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原子力显微镜探测核黄素受体靶向金树状大分子纳米复合材料与受体的相互作用。

Atomic force microscopy probing of receptor-nanoparticle interactions for riboflavin receptor targeted gold-dendrimer nanocomposites.

机构信息

Department of Chemistry & Biochemistry, Calvin College , 3201 Burton Street SE, Grand Rapids, Michigan 49546, United States.

出版信息

J Phys Chem B. 2014 Mar 20;118(11):2872-82. doi: 10.1021/jp412053w. Epub 2014 Mar 7.

Abstract

Riboflavin receptors are overexpressed in malignant cells from certain human breast and prostate cancers, and they constitute a group of potential surface markers important for cancer targeted delivery of therapeutic agents and imaging molecules. Here we report on the fabrication and atomic force microscopy (AFM) characterization of a core-shell nanocomposite consisting of a gold nanoparticle (AuNP) coated with riboflavin receptor-targeting poly(amido amine) dendrimer. We designed this nanocomposite for potential applications such as a cancer targeted imaging material based on its surface plasmon resonance properties conferred by AuNP. We employed AFM as a technique for probing the binding interaction between the nanocomposite and riboflavin binding protein (RfBP) in solution. AFM enabled precise measurement of the AuNP height distribution before (13.5 nm) and after chemisorption of riboflavin-conjugated dendrimer (AuNP-dendrimer; 20.5 nm). Binding of RfBP to the AuNP-dendrimer caused a height increase to 26.7 nm, which decreased to 22.8 nm when coincubated with riboflavin as a competitive ligand, supporting interaction of AuNP-dendrimer and its target protein. In summary, physical determination of size distribution by AFM imaging can serve as a quantitative approach to monitor and characterize the nanoscale interaction between a dendrimer-covered AuNP and target protein molecules in vitro.

摘要

核壳型纳米复合材料的制备及其原子力显微镜(AFM)表征 该核壳型纳米复合材料由金纳米粒子(AuNP)包覆核糖黄素受体靶向性聚酰胺-胺树枝状大分子组成。我们设计这种纳米复合材料是为了基于金纳米粒子的表面等离子体共振特性,将其潜在应用于癌症靶向成像材料。我们采用原子力显微镜(AFM)作为一种技术,用于探测纳米复合材料与溶液中核糖黄素结合蛋白(RfBP)之间的结合相互作用。AFM 能够精确测量金纳米粒子在化学吸附核糖黄素偶联树枝状大分子之前(13.5nm)和之后(AuNP-树枝状大分子;20.5nm)的高度分布。RfBP 与 AuNP-树枝状大分子的结合导致高度增加到 26.7nm,当与核糖黄素作为竞争配体共孵育时,高度降低到 22.8nm,这支持了 AuNP-树枝状大分子与其靶蛋白的相互作用。总之,通过 AFM 成像对尺寸分布进行物理测定,可以作为一种定量方法来监测和表征体外树枝状大分子包覆的 AuNP 与靶蛋白分子之间的纳米级相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adb9/3983334/44bdf394ce92/jp-2013-12053w_0007.jpg

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