VP6-SUMO Self-Assembly as Nanocarriers for Gastrointestinal Delivery

Valentina Palmieri, Francesca Bugli, Massimiliano Papi*, Gabriele Ciasca, G Maulucci, SG Galgano, Alessandro Arcovito, Maurzio Sanguinetti, Marco De Spirito

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)


High proteolytic degradation and poor absorption through epithelial barriers are major challenges to successful oral delivery of therapeutics. Nanoparticle platforms can enhance drug stability and extend the residence time in gastrointestinal (GI) tract. However, drug delivery systems are often inactivated in acidic environment of stomach or suffer poor absorption from intestinal cells due to the mucus layer. To overcome these issues we developed a drug delivery system constituted by a protein construct made by a Rotavirus capsid protein (VP6) and the small ubiquitin-like modifier SUMO. This chimeric construct allows specificity towards intestinal cells, the Rotavirus natural target, combined by an enhanced stability given by the eukaryotic protein transporter SUMO. Furthermore SUMO can act as a molecular switch that facilitates import/export of its ligand to the nucleus, the hypersensitive subcellular site target of many cell killing therapies. In this paper we show that SUMO-VP6 constructs self-assembly into stable nanocarriers. SUMO-VP6 nanocarriers display ideal features for drug delivery: a small size and high monodispersity, a high stability in different pH conditions and a high uptake in the nuclear and cytoplasmic compartment of intestinal cells. These features make SUMO-VP6 nanocarriers a promising novel system for oral delivery of poorly soluble drugs.
Original languageEnglish
Article numberID 378786
Number of pages7
JournalJournal of Nanomaterials
Publication statusPrint publication - 22 Nov 2015
Externally publishedYes


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