Meet Inspiring Speakers and Experts at our 3000+ Global Conference Series Events with over 1000+ Conferences, 1000+ Symposiums
and 1000+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business.

Explore and learn more about Conference Series : World's leading Event Organizer

Back

Lungu N Claudiu

Lungu N Claudiu

Babes-Bolyai University, Romania

Title: MSCM-Multiple selective proteo nano cluster mesh coating CD’s agonist/antagonist

Biography

Biography: Lungu N Claudiu

Abstract

Cell surface molecules (CSM) like L selectin, VLA-4, LFA-1, CD2, CD4, TCR, CD44, CD45RA and CD45RO play a major role in cell interaction, signalling and function. CSM are in a “mosaic” of activated–inactivated states. These states determine cell behaviour. Cells are controlled by a “cocktail” of molecules that act on CSM modulating their states. Nano system was designed using computational methods like molecular dynamics, docking, ligand design, virtual screening and experimental methods like isothermal titration calorimetry (ITC) and single cell imaging techniques. The system is composed of nano polymers, graphene and fullerene patches on witch wild or synthetic “ligands”-amino acids or small peptide for CSM are incorporated. Physico chemical triggers were used to activate MSMC. Cellular meshing by MSCM allows controlling and guiding of cellular dynamic interaction with all the pathways involving the cell. MSMC by its nano polymer mesh can protect or stabilize a certain cell or tissue. MSMC was made cell specific by incorporating Ig motifs against different types of cells. Computational models of L-selectin, VLA-4, LFA-1, CD2, CD4, TCR, CD44, CD45RA and CD45RO were designed and incorporated into a nano polymer mesh. MSMC outer surface was coated with phosphatidilinositol, sphingnomielin and cholesterol mono layer. The system goal is to be administrated iv. In the first stage of development, the attention was focused on single cell manipulation. The viability of the cell (unintended cell death) and the lack of adverse effects like aggregation, hemolysis4, toxicity were tested. Each receptor was characterized individualy and a series of proteic motifs were developed for incorporation into MSMC. In conclusion, a bio-nano-device5 was designed to control a cell by stimulating/inhibiting the CD’s. System was designed to be cell specific and tissue specific; device is ,,controlled’’ by physico-chemical stimuli. The ultimate goal of this system is to control large volumes of cells eventually tissues.