Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mayra Quemé-Peña"'
Autor:
Kamal el Battioui, Sohini Chakraborty, András Wacha, Dániel Molnár, Mayra Quemé-Peña, Imola Cs. Szigyártó, Csenge Lilla Szabó, Andrea Bodor, Kata Horváti, Gergő Gyulai, Szilvia Bősze, Judith Mihály, Bálint Jezsó, Loránd Románszki, Judit Tóth, Zoltán Varga, István Mándity, Tünde Juhász, Tamás Beke-Somfai
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract Developing unique mechanisms of action are essential to combat the growing issue of antimicrobial resistance. Supramolecular assemblies combining the improved biostability of non-natural compounds with the complex membrane-attacking mechanis
Externí odkaz:
https://doaj.org/article/19140e0f599745b188faaf71f8024c6a
Autor:
Tünde Juhász, Mayra Quemé-Peña, Bence Kővágó, Judith Mihály, Maria Ricci, Kata Horváti, Szilvia Bősze, Ferenc Zsila, Tamás Beke-Somfai
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract In the emerging era of antimicrobial resistance, the susceptibility to co-infections of patients suffering from either acquired or inherited hemolytic disorders can lead to dramatic increase in mortality rates. Closely related, heme liberate
Externí odkaz:
https://doaj.org/article/303dc353fe50461882ecf5f2211cc1c0
Publikováno v:
ACS Omega, Vol 6, Iss 24, Pp 15756-15769 (2021)
Externí odkaz:
https://doaj.org/article/44c2bb526a4c46db98f574f88ae93038
Autor:
Mayra Quemé-Peña, Tünde Juhász, Gergely Kohut, Maria Ricci, Priyanka Singh, Imola Cs. Szigyártó, Zita I. Papp, Lívia Fülöp, Tamás Beke-Somfai
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 16, p 8613 (2021)
Anticancer peptides (ACPs) could potentially offer many advantages over other cancer therapies. ACPs often target cell membranes, where their surface mechanism is coupled to a conformational change into helical structures. However, details on their b
Externí odkaz:
https://doaj.org/article/cd011fa815a447bfb36e4259b00a454e
Autor:
Vignesh Udyavara Nagaraj, Tünde Juhász, Mayra Quemé-Peña, Imola Cs. Szigyártó, Dóra Bogdán, András Wacha, Judith Mihály, Loránd Románszki, Zoltán Varga, Joakim Andréasson, István Mándity, Tamás Beke-Somfai
Publikováno v:
ACS applied materialsinterfaces. 14(50)
Self-assembled peptide nanostructures with stimuli-responsive features are promising as functional materials. Despite extensive research efforts, water-soluble supramolecular constructs that can interact with lipid membranes in a controllable way are
Autor:
Szilvia Bősze, Tamás Beke-Somfai, Tünde Juhász, Bálint Szeder, Ferenc Zsila, Beáta Biri-Kovács, Mayra Quemé-Peña, Maria Ricci, Kata Horváti
Publikováno v:
ACS Pharmacol Transl Sci
[Image: see text] The host defense peptide LL-37 is the only human cathelicidin, characterized by pleiotropic activity ranging from immunological to anti-neoplastic functions. However, its overexpression has been associated with harmful inflammatory
Autor:
Maria Ricci, Bence Kővágó, Ferenc Zsila, Tamás Beke-Somfai, Judith Mihály, Tünde Juhász, Mayra Quemé-Peña, Szilvia Bősze, Kata Horváti
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
In the emerging era of antimicrobial resistance, the susceptibility to co-infections of patients suffering from either acquired or inherited hemolytic disorders can lead to dramatic increase in mortality rates. Closely related, heme liberated during
Autor:
Priyanka Singh, Lívia Fülöp, Mayra Quemé-Peña, Gergely Kohut, Tünde Juhász, Imola Cs. Szigyártó, Tamás Beke-Somfai, Zita I. Papp, Maria Ricci
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 8613, p 8613 (2021)
Volume 22
Issue 16
International Journal of Molecular Sciences, Vol 22, Iss 8613, p 8613 (2021)
Volume 22
Issue 16
Anticancer peptides (ACPs) could potentially offer many advantages over other cancer therapies. ACPs often target cell membranes, where their surface mechanism is coupled to a conformational change into helical structures. However, details on their b
Autor:
Judit Henczkó, Ferenc Zsila, Tünde Juhász, Tamás Beke-Somfai, Kata Horváti, Szilvia Bősze, Mayra Quemé-Peña, Zoltán Varga, Csaba Németh, Bernadett Pályi, Judith Mihály, Imola Cs. Szigyártó
Publikováno v:
Chembiochem
Antimicrobial peptides (AMPs) kill bacteria by targeting their membranes through various mechanisms involving peptide assembly, often coupled with disorder‐to‐order structural transition. However, for several AMPs, similar conformational changes
Publikováno v:
ACS Omega
ACS Omega, Vol 6, Iss 24, Pp 15756-15769 (2021)
ACS Omega, Vol 6, Iss 24, Pp 15756-15769 (2021)
Owing to their potential applicability against multidrug-resistant bacteria, antimicrobial peptides (AMPs) or host defense peptides (HDPs) gain increased attention. Besides diverse immunomodulatory roles, their classical mechanism of action mostly in