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Abstract

Using surface plasmon resonance (SPR) and electrospray mass spectrometry (ESI-MS), proinsulin C-peptide was found to influence insulin-insulin interactions. In SPR with chip-bound insulin, C-peptide mixed with analyte insulin increased the binding, while alone C-peptide did not. A control peptide with the same residues in random sequence had little effect. In ESI-MS, C-peptide lowered the presence of insulin hexamer. The data suggest that C-peptide promotes insulin disaggregation. Insulin/insulin oligomer mu M dissociation constants were determined. Compatible with these findings, type 1 diabetic patients receiving insulin and C-peptide developed 66% more stimulation of glucose metabolism than when given insulin alone. A role of C-peptide in promoting insulin disaggregation may be important physiologically during exocytosis of pancreatic beta-cell secretory granulae and pharmacologically at insulin injection sites. It is compatible with the normal co-release of C-peptide and insulin and may contribute to the beneficial effect of C-peptide and insulin replacement in type 1 diabetics.

Keywords

surface plasmon resonance; electrospray ionization mass spectrometry; insulin effect; diabetes type 1; proinsulin C-peptide; insulin disaggregation; insulin hexamer decrease

Published in

Cellular and Molecular Life Sciences
2006, volume: 63, number: 15, pages: 1805-1811
Publisher: BIRKHAUSER VERLAG AG

SLU Authors

  • Johansson, Jan

    • Department of Molecular Biosciences, Swedish University of Agricultural Sciences

UKÄ Subject classification

Veterinary Science
Animal and Dairy Science

Publication identifier

  • DOI: https://doi.org/10.1007/s00018-006-6204-6

Permanent link to this page (URI)

https://res.slu.se/id/publ/10600