| Literature DB >> 25089818 |
Leif B G Johansson1, Rozalyn Simon1, Gunnar Bergström1, Mikaela Eriksson1, Stefan Prokop2, Carl-Fredrik Mandenius1, Frank L Heppner2, Andreas K O Åslund1, K Peter R Nilsson3.
Abstract
Ligands for identifying protein aggregates are of great interest as such deposits are the pathological hallmark of a wide range of severe diseases including Alzheimer's and Parkinson's disease. Here we report the synthesis of an azide functionalized fluorescent pentameric oligothiophene that can be utilized as a ligand for multimodal detection of disease-associated protein aggregates. The azide functionalization allows for attachment of the ligand to a surface by conventional click chemistry without disturbing selective interaction with protein aggregates and the oligothiophene-aggregate interaction can be detected by fluorescence or surface plasmon resonance. In addition, a methodology where the oligothiophene ligand is employed as a capturing molecule selective for aggregated proteins in combination with an antibody detecting a distinct peptide/protein is also presented. We foresee that this methodology will offer the possibility to create a variety of multiplex sensing systems for sensitive and selective detection of protein aggregates, the pathological hallmarks of several neurodegenerative diseases.Entities:
Keywords: Click chemistry; Fluorescence; Oligothiophene; Protein aggregates; Surface plasmon resonance
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Year: 2014 PMID: 25089818 DOI: 10.1016/j.bios.2014.07.042
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618