Faulds Karen, Jarvis Roger, Smith W Ewen, Graham Duncan, Goodacre Royston
Department of Pure and Applied Chemistry, Centre for Molecular Nanometrology, WestCHEM, University of Strathclyde, Glasgow, UK.
Analyst. 2008 Nov;133(11):1505-12. doi: 10.1039/b800506k. Epub 2008 Aug 28.
The labelling of target biomolecules followed by detection using some form of optical spectroscopy has become common practice to aid in their detection. This approach has allowed the field of bioanalysis to dramatically expand; however, most methods suffer from the lack of the ability to discriminate between the components of a complex mixture. Currently, fluorescence spectroscopy is the method of choice but its ability to multiplex is greatly hampered by the broad overlapping spectra which are obtained. Surface enhanced resonance Raman scattering (SERRS) holds many advantages over fluorescence both in sensitivity and, more importantly here, in its ability to identify components in a mixture without separation due to the sharp fingerprint spectra obtained. Here the first multiplexed simultaneous detection of six different DNA sequences, corresponding to different strains of the Escherichia coli bacterium, each labelled with a different commercially available dye label (ROX, HEX, FAM, TET, Cy3, or TAMRA) is reported. This was achieved with the aid of multivariate analysis, also known as chemometrics, which can involve the application of a wide range of statistical and data analysis methods. In this study, both exploratory discriminant analysis and supervised learning, by partial least squares (PLS) regression, were used and the ability to discriminate whether a particular labelled oligonucleotide was present or absent in a mixture was achieved using PLS with very high sensitivity (0.98-1), specificity (0.98-1), accuracy (range 0.99-1), and precision (0.98-1).
对目标生物分子进行标记,然后使用某种形式的光谱学进行检测,已成为辅助其检测的常见做法。这种方法使生物分析领域得到了极大的扩展;然而,大多数方法都存在无法区分复杂混合物成分的问题。目前,荧光光谱法是首选方法,但其多路复用能力受到所获得的宽重叠光谱的极大阻碍。表面增强共振拉曼散射(SERRS)在灵敏度方面比荧光具有许多优势,更重要的是,由于获得的尖锐指纹光谱,它能够在不分离的情况下识别混合物中的成分。本文报道了首次对六种不同的DNA序列进行多路复用同时检测,这些序列对应于大肠杆菌的不同菌株,每种序列都用不同的市售染料标记(ROX、HEX、FAM、TET、Cy3或TAMRA)。这借助多变量分析(也称为化学计量学)得以实现,多变量分析可涉及广泛的统计和数据分析方法的应用。在本研究中,使用了探索性判别分析和偏最小二乘(PLS)回归的监督学习方法,通过PLS实现了区分混合物中是否存在特定标记寡核苷酸的能力,具有非常高的灵敏度(0.98 - 1)、特异性(0.98 - 1)、准确度(范围0.99 - 1)和精密度(0.98 - 1)。