Evidence map›Paper›PMID 9017210›Full record

ArticleBiophysical journal1997

Disparate fluorescence properties of 2-[4'-(iodoacetamido)anilino]-naphthalene-6-sulfonic acid attached to Cys-84 and Cys-35 of troponin C in cardiac muscle troponin.

W J Dong, C K Wang, A M Gordon, H C Cheung

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. The effect of MgThe FEBS journal · 2022
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  7. Mini-thin filaments regulated by troponin-tropomyosin.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  8. Article
  9. Structure of the inhibitory region of troponin by site directed spin labeling electron paramagnetic resonance.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  10. Article
  11. An interdomain distance in cardiac troponin C determined by fluorescence spectroscopy.Protein science : a publication of the Protein Society · 2000
    Article
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

W J DongDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham 35294-2041, USA. wdong@bmg.bhs.uab.edu
C K Wang
A M Gordon
H C Cheung
University of Alabama at Birmingham · USUniversity of Washington · US

Funding

REGULATORY MECHANISMS OF CARDIAC MUSCLER01HL052508 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHEUNG, HERBERT C · 1996 to 2008
$2.6M
REGULATION OF ACTOMYOSIN INTERACTIONS IN CARDIAC MUSCLESP01HL052558 · NHLBI · UNIVERSITY OF WASHINGTON · PI GORDON, ALBERT M · 1994 to 1998
–
NHLBI NIH HHS HL52508NHLBI NIH HHS HL52558
6 · The paper itself

Abstract

Two monocysteine mutants of cardiac muscle troponin C, cTnC(C35S) and cTnC(C84S), were genetically generated and labeled with the fluorescent probe 2-[4'-(iodoacetamido)anilino]naphthalene-6-sulfonic acid (IAANS) at Cys-84 and Cys-35, respectively. Cys-84 is located on helix D in the regulatory N-domain, and Cys-35 is at the -y position of the inactive 12-residue loop of site I. These labeled mutants were studied by a variety of steady-state and time-resolved fluorescence methods. In the absence of divalent cation, the fluorescence of the attached IAANS indicated an exposed environment at Cys-35 and a relatively less-exposed environment at Cys-84. The binding of Ca2+ to the single regulatory site elicited a large enhancement of the emission of IAANS attached to Cys-84, but only marginal fluorescence changes of the probe at Cys-35. Upon reconstitution of the labeled cTnC mutants with troponin I and troponin T to form the three-subunit troponin, the fluorescence of IAANS-Cys-84 in apo-troponin was spectrally similar to that observed with the Ca(2+)-loaded uncomplexed cTnC mutant. Only very moderate changes in the fluorescence of IAANS-Cys-84 were observed when the regulatory site in reconstituted troponin was saturated. The exposed Cys-35 environment of the uncomplexed cTnC mutant became considerably less exposed and less polar when the mutant was incorporated into apo-troponin. In contrast to the Cys-84 site, saturation of the regulatory site II by Ca2+ in reconstituted troponin resulted in a reversal of the environment of the Cys-35 site toward a more exposed and more polar environment. These results indicated involvement of the inactive loop I in the Ca2+ trigger mechanism in cardiac muscle. The fluorescence of IAANS at both Cys-84 and Cys-35 was sensitive to phosphorylation of cTnl in reconstituted troponin, and the sensitivity was observed with both apo-troponin and Ca(2+)-loaded troponin.

Indexed as

AnimalsCalciumCattleCysteineFluorescent DyesKineticsMutationMyocardiumNaphthalenesulfonatesPhosphorylationProtein BindingProtein ConformationTroponin CTroponin ICalciumCysteineFluorescent DyesIAANSNaphthalenesulfonatesTroponin CTroponin I

Identifiers

PMID9017210
PMCPMC1185608
OpenAlexW1974164583

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.