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纳米生物界面指导的纳米颗粒蛋白冠抗原用于复杂基质中的免疫分析和免疫成像。

Nano-Bio Interface-Guided Nanoparticle Protein Corona Antigen for Immunoassays and Immunoimaging in a Complex Matrix.

机构信息

The Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Key Laboratory of Chemo/Biosensing, Laboratory of Biosensing and Bioimaging, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241002, P. R. China.

出版信息

ACS Appl Bio Mater. 2022 Feb 21;5(2):841-852. doi: 10.1021/acsabm.1c01231. Epub 2022 Feb 3.

Abstract

Engineered nanoparticles are widely used in biological imaging and drug delivery because of their excellent physical and chemical properties, but almost all the original functions of engineered nanoparticles suffer from a complex matrix. Herein, we proposed a strategy of preparing nanoparticle protein corona antigens (NPCAgs) through exposing a magnetic core silicon shell (FeO@SiO) fluorescent probe to an antigen protein solution, which could reduce the adsorption of nanoparticles (NPs) with other proteins in serum. In the presence of target anti-BSA IgG, a competitive-type displacement reaction was implemented between NPs@BSA and other proteins by target anti-BSA IgG through the specific antigen-antibody reaction. In addition, secondary structure analysis showed that almost all of the NPCAgs retained their natural conformation, which ensured the function of the NPCAgs, specifically capturing an antibody. Therefore, the NPCAgs showed good performance in immunoassays and immunoimaging, which should shed light on the application in imaging and identification of other nanomaterials.

摘要

由于其优异的物理化学性质,工程纳米粒子被广泛应用于生物成像和药物输送,但几乎所有工程纳米粒子的原始功能都受到复杂基质的影响。在此,我们提出了一种通过将磁性核硅壳(FeO@SiO)荧光探针暴露于抗原蛋白溶液中制备纳米颗粒蛋白冠抗原(NPCAgs)的策略,该策略可以减少纳米颗粒(NPs)与血清中其他蛋白质的吸附。在靶标抗 BSA IgG 的存在下,通过靶标抗 BSA IgG 与 NPs@BSA 之间的特异性抗原-抗体反应,实现了 NPs@BSA 与其他蛋白质之间的竞争型置换反应。此外,二级结构分析表明,几乎所有的 NPCAgs 都保留了其天然构象,这确保了 NPCAgs 的功能,即特异性捕获抗体。因此,NPCAgs 在免疫分析和免疫成像中表现出良好的性能,这应该为其他纳米材料的成像和鉴定应用提供启示。

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