نتایج جستجو برای: random peptide libraries

تعداد نتایج: 478420  

2011
Hirokazu Shiheido Hideaki Takashima Nobuhide Doi Hiroshi Yanagawa

p53 is a tumor suppressor protein that prevents tumorigenesis through cell cycle arrest or apoptosis of cells in response to cellular stress such as DNA damage. Because the oncoprotein MDM2 interacts with p53 and inhibits its activity, MDM2-p53 interaction has been a major target for the development of anticancer drugs. While previous studies have used phage display to identify peptides (such a...

2012
Arie Ryvkin Haim Ashkenazy Larisa Smelyanski Gilad Kaplan Osnat Penn Yael Weiss-Ottolenghi Eyal Privman Peter B. Ngam James E. Woodward Gregory D. May Callum Bell Tal Pupko Jonathan M. Gershoni

BACKGROUND Polyclonal serum consists of vast collections of antibodies, products of differentiated B-cells. The spectrum of antibody specificities is dynamic and varies with age, physiology, and exposure to pathological insults. The complete repertoire of antibody specificities in blood, the IgOme, is therefore an extraordinarily rich source of information-a molecular record of previous encount...

Journal: :The Journal of Experimental Medicine 1997
Bernhard Hemmer Burkhard T. Fleckenstein Marco Vergelli Günther Jung Henry McFarland Roland Martin Karl-Heinz Wiesmüller

CD4+ class II-restricted T cells specific for self antigens are thought to be involved in the pathogenesis of most human autoimmune diseases and molecular mimicry between foreign and self ligands has been implicated as a possible mechanism for their activation. In this report we introduce combinatorial peptide libraries as a powerful tool to identify cross-reactive ligands for these T cells. Th...

2010
Matthew P. Greving Paul E. Belcher Chris W. Diehnelt Maria J. Gonzalez-Moa Jack Emery Jinglin Fu Stephen Albert Johnston Neal W. Woodbury

BACKGROUND There is a significant need for affinity reagents with high target affinity/specificity that can be developed rapidly and inexpensively. Existing affinity reagent development approaches, including protein mutagenesis, directed evolution, and fragment-based design utilize large libraries and/or require structural information thereby adding time and expense. Until now, no systematic ap...

2008
Sita Modali Gopal Abbineni Prashanth Jayanna Valery Petrenko Chuanbin Mao

The goal of this work is to identify a peptide that can specifically bind bone mineral hydroxyapatite [(Ca5(PO4)3OH)2] from a phage-displayed random peptide library. Instead of using pIII library where random peptides are displayed at the tip of filamentous phage, we used landscape phage libraries, in which random octa-peptides or nona-peptides are displayed on all the N-termini of the pVIII (m...

Journal: :iranian journal of allergy, asthma and immunology 0
zohreh jadali mohammad bagher eslami mohammad hossein sanati parvin mansoori mahmoud mahmoudi nader maghsoodi

a random 12 mers phage library was used to screen a pool of immunoglo¬bulin fractions obtained from vitiligo patients. subsequent to panning experiments, a panel of affinity selected phage from vitiligo patients were obtained. this panel was tested using an elis a for their reactivity with pooled sera from patients and normal controls. among the 16 randomly selected clones, two of clones showed...

Journal: :Journal of immunology 1999
Y Tanaka H Ohyama M Ogawa Y Nishimura S Matsushita

The proliferative responses of a human CD4+ T cell clone 29.15.2, reactive with a self-K-ras-derived peptide (3EYKLVVVGAGGVGKSALT20), were tested using a set of X9 combinatorial peptide libraries containing the flanking residues (EYKLVXXXXXXXXXSALT, where X indicates random amino acids). Certain peptide libraries, such as EYKLVXXXXXXM XXSALT and EYKLVXXXXXXXH<cmd /UN...

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