Synthesis of Amide Backbone-Modified Peptides.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2020
Historique:
entrez: 28 12 2019
pubmed: 28 12 2019
medline: 20 1 2021
Statut: ppublish

Résumé

Solubility is a key property of peptides and of central importance to the success of solid-phase peptide synthesis and subsequent peptide purification and handling. Substitution of the backbone amide bond can dramatically increase peptide solubility. Backbone amide bond protection works by preventing the formation of interchain association and can be used both to synthesize aggregation-prone peptide sequences on solid phase and to improve solubility of a peptide post synthesis. Improving peptide solubility by judicial use of backbone protection is of growing importance, particularly for chemical protein synthesis by chemical ligation.

Identifiants

pubmed: 31879929
doi: 10.1007/978-1-0716-0227-0_15
doi:

Substances chimiques

Amides 0
Amino Acids 0
Benzaldehydes 0
Peptides 0
benzaldehyde TA269SD04T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

225-237

Auteurs

Abu-Baker M Abdel-Aal (AM)

The Francis Crick Institute, London, UK.

Richard Raz (R)

The Francis Crick Institute, London, UK.

George Papageorgiou (G)

The Francis Crick Institute, London, UK.

John Offer (J)

The Francis Crick Institute, London, UK. john.offer@crick.ac.uk.

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Classifications MeSH