Aslund Andreas, Herland Anna, Hammarström Per, Nilsson K Peter R, Jonsson Bengt-Harald, Inganäs Olle, Konradsson Peter
Chemistry, IFM, Linköping University, SE-581 83, Linköping, Sweden.
Bioconjug Chem. 2007 Nov-Dec;18(6):1860-8. doi: 10.1021/bc700180g. Epub 2007 Oct 17.
Improved probes for amyloid fibril formation are advantageous for the early detection and better understanding of this disease-associated process. Here, we report a comparative study of eight luminescent conjugated polythiophene derivates (LCPs) and their discrimination of a protein (insulin) in the native or amyloid-like fibrillar state. For two of the LCPs, the synthesis is reported. Compared to their monomer-based analogues, trimer-based LCPs showed significantly better optical signal specificity for amyloid-like fibrils, seen from increased quantum yield and spectral shift. The trimer-based LCPs alone were highly quenched and showed little interaction with native insulin, as seen from analytical ultracentrifugation and insignificant spectral differences from the trimer-based LCP in buffered and native protein solution. Hence, the trimer-based LCPs showed enhanced discrimination between the amyloid-like fibrillar state and the corresponding native protein.
用于淀粉样纤维形成的改进型探针有利于该疾病相关过程的早期检测和更好理解。在此,我们报告了对八种发光共轭聚噻吩衍生物(LCPs)的比较研究及其对处于天然或淀粉样样纤维状态的蛋白质(胰岛素)的鉴别。对于其中两种LCPs,报道了其合成方法。与基于单体的类似物相比,基于三聚体的LCPs对淀粉样样纤维显示出显著更好的光学信号特异性,这从量子产率的提高和光谱位移可以看出。仅基于三聚体的LCPs高度猝灭,并且与天然胰岛素几乎没有相互作用,这从分析超速离心以及在缓冲和天然蛋白质溶液中与基于三聚体的LCP的光谱差异不明显可以看出。因此,基于三聚体的LCPs在淀粉样样纤维状态和相应天然蛋白质之间显示出增强的鉴别能力。