SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:lup.lub.lu.se:5367d08c-4b4a-4f67-9933-7cdb74636b07"
 

Search: onr:"swepub:oai:lup.lub.lu.se:5367d08c-4b4a-4f67-9933-7cdb74636b07" > Binding of Levosime...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Binding of Levosimendan, a Calcium Sensitizer, to Cardiac Troponin C

Sorsa, Tia (author)
University of Helsinki
Heikkinen, Sami (author)
University of Helsinki
Abbott, M. Bret (author)
University of Cincinnati
show more...
Abusamhadneh, Ekram (author)
University of Cincinnati
Laakso, Tero (author)
University of Helsinki
Tilgmann, Carola (author)
Orion Corporation
Serimaa, Ritva (author)
University of Helsinki
Annila, Arto (author)
VTT Technical Research Center of Finland, Espoo
Rosevear, Paul R. (author)
University of Cincinnati
Drakenberg, Torbjörn (author)
Lund University,Lunds universitet,Kemiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH
Pollesello, Piero (author)
Orion Corporation
Kilpeläinen, Ilkka (author)
University of Helsinki
show less...
 (creator_code:org_t)
2001
2001
English 7 s.
In: Journal of Biological Chemistry. - 0021-9258. ; 276:12, s. 9337-9343
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Levosimendan is an inodilatory drug that mediates its cardiac effect by the calcium sensitization of contractile proteins. The target protein of levosimendan is cardiac troponin C (cTnC). In the current work, we have studied the interaction of levosimendan with Ca2+-saturated cTnC by heteronuclear NMR and small angle x-ray scattering. A specific interaction between levosimendan and the Ca2+-loaded regulatory domain of recombinant cTnCC35S was observed. The changes in the NMR spectra of the N-domain of full-length cTnCC35S, due to the binding of levosimendan to the primary site, were indicative of a slow conformational exchange. In contrast, no binding of levosimendan to the regulatory domain of cTnCA-Cys, where all the cysteine residues are mutated to serine, was detected. Moreover, it was shown that levosimendan was in fast exchange on the NMR time scale with a secondary binding site in the C-domain of both cTnCC35S and cTnCA-Cys. The small angle x-ray scattering experiments confirm the binding of levosimendan to Ca2+-saturated cTnC but show no domain-domain closure. The experiments were run in the absence of the reducing agent dithiothreitol and the preservative sodium azide (NaN 3), since we found that levosimendan reacts with these chemicals, commonly used for preparation of NMR protein samples.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Kemiteknik -- Farmaceutisk synteskemi (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Chemical Engineering -- Pharmaceutical Chemistry (hsv//eng)

Keyword

Calcium/metabolism*
Magnetic Resonance Spectroscopy
Troponin C/metabolism*
simendan
Myocardium/metabolism*

Publication and Content Type

art (subject category)
ref (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view