Evidence map›Paper›PMID 2036391›Full record

ArticleBiochemistry1991

Distance distributions and anisotropy decays of troponin C and its complex with troponin I.

H C Cheung, C K Wang, I Gryczynski, W Wiczk, G Laczko, M L Johnson, J R Lakowicz

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In one paragraph

Article in Biochemistry, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 40 citations in OpenAlex.

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  15. Molecular mechanism of troponin-C function.Journal of muscle research and cell motility · 1992
    Review
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

7 authors at 1 institution in 1 country.

H C CheungDepartment of Biochemistry, University of Alabama, Birmingham 35294.
C K Wang
I Gryczynski
W Wiczk
G Laczko
M L Johnson
J R Lakowicz
University of Alabama at Birmingham · US

Funding

WHO'S WHO IN FLUORESCENCEP41RR008119 · NCRR · UNIVERSITY OF MARYLAND BALTIMORE · PI BASKAKOV, ILIA V · 1993 to 2006
$7.4M
STUDIES ON MUSCLE REGULATORY PROTEINSR01AR025193 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHEUNG, HERBERT C · 1986 to 1991
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INTERACTION OF MYOSIN WITH ACTINR01AR031239 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHEUNG, HERBERT C · 1986 to 1994
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DISTANCE DISTRIBUTIONS AND DYNAMICS OF MACROMOLECULESR01GM035154 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI LAKOWICZ, JOSEPH R. · 1985 to 1997
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NCRR NIH HHS P41 RR008119NIAMS NIH HHS AR 25193NIAMS NIH HHS AR 31239NIGMS NIH HHS GM 35154
6 · The paper itself

Abstract

We used frequency domain measurements of fluorescence resonance energy transfer to recover the distribution of distances between Met 25 and Cys 98 in rabbit skeletal troponin C. These residues were labeled with dansylaziridine as energy donor and 5-(iodoacetamido)eosin as acceptor and are located on the N- and C-terminal lobes of the two-domain protein, respectively. We developed a procedure to correct for the fraction of the sample that was incompletely labeled with the acceptor independent of chemical data. At pH 7.5 and in the presence of Mg2+, the mean distance was near 15 A with a half-width of the distribution of 15 A; when Mg2+ was replaced by Ca2+, the mean distance increased to 22 A with a decrease in the half-width by 4 A. Similar but less pronounced differences in the mean distance and half-width between samples containing Mg2+ and Ca2+ were also observed with troponin C complexed to troponin I. The results suggest that the conformation of troponin C is altered by Ca2+ binding to the Ca(2+)-specific sites and displacing bound Mg2+ at the Ca2+/Mg2+ sites. This alteration may play an important role in Ca2+ signaling in muscle. At pH 7.5, the anisotropy decays of the donor-labeled troponin C showed two components, with the long rotational correlation time (12 ns) reflecting the overall motion of the protein. When the pH was lowered from 7.5 to 5.2, the mean distribution distance of apotroponin C increased from 22 to 32 A and the half-width decreased by a factor of 2 from 13 to 7 A. The long correlation time of apotroponin C increased to 19 ns at the acidic pH. These results are discussed in terms of a model in which skeletal troponin C is a dimer at low pH and enable comparison of the solution conformation of the protein at neutral pH with a crystal structure obtained at pH 5.2. While the conformation of the monomeric unit of troponin C dimer at pH 5.2 is extended and consistent with the crystal structure, the conformation at neutral pH is likely more compact than the crystal structure predicts.

Indexed as

AnimalsCalciumEnergy TransferHydrogen-Ion ConcentrationIn Vitro TechniquesMetalsMotionMusclesProtein ConformationRabbitsTroponinTroponin CTroponin ICalciumMetalsTroponinTroponin CTroponin I

Identifiers

PMID2036391
PMCPMC6868476
OpenAlexW1995173836

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Registered trials

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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.