Literature DB >> 24226791

Wavelength-selective fluorescence as a novel tool to study organization and dynamics in complex biological systems.

S Mukherjee1, A Chattopadhyay.   

Abstract

The dynamics exhibited by a given component of a large macromolecule such as a folded globular protein or an organized supramolecular assembly like the biological membrane is a function of its precise localization within the larger system. A set of approaches based on the red edge effect in fluorescence spectroscopy, which can be used to monitordirectly the environment and dynamics around a fluorophore in a complex biological system, is reviewed in this article. A shift in the wavelength of maximum fluorescence emission toward higher wavelengths, caused by a shift in the excitation wavelength toward the red edge of the absorption band, is termed the red edge excitation shift (REES). This effect is mostly observed with polar fluorophores in motionally restricted media such as very viscous solutions or condensed phases. This phenomenon arises from the slow rates of solvent relaxation around an excited-state fluorophore, which is a function of the motional restriction imposed on the solvent molecules in the immediate vicinity of the fluorophore. Utilizing this approach, it becomes possible to probe the mobility parameters of the environment itself (which is represented by the relaxing solvent molecules) using the fluorophore merely as a reporter group. Further, since the ubiquitous solvent for biological systems is water, the information obtained in such cases will come from the otherwise 'optically silent' water molecules. This makes REES and related techniques extremely useful in biology since hydration plays a crucial modulatory role in a large number of important cellular events.

Entities:  

Year:  1995        PMID: 24226791     DOI: 10.1007/BF00723895

Source DB:  PubMed          Journal:  J Fluoresc        ISSN: 1053-0509            Impact factor:   2.217


  71 in total

Review 1.  Fluorescence techniques for studying protein structure.

Authors:  M R Eftink
Journal:  Methods Biochem Anal       Date:  1991

2.  Red-edge excitation fluorescence measurements of several two-tryptophan-containing proteins.

Authors:  Z Wasylewski; H Kołoczek; A Waśniowska; K Slizowska
Journal:  Eur J Biochem       Date:  1992-05-15

3.  Time-dependent rotational rates of excited fluorophores. A linkage between fluorescence depolarization and solvent relaxation.

Authors:  J R Lakowicz
Journal:  Biophys Chem       Date:  1984-01       Impact factor: 2.352

4.  Temperature-dependent shift of fluorescence spectra without conformational changes in protein; studies of dipole relaxation in the melittin molecule.

Authors:  A P Demchenko; A S Ladokhin
Journal:  Biochim Biophys Acta       Date:  1988-08-10

5.  Red-edge-excitation fluorescence spectroscopy of indole and tryptophan.

Authors:  A P Demchenko; A S Ladokhin
Journal:  Eur Biophys J       Date:  1988       Impact factor: 1.733

Review 6.  Fluorescence spectroscopic investigations of the dynamic properties of proteins, membranes and nucleic acids.

Authors:  J R Lakowicz
Journal:  J Biochem Biophys Methods       Date:  1980 Jan-Feb

7.  Resolution of initially excited and relaxed states of tryptophan fluorescence by differential-wavelength deconvolution of time-resolved fluorescence decays.

Authors:  J R Lakowicz; A Balter
Journal:  Biophys Chem       Date:  1982-07       Impact factor: 2.352

8.  Direct recording of the initially excited and the solvent relaxed fluorescence emission spectra of tryptophan by phase sensitive detection of fluorescence.

Authors:  J R Lakowicz; A Balter
Journal:  Photochem Photobiol       Date:  1982-08       Impact factor: 3.421

9.  Fluorescence study of a mutant cytochrome b5 with a single tryptophan in the membrane-binding domain.

Authors:  A S Ladokhin; L Wang; A W Steggles; P W Holloway
Journal:  Biochemistry       Date:  1991-10-22       Impact factor: 3.162

10.  Excimer-forming lipids in membrane research.

Authors:  H J Galla; W Hartmann
Journal:  Chem Phys Lipids       Date:  1980-10       Impact factor: 3.329

View more
  23 in total

1.  Interaction of melittin with membrane cholesterol: a fluorescence approach.

Authors:  H Raghuraman; Amitabha Chattopadhyay
Journal:  Biophys J       Date:  2004-10       Impact factor: 4.033

2.  Organization and dynamics of tryptophan residues in brain spectrin: novel insight into conformational flexibility.

Authors:  Madhurima Mitra; Arunima Chaudhuri; Malay Patra; Chaitali Mukhopadhyay; Abhijit Chakrabarti; Amitabha Chattopadhyay
Journal:  J Fluoresc       Date:  2015-04-03       Impact factor: 2.217

3.  Orientation and dynamics of melittin in membranes of varying composition utilizing NBD fluorescence.

Authors:  H Raghuraman; Amitabha Chattopadhyay
Journal:  Biophys J       Date:  2006-11-17       Impact factor: 4.033

4.  Dynamics of a membrane-bound tryptophan analog in environments of varying hydration: a fluorescence approach.

Authors:  Amitabha Chattopadhyay; Ajuna Arora; Devaki A Kelkar
Journal:  Eur Biophys J       Date:  2005-09-24       Impact factor: 1.733

5.  Aggregation Behavior of pHLIP in Aqueous Solution at Low Concentrations: A Fluorescence Study.

Authors:  Bhagyashree D Rao; Hirak Chakraborty; Sandro Keller; Amitabha Chattopadhyay
Journal:  J Fluoresc       Date:  2018-06-29       Impact factor: 2.217

6.  Alpha-helix formation in melittin and beta-lactoglobulin A induced by fluorinated dialcohols.

Authors:  Merlyn D Schuh; Melinda C Baldwin
Journal:  J Phys Chem B       Date:  2006-06-08       Impact factor: 2.991

7.  Effect of structural transition of the host assembly on dynamics of an ion channel peptide: a fluorescence approach.

Authors:  Satinder S Rawat; Devaki A Kelkar; Amitabha Chattopadhyay
Journal:  Biophys J       Date:  2005-08-12       Impact factor: 4.033

8.  Study of protein-probe interaction and protective action of surfactant sodium dodecyl sulphate in urea-denatured HSA using charge transfer fluorescence probe methyl ester of N,N-dimethylamino naphthyl acrylic acid.

Authors:  Subrata Mahanta; Rupashree Balia Singh; Nikhil Guchhait
Journal:  J Fluoresc       Date:  2008-09-12       Impact factor: 2.217

9.  Organization and dynamics of tryptophan residues in erythroid spectrin: novel structural features of denatured spectrin revealed by the wavelength-selective fluorescence approach.

Authors:  Amitabha Chattopadhyay; Satinder S Rawat; Devaki A Kelkar; Sibnath Ray; Abhijit Chakrabarti
Journal:  Protein Sci       Date:  2003-11       Impact factor: 6.725

10.  Role of tryptophan residues in gramicidin channel organization and function.

Authors:  Amitabha Chattopadhyay; Satinder S Rawat; Denise V Greathouse; Devaki A Kelkar; Roger E Koeppe
Journal:  Biophys J       Date:  2008-03-13       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.