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用于固定在有序介孔二氧化硅上的抗体片段-金纳米颗粒缀合物透射电子显微镜成像的银增强法

Silver Enhancement for Transmission Electron Microscopy Imaging of Antibody Fragment-Gold Nanoparticles Conjugates Immobilized on Ordered Mesoporous Silica.

作者信息

Piludu Marco, Medda Luca, Cugia Francesca, Monduzzi Maura, Salis Andrea

机构信息

Department of Biomedical Sciences, and ‡Department of Chemical and Geological Sciences, University of Cagliari , CSGI and CNBS, Cittadella Universitaria, Strada Statale 554 Bivio Sestu, 09042 Monserrato Cagliari, Italy.

出版信息

Langmuir. 2015 Sep 1;31(34):9458-63. doi: 10.1021/acs.langmuir.5b02830. Epub 2015 Aug 19.

Abstract

Ordered mesoporous silica (OMS) materials are receiving great attention as possible carriers for valuable but unstable drugs as, for example, therapeutic proteins. A key issue is to prove that the therapeutic protein is effectively able to penetrate the pores of OMS during the adsorption step. Here, we immobilized an antibody fragment [F(ab')GAMIgG] conjugated with ultrasmall gold nanoparticles (GNPs) onto amino-functionalized SBA-15 (SBA-NH2) mesoporous silica. The aim of this work is the visualization of the location of the conjugates adsorbed onto SBA-NH2 with transmission electron microscopy (TEM). Because of the ultrasmall size of GNPs (<1 nm), we use the silver enhancement procedure to amplify their size. In this procedure, ultrathin sections of conjugate-loaded SBA-NH2 particles are prepared by a ultramicrotome sectioning technique. The ultrasmall GNPs located on the top side of the 70-90 nm thick slices act as microcrystallization nucleation sites for the deposition of reduced metallic silver. Consequently, the ultrasmall GNPs increase their size. This allows for the direct imaging of the conjugates adsorbed. We clearly localize the F(ab')GAMIgG-GNPs conjugates either on the external surface of the particles or inside the mesopores of SBA-NH2 through TEM.

摘要

有序介孔二氧化硅(OMS)材料作为有价值但不稳定药物(如治疗性蛋白质)的可能载体正受到广泛关注。一个关键问题是要证明治疗性蛋白质在吸附步骤中能够有效地穿透OMS的孔。在此,我们将与超小金纳米颗粒(GNP)偶联的抗体片段[F(ab')GAMIgG]固定在氨基功能化的SBA - 15(SBA - NH2)介孔二氧化硅上。这项工作的目的是通过透射电子显微镜(TEM)可视化吸附在SBA - NH2上的偶联物的位置。由于GNP的超小尺寸(<1 nm),我们使用银增强程序来扩大其尺寸。在这个程序中,通过超薄切片技术制备负载偶联物的SBA - NH2颗粒的超薄切片。位于70 - 90 nm厚切片顶部的超小GNP作为还原金属银沉积的微晶成核位点。因此,超小GNP增大了其尺寸。这使得能够直接对吸附的偶联物进行成像。我们通过TEM清楚地定位了F(ab')GAMIgG - GNP偶联物在颗粒的外表面或SBA - NH2的介孔内部。

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