TECHNOLOGY DESCRIPTION
The present invention relates to the development of innovative cell-penetrating peptides (CPPs) to deliver cargos inside cells with very high efficiency and without noticeable toxicity.
CPPs are most promising alternatives for delivering cargos into cells, however, despite several decades of investigation, the fundamental basis for CPPs activity remains elusive. Consequently, CPPs developed so far do not usually achieve a high efficiency in cargo delivery and are frequently cytotoxic for cells.
The new cell-penetrating peptides (CPPs) comprise a specific short amino acid sequence of the CD300f protein that show a strong binding capacity to phospholipids, the main component of the plasma membrane. Through amino acid substitutions, the inventors found the key amino acids that mediate the binding of this sequence being, in particular, one lysine residue and some tryptophan residues located in very specific and unique positions.
The peptides or proteins comprising the identified sequence show a potent cell-penetration activity, thereby facilitating the internalization of cargos to which they are conjugated (peptide-cargo conjugate).
Diverse types of nanoparticles (as micelles or extracellular vesicles) conjugated to these new peptides present higher delivery rates than nanoparticles conjugated to TAT (tyrosine aminotransferase), the gold standard of CPPs.
The technology provides a pharmaceutical composition comprising a therapeutically effective amount of a conjugate with at least one pharmaceutically acceptable excipient, diluent or carrier.
Both the conjugate and the pharmaceutical composition can be used as a medicament.
BENEFITS
These new and innovative cell-penetrating peptides (CPPs) can deliver cargos inside cells with very high efficiency and without noticeable toxicity.
LIMITATIONS
To be determined during further development.
APPLICATIONS
Treatment of cancer
MATERIALS
Readiness Level (TRL)
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STATUS
Current status
EP Application
AVAILABILITY
Available for
Licensing or Assignment
INVENTOR / TEAM
Juan Sayos, Simo Schwartz, Joaquin Seras, Agueda Martinez, Diana Fernandes de Sousa, Fernanda da Silva