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基于生物素-链霉亲和素系统形成DNA阵列的多步方法的成像和光谱比较。

Imaging and spectroscopic comparison of multi-step methods to form DNA arrays based on the biotin-streptavidin system.

作者信息

Gajos Katarzyna, Petrou Panagiota, Budkowski Andrzej, Awsiuk Kamil, Bernasik Andrzej, Misiakos Konstantinos, Rysz Jakub, Raptis Ioannis, Kakabakos Sotirios

机构信息

M. Smoluchowski Institute of Physics, Jagiellonian University, Łojasiewicza 11, 30-348 Kraków, Poland.

出版信息

Analyst. 2015 Feb 21;140(4):1127-39. doi: 10.1039/c4an00929k.

Abstract

Three multi-step multi-molecular approaches using the biotin-streptavidin system to contact-print DNA arrays on SiO2 surfaces modified with (3-glycidoxypropyl)trimethoxysilane are examined after each deposition/reaction step by atomic force microscopy, X-ray photoelectron spectroscopy and time of flight secondary ion mass spectrometry. Surface modification involves the spotting of preformed conjugates of biotinylated oligonucleotides with streptavidin onto surfaces coated with biotinylated bovine serum albumin b-BSA (approach I) or the spotting of biotinylated oligonucleotides onto a streptavidin coating, the latter prepared through a reaction with immobilized b-BSA (approach II) or direct adsorption (approach III). AFM micrographs, quantified by autocorrelation and height histogram parameters (e.g. roughness), reveal uniform coverage after each modification step with distinct nanostructures after the reaction of biotinylated BSA with streptavidin or of a streptavidin conjugate with biotinylated oligonucleotides. XPS relates the immobilization of biomolecules with covalent binding to the epoxy-silanized surface. Protein coverage, estimated from photoelectron attenuation, shows that regarding streptavidin the highest and the lowest immobilization efficiency is achieved by following approaches I and III, respectively, as confirmed by TOF-SIMS microanalysis. The size of the DNA spot reflects the contact radius of the printed droplet and increases with protein coverage (and roughness) prior to the spotting, as epoxy-silanized surfaces are hardly hydrophilic. Representative TOF-SIMS images show sub-millimeter spots: uniform for approach I, doughnut-like (with a small non-zero minimum) for approach II, both with coffee-rings or peak-shaped for approach III. Spot features, originating from pinned contact lines and DNA surface binding and revealed by complementary molecular distributions (all material, DNA, streptavidin, BSA, epoxy, SiO2), indicate two modes of droplet evaporation depending on the details of each applied approach.

摘要

采用生物素-链霉亲和素系统在经(3-缩水甘油氧基丙基)三甲氧基硅烷修饰的SiO₂表面接触印刷DNA阵列的三种多步多分子方法,在每次沉积/反应步骤后,通过原子力显微镜、X射线光电子能谱和飞行时间二次离子质谱进行检测。表面修饰包括将生物素化寡核苷酸与链霉亲和素的预制缀合物点样到涂有生物素化牛血清白蛋白b-BSA的表面上(方法I),或将生物素化寡核苷酸点样到链霉亲和素涂层上,后者通过与固定化b-BSA反应制备(方法II)或直接吸附(方法III)。通过自相关和高度直方图参数(如粗糙度)量化的原子力显微镜图像显示,在每个修饰步骤后覆盖均匀,在生物素化BSA与链霉亲和素或链霉亲和素缀合物与生物素化寡核苷酸反应后具有独特的纳米结构。X射线光电子能谱将生物分子的固定与与环氧硅烷化表面的共价结合联系起来。根据光电子衰减估计的蛋白质覆盖率表明,对于链霉亲和素,分别通过方法I和方法III实现了最高和最低的固定效率,飞行时间二次离子质谱微分析证实了这一点。DNA斑点的大小反映了印刷液滴的接触半径,并且在点样前随着蛋白质覆盖率(和粗糙度)的增加而增加,因为环氧硅烷化表面几乎不亲水。代表性的飞行时间二次离子质谱图像显示亚毫米级斑点:方法I的斑点均匀,方法II的斑点呈甜甜圈状(有一个小的非零最小值),方法III的斑点既有咖啡环状也有峰状。斑点特征源于固定的接触线和DNA与表面的结合,并通过互补的分子分布(所有物质、DNA、链霉亲和素、BSA、环氧、SiO₂)揭示,表明取决于每种应用方法的细节,液滴蒸发有两种模式。

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