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Synthesis and Characterization of Thiophene-based Donor-Acceptor-Donor Heptameric Ligands for Spectral Assignment of Polymorphic Amyloid-beta Deposits
Linköping University, Department of Physics, Chemistry and Biology, Chemistry. Linköping University, Faculty of Science & Engineering.
Linköping University, Department of Physics, Chemistry and Biology, Chemistry. Linköping University, Faculty of Science & Engineering.
Linköping University, Department of Physics, Chemistry and Biology, Chemistry. Linköping University, Faculty of Science & Engineering.
Linköping University, Department of Physics, Chemistry and Biology, Chemistry. Linköping University, Faculty of Science & Engineering.ORCID iD: 0000-0002-5582-140X
2020 (English)In: Chemistry - A European Journal, ISSN 0947-6539, E-ISSN 1521-3765, Vol. 26, no 33, p. 7425-7432Article in journal (Refereed) Published
Abstract [en]

Protein deposits are associated with many devastating diseases and fluorescent ligands able to visualize these pathological entities are essential. Here, we report the synthesis of thiophene-based donor-acceptor-donor heptameric ligands that can be utilized for spectral assignment of distinct amyloid-beta (A beta) aggregates, one of the pathological hallmarks in Alzheimers disease. The ability of the ligands to selectively distinguish A beta deposits was abolished when the chemical composition of the ligands was altered. Our findings provide the structural and functional basis for the development of new fluorescent ligands that can distinguish between aggregated proteinaceous species consisting of the same peptide or protein. In addition, such ligands might aid in interpreting the potential role of polymorphic A beta deposits in the pathogenesis of Alzheimers disease.

Place, publisher, year, edition, pages
WILEY-V C H VERLAG GMBH , 2020. Vol. 26, no 33, p. 7425-7432
Keywords [en]
Alzheimers disease; fluorescence; luminescent conjugated oligothiophenes; protein aggregates; beta-amyloid
National Category
Biochemistry Molecular Biology
Identifiers
URN: urn:nbn:se:liu:diva-166174DOI: 10.1002/chem.201905612ISI: 000532854400001PubMedID: 32022335OAI: oai:DiVA.org:liu-166174DiVA, id: diva2:1437730
Note

Funding Agencies|Swedish Research CouncilSwedish Research Council [2016-00748]; Erling Persson foundation

Available from: 2020-06-09 Created: 2020-06-09 Last updated: 2025-02-20
In thesis
1. Synthesis of donor–acceptor–donor thiophene based ligands that can be utilized for optical assignment of pathological targets
Open this publication in new window or tab >>Synthesis of donor–acceptor–donor thiophene based ligands that can be utilized for optical assignment of pathological targets
2022 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Thiophene based ligands represent a class of molecular reporters proven superior in discerning pathological targets involved in neurodegenerative diseases, as well as bacterial infection. By fluorometric detection that depends on the milieu surrounding the ligand these biological processes can be studied with fluorescence spectroscopy and hyper-spectral confocal microscopy. The binding of a thiophene-based ligand to a biological target can entail specific fluorescent read-out through the conformation-sensitive ligand. Thus, the photo-physical properties of these molecules and the optical connection of binding make them valuable tools in the study of pathological events. As optical detection of pathological phenomena can be realized through several fluorescence parameters, including changes in fluorescent intensity, wavelength shifts, energy transfer, or emission lifetime, molecular studies of pathological targets in several biological systems have been realized by employing thiophene-based ligands. For instance, utilization of conjugated polydisperse and monodisperse thiophene-based molecules has in several studies demonstrated detection of disease associated protein aggregates in vitro, ex vivo and in vivo. 

My doctoral studies have included the synthesis and characterization of thiophene based donor-acceptor-donor (D–A–D) molecules and evaluation of how changes in side-chain positions, molecular length and number of negatively charged carboxylates impact interaction with biological targets. This thesis describes the utilization of the D–A–D molecules as fluorescent ligands for protein aggregates associated with Alzheimer’s disease and optical assignment of specific bacteria. The design and synthesis of these novel D–A–D thiophene-based fluorophores, with alterations in back bone, distribution of side chains and negatively charged groups, have generated novel insights regarding the ligands chemical structure on ligand performance, by the assessment of binding mode of the respective ligand to distinct pathological entities. Furthermore, the D–A–D molecules hold alternative photo-physical properties compared to thiophene-based ligand and these optical properties of the ligands have been employed to provide new insights in questions regarding protein aggregate polymorphism in Alzheimer’s disease. Overall, by organic synthesis we have fine-tuned the properties of thiophene-based D-A-D molecules and evaluated how modifications affect interactions with distinct biological, pathological targets and we foresee that D–A–D thiophene-based ligands will expand the toolbox for studying pathological targets in neurodegenerative diseases, as well as bacterial infection. 

Place, publisher, year, edition, pages
Linköping: Linköping University Electronic Press, 2022. p. 56
Series
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 2269
National Category
Organic Chemistry
Identifiers
urn:nbn:se:liu:diva-190162 (URN)978-91-7929-539-4 (ISBN)978-91-7929-540-0 (ISBN)
Public defence
2022-12-12, Planck, Fysikhuset, Campus Valla, Linköping, 09:15
Opponent
Supervisors
Available from: 2022-11-24 Created: 2022-11-24 Last updated: 2022-11-24Bibliographically approved

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