Literature DB >> 986163

A spectroscopic technique for measuring slow rotational diffusion of macromolecules. 1: Preparation and properties of a triplet probe.

R J Cherry, A Cogoli, M Oppliger, G Schneider, G Semenza.   

Abstract

Slow rotational diffusion may be investigated by measuring the decay of dichroism of flash-induced transient absorption changes of suitable probes. The preparation of the covalent ""triplets" probe eosin isothiocyanate is described together with investigations of spectroscopic properties of eosin-protein conjugates. Triplet state lifetimes of air-equilibrated solutions of eosin-protein conjugates are in the order of 10 mus, demonstrating that the probe is protected from oxygen quenching by the protein. Experiments with the sucrase-isomaltase complex from small intestine show that its enzymatic activity is little affected by binding up to 2 mol of eosin/mol of protein.

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Year:  1976        PMID: 986163     DOI: 10.1021/bi00662a001

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  17 in total

1.  Rotational motion and evidence for oligomeric structures of sarcoplasmic reticulum Ca2+-activated ATPase.

Authors:  W Hoffmann; M G Sarzala; D Chapman
Journal:  Proc Natl Acad Sci U S A       Date:  1979-08       Impact factor: 11.205

2.  Large-scale rotational motions of proteins detected by electron paramagnetic resonance and fluorescence.

Authors:  D D Thomas
Journal:  Biophys J       Date:  1978-11       Impact factor: 4.033

3.  Rotational diffusion of cell surface components by time-resolved phosphorescence anisotropy.

Authors:  R H Austin; S S Chan; T M Jovin
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

4.  Protein rotational dynamics investigated with a dual EPR/optical molecular probe. Spin-labeled eosin.

Authors:  C E Cobb; E J Hustedt; J M Beechem; A H Beth
Journal:  Biophys J       Date:  1993-03       Impact factor: 4.033

5.  Measurement of rotational dynamics by the simultaneous nonlinear analysis of optical and EPR data.

Authors:  E J Hustedt; C E Cobb; A H Beth; J M Beechem
Journal:  Biophys J       Date:  1993-03       Impact factor: 4.033

6.  Phosphorescence of protein-bound eosin and erythrosin. A possible probe for measurements of slow rotational mobility.

Authors:  P B Garland; C H Moore
Journal:  Biochem J       Date:  1979-12-01       Impact factor: 3.857

7.  GRPY: An Accurate Bead Method for Calculation of Hydrodynamic Properties of Rigid Biomacromolecules.

Authors:  Pawel J Zuk; Bogdan Cichocki; Piotr Szymczak
Journal:  Biophys J       Date:  2018-07-24       Impact factor: 4.033

8.  Measurement of protein rotational motion using frequency domain polarized fluorescence depletion.

Authors:  T M Yoshida; F Zarrin; B G Barisas
Journal:  Biophys J       Date:  1988-08       Impact factor: 4.033

Review 9.  Linear-dichroism spectroscopy for the study of structural properties of proteins.

Authors:  M Bloemendal; R van Grondelle
Journal:  Mol Biol Rep       Date:  1993-06       Impact factor: 2.316

10.  Protein rotational motion in solution measured by polarized fluorescence depletion.

Authors:  T M Yoshida; B G Barisas
Journal:  Biophys J       Date:  1986-07       Impact factor: 4.033

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