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Study of the full deprotection of a model peptide

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dc.contributor Farràs i Soler, Jaume
dc.creator García Gros, Júlia
dc.date 2017-09-29T15:12:06Z
dc.date 2017-09-29T15:12:06Z
dc.date 2017-06
dc.date.accessioned 2024-12-16T10:25:36Z
dc.date.available 2024-12-16T10:25:36Z
dc.identifier http://hdl.handle.net/2445/116059
dc.identifier.uri http://fima-docencia.ub.edu:8080/xmlui/handle/123456789/19723
dc.description Treballs Finals de Grau de Química, Facultat de Química, Universitat de Barcelona, Any: 2017, Tutor: Jaume Farràs Soler
dc.description Fmoc chemistry has been used to synthesise the 2-chlorotrityl peptidyl-resin shown in the figure below, in order to study its cleavage conditions and the subsequent side products.The cleavage of the peptide, as well as the deprotection of its side chains, are practically quantitative after 30 minutes of reaction time, using 95 % TFA, 2.5 % TIPS and 2.5 Milli-Q water. The main impurity belongs to a dimer that arises from the formation of a disulphide bond between the Cys residues of two identical peptide chains. The addition of DTT to the cleavage mixture as a reducing agent does not prevent the formation of the dimer. On the other hand, using TCEP as a reducing agent minimises the formation of this side product in a very efficient way.
dc.format 51 p.
dc.format application/pdf
dc.language eng
dc.rights cc-by-nc-nd (c) García, 2017
dc.rights http://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.rights info:eu-repo/semantics/openAccess
dc.source Treballs Finals de Grau (TFG) - Química
dc.subject Síntesi de pèptids
dc.subject Enllaços químics
dc.subject Treballs de fi de grau
dc.subject Peptide synthesis
dc.subject Chemical bonds
dc.subject Bachelor's theses
dc.title Study of the full deprotection of a model peptide
dc.title Estudi de la desprotecció total d’un pèptid model
dc.type info:eu-repo/semantics/bachelorThesis


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