Chemical synthesis and structure elucidation of bovine K-casein (1-44)


Autoria(s): Bansal, P.S.; Daly, N.L.; McGhie, E.; Craik, D.J.; Alewood, P.F.; Grieve, P.; Marschke, R.J.
Data(s)

2006

Resumo

The caseins (αs1, αs2, β, and κ) are phosphoproteins present in bovine milk that have been studied for over a century and whose structures remain obscure. Here we describe the chemical synthesis and structure elucidation of the N-terminal segment (1–44) of bovine κ-casein, the protein which maintains the micellar structure of the caseins. κ-Casein (1–44) was synthesised by highly optimised Boc solid-phase peptide chemistry and characterised by mass spectrometry. Structure elucidation was carried out by circular dichroism and nuclear magnetic resonance spectroscopy. CD analysis demonstrated that the segment was ill defined in aqueous medium but in 30% trifluoroethanol it exhibited considerable helical structure. Further, NMR analysis showed the presence of a helical segment containing 26 residues which extends from Pro8 to Arg34. This is the first report which demonstrates extensive secondary structure within the casein class of proteins.

Identificador

Bansal, P.S. and Daly, N.L. and McGhie, E. and Craik, D.J. and Alewood, P.F. and Grieve, P. and Marschke, R.J. (2006) Chemical synthesis and structure elucidation of bovine K-casein (1-44). Biochemical and Biophysical Research Communications, 340 (4). pp. 1098-1103.

http://era.daf.qld.gov.au/776/

Publicador

Elsevier

Relação

http://dx.doi.org/10.1016/j.bbrc.2005.12.115

http://era.daf.qld.gov.au/776/

Palavras-Chave #Dairy processing. Dairy products #Agricultural chemistry. Agricultural chemicals
Tipo

Article

PeerReviewed