Literature DB >> 6589602

Picosecond fluorescence decay of tryptophans in myoglobin.

R M Hochstrasser, D K Negus.   

Abstract

The fluorescence decay characteristics of Mb, MbCO, metMb (sperm whale), metMb (yellowfin tuna), and their apo derivatives were determined by using a picosecond streak camera and time-correlated single photon counting. The emission is dominated by tryptophans that transfer their energy to the heme on a subnanosecond time scale. Sperm whale Mb and derivatives have two tryptophans and their decays can be interpreted mainly as two exponentials, one of ca. 20 ps and the other of 130 ps, whereas tuna Mb has one tryptophan and its emission is nonexponential but dominated by one component of 31 ps. These results along with Förster energy transfer calculations allow us to assign the ca. 30-ps emission to Trp-14 and the 130-ps emission to Trp-7 in Mb. The streak camera was modified to determine the decay of the fluorescence anisotropy. In metMb (tuna) the fluorescence anisotropy decays in 100 ps, which is postulated to result from rapid motion of the Trp-14. Because energy transfer was used to gate the anisotropy, the fast motion of Trp-14 is proposed to correspond to only 10% of the equilibrium distribution of molecules.

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Year:  1984        PMID: 6589602      PMCID: PMC345597          DOI: 10.1073/pnas.81.14.4399

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  27 in total

1.  The kinetics of the recombination reaction between apomyoglobin and alkaline haematin.

Authors:  P A Adams
Journal:  Biochem J       Date:  1977-04-01       Impact factor: 3.857

2.  Resolution of the fluorescence excitation spectrum of indole into the 1La and 1Lb excitation bands.

Authors:  B Valeur; G Weber
Journal:  Photochem Photobiol       Date:  1977-05       Impact factor: 3.421

3.  Time-resolved spectroscopy of hemoglobin and its complexes with subpicosecond optical pulses.

Authors:  C V Shank; E P Ippen; R Bersohn
Journal:  Science       Date:  1976-07-02       Impact factor: 47.728

4.  Yellowfin tuna (Thunnus albacares) myoglobin: characterization and comparative stability.

Authors:  G J Fosmire; W D Brown
Journal:  Comp Biochem Physiol B       Date:  1976

5.  Protein difference spectra. Effect of solvent and charge on tryptophan.

Authors:  L J Andrews; L S Forster
Journal:  Biochemistry       Date:  1972-05-09       Impact factor: 3.162

6.  Intrinsic fluorescence emission of intact oxy hemoglobins.

Authors:  R E Hirsch; R S Zukin; R L Nagel
Journal:  Biochem Biophys Res Commun       Date:  1980-03-28       Impact factor: 3.575

7.  Ultrafast relaxation in picosecond photolysis of nitrosylhemoglobin.

Authors:  P A Cornelius; R M Hochstrasser; A W Steele
Journal:  J Mol Biol       Date:  1983-01-05       Impact factor: 5.469

8.  Geminate recombination of O2 and hemoglobin.

Authors:  D A Chernoff; R M Hochstrasser; A W Steele
Journal:  Proc Natl Acad Sci U S A       Date:  1980-10       Impact factor: 11.205

9.  Structural dynamics of liganded myoglobin.

Authors:  H Frauenfelder; G A Petsko
Journal:  Biophys J       Date:  1980-10       Impact factor: 4.033

10.  Nanosecond segmental mobilities of tryptophan residues in proteins observed by lifetime-resolved fluorescence anisotropies.

Authors:  J R Lakowicz; G Freshwater; G Weber
Journal:  Biophys J       Date:  1980-10       Impact factor: 4.033

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  26 in total

1.  Kinetics of the reconstitution of hemoglobin from semihemoglobins alpha and beta with heme.

Authors:  Y Kawamura-Konishi; K Chiba; H Kihara; H Suzuki
Journal:  Eur Biophys J       Date:  1992       Impact factor: 1.733

2.  Quenchers induce wavelength dependence on protein fluorescence lifetimes.

Authors:  Søren Klitgaard; M T Neves-Petersen; S B Petersen
Journal:  J Fluoresc       Date:  2006-06-23       Impact factor: 2.217

3.  Fluorescence intensity and anisotropy decays of the intrinsic tryptophan emission of hemoglobin measured with a 10-GHz fluorometer using front-face geometry on a free liquid surface.

Authors:  E Bucci; Z Gryczynski; C Fronticelli; I Gryczynski; J R Lakowicz
Journal:  J Fluoresc       Date:  1992-03       Impact factor: 2.217

4.  Tryptophan-to-heme electron transfer in ferrous myoglobins.

Authors:  Roberto Monni; André Al Haddad; Frank van Mourik; Gerald Auböck; Majed Chergui
Journal:  Proc Natl Acad Sci U S A       Date:  2015-04-20       Impact factor: 11.205

5.  Femtosecond dynamics of rubredoxin: tryptophan solvation and resonance energy transfer in the protein.

Authors:  Dongping Zhong; Samir Kumar Pal; Deqiang Zhang; Sunney I Chan; Ahmed H Zewail
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-18       Impact factor: 11.205

6.  Temperature-dependent heme kinetics with nonexponential binding and barrier relaxation in the absence of protein conformational substates.

Authors:  Xiong Ye; Dan Ionascu; Florin Gruia; Anchi Yu; Abdelkrim Benabbas; Paul M Champion
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-05       Impact factor: 11.205

7.  Fluorescence quenching dynamics of tryptophan in proteins. Effect of internal rotation under potential barrier.

Authors:  F Tanaka; N Mataga
Journal:  Biophys J       Date:  1987-03       Impact factor: 4.033

8.  Effect of disordered hemes on energy transfer rates between tryptophans and heme in myoglobin.

Authors:  Z Gryczynski; C Fronticelli; T Tenenholz; E Bucci
Journal:  Biophys J       Date:  1993-11       Impact factor: 4.033

9.  Decay of the tryptophan fluorescence anisotropy in bacteriorhodopsin and its modified forms.

Authors:  R van den Berg; D J Jang; M A el-Sayed
Journal:  Biophys J       Date:  1990-04       Impact factor: 4.033

10.  Analysis of time-resolved fluorescence anisotropy in lipid-protein systems. II. Application to tryptophan fluorescence of bacteriophage M13 coat protein incorporated in phospholipid bilayers.

Authors:  K Peng; A J Visser; A van Hoek; C J Wolfs; M A Hemminga
Journal:  Eur Biophys J       Date:  1990       Impact factor: 1.733

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