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使用与蛋白 G 功能化的长程表面等离子体波导检测白血病标志物。

Detection of leukemia markers using long-range surface plasmon waveguides functionalized with Protein G.

机构信息

Department of Biological and Chemical Engineering, University of Ottawa, 161 Louis Pasteur, Ottawa, Ontario K1N 6N5, Canada.

出版信息

Lab Chip. 2015 Nov 7;15(21):4156-65. doi: 10.1039/c5lc00940e. Epub 2015 Sep 16.

Abstract

A novel optical biosensor based on long-range surface plasmon-polariton (LRSPP) waveguides is demonstrated for the detection of leukemia markers in patient serum using a functionalization strategy based on Protein G. The sensor consists of thin straight Au waveguides (5 μm × 35 nm × 3.2 mm) embedded in fluoropolymer CYTOP™ with a fluidic channel etched into the top cladding. B-cell leukemia is characterized by a high B-cell count and abnormal distribution of immunoglobulin G kappa (IgGκ) and lambda (IgGλ) light chains in serum. The detection of leukemic abnormalities in serum was performed based on determining IgGκ-to-IgGλ ratios (κ : λ). Three patient sera were tested: high kappa (HKS, κ : λ ~12.7 : 1), high lambda (HLS, λ : κ ~6.9 : 1) and normal (control) sera (NS, κ : λ ~1.7 : 1). Au waveguides were functionalized with Protein G and two complementary immobilization approaches were investigated: a) the reverse approach, where the Protein G surface is functionalized with patient serum and then tested against goat anti-human IgG light chains in buffer, and b) the direct approach, where the Protein G surface is functionalized with goat anti-human IgGs first and then tested against patient serum. The reverse approach was found to be more effective and robust because Protein G-functionalized surface performs as an "immunological filter" by capturing primarily IgGs out of the pool of serum proteins. For the reverse approach, the ratios measured were 3.7 : 1(κ : λ), 9.7 : 1(λ : κ) and 1.9 : 1(κ : λ) for HKS, HLS and NS, respectively, which compare favorably with corresponding protein densitometry measurements. The respective ratios for the direct approach were 2.6 : 1(κ : λ), 2.6 : 1(λ : κ) and 1.7 : 1(κ : λ). The binding strength and cross-reactivity of goat anti-human IgGs light chains were also determined using pure solutions. The LRSPP biosensor along with the innovative "reverse approach" can provide a low-cost and compact solution to B-cell leukemia screening.

摘要

一种基于长程表面等离子体激元(LRSPP)波导的新型光学生物传感器,用于使用基于蛋白 G 的功能化策略检测患者血清中的白血病标志物。该传感器由嵌入氟聚合物 CYTOP™中的薄直金波导(5 μm×35 nm×3.2 mm)组成,在顶部包层中刻蚀有流体通道。B 细胞白血病的特征是血清中 B 细胞计数高且免疫球蛋白 G kappa(IgGκ)和 lambda(IgGλ)轻链分布异常。通过确定 IgGκ-to-IgGλ 比值(κ:λ)来检测血清中的白血病异常。测试了三种患者血清:高 κ(HKS,κ:λ12.7:1)、高 λ(HLS,λ:κ6.9:1)和正常(对照)血清(NS,κ:λ~1.7:1)。金波导用蛋白 G 功能化,并研究了两种互补的固定化方法:a)反向方法,其中蛋白 G 表面用患者血清功能化,然后在缓冲液中用抗人 IgG 轻链的山羊抗体制测试;b)直接方法,其中蛋白 G 表面首先用抗人 IgGs 功能化,然后用患者血清测试。发现反向方法更有效且更稳健,因为蛋白 G 功能化表面通过从血清蛋白池中捕获主要的 IgG 来充当“免疫过滤器”。对于反向方法,分别测量到 HKS、HLS 和 NS 的比值为 3.7:1(κ:λ)、9.7:1(λ:κ)和 1.9:1(κ:λ),这与相应的蛋白质密度测量结果相当。对于直接方法,分别得到 2.6:1(κ:λ)、2.6:1(λ:κ)和 1.7:1(κ:λ)的比值。还使用纯溶液确定了抗人 IgG 轻链的山羊抗体的结合强度和交叉反应性。LRSPP 生物传感器以及创新的“反向方法”可为 B 细胞白血病筛查提供一种低成本、紧凑型解决方案。

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