Small amounts of phenolic compounds are being used as preservatives in pharmaceutical insulin preparations. It has been shown previously that these compounds bind to specific sites on the insulin hexamer and act as allosteric effectors, inducing a transformation of the T 6 hexamer to the R 6 hexamer
The structure of a rhombohedral R6 insulin hexamer that binds phenol
โ Scribed by G. D. Smith; G. G. Dodson
- Book ID
- 101719103
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1992
- Tongue
- English
- Weight
- 327 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0006-3525
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โฆ Synopsis
Different hexameric forms of insulin have been crystallized from a variety of conditions. In the presence of 1% phenol, 1.OM sodium chloride, and at a p H of 8.5, a rhombohedral form is produced with two monomers in the asymmetric unit, space group R3, a = 79.92
A and c = 40.39 A. The structure has been solved and refined, using data between 8.0 and 2.5 8, resolution, to a residual of 0.157. Each of the monomers adopts an R conformation, that is residues Bl-B8 are a-helical. As a result of the T to R transition, an elliptical cavity is created between symmetry-related monomers and is occupied by a phenol molecule. A region of density within bonding distance to one of the zinc ions has been interpreted as an additional phenol molecule.
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