FN3: a new protein scaffold reaches the clinic.

Abstract

In the ten years since the first fibronectin type III (FN3) domain library was published, FN3 has continued to show promise as a scaffold for the generation of stable protein domains that bind to targets with high affinity. A variety of display systems, library designs and affinity maturation strategies have been used to generate FN3 domains with nanomolar to picomolar affinities. The first crystal structures of engineered FN3 molecules in complex with their targets have been solved, and structural studies of engineered FN3 have begun to reveal determinants of stability and to define zones that accept mutations with minimal trade-off between affinity and stability. CT-322, the first engineered FN3 to enter clinical development, is now entering Phase II trials for glioblastoma multiforme.

• Authors: Laird Bloom, Valerie Calabro
• Journal: Drug discovery today (Drug Discov Today) Vol. 14 Issue 19-20 Pg. 949-55 (Oct 2009) ISSN: 1878-5832 [Electronic] England
• PMID: 19576999 (Publication Type: Journal Article, Review)

Chemical References

• Antineoplastic Agents
• Fibronectins
• Peptide Library
• Recombinant Proteins

Topics

• Amino Acid Sequence
• Animals
• Antineoplastic Agents (chemistry, metabolism, therapeutic use)
• Binding Sites
• Central Nervous System Neoplasms (drug therapy)
• Fibronectins (chemistry, genetics, metabolism, therapeutic use)
• Glioblastoma (drug therapy)
• Humans
• Models, Molecular
• Molecular Sequence Data
• Mutagenesis, Site-Directed
• Peptide Library
• Protein Conformation
• Protein Stability
• Protein Structure, Tertiary
• Recombinant Proteins (therapeutic use)
• Structure-Activity Relationship
• Tissue Engineering
• Tissue Scaffolds