Fupeng Li: The Art of Biochemical Synthesis, Chemical Synthesis of Proteins Containing Post-translational Modifications and PNA-templated Disulfide Bond Formation - neues Buch
As the most important molecules, proteins often undergo post-translational modifications (PTM) to carry out their functions. In my study, two methods have been developed for the synthesis… Mehr…
As the most important molecules, proteins often undergo post-translational modifications (PTM) to carry out their functions. In my study, two methods have been developed for the synthesis of proteins containing PTMs. The first method is chemical ligation at valine residue. The thioacid capture ligation was found to be more efficient to overcome steric hindrance of the tertiary thiol group in penicillamine compared with thioester-mediated ligation. The second method is a direct and easy-to-use approach to introducing site-specific acetylation onto recombinant proteins. The free thiol of cysteine was reacted with N-vinylacetamide (NVA) by radical-mediated thiol-ene coupling to generate acetyl-4-thialysine (sLys (Ac)) which is anacetyl-lysine analog. In the last part of this work, we have also introduced a new strategy for selective disulfide formation directed by PNA pairing. This method can be more useful than the DNA-templated reaction systems. Inhoud: Taal: en; Bindwijze: Paperback; Oorspronkelijke releasedatum: 30 augustus 2012; Aantal pagina's: 152; Illustraties: Nee; Betrokkenen: Hoofdauteur: Fupeng Li; Hoofduitgeverij: Lap Lambert Academic Publishing; Overige kenmerken: Extra groot lettertype: Nee; Gewicht: 231 g; Product breedte: 152 mm; Product hoogte: 9 mm; Product lengte: 229 mm; Studieboek: Ja; Verpakking breedte: 152 mm; Verpakking hoogte: 9 mm; Verpakking lengte: 229 mm; EAN: Engels | Paperback | 9783659219689 | 30 augustus 2012 | 152 pagina's, Boeken, Wetenschap & Natuur, Biologie, Lap Lambert Academic Publishing<
Fupeng Li: The Art of Biochemical Synthesis : Chemical Synthesis of Proteins Containing Post¿translational Modifications and PNA¿templated Disulfide Bond Formation - Taschenbuch
[EAN: 9783659219689], Nieuw boek, [SC: 14.0], [PU: LAP LAMBERT Academic Publishing], nach der Bestellung gedruckt Neuware - Printed after ordering - As the most important molecules, prote… Mehr…
[EAN: 9783659219689], Nieuw boek, [SC: 14.0], [PU: LAP LAMBERT Academic Publishing], nach der Bestellung gedruckt Neuware - Printed after ordering - As the most important molecules, proteins often undergo post-translational modifications (PTM) to carry out their functions. In my study, two methods have been developed for the synthesis of proteins containing PTMs. The first method is chemical ligation at valine residue. The thioacid capture ligation was found to be more efficient to overcome steric hindrance of the tertiary thiol group in penicillamine compared with thioester-mediated ligation. The second method is a direct and easy-to-use approach to introducing site-specific acetylation onto recombinant proteins. The free thiol of cysteine was reacted with N-vinylacetamide (NVA) by radical-mediated thiol-ene coupling to generate acetyl-4-thialysine (sLys (Ac)) which is anacetyl-lysine analog. In the last part of this work, we have also introduced a new strategy for selective disulfide formation directed by PNA pairing. This method can be more useful than the DNA-templated reaction systems. 152 pp. Englisch, Books<
Fupeng Li: The Art of Biochemical Synthesis : Chemical Synthesis of Proteins Containing Post¿translational Modifications and PNA¿templated Disulfide Bond Formation - Taschenbuch
[EAN: 9783659219689], Neubuch, [PU: LAP LAMBERT Academic Publishing], nach der Bestellung gedruckt Neuware - Printed after ordering - As the most important molecules, proteins often under… Mehr…
[EAN: 9783659219689], Neubuch, [PU: LAP LAMBERT Academic Publishing], nach der Bestellung gedruckt Neuware - Printed after ordering - As the most important molecules, proteins often undergo post-translational modifications (PTM) to carry out their functions. In my study, two methods have been developed for the synthesis of proteins containing PTMs. The first method is chemical ligation at valine residue. The thioacid capture ligation was found to be more efficient to overcome steric hindrance of the tertiary thiol group in penicillamine compared with thioester-mediated ligation. The second method is a direct and easy-to-use approach to introducing site-specific acetylation onto recombinant proteins. The free thiol of cysteine was reacted with N-vinylacetamide (NVA) by radical-mediated thiol-ene coupling to generate acetyl-4-thialysine (sLys (Ac)) which is anacetyl-lysine analog. In the last part of this work, we have also introduced a new strategy for selective disulfide formation directed by PNA pairing. This method can be more useful than the DNA-templated reaction systems. 152 pp. Englisch, Books<
Li, Fupeng: The Art of Biochemical Synthesis Chemical Synthesis of Proteins Containing Post¿translational Modifications and PNA¿templated Disulfide Bond Formation - neues Buch
The Art of Biochemical Synthesis, Chemical Synthesis of Proteins Containing Post-translational Modifications and PNA-templated Disulfide Bond Formation - neues Buch
As the most important molecules, proteins often undergo post-translational modifications (PTM) to carry out their functions. In my study, two methods have been developed for the synthesis… Mehr…
As the most important molecules, proteins often undergo post-translational modifications (PTM) to carry out their functions. In my study, two methods have been developed for the synthesis of proteins containing PTMs. The first method is chemical ligation at valine residue. The thioacid capture ligation was found to be more efficient to overcome steric hindrance of the tertiary thiol group in penicillamine compared with thioester-mediated ligation. The second method is a direct and easy-to-use approach to introducing site-specific acetylation onto recombinant proteins. The free thiol of cysteine was reacted with N-vinylacetamide (NVA) by radical-mediated thiol-ene coupling to generate acetyl-4-thialysine (sLys (Ac)) which is anacetyl-lysine analog. In the last part of this work, we have also introduced a new strategy for selective disulfide formation directed by PNA pairing. This method can be more useful than the DNA-templated reaction systems. Inhoud: Taal: en; Bindwijze: Paperback; Oorspronkelijke releasedatum: 30 augustus 2012; Aantal pagina's: 152; Illustraties: Nee; Betrokkenen: Hoofdauteur: Fupeng Li; Hoofduitgeverij: Lap Lambert Academic Publishing; Overige kenmerken: Extra groot lettertype: Nee; Gewicht: 231 g; Product breedte: 152 mm; Product hoogte: 9 mm; Product lengte: 229 mm; Studieboek: Ja; Verpakking breedte: 152 mm; Verpakking hoogte: 9 mm; Verpakking lengte: 229 mm; EAN: Engels | Paperback | 9783659219689 | 30 augustus 2012 | 152 pagina's, Boeken, Wetenschap & Natuur, Biologie, Lap Lambert Academic Publishing<
The Art of Biochemical Synthesis : Chemical Synthesis of Proteins Containing Post¿translational Modifications and PNA¿templated Disulfide Bond Formation - Taschenbuch
[EAN: 9783659219689], Nieuw boek, [SC: 14.0], [PU: LAP LAMBERT Academic Publishing], nach der Bestellung gedruckt Neuware - Printed after ordering - As the most important molecules, prote… Mehr…
[EAN: 9783659219689], Nieuw boek, [SC: 14.0], [PU: LAP LAMBERT Academic Publishing], nach der Bestellung gedruckt Neuware - Printed after ordering - As the most important molecules, proteins often undergo post-translational modifications (PTM) to carry out their functions. In my study, two methods have been developed for the synthesis of proteins containing PTMs. The first method is chemical ligation at valine residue. The thioacid capture ligation was found to be more efficient to overcome steric hindrance of the tertiary thiol group in penicillamine compared with thioester-mediated ligation. The second method is a direct and easy-to-use approach to introducing site-specific acetylation onto recombinant proteins. The free thiol of cysteine was reacted with N-vinylacetamide (NVA) by radical-mediated thiol-ene coupling to generate acetyl-4-thialysine (sLys (Ac)) which is anacetyl-lysine analog. In the last part of this work, we have also introduced a new strategy for selective disulfide formation directed by PNA pairing. This method can be more useful than the DNA-templated reaction systems. 152 pp. Englisch, Books<
Fupeng Li: The Art of Biochemical Synthesis : Chemical Synthesis of Proteins Containing Post¿translational Modifications and PNA¿templated Disulfide Bond Formation - Taschenbuch
[EAN: 9783659219689], Neubuch, [PU: LAP LAMBERT Academic Publishing], nach der Bestellung gedruckt Neuware - Printed after ordering - As the most important molecules, proteins often under… Mehr…
[EAN: 9783659219689], Neubuch, [PU: LAP LAMBERT Academic Publishing], nach der Bestellung gedruckt Neuware - Printed after ordering - As the most important molecules, proteins often undergo post-translational modifications (PTM) to carry out their functions. In my study, two methods have been developed for the synthesis of proteins containing PTMs. The first method is chemical ligation at valine residue. The thioacid capture ligation was found to be more efficient to overcome steric hindrance of the tertiary thiol group in penicillamine compared with thioester-mediated ligation. The second method is a direct and easy-to-use approach to introducing site-specific acetylation onto recombinant proteins. The free thiol of cysteine was reacted with N-vinylacetamide (NVA) by radical-mediated thiol-ene coupling to generate acetyl-4-thialysine (sLys (Ac)) which is anacetyl-lysine analog. In the last part of this work, we have also introduced a new strategy for selective disulfide formation directed by PNA pairing. This method can be more useful than the DNA-templated reaction systems. 152 pp. Englisch, Books<
Li, Fupeng: The Art of Biochemical Synthesis Chemical Synthesis of Proteins Containing Post¿translational Modifications and PNA¿templated Disulfide Bond Formation - neues Buch
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Detailangaben zum Buch - The Art of Biochemical Synthesis
EAN (ISBN-13): 9783659219689 ISBN (ISBN-10): 3659219681 Gebundene Ausgabe Taschenbuch Erscheinungsjahr: 2012 Herausgeber: LAP Lambert Academic Publishing
Buch in der Datenbank seit 2008-01-13T15:43:02+01:00 (Zurich) Detailseite zuletzt geändert am 2023-10-05T21:54:42+02:00 (Zurich) ISBN/EAN: 9783659219689
ISBN - alternative Schreibweisen: 3-659-21968-1, 978-3-659-21968-9 Alternative Schreibweisen und verwandte Suchbegriffe: Titel des Buches: the chemical bond
