نتایج جستجو برای: complementarity determining regions

تعداد نتایج: 521921  

2016
Christian Margreitter Patrick Mayrhofer Renate Kunert Chris Oostenbrink

Monoclonal antibodies represent the fastest growing class of biotherapeutic proteins. However, as they are often initially derived from rodent organisms, there is a severe risk of immunogenic reactions, hampering their applicability. The humanization of these antibodies remains a challenging task in the context of rational drug design. "Superhumanization" describes the direct transfer of the co...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1978
J G Seidman A Leder M H Edgell F Polsky S M Tilghman D C Tiemeier P Leder

We have identified at least six EcoRI fragments of mouse DNA that encode variable-region gene sequences closely related to the mouse kappa light chain, MOPC-149. Two of these fragments have been cloned, and the entire nucleotide sequence of the variable-region genes encoded on each has been determined. Both genes encode closely related variable-region sequences extending from codon position 1 t...

Journal: :Biochemistry 1993
R A Love J E Villafranca R M Aust K K Nakamura R A Jue J G Major R Radhakrishnan W F Butler

Antibodies with bound metal-chelate haptens provide new means for exploiting the diverse properties of metallic elements. The murine monoclonal antibody CHA255 (IgG1 lambda) binds the metal-chelate hapten indium (III)-4-[N'-(2-hydroxyethyl)thioureido]-L-benzyl-EDTA (designated In-EOTUBE) with high affinity (K(a) = 1.1 x 10(10) M-1). Antibody binding is highly specific for the indium chelate; th...

Journal: :Journal of molecular biology 2008
Christine Rothe Stefanie Urlinger Corinna Löhning Josef Prassler Yvonne Stark Ute Jäger Bernd Hubner Michael Bardroff Ingrid Pradel Melanie Boss Renate Bittlingmaier Tschimegma Bataa Christian Frisch Bodo Brocks Annemarie Honegger Margit Urban

This article describes the generation of the Human Combinatorial Antibody Library HuCAL GOLD. HuCAL GOLD is a synthetic human Fab library based on the HuCAL concept with all six complementarity-determining regions (CDRs) diversified according to the sequence and length variability of naturally rearranged human antibodies. The human antibody repertoire was analyzed in-depth, and individual CDR l...

Journal: :The Journal of Experimental Medicine 1988
V H Van Cleave C W Naeve D W Metzger

In an effort to understand the structural basis for antigen mimicry by internal image antibodies, we determined the variable (V) region sequences of two mouse mAbs that mimic the rabbit Ig a1 allotype. The results showed that while the mAb light chains did not contain any allotype-related residues, both heavy chain V regions contained within complementarity-determining region 2 an unusual seque...

Journal: :The Journal of Experimental Medicine 1991
A M Pullen J Bill R T Kubo P Marrack J W Kappler

Superantigen bound to major histocompatibility complex (MHC) products have been shown to stimulate T cells in a V beta-specific manner. Mouse T cells bearing V beta 8.1 usually respond to the self superantigen, Mls-1a, whereas T cells bearing V beta 8.2a do not. Previously, using site-directed mutational analysis, we identified the residues of natural variants of T cell receptor (TCR) V beta 8....

2014
Tao Liu Yan Liu Ying Wang Mitchell Hull Peter G. Schultz Feng Wang

The bovine antibody (BLV1H12) which has an ultralong heavy chain complementarity determining region 3 (CDRH3) provides a novel scaffold for antibody engineering. By substituting the extended CDRH3 of BLV1H12 with modified CXCR4 binding peptides that adopt a β-hairpin conformation, we generated antibodies specifically targeting the ligand binding pocket of CXCR4 receptor. These engineered antibo...

2014
Johannes K X Maier Paul Labute

The success of antibody-based drugs has led to an increased demand for predictive computational tools to assist antibody engineering efforts surrounding the six hypervariable loop regions making up the antigen binding site. Accurate computational modeling of isolated protein loop regions can be quite difficult; consequently, modeling an antigen binding site that includes six loops is particular...

Journal: :Journal of immunology 2002
Deepak T Nair Kavita Singh Zaved Siddiqui Bishnu P Nayak Kanury V S Rao Dinakar M Salunke

Crystal structures of distinct mAbs that recognize a common epitope of a peptide Ag have been determined and analyzed in the unbound and bound forms. These Abs display dissimilar binding site structures in the absence of the Ag. The dissimilarity is primarily expressed in the conformations of complementarity-determining region H3, which is responsible for defining the epitope specificity. Inter...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Dror Baran M Gabriele Pszolla Gideon D Lapidoth Christoffer Norn Orly Dym Tamar Unger Shira Albeck Michael D Tyka Sarel J Fleishman

Natural proteins must both fold into a stable conformation and exert their molecular function. To date, computational design has successfully produced stable and atomically accurate proteins by using so-called "ideal" folds rich in regular secondary structures and almost devoid of loops and destabilizing elements, such as cavities. Molecular function, such as binding and catalysis, however, oft...

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