An Introductory Guide to Protease Sensitive Linker Design Using Matrix Metalloproteinase 13 as an Example.
bioinformatics
cleavage site specificity
matrix metalloproteinase 13
protease sensitive linkers
proteomics
solid phase peptide synthesis
Journal
ACS biomaterials science & engineering
ISSN: 2373-9878
Titre abrégé: ACS Biomater Sci Eng
Pays: United States
ID NLM: 101654670
Informations de publication
Date de publication:
30 May 2024
30 May 2024
Historique:
medline:
30
5
2024
pubmed:
30
5
2024
entrez:
30
5
2024
Statut:
aheadofprint
Résumé
Proteases play a crucial role, not only in physiological, but also in pathological processes, such as cancer, inflammation, arthritis, Alzheimer's, and infections, to name but a few. Their ability to cleave peptides can be harnessed for a broad range of biotechnological purposes. To do this efficiently, it is essential to find an amino acid sequence that meets the necessary requirements, including interdependent factors like specificity, selectivity, cleavage kinetics, or synthetic accessibility. Cleavage sequences from natural substrates of the protease may not be optimal in terms of specificity and selectivity, which is why these frequently require arduous and sometimes unsuccessful optimization such as by iterative exchange of single amino acids. Hence, here we describe the systematic design of
Identifiants
pubmed: 38813796
doi: 10.1021/acsbiomaterials.4c00407
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM