Brazilian Synchrotron Light Laboratory (LNLS), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, Brazil.
Programa de Pós-Graduação em Biotecnociências, Universidade Federal do ABC, 09210-580 Santo André, Brazil.
ACS Appl Mater Interfaces. 2022 Jun 29;14(25):28559-28569. doi: 10.1021/acsami.2c05362. Epub 2022 Jun 13.
Protein corona formation and nanoparticles' aggregation have been heavily discussed over the past years since the lack of fine-mapping of these two combined effects has hindered the targeted delivery evolution and the personalized nanomedicine development. We present a multitechnique approach that combines dynamic light and small-angle X-ray scattering techniques with cryotransmission electron microscopy in a given fashion that efficiently distinguishes protein corona from aggregates formation. This methodology was tested using ∼25 nm model silica nanoparticles incubated with either model proteins or biologically relevant proteomes (such as fetal bovine serum and human plasma) in low and high ionic strength buffers to precisely tune particle-to-protein interactions. In this work, we were able to differentiate protein corona, small aggregates formation, and massive aggregation, as well as obtain fractal information on the aggregates reliably and straightforwardly. The strategy presented here can be expanded to other particle-to-protein mixtures and might be employed as a quality control platform for samples that undergo biological tests.
近年来,由于缺乏对这两种联合效应的精细映射,蛋白质冠形成和纳米颗粒聚集一直受到广泛讨论,这阻碍了靶向递药的发展和个性化纳米医学的发展。我们提出了一种多技术方法,将动态光散射和小角 X 射线散射技术与 cryotransmission 电子显微镜结合使用,以一种有效的方式将蛋白质冠与聚集物的形成区分开来。该方法使用约 25nm 的模型硅纳米颗粒在低离子强度和高离子强度缓冲液中与模型蛋白或生物相关的蛋白质组(如胎牛血清和人血浆)孵育进行了测试,以精确调节颗粒与蛋白质的相互作用。在这项工作中,我们能够可靠而直接地区分蛋白质冠、小聚集物的形成和大规模聚集,并获得有关聚集物的分形信息。这里提出的策略可以扩展到其他颗粒-蛋白质混合物,并可以作为经历生物测试的样品的质量控制平台。