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Conformational behavior of fragments of adrenocorticotropin and their antisense peptides determined by NMR spectroscopy and CD spectropolarimetry.

Authors :
Najem ES
Corigliano-Murphy A
Ferretti JA
Source :
FEBS letters [FEBS Lett] 1989 Jul 03; Vol. 250 (2), pp. 405-10.
Publication Year :
1989

Abstract

An 'antisense' peptide ('HTCA'), whose sequence was generated by reading the antisense RNA sequence corresponding to ACTH (1-24) was shown to bind ACTH (1-24) with a Kd of 0.3 nM in a solid-matrix binding assay [( 1986) Biochem. J. 234, 679 683]. Two-dimensional NMR spectra were used to examine the conformational behavior in methanol and in water solution of two fragments of adrenocorticotropin, ACTH(1-24) and ACTH (1-13), as well as their antisense peptides, HTCA and HTCA(12-24). The conformations are extended chains in these solutions, both as isolated molecules and when mixed with their antisense complements. The Kd values are greater than 1 mM.

Details

Language :
English
ISSN :
0014-5793
Volume :
250
Issue :
2
Database :
MEDLINE
Journal :
FEBS letters
Publication Type :
Academic Journal
Accession number :
2546806
Full Text :
https://doi.org/10.1016/0014-5793(89)80765-3