Literature DB >> 8177892

pH on-off switching of antibody-hapten binding by site-specific chemical modification of tyrosine.

D S Tawfik1, R Chap, Z Eshhar, B S Green.   

Abstract

Tetranitromethane (TNM) chemically mutates the binding sites of antibodies so that the nitrated antibodies exhibit pH-dependent binding near physiological pH. Three monoclonal antibodies were selectively modified, each under different conditions, with the resultant loss of binding activity at pH > 8 which is recovered at pH < 6. Recovery and loss of binding are ascribed to the protonation and deprotonation, respectively, of the hydroxyl group of the resulting 3-nitrotyrosine side chain (pKa approximately 7) at the binding site of these antibodies. pH on-off dependency of binding activity, common to all TNM-modified antibodies studied by us so far, may find use in a variety of applications in which controlled modulation under mild conditions is required.

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Year:  1994        PMID: 8177892     DOI: 10.1093/protein/7.3.431

Source DB:  PubMed          Journal:  Protein Eng        ISSN: 0269-2139


  10 in total

1.  Computational design of a pH-sensitive IgG binding protein.

Authors:  Eva-Maria Strauch; Sarel J Fleishman; David Baker
Journal:  Proc Natl Acad Sci U S A       Date:  2013-12-31       Impact factor: 11.205

2.  A combinatorial histidine scanning library approach to engineer highly pH-dependent protein switches.

Authors:  Megan L Murtaugh; Sean W Fanning; Tressa M Sharma; Alexandra M Terry; James R Horn
Journal:  Protein Sci       Date:  2011-08-03       Impact factor: 6.725

3.  Characterization of the hydrolytic activity of a polyclonal catalytic antibody preparation by pH-dependence and chemical modification studies: evidence for the involvement of Tyr and Arg side chains as hydrogen-bond donors.

Authors:  M Resmini; R Vigna; C Simms; N J Barber; E P Hagi-Pavli; A B Watts; C Verma; G Gallacher; K Brocklehurst
Journal:  Biochem J       Date:  1997-08-15       Impact factor: 3.857

4.  Mutations in the catalytic domain of human matrix metalloproteinase-1 (MMP-1) that allow for regulated activity through the use of Ca2+.

Authors:  Rudolph D Paladini; Ge Wei; Anirban Kundu; Qiping Zhao; Louis H Bookbinder; Gilbert A Keller; H Michael Shepard; Gregory I Frost
Journal:  J Biol Chem       Date:  2013-01-15       Impact factor: 5.157

Review 5.  Considering protonation as a posttranslational modification regulating protein structure and function.

Authors:  André Schönichen; Bradley A Webb; Matthew P Jacobson; Diane L Barber
Journal:  Annu Rev Biophys       Date:  2013-02-28       Impact factor: 12.981

6.  Reversibility of biotin-binding by selective modification of tyrosine in avidin.

Authors:  E Morag; E A Bayer; M Wilchek
Journal:  Biochem J       Date:  1996-05-15       Impact factor: 3.857

7.  Tyrosine nitration of IkappaBalpha: a novel mechanism for NF-kappaB activation.

Authors:  Vasily A Yakovlev; Igor J Barani; Christopher S Rabender; Stephen M Black; J Kevin Leach; Paul R Graves; Glen E Kellogg; Ross B Mikkelsen
Journal:  Biochemistry       Date:  2007-10-02       Impact factor: 3.162

8.  The effects of tyrosine nitration on the structure and function of hen egg-white lysozyme.

Authors:  P G Richards; D J Walton; J Heptinstall
Journal:  Biochem J       Date:  1996-04-15       Impact factor: 3.857

Review 9.  pH-responsive antibodies for therapeutic applications.

Authors:  Tomasz Klaus; Sameer Deshmukh
Journal:  J Biomed Sci       Date:  2021-01-22       Impact factor: 8.410

10.  Engineered protein A ligands, derived from a histidine-scanning library, facilitate the affinity purification of IgG under mild acidic conditions.

Authors:  Masayuki Tsukamoto; Hideki Watanabe; Ayako Ooishi; Shinya Honda
Journal:  J Biol Eng       Date:  2014-07-01       Impact factor: 4.355

  10 in total

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