Centre de recherche du CHU de Québec, Département de Microbiologie-infectiologie et immunologie, Faculté de médecine, Université Laval, 2705 Laurier Blvd., Quebec City, QC, G1V 4G2, Canada.
Macromol Biosci. 2013 Jun;13(6):717-22. doi: 10.1002/mabi.201200469. Epub 2013 Mar 19.
DNA hybridization is a universal and specific mechanism for the recognition of biological targets. Some cationic polythiophene transducers sensitive to DNA structure have been previously utilized to detect such biomolecules. Further characterization of these systems indicates that both DNA sequence composition and length modulate the biosensor performance. It appears that different repeated sequence patterns cause different conformational changes of the polythiophene, from a more relaxed form to an extremely rigid one. A length difference between the DNA oligonucleotide probe and target has a detrimental effect on the fluorescent signal, but it can be attenuated by changing the sequence composition of the protruding target sequence. This demonstrates that the nature of DNA can be critical for hybridization-based detection systems.
DNA 杂交是识别生物靶标的通用且特异的机制。先前已经利用一些对 DNA 结构敏感的阳离子聚噻吩换能器来检测此类生物分子。对这些系统的进一步表征表明,DNA 序列组成和长度均调节生物传感器的性能。似乎不同的重复序列模式会导致聚噻吩发生不同的构象变化,从更松弛的形式变为极其刚性的形式。寡核苷酸探针与靶标之间的长度差异会对荧光信号产生不利影响,但通过改变突出靶序列的序列组成可以减弱这种影响。这表明 DNA 的性质对于基于杂交的检测系统可能是至关重要的。