首页> 外文会议>Conference on Multiphoton Microscopy in the Biomedical Sciences IV; 20040125-20040127; San Jose,CA; US >Multi-photon excitation fluorescence correlation spectroscopy of fluorescent DNA base analogs
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Multi-photon excitation fluorescence correlation spectroscopy of fluorescent DNA base analogs

机译:荧光DNA碱基类似物的多光子激发荧光相关光谱

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Two- and three-photon excitation was used to investigate the properties of two fluorescent DNA base analogs: 2-aminopurine and 6-methylisoxanthopterin. 2-aminopurine is a widely used fluorescent analog of the DNA base adenine. Three-photon excitation of 2-aminopurine is achievable by using intense femtosecond laser pulses in 850-950 nm spectral region. Interestingly, the three-photon excitation spectrum is blue-shifted relative to the three-times-wavelength single-photon excitation spectrum. The maximum of the absorbance band in the UV is at 305 nm, while the three-photon excitation spectrum has a maximum at around 880 nm. Fluorescence correlation measurements were attempted to evaluate the feasibility of using three-photon excitation of 2-aminopurine for DNA-protein interaction studies. However, due to relatively small three-photon absorption cross-section, a good signal-to-noise fluorescence correlation curves take very long time to obtain. Fluorescence properties of 6-methylisoxanthopterin, the fluorescent analog of guanine, were investigated using two-photon excitation. This molecule has the lowest energy absorption band centered around 350 nm, thus, two-photon excitation is attainable using 700 to 760 nm output of Ti-sapphire laser. The excitation spectrum of this molecule in the infrared well matches the doubled-wavelength single-photon excitation spectrum in the UV. The high fluorescence quantum yield of 6-methylisoxanthopterin allows efficient fluorescence correlation measurements and makes this molecule a very good candidate for using in in vitro DNA-protein interaction studies.
机译:使用两个和三个光子激发来研究两个荧光DNA碱基类似物的性质:2-氨基嘌呤和6-甲基异黄嘌呤。 2-氨基嘌呤是DNA碱基腺嘌呤的广泛使用的荧光类似物。通过在850-950 nm光谱范围内使用强飞秒激光脉冲,可以实现2-氨基嘌呤的三光子激发。有趣的是,三光子激发光谱相对于三倍波长单光子激发光谱发生了蓝移。 UV中吸收带的最大值在305 nm,而三光子激发光谱的最大值在880 nm附近。尝试进行荧光相关测量以评估使用2-氨基嘌呤的三光子激发进行DNA-蛋白质相互作用研究的可行性。但是,由于相对较小的三光子吸收截面,因此获得良好的信噪比荧光相关曲线需要很长时间。利用双光子激发研究了鸟嘌呤的荧光类似物6-甲基异黄嘌呤的荧光性质。该分子具有以350 nm为中心的最低能量吸收带,因此,使用700至760 nm的Ti-蓝宝石激光器输出可以获得双光子激发。该分子在红外井中的激发光谱与紫外中的双波长单光子激发光谱匹配。 6-甲基异黄嘌呤的高荧光量子产率使得有效的荧光相关性测量成为可能,并且使该分子成为用于体外DNA-蛋白质相互作用研究的非常好的候选者。

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