Literature DB >> 9755897

Self-association properties of monomeric insulin analogs under formulation conditions.

J P Richards1, M P Stickelmeyer, D B Flora, R E Chance, B H Frank, M R DeFelippis.   

Abstract

PURPOSE: The purpose of the current study was to investigate the effects of two important excipients, zinc and m-cresol, on the self-association properties of a series of monomeric insulin analogs. In this way, the effects on formulation behavior of individual amino acid substitutions in the C-terminal region of the insulin B-chain could be compared.
METHODS: The self-association of ten insulin analogs was monitored by equilibrium and velocity analytical ultracentrifugation under three different conditions: (i) in neutral buffer alone; (ii) in neutral buffer containing zinc ion; and (iii) in neutral buffer containing both zinc ion and phenolic preservative (a typical condition for insulin formulations). The self-association properties of these analogs were compared to those of human insulin and the rapid-acting insulin analog Lys(B28)Pro(B29)-human insulin.
RESULTS: The analogs in the current study exhibited a wide range of association properties when examined in neutral buffer alone or in neutral buffer containing zinc ion. However, all of these analogs had association properties similar to human insulin in the presence of both zinc and m-cresol. Under these formulation conditions each analog had an apparent sedimentation coefficient of s* = 2.9-3.1 S, which corresponds to the insulin hexamer.
CONCLUSIONS: Analogs with changes in the B27-B29 region of human insulin form soluble hexamers in the presence of both zinc and m-cresol, and m-cresol binding overrides the otherwise destabilizing effects of these mutations on self assembly.

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Year:  1998        PMID: 9755897     DOI: 10.1023/a:1011961923870

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  26 in total

1.  Phenol stabilizes more helix in a new symmetrical zinc insulin hexamer.

Authors:  U Derewenda; Z Derewenda; E J Dodson; G G Dodson; C D Reynolds; G D Smith; C Sparks; D Swenson
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2.  Physicochemical basis for the rapid time-action of LysB28ProB29-insulin: dissociation of a protein-ligand complex.

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3.  Insulin association in neutral solutions studied by light scattering.

Authors:  S Hvidt
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4.  Enzymatic semisynthesis of porcine despentapeptide (B26-30) insulin using unprotected desoctapeptide (B23-30) insulin as a substrate. Model studies.

Authors:  T Kubiak; D Cowburn
Journal:  Int J Pept Protein Res       Date:  1986-05

5.  The structure of 2Zn pig insulin crystals at 1.5 A resolution.

Authors:  E N Baker; T L Blundell; J F Cutfield; S M Cutfield; E J Dodson; G G Dodson; D M Hodgkin; R E Hubbard; N W Isaacs; C D Reynolds
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1988-07-06       Impact factor: 6.237

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7.  Action profile of the rapid acting insulin analogue: human insulin B28Asp.

Authors:  L Heinemann; T Heise; L N Jorgensen; A A Starke
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Authors:  L J Slieker; G S Brooke; R D DiMarchi; D B Flora; L K Green; J A Hoffmann; H B Long; L Fan; J E Shields; K L Sundell; P L Surface; R E Chance
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Journal:  Biochemistry       Date:  1972-10-24       Impact factor: 3.162

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10.  Rapid-Acting and Human Insulins: Hexamer Dissociation Kinetics upon Dilution of the Pharmaceutical Formulation.

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