Quesada M A, Rye H S, Gingrich J C, Glazer A N, Mathies R A
University of California, Berkeley.
Biotechniques. 1991 May;10(5):616-25.
A high-sensitivity, laser-excited confocal fluorescence gel scanner has been developed and applied to the detection of fluorescently labeled DNA. An argon ion laser (1-10 mW at 488 nm) is focused in the gel with a high-numerical aperture microscope objective. The laser-excited fluorescence is gathered by the objective and focused on a confocal spatial filter, followed by a spectral filter and photodetector. The gel is placed on a computer-controlled scan stage, and the scanned image of the gel fluorescence is stored and analyzed in a computer. This scanner has been used to detect DNA separated on sequencing gels, agarose mapping gels and pulsed field gels. Sanger sequencing gels were run on M13mp18 DNA using a fluoresceinated primer. The 400-microns-thick gels, loaded with 30 fmol of DNA fragments in 3-mm lanes, were scanned at 78-microns resolution. The high resolution of our scanner coupled with image processing allows us to read up to approximately 300 bases in four adjacent sequencing lanes. The minimum band size that could be detected and read was approximately 200 microns. This instrument has a limiting detection sensitivity of approximately 10 amol of fluorescein-labeled DNA in a 1 x 3-mm band. In applications to agarose mapping gels, we have exploited the fact that DNA can be prestained with ethidium homodimer, followed by electrophoresis and fluorescence detection to achieve picogram sensitivity. We have also developed methods using both ethidium homodimer and thiazole orange staining which permit two-color detection of DNA in one lane.(ABSTRACT TRUNCATED AT 250 WORDS)
已开发出一种高灵敏度、激光激发的共聚焦荧光凝胶扫描仪,并将其应用于荧光标记DNA的检测。氩离子激光(488nm波长,功率1 - 10mW)通过高数值孔径显微镜物镜聚焦在凝胶上。激光激发的荧光由物镜收集并聚焦在共焦空间滤波器上,然后是光谱滤波器和光电探测器。凝胶放置在计算机控制的扫描台上,凝胶荧光的扫描图像在计算机中存储和分析。该扫描仪已用于检测在测序凝胶、琼脂糖图谱凝胶和脉冲场凝胶上分离的DNA。使用荧光素化引物在M13mp18 DNA上运行桑格测序凝胶。将含有30 fmol DNA片段的400微米厚凝胶加载到3毫米宽的泳道中,以78微米分辨率进行扫描。我们扫描仪的高分辨率与图像处理相结合,使我们能够在四个相邻测序泳道中读取多达约300个碱基。能够检测和读取的最小条带大小约为200微米。该仪器在1×3毫米条带中对荧光素标记DNA的极限检测灵敏度约为10 amol。在琼脂糖图谱凝胶的应用中,我们利用了DNA可以用乙锭同二聚体预染色,然后进行电泳和荧光检测以实现皮克灵敏度这一事实。我们还开发了同时使用乙锭同二聚体和噻唑橙染色的方法,允许在一个泳道中对DNA进行双色检测。(摘要截断于250字)