Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Quentin Seisel"'
1
Akademický článek
Highway to Cell: Selection of the Best Cell-Penetrating Peptide to Internalize the CFTR-Stabilizing iCAL36 Peptide
Autor: Quentin Seisel, Israpong Lakumpa, Emilie Josse, Eric Vivès, Jessica Varilh, Magali Taulan-Cadars, Prisca Boisguérin
Publikováno v: Pharmaceutics, Vol 14, Iss 4, p 808 (2022)
Therapeutic peptides have regained interest as they can address unmet medical needs and can be an excellent complement to pharmaceutic small molecules and other macromolecular therapeutics. Over the past decades, correctors and potentiators of the cy
Externí odkaz: https://doaj.org/article/305f1631f2c34a4aa01a089357f94cb3
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2
Akademický článek
A retro-inverso cell-penetrating peptide for siRNA delivery
Autor: Anaïs Vaissière, Gudrun Aldrian, Karidia Konate, Mattias F. Lindberg, Carole Jourdan, Anthony Telmar, Quentin Seisel, Frédéric Fernandez, Véronique Viguier, Coralie Genevois, Franck Couillaud, Prisca Boisguerin, Sébastien Deshayes
Publikováno v: Journal of Nanobiotechnology, Vol 15, Iss 1, Pp 1-18 (2017)
Abstract Background Small interfering RNAs (siRNAs) are powerful tools to control gene expression. However, due to their poor cellular permeability and stability, their therapeutic development requires a specific delivery system. Among them, cell-pen
Externí odkaz: https://doaj.org/article/d14efe6268784060953ef834f12fb825
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3
Fluorescent Leakage Assay to Investigate Membrane Destabilization by Cell-Penetrating Peptide
Autor: Quentin Seisel, Sébastien Deshayes, Eric Vivès, Prisca Boisguerin, Karidia Konate
Publikováno v: Journal of visualized experiments : JoVE
Journal of visualized experiments : JoVE, JoVE, In press, ⟨10.3791/62028⟩
Cell-penetrating peptides (CPPs) are defined as carriers that are able to cross the plasma membrane and to transfer a cargo into cells. One of the main common features required for this activity resulted from the interactions of CPPs with the plasma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fb822ab95356ee51916fdeadd901f9f
https://hal.archives-ouvertes.fr/hal-03367256
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4
How to evaluate the cellular uptake of CPPs with fluorescence techniques: Dissecting methodological pitfalls associated to tryptophan-rich peptides
Autor: Quentin Seisel, Sébastien Deshayes, François Pelletier, Prisca Boisguerin
Publikováno v: Biochimica et Biophysica Acta:Biomembranes
Biochimica et Biophysica Acta:Biomembranes, Elsevier, 2019, 1861 (9), pp.1533-1545. ⟨10.1016/j.bbamem.2019.06.011⟩
Biochim Biophys Acta Biomembr
International audience; Cell-penetrating peptides (CPP) are broadly recognized as efficient non-viral vectors for the internalization of compounds such as peptides, oligonucleotides or proteins. Characterizing these carriers requires reliable methods
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::707bb2f31ec4f97be73071791941184c
https://hal.archives-ouvertes.fr/hal-03007575
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6
Optimization of the process of inverted peptides (PIPE PLUS ) to screen PDZ domain ligands
Autor: Dean R. Madden, Nicholas P. Gill, Marisa Rädisch, Quentin Seisel, Prisca Boisguerin
Publikováno v: Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2017, 27 (14), pp.3111--3116. ⟨10.1016/j.bmcl.2017.05.045⟩
PDZ domains play crucial roles in cell signaling processes and are therefore attractive targets for the development of therapeutic inhibitors. In many cases, C-terminal peptides are the physiological binding partners of PDZ domains. To identify both
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6edf69db938cb021eb25eebd09a52f8a
https://hal.archives-ouvertes.fr/hal-01875266
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7
Optimization of the process of inverted peptides (PIPE
Autor: Quentin, Seisel, Marisa, Rädisch, Nicholas P, Gill, Dean R, Madden, Prisca, Boisguerin
Publikováno v: Bioorganicmedicinal chemistry letters. 27(14)
PDZ domains play crucial roles in cell signaling processes and are therefore attractive targets for the development of therapeutic inhibitors. In many cases, C-terminal peptides are the physiological binding partners of PDZ domains. To identify both
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ef7ac47b5f8234937da83fdf75112df5
https://pubmed.ncbi.nlm.nih.gov/28549735
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8
PEGylation rate influences peptide-based nanoparticles mediated siRNA delivery in vitro and in vivo
Autor: S. Barrere-Lemaire, Gudrun Aldrian, Hélène Déméné, Véronique Viguier, Karidia Konate, Eric Vivès, Franck Couillaud, Dina Aggad, Quentin Seisel, Anaïs Vaissière, Coralie Genevois, Frédéric Fernandez, Sébastien Deshayes, Prisca Boisguerin, Aurélie Covinhes
Publikováno v: Journal of Controlled Release
Journal of Controlled Release, Elsevier, 2017, 256, pp.79-91. ⟨10.1016/j.jconrel.2017.04.012⟩
Small interfering RNAs (siRNAs) present a strong therapeutic potential because of their ability to inhibit the expression of any desired protein. Recently, we developed the retro-inverso amphipathic RICK peptide as novel non-covalent siRNA carrier. T
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92b3178351d3f6aa0c3769d891d64be7
https://pubmed.ncbi.nlm.nih.gov/28411182
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