Literature DB >> 19348779

Methods for sample labeling and meniscus determination in the fluorescence-detected analytical ultracentrifuge.

Michael F Bailey1, Lauren M Angley, Matthew A Perugini.   

Abstract

The fluorescence detection system for the analytical ultracentrifuge (AU-FDS) enables the measurement of hydrodynamic properties and interactions of biomolecules at subnanomolar concentrations. In this study, we describe methods for (i) preparing and purifying fluorescently labeled biomolecules and (ii) determining the meniscus position in the AU-FDS using BODIPY 493/503 fluorescent dye suspended in light oil. We subsequently use these methods to measure the interaction of DNA with Escherichia coli Klenow fragment (KF) and show that KF binds matched DNA to form 1:1 and 2:1 (protein/DNA) complexes with dissociation constants of 4.2 and 22 nM, respectively.

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Year:  2009        PMID: 19348779     DOI: 10.1016/j.ab.2009.03.045

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  11 in total

1.  Use of fluorescence-detected sedimentation velocity to study high-affinity protein interactions.

Authors:  Sumit K Chaturvedi; Jia Ma; Huaying Zhao; Peter Schuck
Journal:  Nat Protoc       Date:  2017-08-03       Impact factor: 13.491

2.  Energetics of SecA dimerization.

Authors:  Andy J Wowor; Dongmei Yu; Debra A Kendall; James L Cole
Journal:  J Mol Biol       Date:  2011-02-15       Impact factor: 5.469

3.  Are fluorescence-detected sedimentation velocity data reliable?

Authors:  Daniel F Lyons; Jeffrey W Lary; Bushra Husain; John J Correia; James L Cole
Journal:  Anal Biochem       Date:  2013-03-07       Impact factor: 3.365

4.  Ionomer and protein size analysis by analytical ultracentrifugation and electrospray scanning mobility particle sizer.

Authors:  Simon E Wawra; Martin Thoma; Johannes Walter; Christian Lübbert; Thaseem Thajudeen; Cornelia Damm; Wolfgang Peukert
Journal:  Eur Biophys J       Date:  2018-06-16       Impact factor: 1.733

5.  Tools for the quantitative analysis of sedimentation boundaries detected by fluorescence optical analytical ultracentrifugation.

Authors:  Huaying Zhao; Ernesto Casillas; Hari Shroff; George H Patterson; Peter Schuck
Journal:  PLoS One       Date:  2013-10-18       Impact factor: 3.240

6.  Analysis of high-affinity assembly for AMPA receptor amino-terminal domains.

Authors:  Huaying Zhao; Anthony J Berger; Patrick H Brown; Janesh Kumar; Andrea Balbo; Carrie A May; Ernesto Casillas; Thomas M Laue; George H Patterson; Mark L Mayer; Peter Schuck
Journal:  J Gen Physiol       Date:  2012-04-16       Impact factor: 4.086

7.  Combining biophysical methods for the analysis of protein complex stoichiometry and affinity in SEDPHAT.

Authors:  Huaying Zhao; Peter Schuck
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2015-01-01

8.  Accounting for photophysical processes and specific signal intensity changes in fluorescence-detected sedimentation velocity.

Authors:  Huaying Zhao; Jia Ma; Maria Ingaramo; Eric Andrade; Jeff MacDonald; Glen Ramsay; Grzegorz Piszczek; George H Patterson; Peter Schuck
Journal:  Anal Chem       Date:  2014-08-28       Impact factor: 6.986

9.  Analysis of protein interactions with picomolar binding affinity by fluorescence-detected sedimentation velocity.

Authors:  Huaying Zhao; Mark L Mayer; Peter Schuck
Journal:  Anal Chem       Date:  2014-03-05       Impact factor: 6.986

10.  Polymerase delta-interacting protein 38 (PDIP38) modulates the stability and activity of the mitochondrial AAA+ protease CLPXP.

Authors:  Philip R Strack; Erica J Brodie; Hanmiao Zhan; Verena J Schuenemann; Liz J Valente; Tamanna Saiyed; Bradley R Lowth; Lauren M Angley; Matthew A Perugini; Kornelius Zeth; Kaye N Truscott; David A Dougan
Journal:  Commun Biol       Date:  2020-11-06
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