Department of Chemistry, Institute of Biomedical Sciences, Fudan University, Shanghai, PR China.
Anal Chim Acta. 2011 Mar 18;689(2):243-9. doi: 10.1016/j.aca.2011.01.046. Epub 2011 Jan 27.
We describe a sensitive biosensing system combining magnetic relaxation switch diagnosis and colorimetric detection of human α-thrombin, based on the aptamer-protein interaction induced aggregation of Fe(3)O(4)@Au nanoparticles. To demonstrate the concept, gold-coated iron oxide nanoparticle was synthesized by iterative reduction of HAuCl(4) onto the dextran-coated Fe(3)O(4) nanoparticles. The resulting core-shell structure had a flowerlike shape with pretty narrow size distribution (referred to as "nanorose"). The two aptamers corresponding to human α-thrombin were conjugated separately to two distinct nanorose populations. Once a solution containing human α-thrombin was introduced, the nanoroses switched from a well dispersed state to an aggregated one, leading to a change in the spin-spin relaxation time (T(2)) as well as the UV-Vis absorption spectra of the solution. Thus the qualitative and quantitative detection method for human α-thrombin was established. The dual-mode detection is clearly advantageous in obtaining a more reliable result; the detection range is widened as well. By using the dual-mode detection method, a detectable T(2) change is observed with 1.0 nM human α-thrombin, and the detection range is from 1.6 nM to 30.4 nM.
我们描述了一种基于适配体-蛋白相互作用诱导的 Fe(3)O(4)@Au 纳米粒子聚集的灵敏生物传感系统,用于检测人凝血酶。为了验证该概念,通过将 HAuCl(4)反复还原到葡聚糖包覆的 Fe(3)O(4)纳米粒子上,合成了金包覆的氧化铁纳米粒子。所得的核壳结构具有花状形状,尺寸分布相当窄(称为“纳米玫瑰”)。两个与人凝血酶对应的适配体分别连接到两个不同的纳米玫瑰群体上。一旦引入含有人凝血酶的溶液,纳米玫瑰就会从分散状态转变为聚集状态,导致溶液的自旋-自旋弛豫时间(T(2))和紫外-可见吸收光谱发生变化。因此,建立了定性和定量检测人凝血酶的方法。双模式检测显然在获得更可靠的结果方面具有优势,同时也拓宽了检测范围。通过使用双模式检测方法,可观察到 1.0 nM 人凝血酶的可检测 T(2)变化,检测范围为 1.6 nM 至 30.4 nM。