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Conformation of thymosin β9 in water/fluoroalcohol solution determined by NMR spectroscopy

✍ Scribed by Raphael Stoll; Wolfgang Voelter; Tad A. Holak


Publisher
Wiley (John Wiley & Sons)
Year
1997
Tongue
English
Weight
331 KB
Volume
41
Category
Article
ISSN
0006-3525

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✦ Synopsis


The conformation of thymosin beta 9 in solution of 40% (v/v) 1,1,1,3,3,3-hexafluoro-2-propanol-d2 in water has been investigated by two-dimensional 1H-nmr spectroscopy. Under this condition thymosin beta 9 adopts an ordered structure. The determination of the conformation of the peptide was based on a set of 304 approximate interproton distance constraints derived from nuclear Overhauser enhancement measurements. The conformation of thymosin beta 9 includes two helical regions from residues 4 to 27 and 32 to 41. The two helices are separated by a poorly defined loop region between amino acids 28 and 31; the N-terminus of thymosin beta 9 shows random-coil structure only.


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