Literature DB >> 24638228

Submillisecond conformational changes in proteins resolved by photothermal beam deflection.

Walter G Gonzalez1, Jaroslava Miksovska2.   

Abstract

Photothermal beam deflection together with photo-acoustic calorimetry and thermal grating belongs to the family of photothermal methods that monitor the time-profile volume and enthalpy changes of light induced conformational changes in proteins on microsecond to millisecond time-scales that are not accessible using traditional stop-flow instruments. In addition, since overall changes in volume and/or enthalpy are probed, these techniques can be applied to proteins and other biomacromolecules that lack a fluorophore and or a chromophore label. To monitor dynamics and energetics of structural changes associated with Ca(2+) binding to calcium transducers, such neuronal calcium sensors, a caged calcium compound, DM-nitrophen, is employed to photo-trigger a fast (τ < 20 μsec) increase in free calcium concentration and the associated volume and enthalpy changes are probed using photothermal beam deflection technique.

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Year:  2014        PMID: 24638228      PMCID: PMC4124947          DOI: 10.3791/50969

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  12 in total

1.  Time-resolved thermodynamic changes photoinduced in 5,12-trans-locked bacteriorhodopsin. Evidence that retinal isomerization is required for protein activation.

Authors:  A Losi; I Michler; W Gärtner; S E Braslavsky
Journal:  Photochem Photobiol       Date:  2000-11       Impact factor: 3.421

2.  Structure-function relationships in metalloproteins.

Authors:  Jaroslava Miksovská; Randy W Larsen
Journal:  Methods Enzymol       Date:  2003       Impact factor: 1.600

3.  Photothermal studies of CO photodissociation from mixed valence Escherichia coli cytochrome bo3.

Authors:  Jaroslava Miksovská; Robert B Gennis; Randy W Larsen
Journal:  FEBS Lett       Date:  2005-06-06       Impact factor: 4.124

4.  A photoacoustic calorimetric study of horse myoglobin.

Authors:  J A Westrick; K S Peters
Journal:  Biophys Chem       Date:  1990-08-31       Impact factor: 2.352

5.  Characterization of conformational changes coupled to ligand photodissociation from the heme binding domain of FixL.

Authors:  Jaroslava Miksovská; Christine Suquet; James D Satterlee; Randy W Larsen
Journal:  Biochemistry       Date:  2005-08-02       Impact factor: 3.162

6.  Laser photolysis of caged calcium: rates of calcium release by nitrophenyl-EGTA and DM-nitrophen.

Authors:  G C Ellis-Davies; J H Kaplan; R J Barsotti
Journal:  Biophys J       Date:  1996-02       Impact factor: 4.033

7.  Light-induced conformational changes in full-length Arabidopsis thaliana cryptochrome.

Authors:  Masato Kondoh; Chiaki Shiraishi; Pavel Müller; Margaret Ahmad; Kenichi Hitomi; Elizabeth D Getzoff; Masahide Terazima
Journal:  J Mol Biol       Date:  2011-08-22       Impact factor: 5.469

8.  The contribution of heme propionate groups to the conformational dynamics associated with CO photodissociation from horse heart myoglobin.

Authors:  Natalia Belogortseva; Marisa Rubio; William Terrell; Jaroslava Miksovská
Journal:  J Inorg Biochem       Date:  2007-04-02       Impact factor: 4.155

9.  Photolabile chelators for the rapid photorelease of divalent cations.

Authors:  J H Kaplan; G C Ellis-Davies
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

10.  Thermodynamic profile for urea photo-release from a N-(2-nitrobenzyl) caged urea compound.

Authors:  Gangadhar Dhulipala; Marisa Rubio; Katja Michael; Jaroslava Miksovská
Journal:  Photochem Photobiol Sci       Date:  2009-06-10       Impact factor: 3.982

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