Lynch Iseult, Dawson Kenneth A, Linse Sara
Irish Centre for Colloid Science and Biomaterials, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, Ireland.
Sci STKE. 2006 Mar 21;2006(327):pe14. doi: 10.1126/stke.3272006pe14.
As potential applications of nanotechnology and nanoparticles increase, so too does the likelihood of human exposure to nanoparticles. Because of their small size, nanoparticles are easily taken up into cells (by receptor-mediated endocytosis), whereupon they have essentially free access to all cellular compartments. Similarly to macroscopic biomaterial surfaces (that is, implants), nanoparticles become coated with a layer of adsorbed proteins immediately upon contact with physiological solutions (unless special efforts are taken to prevent this). The process of adsorption often results in conformational changes of the adsorbed protein, which may be affected by the larger curvature of nanoparticles compared with implant surfaces. Protein adsorption may result in the exposure at the surface of amino acid residues that are normally buried in the core of the native protein, which are recognized by the cells as "cryptic epitopes." These cryptic epitopes may trigger inappropriate cellular signaling events (as opposed to being rejected by the cells as foreign bodies). However, identification of such surface-exposed epitopes is nontrivial, and the molecular nature of the adsorbed proteins should be investigated using biological and physical science methods in parallel with systems biology studies of the induced alterations in cell signaling.
随着纳米技术和纳米颗粒的潜在应用不断增加,人类接触纳米颗粒的可能性也在增加。由于尺寸小,纳米颗粒很容易被细胞摄取(通过受体介导的内吞作用),进入细胞后它们基本上可以自由进入所有细胞区室。与宏观生物材料表面(即植入物)类似,纳米颗粒一旦与生理溶液接触就会立即被一层吸附蛋白覆盖(除非采取特殊措施防止这种情况发生)。吸附过程通常会导致被吸附蛋白的构象变化,与植入物表面相比,纳米颗粒更大的曲率可能会影响这种变化。蛋白质吸附可能导致原本埋藏在天然蛋白质核心中的氨基酸残基暴露在表面,细胞将这些残基识别为“隐蔽表位”。这些隐蔽表位可能会引发不适当的细胞信号事件(而不是被细胞作为异物排斥)。然而,识别这种表面暴露的表位并非易事,应该同时使用生物学和物理科学方法以及对诱导的细胞信号变化进行系统生物学研究来研究吸附蛋白的分子性质。 。