Please use this identifier to cite or link to this item: doi:10.22028/D291-30954
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Title: Fine-tuning Nanocarriers Specifically toward Cargo: A Competitive Study on Solubilizing Related Photosensitizers for Photodynamic Therapy
Author(s): Wieczorek, Sebastian
Remmler, Dario
Masini, Tiziana
Kochovski, Zdravko
Hirsch, Anna
Börner, Hans G.
Language: English
Title: Bioconjugate chemistry
Volume: 28
Issue: 3
Startpage: 760
Endpage: 767
Publisher/Platform: ACS
Year of Publication: 2017
Publikation type: Journal Article
Abstract: Tailor-made drug solubilizers are studied based on peptide-poly(ethylene glycol) conjugates, which exhibit peptide segments constituting binding motifs for the small-molecule drugs of interest to render them water-soluble. Suitable 7mer peptides are selected via combinatorial means by screening large one-bead-one-compound (OBOC) peptide libraries. The capability of the screening method to read out structural detail of the drugs is investigated by comparing three related photosensitizers (Chlorin E6 (Ce6), Pheophorbide A (Pba) and meta-tetra(hydroxyphenyl)chlorin (m-THPC), which are applicable for photodynamic cancer therapy. The screening procedure delivers de novo solubilizers that show the best solubilization efficiency for the drug the screening is performed with. While molecular recognition events between peptide and drug are not expected to be found, significant binding capacity differences of, e.g., the Ce6-solubilizer for Pba are suggesting selectivity in drug binding, even among structurally closely related drugs. Cyro-Electron microscopy revealed the formation of colloidal aggregates between drug moieties and peptide conjugates. Insights into relevant amino acids in the identified peptide sequences are gained by studying capacities of systematic point mutations (alanine scans), enabling understanding of drug-binding motifs. These reveal the importance of sequence positioning of appropriate H-bonding between polar functional groups of the peptide and the drugs, which agrees well with computational binding studies performed on drug/peptide model complexes.
DOI of the first publication: 10.1021/acs.bioconjchem.6b00549
URL of the first publication: https://pubs.acs.org/doi/abs/10.1021/acs.bioconjchem.6b00549
Link to this record: hdl:20.500.11880/29161
http://dx.doi.org/10.22028/D291-30954
ISSN: 1520-4812
1043-1802
Date of registration: 15-May-2020
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Pharmazie
Professorship: NT - Prof. Dr. Anna Hirsch
Collections:UniBib – Die Universitätsbibliographie

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