Literature DB >> 19252840

Dynamics of antibody domains studied by solution NMR.

Bang K Vu1, Joseph D Walsh, Dimiter S Dimitrov, Rieko Ishima.   

Abstract

Information on local dynamics of antibodies is important to evaluate stability, to rationally design variants, and to clarify conformational disorders at the epitope binding sites. Such information may also be useful for improved understanding of antigen recognition. NMR can be used for characterization of local protein dynamics at the atomic level through relaxation measurements. Due to the complexity of the NMR spectra, an extensive use of this method is limited to small protein molecules, for example, antibody domains and some scFv. Here, we describe a protocol that was used to study the dynamics of an antibody domain in solution using NMR. We describe protein preparation for NMR studies, NMR sample optimization, signal assignments, and dynamics experiments.

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Year:  2009        PMID: 19252840      PMCID: PMC3423202          DOI: 10.1007/978-1-59745-554-1_29

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  28 in total

1.  NMR observation of selected segments in a larger protein: central-segment isotope labeling through intein-mediated ligation.

Authors:  T Otomo; N Ito; Y Kyogoku; T Yamazaki
Journal:  Biochemistry       Date:  1999-12-07       Impact factor: 3.162

2.  TROSY and CRINEPT: NMR with large molecular and supramolecular structures in solution.

Authors:  R Riek; K Pervushin; K Wüthrich
Journal:  Trends Biochem Sci       Date:  2000-10       Impact factor: 13.807

Review 3.  Nmr probes of molecular dynamics: overview and comparison with other techniques.

Authors:  A G Palmer
Journal:  Annu Rev Biophys Biomol Struct       Date:  2001

4.  Molecular dynamics simulations of a double unit cell in a protein crystal: volume relaxation at constant pressure and correlation of motions between the two unit cells.

Authors:  Regula Walser; Philippe H Hünenberger; Wilfred F van Gunsteren
Journal:  Proteins       Date:  2002-08-01

5.  Structures of larger proteins in solution: three- and four-dimensional heteronuclear NMR spectroscopy.

Authors:  G M Clore; A M Gronenborn
Journal:  Science       Date:  1991-06-07       Impact factor: 47.728

6.  Solution structure of a llama single-domain antibody with hydrophobic residues typical of the VH/VL interface.

Authors:  Wim Vranken; Dmitri Tolkatchev; Ping Xu; Jamshid Tanha; Zhigang Chen; Saran Narang; Feng Ni
Journal:  Biochemistry       Date:  2002-07-09       Impact factor: 3.162

7.  A rapid method to attain isotope labeled small soluble peptides for NMR studies.

Authors:  Bernd W Koenig; Marco Rogowski; John M Louis
Journal:  J Biomol NMR       Date:  2003-07       Impact factor: 2.835

8.  Expression, purification, and isotope labeling of the Fv of the human HIV-1 neutralizing antibody 447-52D for NMR studies.

Authors:  Naama Kessler; Anat Zvi; Min Ji; Michal Sharon; Osnat Rosen; Rina Levy; Miroslaw Gorny; Suzan Zolla-Pazner; Jacob Anglister
Journal:  Protein Expr Purif       Date:  2003-06       Impact factor: 1.650

9.  Backbone dynamics of proteins as studied by 15N inverse detected heteronuclear NMR spectroscopy: application to staphylococcal nuclease.

Authors:  L E Kay; D A Torchia; A Bax
Journal:  Biochemistry       Date:  1989-11-14       Impact factor: 3.162

10.  Practical aspects of the 2D 15N-[1h]-NOE experiment.

Authors:  Christian Renner; Michael Schleicher; Luis Moroder; Tad A Holak
Journal:  J Biomol NMR       Date:  2002-05       Impact factor: 2.835

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  2 in total

Review 1.  Engineered CH2 domains (nanoantibodies).

Authors:  Dimiter S Dimitrov
Journal:  MAbs       Date:  2009 Jan-Feb       Impact factor: 5.857

2.  A large library based on a novel (CH2) scaffold: identification of HIV-1 inhibitors.

Authors:  Xiaodong Xiao; Yang Feng; Bang K Vu; Rieko Ishima; Dimiter S Dimitrov
Journal:  Biochem Biophys Res Commun       Date:  2009-07-15       Impact factor: 3.575

  2 in total

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