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Display technologies: Application for the discovery of drug and gene delivery agents()

Recognition of molecular diversity of cell surface proteomes in disease is essential for the development of targeted therapies. Progress in targeted therapeutics requires establishing effective approaches for high-throughput identification of agents specific for clinically relevant cell surface mark...

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Detalles Bibliográficos
Autores principales: Sergeeva, Anna, Kolonin, Mikhail G., Molldrem, Jeffrey J., Pasqualini, Renata, Arap, Wadih
Formato: Texto
Lenguaje:English
Publicado: Elsevier B.V. 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847402/
https://www.ncbi.nlm.nih.gov/pubmed/17123658
http://dx.doi.org/10.1016/j.addr.2006.09.018
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author Sergeeva, Anna
Kolonin, Mikhail G.
Molldrem, Jeffrey J.
Pasqualini, Renata
Arap, Wadih
author_facet Sergeeva, Anna
Kolonin, Mikhail G.
Molldrem, Jeffrey J.
Pasqualini, Renata
Arap, Wadih
author_sort Sergeeva, Anna
collection PubMed
description Recognition of molecular diversity of cell surface proteomes in disease is essential for the development of targeted therapies. Progress in targeted therapeutics requires establishing effective approaches for high-throughput identification of agents specific for clinically relevant cell surface markers. Over the past decade, a number of platform strategies have been developed to screen polypeptide libraries for ligands targeting receptors selectively expressed in the context of various cell surface proteomes. Streamlined procedures for identification of ligand-receptor pairs that could serve as targets in disease diagnosis, profiling, imaging and therapy have relied on the display technologies, in which polypeptides with desired binding profiles can be serially selected, in a process called biopanning, based on their physical linkage with the encoding nucleic acid. These technologies include virus/phage display, cell display, ribosomal display, mRNA display and covalent DNA display (CDT), with phage display being by far the most utilized. The scope of this review is the recent advancements in the display technologies with a particular emphasis on molecular mapping of cell surface proteomes with peptide phage display. Prospective applications of targeted compounds derived from display libraries in the discovery of targeted drugs and gene therapy vectors are discussed.
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spelling pubmed-18474022007-04-02 Display technologies: Application for the discovery of drug and gene delivery agents() Sergeeva, Anna Kolonin, Mikhail G. Molldrem, Jeffrey J. Pasqualini, Renata Arap, Wadih Adv Drug Deliv Rev Article Recognition of molecular diversity of cell surface proteomes in disease is essential for the development of targeted therapies. Progress in targeted therapeutics requires establishing effective approaches for high-throughput identification of agents specific for clinically relevant cell surface markers. Over the past decade, a number of platform strategies have been developed to screen polypeptide libraries for ligands targeting receptors selectively expressed in the context of various cell surface proteomes. Streamlined procedures for identification of ligand-receptor pairs that could serve as targets in disease diagnosis, profiling, imaging and therapy have relied on the display technologies, in which polypeptides with desired binding profiles can be serially selected, in a process called biopanning, based on their physical linkage with the encoding nucleic acid. These technologies include virus/phage display, cell display, ribosomal display, mRNA display and covalent DNA display (CDT), with phage display being by far the most utilized. The scope of this review is the recent advancements in the display technologies with a particular emphasis on molecular mapping of cell surface proteomes with peptide phage display. Prospective applications of targeted compounds derived from display libraries in the discovery of targeted drugs and gene therapy vectors are discussed. Elsevier B.V. 2006-12-30 2006-10-06 /pmc/articles/PMC1847402/ /pubmed/17123658 http://dx.doi.org/10.1016/j.addr.2006.09.018 Text en Copyright © 2006 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Sergeeva, Anna
Kolonin, Mikhail G.
Molldrem, Jeffrey J.
Pasqualini, Renata
Arap, Wadih
Display technologies: Application for the discovery of drug and gene delivery agents()
title Display technologies: Application for the discovery of drug and gene delivery agents()
title_full Display technologies: Application for the discovery of drug and gene delivery agents()
title_fullStr Display technologies: Application for the discovery of drug and gene delivery agents()
title_full_unstemmed Display technologies: Application for the discovery of drug and gene delivery agents()
title_short Display technologies: Application for the discovery of drug and gene delivery agents()
title_sort display technologies: application for the discovery of drug and gene delivery agents()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847402/
https://www.ncbi.nlm.nih.gov/pubmed/17123658
http://dx.doi.org/10.1016/j.addr.2006.09.018
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