Literature DB >> 1789928

Kinetic measurements of T----R structural transitions in insulin.

Y Karataş1, P Krüger, A Wollmer.   

Abstract

The T6----T3R3 and T3R3----R6-structural transitions of cobalt insulin hexamers as induced by SCN ions or m-cresol were studied in stopped-flow experiments using the absorption in the visible for monitoring their time course. The T6----T3R3 transition induced by either SCN or limited concentrations of m-cresol is mono-exponential with a rate constant of 0.1 s-1 and 0.4 s-1, respectively. A mono-exponential time course is also encountered for the m-cresol-induced T3R3----R6 transition when starting from the T3R3 state preestablished by either SCN or m-cresol. The corresponding rate constants are 1.3 s-1 and 0.49 s-1, respectively. If m-cresol is used beyond the concentration range where transformation is limited to one trimer, two exponentials are required for fitting the time course. The second exponential corresponds to the T3R3----R6 step with a concentration-independent rate constant of 0.4 s-1. The rate constant for the faster T6----T3R3 transition, however, increases with increasing excess of m-cresol.

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Year:  1991        PMID: 1789928     DOI: 10.1515/bchm3.1991.372.2.1035

Source DB:  PubMed          Journal:  Biol Chem Hoppe Seyler        ISSN: 0177-3593


  3 in total

1.  MD simulation of protein-ligand interaction: formation and dissociation of an insulin-phenol complex.

Authors:  Wolfgang Swegat; Jürgen Schlitter; Peter Krüger; Axel Wollmer
Journal:  Biophys J       Date:  2003-03       Impact factor: 4.033

2.  The structure of a mutant insulin uncouples receptor binding from protein allostery. An electrostatic block to the TR transition.

Authors:  Zhu-li Wan; Kun Huang; Shi-Quan Hu; Jonathan Whittaker; Michael A Weiss
Journal:  J Biol Chem       Date:  2008-05-20       Impact factor: 5.157

3.  Assembly and dissociation of human insulin and LysB28ProB29-insulin hexamers: a comparison study.

Authors:  D T Birnbaum; M A Kilcomons; M R DeFelippis; J M Beals
Journal:  Pharm Res       Date:  1997-01       Impact factor: 4.200

  3 in total

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