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https://hdl.handle.net/10442/18109
| Εξειδίκευση τύπου : | Κεφάλαιο βιβλίου |
| Τίτλος: | Integrated bacterial production and functional screening of expanded cyclic peptide libraries for identifying chemical rescuers of pathogenic protein misfolding and aggregation |
| Δημιουργός/Συγγραφέας: | Delivoria, Dafni C. [EL] Σκρέτας, Γιώργος[EN] Skretas, George |
| Επιμελητής έκδοσης: | Iranzo, Olga Roque, Ana Cecília |
| Εκδότης: | Springer |
| Τόπος έκδοσης: | Humana, New York |
| Ημερομηνία: | 2020 |
| Γλώσσα: | Αγγλικά |
| ISBN: | 978-1-0716-0719-0 978-1-0716-0720-6 |
| ISSN: | 1949-2448 1949-2456 |
| DOI: | 10.1007/978-1-0716-0720-6_13 |
| Περίληψη: | Protein misfolding and aggregation are defining features of a wide range of human conditions, collectively termed protein misfolding diseases. These include disorders with diverse pathologies and symptoms, such as Alzheimer’s disease, Parkinson’s disease, and type 2 diabetes, the vast majority of which impose a very high socio-economic burden on humanity and remain incurable to date. To address this unmet medical need, we report here a simple and high-throughput system for identifying macrocyclic rescuers of protein misfolding. In this system, Escherichia coli cells are genetically engineered in order to perform two simultaneous tasks: (1) produce combinatorial libraries of head-to-tail cyclic oligopeptides using protein-splicing technology and (2) enable the identification of the bioactive cyclic peptides that correct the problematic folding and/or inhibit the aggregation of disease-associated misfolding-prone proteins using a genetic assay that links the folding of the target protein to a fluorescent phenotype. In this way, the bioactive cyclic peptide hits are identified in an ultrahigh-throughput manner using flow cytometric cell sorting, thus significantly decreasing the overall cost, time, and complexity of early drug discovery for these notorious diseases. |
| Τίτλος πηγής δημοσίευσης: | Peptide and Protein Engineering: From Concepts to Biotechnological Applications |
| Σελίδες: | 237–266 |
| Σειρά δημοσίευσης: | Springer Protocols Handbooks |
| Θεματική Κατηγορία: | [EL] Βιοχημεία[EN] Biochemistry [EL] Μικροβιολογία[EN] Microbiology [EL] Χημική Βιολογία[EN] Chemical Biology [EL] Βιοτεχνολογία[EN] Biotechnology |
| Λέξεις-Κλειδιά: | Protein misfolding diseases Protein aggregation High-throughput screening SICLOPPS technology Cyclic peptides |
| Κάτοχος πνευματικών δικαιωμάτων: | Copyright © 2020 Springer Science+Business Media, LLC, part of Springer Nature |
| Ηλεκτρονική διεύθυνση στον εκδότη (link): | https://link.springer.com/protocol/10.1007/978-1-0716-0720-6_13#editor-information |
| Ηλεκτρονική διεύθυνση περιοδικού (link) : | https://link.springer.com/book/10.1007/978-1-0716-0720-6 |
| Εμφανίζεται στις συλλογές: | Ινστιτούτο Χημικής Βιολογίας - Επιστημονικό έργο
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