Pregled bibliografske jedinice broj: 1020163
Correlation Of Membrane Interaction Simulations With Experimental Effects For Kiadin Antimicrobial Peptides
Correlation Of Membrane Interaction Simulations With Experimental Effects For Kiadin Antimicrobial Peptides // 9th International Meeting on Antimicrobial Peptides
Utrecht, 2019. str. 17-17 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1020163 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Correlation Of Membrane Interaction Simulations With Experimental Effects For Kiadin Antimicrobial Peptides
Autori
Rončević, Tomislav ; Guida, Filomena ; Sonavane, Yogesh ; Zoranić, Larisa ; Tossi, Alessandro
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
9th International Meeting on Antimicrobial Peptides
/ - Utrecht, 2019, 17-17
Skup
International Meeting on Antimicrobial Peptides (IMAP 2019)
Mjesto i datum
Utrecht, Nizozemska, 28.08.2019. - 30.08.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Membrane interaction ; Molecular dynamics simulations
(Interakcija s membranom ; simulacije molekulske dinamike)
Sažetak
Kiadins are linear, glycine- and lysine-rich peptides, in silico designed based either on a template derived from the tandem-repeat of the small natural peptide PGLa-H, or on a de novo approach using quantitative structure–activity relationship models [1, 2]. They showed a quite variable activity against Gram-positive and -negative bacterial pathogens, including drug resistant strains, as well as a variable cyto/ genotoxicity when tested on human blood cells. Atomic force microscopy confirmed that they act through membrane damage, leading to its permeabilization, as also confirmed by flow cytometry, but with subtly different modes of action. An initial molecular dynamics (MD) study provided some insight into this mechanism, suggesting the peptides have different interacting preferences with a model biological membrane. Activity and selectivity appear to be influenced in particular by the number and placing of glycine residues along the sequence [2]. We then took into consideration the possibility that the manner in which a peptide faces the membrane surface on its approach could affect the initial mode of action, and subsequently also affect how it inserts into the lipid layer, eventually disrupting it. We relate these in silico results to the strength of interaction with an immobilized liposomes having a membrane composed of the same phospholipids, using surface plasmon resonance. In particular, we attempted to understand why a higher proportion of Gly residues in the sequence correlated with a reduced antibacterial potency but did not necessarily result in a lower toxicity towards host cells. [1] T. Rončević, G. Gajski, N. Ilić, I. Goić-Barišić, M. Tonkić, L. Zoranić, J. Simunić, M. Benincasa, M. Mijaković, A. Tossi, D. Juretić, Biochim. Biophys. Acta BBA - Biomembr. 1859 (2017) 228–237. doi:10.1016/j.bbamem. 2016.11.011 ; [2] T. Rončević, D. Vukičević, N. Ilić, L. Krce, G. Gajski, M. Tonkić, I. Goić-Barišić, L. Zoranić, Y. Sonavane, M. Benincasa, D. Juretić, A. Maravić, A. Tossi, J. Med. Chem. 61 (2018) 2924–2936. doi:10.1021/acs. jmedchem.7b01831.
Izvorni jezik
Engleski
Znanstvena područja
Fizika, Biologija, Interdisciplinarne prirodne znanosti
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Split