We are part of the H2020-MSCA-ITN team STOP SPREAD BAD BUGS!

We are part of the team being awarded the H2020 Marie Skłodowska-Curie Actions (MSCA) Innovative Training Networks (ITN) with the project “STOP SPREAD BAD BUGS: novel antimicrobial approaches to combat multidrug resistance in bacteria“. As part of the CONCEPT lab we will support a multidisciplinary team composed by medical doctors, biologists, chemists, and physicists to […]

We are part of the PRIN 2020 project CANNOT-ESKAPE!

We are part of the team being awarded the national PRIN2020 project “CANNOT-ESKAPE: Targeting baCteriAl cell eNvelope of Nocosomial paThogens to ESKAPE resistance”. Our unit, led by Rita de Zorzi (University of Trieste), we will support a multidisciplinary team led by Flavia Squeglia (CNR, Naples), supporting biologists, chemists, and physicists tackling the problem of antimicrobial […]

Read our latest paper on the topology to employ for in silico designed peptides!

A new application of BINDesignER/PARCE! Herein, we compared the ability of linear and cyclic peptides generated in silico to target different protein sites: internal pockets and solvent-exposed sites. We selected human lysozyme (HuL) as a model target protein combined with the computational evolution of linear and cyclic peptides. The computational results demonstrated that cyclic peptides […]

We have been awarded a “ARDF’s Annual Open grant” from the Alternatives Research & Development Foundation (ARDF)

Our commitment in the development of new computational protocols that can compete and, in time, eliminate the demand for in vivo procedures for antibody discovery and maturation has been prized once again with a 40,000$ grant with the project ” De-novo engineered antibody fragments: validation of the first in-silico pipeline for antibody discovery ” from the […]

Read our latest paper on in silico designed peptides for nanopatterned surface sensors!

We present a rationally designed, self-assembled nanochip capable of capturing a target protein by means of pre-selected binding sites. We show how the confined peptides are capable of specifically capturing β2m from the surface–liquid interface with micromolar affinity, hence providing a viable proof-of-concept for our approach to peptide design   A. Feyisara Adedeji Olulana, M.A. […]