白质相比,血清白蛋白具有独特的结合模式。这项初步研究为未来研究软蛋白质冠层的复杂性提供了蓝图,而软蛋白质冠层对于开发纳米药物至关重要。