Rajendra Jascindra, Rodger Alison
Department of Chemistry, University of Warwick, Coventry, UK.
Chemistry. 2005 Aug 5;11(16):4841-7. doi: 10.1002/chem.200500093.
The binding of single-stranded DNAs and a neutral DNA analogue (peptide nucleic acid, PNA) to single-walled carbon nanotubes in solution phase has been probed by absorbance spectroscopy and linear dichroism. The nanotubes are solubilised by aqueous sodium dodecyl sulfate, in which the nucleic acids also dissolve. The linear dichroism (LD) of the nanotubes, when subtracted from that due to the nanotubes/nucleic acid samples, gives the LD of the bound nucleic acid. The binding of the single-stranded DNA to the single-walled nanotubes is quite different from that previously observed for double-stranded DNA. It is likely that the nucleic acid bases lie flat on the nanotube surface with the backbone wrapping round the nanotube at an oblique angle in the region of 45 degrees . The net effect is like beads on a string. The base orientation with the single-stranded PNA is inverted with respect to that of the single-stranded DNA, as shown by their oppositely signed LD signals.
通过吸收光谱法和线性二色性研究了溶液相中单链DNA和中性DNA类似物(肽核酸,PNA)与单壁碳纳米管的结合。纳米管通过十二烷基硫酸钠水溶液溶解,核酸也溶解在其中。从纳米管/核酸样品的线性二色性(LD)中减去纳米管的LD,得到结合核酸的LD。单链DNA与单壁纳米管的结合与先前观察到的双链DNA的结合有很大不同。核酸碱基可能平躺在纳米管表面,主链在约45度的倾斜角度环绕纳米管。净效应就像串在绳子上的珠子。单链PNA的碱基取向与单链DNA的碱基取向相反,这由它们相反符号的LD信号表明。