Your browser doesn't support javascript.
loading
Histidine-enhanced gene delivery systems: The state of the art.
Hooshmand, Seyyed Emad; Jahanpeimay Sabet, Makkieh; Hasanzadeh, Akbar; Kamrani Mousavi, Seyede Mahtab; Haeri Moghaddam, Niloofar; Hooshmand, Seyed Aghil; Rabiee, Navid; Liu, Yong; Hamblin, Michael R; Karimi, Mahdi.
Afiliação
  • Hooshmand SE; Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Jahanpeimay Sabet M; Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
  • Hasanzadeh A; Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
  • Kamrani Mousavi SM; Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
  • Haeri Moghaddam N; Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
  • Hooshmand SA; Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
  • Rabiee N; Laboratory of Systems Biology and Bioinformatics (LBB), Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran.
  • Liu Y; Department of Physics, Sharif University of Technology, Tehran, Iran.
  • Hamblin MR; School of Engineering, Macquarie University, Sydney, NSW, Australia.
  • Karimi M; Institute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou, Jiangsu, China.
J Gene Med ; 24(5): e3415, 2022 05.
Article em En | MEDLINE | ID: mdl-35132731
ABSTRACT
Gene therapy has emerged as a promising tool for treating different intractable diseases, particularly cancer or even viral diseases such as COVID-19 (coronavirus disease 2019). In this context, various non-viral gene carriers are being explored to transfer DNA or RNA sequences into target cells. Here, we review the applications of the naturally occurring amino acid histidine in the delivery of nucleic acids into cells. The biocompatibility of histidine-enhanced gene delivery systems has encouraged their wider use in gene therapy. Histidine-based gene carriers can involve the modification of peptides, dendrimers, lipids or nanocomposites. Several linear polymers, such as polyethylenimine, poly-l-lysine (synthetic) or dextran and chitosan (natural), have been conjugated with histidine residues to form complexes with nucleic acids for intracellular delivery. The challenges, opportunities and future research trends of histidine-based gene deliveries are investigated.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Nucleicos / COVID-19 Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Nucleicos / COVID-19 Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article