Department of Biological and Chemical Engineering, University of Ottawa, 161 Louis Pasteur, Ottawa, Ontario K1N 6N5, Canada.
Lab Chip. 2015 Nov 7;15(21):4156-65. doi: 10.1039/c5lc00940e. Epub 2015 Sep 16.
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.
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。