Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 1Comparison of Cell-Penetrating and Fusogenic Tat-Ha2 Peptide Performance in Peptideplex, Multicomponent, and Conjugate Sirna Delivery Systems(Amer Chemical Soc, 2024) Uz, Metin; Bulmus, Volga; Altinkaya, Sacide AlsoyIn this study, the performance of the cell-penetrating and fusogenic peptide, TAT-HA2, which consists of a cell-permeable HIV trans-activator of transcription (TAT) protein transduction domain and a pH-responsive influenza A virus hemagglutinin protein (HA2) domain, was comparatively evaluated for the first time in peptideplex, multicomponent, and conjugate siRNA delivery systems. TAT-HA2 in all three systems protected siRNA from degradation, except in the conjugate system with a low Peptide/siRNA ratio. The synergistic effect of different peptide domains enhanced the transfection efficiency of multicomponent and conjugate systems compared to that of peptideplexes, which was attributed to the surface configuration of TAT-HA2 peptides depending on the nature of attachment. Particularly, the multicomponent system showed better cellular uptake and endosomal escape than the peptideplexes, resulting in enhanced siRNA delivery in the cytoplasm. In addition, the presence of cleavable disulfide bonds in multicomponent and conjugate systems promoted the effective siRNA delivery in the cytoplasm, resulting in improved gene silencing activity. The multicomponent system reduced the level of luciferase expression in SKOV3 cells to 45% (+/- 4). In contrast, the conjugate system and the commercially available siRNA transfection agent, Lipofectamine RNAiMax, caused luciferase suppression down to 55% (+/- 2) at a siRNA dose of 100 nM. For the same dose, the peptideplex system could only reduce the luciferase expression to 65% (+/- 5). None of the developed systems showed significant toxicity at any dose. Overall, the TAT-HA2 peptide is promising as a siRNA delivery vector; however, its performance depends on the nature of attachment and, as a result, its surface configuration on the developed delivery system.Book Citation - Scopus: 5Editors’ Foreword(CRC Press, 2017) Figoli, A.; Hoinkis, Jan; Altinkaya, Sacide Alsoy; Bundschuh, JochenThe book focuses on Application of Nanotechnology in Membranes for Water Treatment but not only provides a series of innovative solutions for water reclamation through advanced membrane technology but also serves as a medium to promote international cooperation and networking for the development of advanced membrane technology for Universal well-being and to achieve the common goal of supplying economically, environmentally and societally sustainable freshwater and better sanitation systems. This book is unique because the chapters were authored by established researchers all around the globe based on their recent research findings. In addition, this book provides a holistic coverage of membrane development for water treatment, from the membrane preparation and characterizations to the performance for specific processes and applications. Since that water scarcity has become a global risk and one of the most serious challenges for the scientific community in this century, the publication of this book is therefore significant as it will serve as a medium for a good reference of an alternative solution in water reclamation. This book will provide the readers with a thorough understanding of the different available approaches for manufacturing membranes both with innovative polymeric systems and inorganic nano-materials which could give enhanced functionalities, catalytic and antimicrobial activities to improve the performance of the existing membranes. It will be useful for leading decision and policy makers, water sector representatives and administrators, policy makers from the governments, business leaders, business houses in water treatment, and engineers/ scientists from both industrialized and developing countries as well. © 2019 Elsevier B.V., All rights reserved.