Literature DB >> 10694456

Optical spectroscopy in studies of antibody-hapten interactions.

S Y Tetin1, T L Hazlett.   

Abstract

This article describes the use of optical spectroscopy in studying antibody-hapten interactions and in determining the equilibrium binding constants. Along with equilibrium binding data, spectroscopic tools often deliver structural information on binding-induced conformational changes of antibodies (or haptens). Structural implications of results from example antibody-hapten systems are included. Fluorescence spectroscopy has been particularly useful in the area of ligand binding, and thus steady-state fluorescence quenching and fluorescence polarization are the primary techniques under discussion. A brief description of fluorescence correlation spectroscopy is also provided. Absorption techniques, including circular dichroism, are mentioned to a lesser extent. A basic description of the mathematical models involved in the analysis of binding equilibria is provided along with references to more complete works. Simulated and experimental data are used to illustrate the various experimental protocols and the appropriate analytical methods. Typical sources of errors and experimental precautions are indicated throughout the general discussion. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10694456     DOI: 10.1006/meth.1999.0927

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  14 in total

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2.  Determination of the folding of proteins as a function of denaturants, osmolytes or ligands using circular dichroism.

Authors:  Norma J Greenfield
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

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Journal:  Assay Drug Dev Technol       Date:  2011-03-11       Impact factor: 1.738

4.  Evidence of Fe3+ interaction with the plug domain of the outer membrane transferrin receptor protein of Neisseria gonorrhoeae: implications for Fe transport.

Authors:  Sambuddha Banerjee; Claire J Parker Siburt; Shreni Mistry; Jennifer M Noto; Patrick DeArmond; Michael C Fitzgerald; Lisa A Lambert; Cynthia N Cornelissen; Alvin L Crumbliss
Journal:  Metallomics       Date:  2012-03-08       Impact factor: 4.526

5.  Tailoring of biomimetic high-density lipoprotein nanostructures changes cholesterol binding and efflux.

Authors:  Andrea J Luthi; Heng Zhang; Dongwoo Kim; David A Giljohann; Chad A Mirkin; C Shad Thaxton
Journal:  ACS Nano       Date:  2011-12-01       Impact factor: 15.881

6.  Spectroscopic properties of various blood antigens/antibodies.

Authors:  Seyedeh Solaleh Seyedi; Parviz Parvin; Amir Jafargholi; Nazanin Hashemi; Seyed Morteza Tabatabaee; Ali Abbasian; Ahmad Khorrami
Journal:  Biomed Opt Express       Date:  2020-04-01       Impact factor: 3.732

7.  Determining antibody stoichiometry using time-integrated fluorescence cumulant analysis.

Authors:  Joseph P Skinner; Bin Wu; Joachim D Mueller; Sergey Y Tetin
Journal:  J Phys Chem B       Date:  2010-12-30       Impact factor: 2.991

8.  Co2+ selectivity of Thermotoga maritima CorA and its inability to regulate Mg2+ homeostasis present a new class of CorA proteins.

Authors:  Yu Xia; Anna-Karin Lundbäck; Newsha Sahaf; Gustav Nordlund; Peter Brzezinski; Said Eshaghi
Journal:  J Biol Chem       Date:  2011-03-22       Impact factor: 5.157

9.  Non-specific protein-DNA interactions control I-CreI target binding and cleavage.

Authors:  Rafael Molina; Pilar Redondo; Stefano Stella; Marco Marenchino; Marco D'Abramo; Francesco Luigi Gervasio; Jean Charles Epinat; Julien Valton; Silvestre Grizot; Phillipe Duchateau; Jesús Prieto; Guillermo Montoya
Journal:  Nucleic Acids Res       Date:  2012-04-11       Impact factor: 16.971

10.  Far-UV circular dichroism signatures indicate fluorophore labeling induced conformational changes of penetratin.

Authors:  Ferenc Zsila
Journal:  Amino Acids       Date:  2022-03-18       Impact factor: 3.789

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