Published On: July 10, 2025Categories: Blog

Protein engineering: tailoring therapeutic molecules

 

Protein engineering enables the rational design and optimization of biologically active proteins, including enzymes, cytokines, antibodies, and fusion proteins. Through direct evolution, structure-guided modifications, or synthetic biology tools, researchers can improve a protein:

  • Affinity and specificity to target molecules
  • Pharmacokinetics and half-life in vivo
  • Stability under physiological conditions
  • And even its ability to cross cellular membranes.

These advances are paving the way for smarter, modular therapeutics. However, even the most sophisticated protein requires an effective strategy to reach its target intact, and this is where nanotechnology plays a crucial role.

 

Nanotechnology: making protein delivery possible

 

Delivering proteins systemically remains a major bottleneck. Their large size, structural fragility, and susceptibility to degradation make conventional routes (e.g., intravenous bolus or topical formulations) insufficient for many therapeutic proteins.

Nanoparticles, especially lipid-based nanocarriers, offer a powerful platform to overcome these limitations. At DIVERSA, we design bio-compatible and biodegradable nanoparticles capable of:

  • Associating proteins through mild, click-compatible chemistry, preserving their structure and bioactivity
  • Facilitating targeted delivery to diseased tissues or intracellular compartments
  • Enabling co-delivery of proteins with other modalities (e.g., mRNA, small molecules)
  • And offering scalability and safety for clinical translation.

The result is a new generation of protein delivery systems that merge structural elegance with functional efficiency.

 

Synergy in action: from concept to clinic

 

The alliance of protein engineering and nanotechnology has already demonstrated potential in several applications:

  • Immuno-oncology: delivering engineered cytokines or bispecific antibodies to tumors while reducing systemic toxicity.
  • Enzyme replacement therapies: using nanoparticles to carry functional enzymes into lysosomes or other organelles.
  • Cellular reprogramming: combining transcription factors with lipid nanoparticles (LNPs) to rewire cell identity or immune behavior.
  • Targeted degradation: delivering fusion proteins like PROTACs or ubiquitin ligases to degrade oncogenic proteins.

These strategies are not just theoretical, they are progressing through preclinical pipelines and into clinical development, opening new therapeutic avenues.

 

DIVERSA’s contribution

 

We are advancing the integration of protein-based biologics and nanomedicine technologies. Our platform allows:

Our goal? To help translate protein design into real-world therapies that are safe, scalable, and highly effective.

 

Looking ahead

 

As the landscape of innovative therapies continues to evolve, the combination of protein engineering and nanotechnology will remain at its core. Whether in oncology, rare diseases, or regenerative medicine, this partnership enables a level of control, precision, and creativity that traditional platforms cannot offer.

The future of therapy is not just smart. It’s engineered and nano-enabled.

 

Visit www.diversatechnologies.com or send an email to info@diversatechnologies.com to explore our solutions.

 

References

 

Internal References

  1. Nanotechnology in protein therapeutics: advancing drug discovery and delivery.
  2. How nanotechnology is shaping the future of personalized medicine.
  3. Overcoming regulatory hurdles in clinical translation of nanomedicine.

 

External References

  1. Ren, L., Zhao, Z., Chao, Y., Yu, P., Mei, Z., Du, B., & Cheng, Y. (2025). Optimization of lipid nanoparticles with robust efficiency for the delivery of protein therapeutics to augment cancer immunotherapy. Advanced Science12(17), 2500844. org/10.1002/advs.202500844
  2. Martins, S., Sarmento, B., Ferreira, D. C., & Souto, E. B. (2007). Lipid-based colloidal carriers for peptide and protein delivery–liposomes versus lipid nanoparticles. International journal of nanomedicine2(4), 595-607. org/10.2147/IJN.S2.4.595