نتایج جستجو برای: مدلسازی لوپ cdr h3

تعداد نتایج: 28355  

2015
Jonas Kügler Sonja Wilke Doris Meier Florian Tomszak André Frenzel Thomas Schirrmann Stefan Dübel Henk Garritsen Björn Hock Lars Toleikis Mark Schütte Michael Hust

BACKGROUND Antibody phage display is a proven key technology that allows the generation of human antibodies for diagnostics and therapy. From naive antibody gene libraries - in theory - antibodies against any target can be selected. Here we describe the design, construction and characterization of an optimized antibody phage display library. RESULTS The naive antibody gene libraries HAL9 and ...

2018
Xi Fu Jianqiang Sun Engkong Tan Kentaro Shimizu Md Shaheed Reza Shugo Watabe Shuichi Asakawa

B-cell antigen receptor (BCR) or antibody diversity arises from somatic recombination of immunoglobulin (Ig) gene segments and is concentrated within the Ig heavy (H) chain complementarity-determining region 3 (CDR-H3). We performed high-throughput sequencing of the expressed antibody heavy-chain repertoire from adult torafugu. We found that torafugu use between 70 and 82% of all possible V (va...

2016
Hiroshi Nishigami Narutoshi Kamiya Haruki Nakamura

The antigen-binding site of antibodies, also known as complementarity-determining region (CDR), has hypervariable sequence properties. In particular, the third CDR loop of the heavy chain, CDR-H3, has such variability in its sequence, length, and conformation that ordinary modeling techniques cannot build a high-quality structure. At Stage 2 of the Second Antibody Modeling Assessment (AMA-II) h...

Journal: :Science immunology 2016
Mohamed Khass Tessa Blackburn Peter D Burrows Mark R Walter Emidio Capriotti Harry W Schroeder

Developmental checkpoints eliminate B cells that synthesize defective immunoglobulin (Ig) heavy (HC) and light (LC) chains. The first checkpoint tests μHCs paired with VpreB/λ5 in a pre-B cell receptor (pre-BCR) to determine whether the μHC will be able to bind conventional LCs to form membrane IgM. VpreB and λ5 also create a sensing site that interacts with the μHC antigen-binding region compl...

2016
Alexey Teplyakov Galina Obmolova Thomas J. Malia Jinquan Luo Salman Muzammil Raymond Sweet Juan Carlos Almagro Gary L. Gilliland

To support antibody therapeutic development, the crystal structures of a set of 16 germline variants composed of 4 different kappa light chains paired with 4 different heavy chains have been determined. All four heavy chains of the antigen-binding fragments (Fabs) have the same complementarity-determining region (CDR) H3 that was reported in an earlier Fab structure. The structure analyses incl...

Journal: :Journal of virology 2010
Jean-Philippe Julien Nerea Huarte Rubén Maeso Stefka G Taneva Annie Cunningham José L Nieva Emil F Pai

The identification and characterization of broadly neutralizing antibodies (bnAbs) against HIV-1 has formed a major research focus, with the ultimate goal to help in the design of an effective AIDS vaccine. One of these bnAbs, 2F5, has been extensively characterized, and residues at the apex of its unusually long complementarity-determining region (CDR) H3 loop have been shown to be crucial for...

2018
Mohamed Khass Tessa Blackburn Ada Elgavish Peter D. Burrows Harry W. Schroeder

Sequential developmental checkpoints are used to "optimize" the B cell antigen receptor repertoire by minimizing production of autoreactive or useless immunoglobulins and enriching for potentially protective antibodies. The first and apparently most impactful checkpoint requires μHC to form a functional pre-B cell receptor (preBCR) by associating with surrogate light chain, which is composed of...

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