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首页> 外文期刊>ACS Omega >Optimization and Structural Stability of Gold Nanoparticle–Antibody Bioconjugates
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Optimization and Structural Stability of Gold Nanoparticle–Antibody Bioconjugates

机译:金纳米粒子-抗体生物共轭物的优化和结构稳定性

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Gold nanoparticles (AuNPs) bound with biomolecules have emerged as suitable biosensors exploiting unique surface chemistries and optical properties. Many efforts have focused on antibody bioconjugation to AuNPs resulting in a sensitive bioconjugate to detect specific types of bacteria. Unfortunately, bacteria thrive under various harsh environments, and an understanding of bioconjugate stability is needed. Here, we show a method for optimizing Listeria monocytogenes polyclonal antibodies bioconjugation mechanisms to AuNPs via covalent binding at different pH values, from 2 to 11, and 2-(N-morpholino)ethanesulfonic acid (MES), 3-(N-morpholino)propanesulfonic acid, NaOH, HCl conditions. By fitting Lorentz curves to the amide I and II regions, we analyze the stability of the antibody secondary structure. This shows an increase in the apparent breakdown of the antibody secondary structure during bioconjugation as pH decreases from 7.9 to 2. We find variable adsorption efficiency, measured as the percentage of antibody adsorbed to the AuNP surface, from 17 to 27% as pH increases from 2 to 6 before decreasing to 8 and 13% at pH 7.9 and 11, respectively. Transmission electron microscopy (TEM) analysis reveals discrepancies between size and morphological changes due to the corona layer assembly from antibody binding to single nanoparticles versus aggregation or cluster self-assembly into large aggregates. The corona layer formation size increases from 3.9 to 5.1 nm from pH 2 to 6, at pH 7.9, there is incomplete corona formation, whereas at pH 11, there is a corona layer formed of 6.4 nm. These results indicate that the covalent binding process was more efficient at lower pH values; however, aggregation and deactivation of the antibodies were observed. We demonstrate that optimum bioconjugation condition was determined at pH 6 and MES buffer-type by indicators of covalent bonding and stability of the antibody secondary structure using Fourier transform-infrared, the morphological characteristics and corona layer formation using TEM, and low wavelength shifts of ultraviolet–visible after bioconjugation.
机译:与生物分子结合的金纳米颗粒(AuNP)已成为利用独特的表面化学和光学特性的合适生物传感器。许多努力集中在抗体与AuNPs的生物缀合上,从而产生了一种敏感的生物缀合物来检测特定类型的细菌。不幸的是,细菌会在各种恶劣的环境中繁衍生息,因此需要了解生物结合物的稳定性。在这里,我们展示了一种通过在不同pH值(从2到11)和2-(N-吗啉代)乙磺酸(MES),3-(N-吗啉代)上通过共价结合来优化单核细胞增生李斯特菌多克隆抗体对AuNPs生物缀合机制的方法。丙烷磺酸,NaOH,HCl条件。通过将Lorentz曲线拟合到酰胺I和II区域,我们分析了抗体二级结构的稳定性。这表明随着pH从7.9降低到2,生物共轭过程中抗体二级结构的表观分解增加。我们发现,随着pH值的增加,吸附效率变化(以抗体吸附到AuNP表面的百分比表示)从17%升至27%。 2至6,然后分别在pH 7.9和11下降低至8%和13%。透射电子显微镜(TEM)分析揭示了由于电晕层组装(从抗体结合到单个纳米粒子到聚集或簇自组装成大聚集体)而导致的尺寸和形态变化之间的差异。从pH 2到6,电晕层的形成尺寸从3.9纳米增加到5.1 nm,在pH 7.9时,电晕的形成不完全,而在pH 11时,电晕层的形成为6.4 nm。这些结果表明,共价结合过程在较低的pH值下更有效。然而,观察到抗体的聚集和失活。我们证明了最佳的生物缀合条件是在pH 6和MES缓冲液类型下通过使用傅立叶变换红外的共价键和抗体二级结构的稳定性,使用TEM的形态特征和电晕层形成以及紫外线的低波长偏移的指标来确定的–生物结合后可见。

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