Dar Mubasher, Giesler Theresa, Richardson Rob, Cai Christine, Cooper Mike, Lavasani Shahin, Kille Peter, Voet Thierry, Vermeesch Joris
GE Healthcare, 800 Centennial Ave, Piscataway, NJ 08855, USA.
BMC Biotechnol. 2008 Nov 12;8:86. doi: 10.1186/1472-6750-8-86.
Array-based comparative genomic hybridization (CGH) and gene expression profiling have become vital techniques for identifying molecular defects underlying genetic diseases. Regardless of the microarray platform, cyanine dyes (Cy3 and Cy5) are one of the most widely used fluorescent dye pairs for microarray analysis owing to their brightness and ease of incorporation, enabling high level of assay sensitivity. However, combining both dyes on arrays can become problematic during summer months when ozone levels rise to near 25 parts per billion (ppb). Under such conditions, Cy5 is known to rapidly degrade leading to loss of signal from either "homebrew" or commercial arrays. Cy5 can also suffer disproportionately from dye photobleaching resulting in distortion of (Cy5/Cy3) ratios used in copy number analysis. Our laboratory has been active in fluorescent dye research to find a suitable alternative to Cy5 that is stable to ozone and resistant to photo-bleaching. Here, we report on the development of such a dye, called HyPer5, and describe its' exceptional ozone and photostable properties on microarrays.
Our results show HyPer5 signal to be stable to high ozone levels. Repeated exposure of mouse arrays hybridized with HyPer5-labeled cDNA to 300 ppb ozone at 5, 10 and 15 minute intervals resulted in no signal loss from the dye. In comparison, Cy5 arrays showed a dramatic 80% decrease in total signal during the same interval. Photobleaching experiments show HyPer5 to be resistant to light induced damage with 3- fold improvement in dye stability over Cy5. In high resolution array CGH experiments, HyPer5 is demonstrated to detect chromosomal aberrations at loci 2p21-16.3 and 15q26.3-26.2 from three patient sample using bacterial artificial chromosome (BAC) arrays. The photostability of HyPer5 is further documented by repeat array scanning without loss of detection. Additionally, HyPer5 arrays are shown to preserve sensitivity and data quality from gene expression experiments.
HyPer5 is a red fluorescent dye that behaves functionally similar to Cy5 except in stability to ozone and light. HyPer5 is demonstrated to be resistant to ozone at up to 300 ppb, levels significantly higher than commonly observed during summer months. Consequently, HyPer5 dye can be used in parallel with Cy3 under any environmental conditions in array experiments.
基于芯片的比较基因组杂交(CGH)和基因表达谱分析已成为识别遗传疾病潜在分子缺陷的重要技术。无论使用何种微阵列平台,花青染料(Cy3和Cy5)都是微阵列分析中使用最广泛的荧光染料对之一,因其亮度高且易于掺入,可实现高水平的检测灵敏度。然而,在夏季臭氧水平升至近25十亿分率(ppb)时,在芯片上同时使用这两种染料可能会出现问题。在这种条件下,已知Cy5会迅速降解,导致“自制”或商用芯片信号丢失。Cy5在染料光漂白方面也会受到不成比例的影响,导致拷贝数分析中使用的(Cy5/Cy3)比率失真。我们实验室一直积极开展荧光染料研究,以寻找一种对臭氧稳定且抗光漂白的Cy5合适替代品。在此,我们报告了一种名为HyPer5的染料的开发情况,并描述了其在微阵列上出色的抗臭氧和光稳定性能。
我们的结果表明HyPer5信号在高臭氧水平下稳定。用HyPer5标记的cDNA杂交的小鼠芯片,以5、10和15分钟的间隔反复暴露于300 ppb臭氧中,染料未出现信号损失。相比之下,Cy5芯片在相同间隔内总信号急剧下降了80%。光漂白实验表明HyPer5抗光诱导损伤,染料稳定性比Cy5提高了3倍。在高分辨率芯片CGH实验中,使用细菌人工染色体(BAC)芯片,证明HyPer5能检测来自三名患者样本在2p21 - 16.3和15q26.3 - 26.2位点的染色体畸变。通过重复芯片扫描且不损失检测能力,进一步证明了HyPer5的光稳定性。此外,HyPer5芯片在基因表达实验中能保持灵敏度和数据质量。
HyPer5是一种红色荧光染料,其功能与Cy5相似,只是在对臭氧和光的稳定性方面有所不同。已证明HyPer5在高达300 ppb的臭氧水平下具有抗性,该水平显著高于夏季常见水平。因此,在阵列实验的任何环境条件下,HyPer5染料都可与Cy3并行使用。