Sun Steven, Francis Jesse, Sapsford Kim E, Kostov Yordan, Rasooly Avraham
Division of Biology, Office of Science and Engineering Laboratories, FDA, Silver Spring, MD 20993, USA.
Sens Actuators B Chem. 2010 Apr 8;146(1-8):297-306. doi: 10.1016/j.snb.2010.02.009.
A portable and rapid detection system for the activity analysis of Botulinum Neurotoxins (BoNT) is needed for food safety and bio-security applications. To improve BoNT activity detection, a previously designed portable charge-coupled device (CCD) based detector was modified and equipped with a higher intensity more versatile multi-wavelength spatial light-emitting diode (LED) illumination, a faster CCD detector and the capability to simultaneously detect 30 samples. A FITC/DABCYL Förster Resonance Energy Transfer (FRET)-labeled peptide substrate (SNAP-25), with BoNT-A target cleavage site sequence was used to measure BoNT-A light chain (LcA) activity through the FITC fluorescence increase that occurs upon peptide substrate cleavage. For fluorescence excitation, a multi-wavelength spatial LED illuminator was used and compared to our previous electroluminescent (EL) strips. The LED illuminator was equipped with blue, green, red and white LEDs, covering a spectrum of 450-680 nm (red 610-650 nm, green 492-550 nm, blue 450-495 nm, and white LED 440-680 nm). In terms of light intensity, the blue LED was found to be ~80 fold higher than the previously used blue EL strips. When measuring the activity of LcA the CCD detector limit of detection (LOD) was found to be 0.08 nM LcA for both the blue LED (2 s exposure) and the blue EL (which require ≥60 s exposure) while the limits of quantitation (LOQ) is about 1 nM. The LOD for white LED was higher at 1.4 nM while the white EL was not used for the assay due to a high variable background. Unlike the weaker intensity EL illumination the high intensity LED illumination enabled shorter exposure times and allowed multi-wavelength illumination without the need to physically change the excitation strip, thus making spectrum excitation of multiple fluorophores possible increasing the versatility of the detector platform for a variety of optical detection assays.
为了食品安全和生物安全应用,需要一种用于肉毒杆菌神经毒素(BoNT)活性分析的便携式快速检测系统。为了改进BoNT活性检测,对先前设计的基于便携式电荷耦合器件(CCD)的检测器进行了改进,配备了强度更高、通用性更强的多波长空间发光二极管(LED)照明、更快的CCD检测器以及同时检测30个样品的能力。使用具有BoNT-A靶切割位点序列的FITC/DABCYL荧光共振能量转移(FRET)标记肽底物(SNAP-25),通过肽底物切割时发生的FITC荧光增加来测量BoNT-A轻链(LcA)活性。对于荧光激发,使用了多波长空间LED照明器,并与我们之前的电致发光(EL)条进行了比较。该LED照明器配备了蓝色、绿色、红色和白色LED,覆盖450-680nm的光谱范围(红色610-650nm,绿色492-550nm,蓝色450-495nm,白色LED 440-680nm)。在光强度方面,发现蓝色LED比先前使用的蓝色EL条高约80倍。在测量LcA活性时,对于蓝色LED(2秒曝光)和蓝色EL(需要≥60秒曝光)而言,CCD检测器的检测限(LOD)均为0.08 nM LcA,而定量限(LOQ)约为1 nM。白色LED的LOD较高,为1.4 nM,而白色EL由于背景变化较大未用于该检测。与强度较弱 的EL照明不同,高强度LED照明能够实现更短的曝光时间,并且无需物理更换激发条即可进行多波长照明,从而使得多个荧光团的光谱激发成为可能,增加了检测器平台在各种光学检测分析中的通用性。