نتایج جستجو برای: phage library

تعداد نتایج: 138241  

2015
Junrong Yan Pingyan Wang Min Zhu Guanghui Li Ema Romão Sheng Xiong Yakun Wan

BACKGROUND Nanobodies (Nbs) are single-domain antigen-binding fragments derived from the camelids heavy-chain only antibodies (HCAbs). Their unique advantageous properties make Nbs highly attractive in various applications. The general approach to obtain Nbs is to isolate them from immune libraries by phage display technology. However, it is unfeasible when the antigens are toxic, lethal, trans...

Journal: :BMC Biotechnology 2009
Wim Noppe Fatima Plieva Igor Yu Galaev Hans Pottel Hans Deckmyn Bo Mattiasson

BACKGROUND Phage Display technology is a well established technique for high throughput screening of affinity ligands. Here we describe a new compact chromato-panning procedure for selection of suitable binders from a phage peptide display library. RESULTS Both phages and E. coli cells pass non-hindered through the interconnected pores of macroporous gel, so called cryogel. After coupling a l...

Journal: :Journal of microbiological methods 2005
Iryna B Sorokulova Eric V Olsen I-Hsuan Chen Ben Fiebor James M Barbaree Vitaly J Vodyanoy Bryan A Chin Valery A Petrenko

We selected from landscape phage library probes that bind preferentially Salmonella typhimurium cells compared with other Enterobacteriaceae. The specificity of the phage probes for S. typhimurium was analyzed by the phage-capture test, the enzyme-linked immunosorbent assay (ELISA), and the precipitation test. Interaction of representative probes with S. typhimurium was characterized by fluores...

Journal: :Protein Engineering, Design and Selection 2002

Journal: :Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 2010
Takuya Yamashita Naoki Utoguchi Ryo Suzuki Kazuya Nagano Shin-ichi Tsunoda Yasuo Tsutsumi Kazuo Maruyama

Tumor blood vessels are essential for tumor growth. Therefore, these blood vessels are potential targets for anti-cancer therapy. The purpose of this study is to develop anti-tumor endothelial cell (TEC) antibodies for delivering anti-cancer agents or drugs. To achieve this goal, we utilized the phage antibody display library method to create monoclonal antibodies in vitro. Accordingly, we deve...

Journal: :Journal of molecular biology 2008
Daniel Steiner Patrik Forrer Andreas Plückthun

There is an ever-increasing demand to select specific, high-affinity binding molecules against targets of biomedical interest. The success of such selections depends strongly on the design and functional diversity of the library of binding molecules employed, and on the performance of the selection strategy. We recently developed SRP phage display that employs the cotranslational signal recogni...

Journal: :Molecules 2011
Anka N Veleva Desh B Nepal C Brandon Frederick Jacob Schwab Pamela Lockyer Hong Yuan David S Lalush Cam Patterson

We developed a screening procedure to identify ligands from a phage display random peptide library that are selective for circulating bone marrow derived cells homing to angiogenic tumors. Panning the library on blood outgrowth endothelial cell suspension in vitro followed by in vivo selection based on homing of bone marrow-bound phage to angiogenic tumors, yielded the peptide QFPPKLTNNSML. Upo...

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...

Tumor-targeted therapies are playing growing roles in cancer research. The exploitation of these powerful therapeutic modalities largely depends on the discovery of tumor-targeting ligands. Phage display has proven a promising high throughput screening tool for the identification of novel specific peptides with high binding affinity to cancer cells. In the present study, we describe the use of ...

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