TY - JOUR
T1 - Nuclear magnetic resonance studies on the interaction of avoparcin with model receptors of bacterial cell walls
AU - Fesik, S. W.
AU - Armitage, I. M.
AU - Ellestad, G. A.
AU - McGahren, W. J.
PY - 1984/1/1
Y1 - 1984/1/1
N2 - On the basis of nuclear Overhauser enhancement and 1H chemical shift data obtained in aqueous solution, a model is proposed for the interaction of β-avoparcin and epi-β-avoparcin with acetly-D-alanyl-D-alanine (Ac-D-Ala-D-Ala) and diacetyl-L-lysyl-D-alanyl-D-alanine (Ac2-L-Lys-D-Ala-D-Ala). For the β-avoparcin: Ac2-L-Lys-D-Ala-Ala complex, the COOH-terminal end of the tripeptide is located near the NH2 terminus of the antibiotic with the tripeptide extending across the peptide backbone of β-avoparcin toward its COOH-terminal end. In our proposed structure, the three amino acid residues of the peptide span the entire length of the antibiotic, and the aliphatic side chain of the lysine residue extends over the D-ring of β-avoparcin. The structure of the epi-β-avoparcin:Ac2-L-Lys-D-Ala-D-Ala complex was found to be similar to the β-avoparcin complex at the binding site for the lysine residue at the COOH-terminal end of the antibiotic, but differed in the interactions at the NH2 terminus. These results are consistent with the similarities in the COOH-terminal conformations and the differences in conformations at the NH2 terminus found for β-avoparcin and epi-β-avoparcin which were described in this paper [Fesik, S.W., I.M. Armitage, G.A. Ellestad, and W.J. McGahren, Mol. Pharmacol. 25:275-280 (1984)]. The association constants (measured by UV methods) for both β-avoparcin:peptide complexes were greater than those measured for epi-β-avoparcin and correlated with their differences in antibacterial activity. Epi-β-avoparcin exhibited no measurable binding to the dipeptide; however, a significant affinity was measured for the tripeptide, indicating that the interactions with the NH2 terminus of the antibiotics provide binding energy for the antibiotic peptide complex but that the COOH-terminal end of the antibiotics also plays an important role in the binding interaction. These results are interesting in light of the similarities in the structural and conformational features at the COOH terminus for all of the glycopeptide antibiotics.
AB - On the basis of nuclear Overhauser enhancement and 1H chemical shift data obtained in aqueous solution, a model is proposed for the interaction of β-avoparcin and epi-β-avoparcin with acetly-D-alanyl-D-alanine (Ac-D-Ala-D-Ala) and diacetyl-L-lysyl-D-alanyl-D-alanine (Ac2-L-Lys-D-Ala-D-Ala). For the β-avoparcin: Ac2-L-Lys-D-Ala-Ala complex, the COOH-terminal end of the tripeptide is located near the NH2 terminus of the antibiotic with the tripeptide extending across the peptide backbone of β-avoparcin toward its COOH-terminal end. In our proposed structure, the three amino acid residues of the peptide span the entire length of the antibiotic, and the aliphatic side chain of the lysine residue extends over the D-ring of β-avoparcin. The structure of the epi-β-avoparcin:Ac2-L-Lys-D-Ala-D-Ala complex was found to be similar to the β-avoparcin complex at the binding site for the lysine residue at the COOH-terminal end of the antibiotic, but differed in the interactions at the NH2 terminus. These results are consistent with the similarities in the COOH-terminal conformations and the differences in conformations at the NH2 terminus found for β-avoparcin and epi-β-avoparcin which were described in this paper [Fesik, S.W., I.M. Armitage, G.A. Ellestad, and W.J. McGahren, Mol. Pharmacol. 25:275-280 (1984)]. The association constants (measured by UV methods) for both β-avoparcin:peptide complexes were greater than those measured for epi-β-avoparcin and correlated with their differences in antibacterial activity. Epi-β-avoparcin exhibited no measurable binding to the dipeptide; however, a significant affinity was measured for the tripeptide, indicating that the interactions with the NH2 terminus of the antibiotics provide binding energy for the antibiotic peptide complex but that the COOH-terminal end of the antibiotics also plays an important role in the binding interaction. These results are interesting in light of the similarities in the structural and conformational features at the COOH terminus for all of the glycopeptide antibiotics.
UR - http://www.scopus.com/inward/record.url?scp=0021330253&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0021330253&partnerID=8YFLogxK
M3 - Article
C2 - 6700574
AN - SCOPUS:0021330253
SN - 0026-895X
VL - 25
SP - 281
EP - 286
JO - Molecular Pharmacology
JF - Molecular Pharmacology
IS - 2
ER -