نتایج جستجو برای: keywords phage peptide library

تعداد نتایج: 2249050  

Journal: :Science 1996
T N Schumacher L M Mayr D L Minor M A Milhollen M W Burgess P S Kim

Genetically encoded libraries of peptides and oligonucleotides are well suited for the identification of ligands for many macromolecules. A major drawback of these techniques is that the resultant ligands are subject to degradation by naturally occurring enzymes. Here, a method is described that uses a biologically encoded library for the identification of D-peptide ligands, which should be res...

2013
Marina Pavlidou Karen Hänel Luis Möckel Dieter Willbold

In this work, we exploited a method that uses polytopic membrane proteins as targets for phage display selections. Membrane proteins represent the largest class of drug targets and drug discovery is mostly based on the identification of ligands binding to target molecules. The screening of a phage display library for ligands against membrane proteins is typically hindered by the requirement of ...

2006
Daniel J. Kenan Elisabeth B. Walsh Steven R. Meyers George A. O’Toole Erin G. Carruthers Woo K. Lee Stefan Zauscher Carla A. H. Prata Mark W. Grinstaff

Identification of Polystyrene (PS)-Binding Sequences Polymer-binding sequences were identified using a phage display library developed from phage type M13. The library displayed random peptide sequences on its pIII coat proteins of the format X6YX6 or X6PX6, where X represents one of the twenty naturally occurring amino acids. For the panning procedure, wells of a native polystyrene plate (CoSt...

Journal: :Molecular cancer research : MCR 2011
Alisson L Matsuo Maria A Juliano Carlos R Figueiredo Wagner L Batista Aparecida S Tanaka Luiz R Travassos

Phage-display peptide libraries have been widely used to identify specific peptides targeting in vivo tumor cells and the tumor vasculature and playing an important role in the discovery of antitumor bioactive peptides. In the present work, we identified a new melanoma-homing peptide, (-CVNHPAFAC-), using a C7C phage-display library directed to the developing tumor in syngeneic mice. Phage were...

2011
Alisson L. Matsuo Maria A. Juliano Carlos R. Figueiredo Wagner L. Batista Aparecida S. Tanaka Luiz R. Travassos

Phage-display peptide libraries have been widely used to identify specific peptides targeting in vivo tumor cells and the tumor vasculature and playing an important role in the discovery of antitumor bioactive peptides. In the present work, we identified a new melanoma-homing peptide, (-CVNHPAFAC-), using a C7C phage-display library directed to the developing tumor in syngeneic mice. Phage were...

2011
Xiangan Tu Jintao Zhuang Wenwei Wang Liang Zhao Liangyun Zhao Jiquan Zhao Chunhua Deng Shaopeng Qiu Yuanyuan Zhang

BACKGROUND Specific peptide ligands to cell surface receptors have been extensively used in tumor research and clinical applications. Phage display technology is a powerful tool for the isolation of cell-specific peptide ligands. To screen and identify novel markers for renal cell carcinoma, we evaluated a peptide that had been identified by phage display technology. METHODS A renal carcinoma...

Journal: :Journal of biotechnology 2012
Tatiana I Samoylova Anna M Cochran Alexandre M Samoylov Bettina Schemera Adam H Breiteneicher Stephen S Ditchkoff Valery A Petrenko Nancy R Cox

Multiple phage-peptide constructs, where the peptides mimic sperm epitopes that bind to zona pellucida (ZP) proteins, were generated via selection from a phage display library using a novel approach. Selections were designed to allow for identification of ZP-binding phage clones with potential species-specific properties, an important feature for wildlife oral vaccines as the goal is to control...

2017
Jason M. Goldstein Joo Lee Xiaoling Tang Anne E. Boyer John R. Barr Dennis A. Bagarozzi Conrad P. Quinn

AVR1674 and AVR1675 are monoclonal antibodies (mAbs) that bind with high specificity to anthrax toxin lethal factor (LF) and lethal toxin (LTx). These mAbs have been used as pivotal reagents to develop anthrax toxin detection tests using mass spectrometry. The mAbs were demonstrated to bind LF with good affinity (KD 10−7–10−9 M) and to enhance LF-mediated cleavage of synthetic peptide substrate...

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