نتایج جستجو برای: keywords phage peptide library

تعداد نتایج: 2249050  

Journal: :American journal of physiology. Renal physiology 2008
Yu-Jung Lee Hyo-Jung Choi Jung-Suk Lim Ji-Hyun Earm Byung-Heon Lee In-San Kim Jørgen Frøkiaer Søren Nielsen Tae-Hwan Kwon

Aquaporin-2 (AQP2), the vasopressin-regulated water channel in collecting duct principal cells, plays a key role in the regulation of body water balance. We aimed to isolate high-affinity peptide ligands that bind to immunoisolated AQP2-expressing plasma membrane (PM) or intracellular vesicle (ICV) preparations from rat kidney by the in vitro phage display technique. Immunoblotting revealed tha...

Journal: :Bioconjugate chemistry 2008
A González-Techera M Umpiérrez-Failache S Cardozo G Obal O Pritsch J A Last S J Gee B D Hammock G González-Sapienza

The use of phage display peptide libraries allows rapid isolation of peptide ligands for any target selector molecule. However, due to differences in peptide expression and the heterogeneity of the phage preparations, there is no easy way to compare the binding properties of the selected clones, which operates as a major "bottleneck" of the technology. Here, we present the development of a new ...

Journal: :Bioconjugate chemistry 2009
Anna Merzlyak Seung-Wuk Lee

Genetic engineering of phage provides novel opportunities to build various nanomaterials by displaying functional peptide motifs on its surface coat protein. However, any genetic modifications of phage coat proteins must be able to accommodate their many biological roles in the phage replication process. To express functional but inherently unfavorable peptide motifs on major coat protein pVIII...

2001
Erkki Ruoslahti

The asp1 integrin binds fibronectin through the integrin recognition sequence Arg-Gly-Asp (RGD). We have used a 6-amino acid peptide library expressed on filamentous phage to identify peptide ligands for asp1. We found that this integrin selectively binds RGD-containing peptides from the library. Of the 32 different sequences obtained, 28 had the RGD motif, 3 contained sequences related to RGD,...

Journal: :Angewandte Chemie International Edition 2019

Journal: :Methods 2001
B K Kay J Kasanov M Yamabhai

Among the many techniques available to investigators interested in mapping protein-protein interactions is phage display. With a modest amount of effort, time, and cost, one can select peptide ligands to a wide array of targets from phage-display combinatorial peptide libraries. In this article, protocols and examples are provided to guide scientists who wish to identify peptide ligands to thei...

Journal: :Molecules 2011
Guillaume Castel Mohamed Chtéoui Bernadette Heyd Noël Tordo

Given the growing number of diseases caused by emerging or endemic viruses, original strategies are urgently required: (1) for the identification of new drugs active against new viruses and (2) to deal with viral mutants in which resistance to existing antiviral molecules has been selected. In this context, antiviral peptides constitute a promising area for disease prevention and treatment. The...

Journal: :The Biochemical journal 1993
I Saggio R Laufer

Recombinant biotin-binding phages were affinity-selected from a random peptide library expressed on the surface of filamentous phage. Phage binding to biotinylated proteins was half-maximally inhibited by micromolar concentrations of a monobiotinylated molecule. Sequencing of the peptide inserts of selected phages led to the identification of a previously unknown biotin-binding motif, CXWXPPF(K...

2012
Roberto Rangel Liliana Guzman-Rojas Lucia G. le Roux Fernanda I. Staquicini Hitomi Hosoya E. Magda Barbu Michael G. Ozawa Jing Nie Kenneth Dunner Jr Robert R. Langley E. Helene Sage Erkki Koivunen Juri G. Gelovani Roy R. Lobb Richard L. Sidman Renata Pasqualini Wadih Arap

Phage display screening allows the study of functional protein-protein interactions at the cell surface, but investigating intracellular organelles remains a challenge. Here we introduce internalizing-phage libraries to identify clones that enter mammalian cells through a receptor-independent mechanism and target-specific organelles as a tool to select ligand peptides and identify their intrace...

Journal: :Journal of Immunology 2023

Abstract TIGIT is an emerging immune checkpoint receptor expressed higher than PD-1 in some tumors especially anti-PD1 resistant tumors. By competing with the co-stimulatory CD226/DNAM-1 for binding to CD155/PVR, transduces inhibitory signals and suppresses response. Therefore, we sought discover inhibitors improving tumor immunotherapy. Through directional cloning, bacterial transformation pha...

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