Home LiteratureArticle Details
PMID: 5435498 Published · ppublish English Journal Article

Membrane studies with polarity-dependent and excimer-forming fluorescent probes.

The Biochemical journal ·Vol. 116 ·No. 4 ·1970-02-00 ·Pages 721-31

Brocklehurst JR, Freedman RB, Hancock DJ, Radda GK

Abstract

1. The interaction of electron-transporting particles from heavy mitochondria of ox heart with several fluorescent probes was examined. 2. 1-Anilinonaphthalene-8-sulphonate and 2-(N-methylanilino)naphthalene-6-sulphonate both show an energy-dependent response. 3. Energy transfer between the electron-transporting particles and the dyes and the kinetics of the dye-particle interaction were studied in order to locate the binding regions in the membrane. 4. The energy-dependent probe responses were shown to be a result of changes in the quantum yield of fluorescence of the bound dyes together with increased binding of the dyes to the energized membrane. 5. Fluorescence lifetime measurements were also used to observe changes on energization. 6. A new type of probe was found in pyrene-3-sulphonate, which may be regarded as a ;volume indicator' for the internal membrane binding region, since it shows a concentration-dependent excimer fluorescence. 7. By comparing the responses of all these dyes when energized particles are uncoupled, a membrane transition with a time-constant of 2-3s is inferred.

MeSH Terms
Animals Binding Sites Cattle Electron Transport Energy Transfer Fluorescent Dyes Kinetics Membranes Mitochondria, Muscle Myocardium Naphthalenes Spectrum Analysis Succinates/pharmacology Sulfonic Acids
Chemicals
Fluorescent Dyes Naphthalenes Succinates Sulfonic Acids
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Brocklehurst J R
Freedman R B
Hancock D J
Radda G K
References (16)
16 references, click to expand
  1. Fluorescent indicators of adsorption in aqueous solution and on the solid phase.
    Biochem J. 1954 Jan 16;56(325th Meeting):xxxi PMID: 13159909
  2. The interaction of 1-anilino-8-naphthalene sulphonate with erythrocyte membranes.
    FEBS Lett. 1969 Apr;3(2):150-152 PMID: 11946993
  3. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes.
    Arch Biochem Biophys. 1963 Jan;100:119-30 PMID: 14028302
  4. Intramolecular resonance transfer of energy in proteins.
    Biochim Biophys Acta. 1959 Sep;35:242-4 PMID: 13835345
  5. The reversible acid dissociation and hybridization of lactic dehydrogenase.
    Arch Biochem Biophys. 1966 Sep 26;116(1):207-23 PMID: 6006804
  6. Ultraviolet fluorescence of the aromatic amino acids.
    Biochem J. 1957 Mar;65(3):476-82 PMID: 13412650
  7. Quantitative estimation of protein binding site polarity. Fluorescence of N-arylaminonaphthalenesulfonates.
    Biochemistry. 1968 Oct;7(10):3381-90 PMID: 5693059
  8. Fluorescent probes for conformational states of proteins. II. The binding of 2-p-toluidinylnaphthalene-6-sulfonate to alpha-chymotrypsin.
    Biochemistry. 1967 Feb;6(2):559-66 PMID: 6047639
  9. Interaction of fluorescent probes with membranes. I. Effect of ions on erythrocyte membranes.
    Biochemistry. 1969 Jul;8(7):2742-7 PMID: 5808332
  10. 1-Anilinonaphthalene-8-sulphonate, a fluorescent conformational probe for glutamate dehydrogenase.
    Biochem J. 1969 Sep;114(2):407-17 PMID: 4309311
  11. A fluorescence probe of energy-dependent structure changes in fragmented membranes.
    Proc Natl Acad Sci U S A. 1969 Feb;62(2):612-9 PMID: 4307717
  12. Studies of myosin conformation by fluorescent techniques.
    Biochemistry. 1969 May;8(5):2177-82 PMID: 4977582
  13. The interaction of a naphthalene dye with apomyoglobin and apohemoglobin. A fluorescent probe of non-polar binding sites.
    J Mol Biol. 1965 Sep;13(2):482-95 PMID: 5867031
  14. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
  15. FRAGMENTATION OF BOVINE SERUM ALBUMIN BY PEPSIN. I. THE ORIGIN OF THE ACID EXPANSION OF THE ALBUMIN MOLECULE.
    J Biol Chem. 1964 May;239:1415-23 PMID: 14189873
  16. Interaction of glutamate dehydrogenase with fluorescent dyes.
    Biochem Biophys Res Commun. 1967 May 25;27(4):500-4 PMID: 4293197
Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1970-02-00
Pages
721-31
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1185418
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com