TY - JOUR
T1 - Use of “loss-of-contact” substitutions to identify residues involved in an amino acid-base pair contact
T2 - Effect of substitution of glnl8 of lac repressor by gly, ser, and leu
AU - Ebright, Richard H.
N1 - Funding Information:
I thank J. Beckwith for discussion and research support. I acknowledge also J. Betz, R. Brent, E. Eisenstadt, C. Kumamoto, E. Murgola, M. Pfahl, and W. Reznikoff for bacterial strains or plasmids, and J. Betz, E. Eisenstadt, and J. Miller for discussion. I thank E. Murgola for suggesting the method used to introduce gly VSS into the XA genetic background. This work was supported by National Institutes of Health grant GM13017 to J. Beckwith.
PY - 1985/10
Y1 - 1985/10
N2 - A procedure to identify which base pair of lac operator (lacO) a suspected contacting amino acid of Lac repressor (LacR) interacts with is presented. The procedure is to eliminate the ability of the amino acid under study to contact DNA, and then to determine at which base pair-if any-specificity is eliminated. To implement this procedure, four sets of Escherichia coli K-12 strains have been constructed. These strains permit: (i) the substitution of a selected amino acid of LacR by, respectively, Gly, Ser, Leu, or Gin, and (ii) the analysis of the specificity of the resulting substituted LacR with respect to base pairs 5, 6, 7, 8, 9, and 10 of lacO. This procedure has been applied to Glnl8 of LacR. The preliminary data indicate that LacR(Glnl8=“Gly) is unable to distinguish between the 0+ base pair G: C and the 0° base pair T:A at position 7 of lacO (KDOc/KDO+ = 0.93). In contrast, LacR(Glnl8=>Gly) discriminates 0+ from Oc by a factor of 13 to 23 at each other position. The same qualitative ‘ pattern of results was obtained with LacR(Glnl8=>Ser) and LacR(Glnl8=“Leu). Therefore, I propose that Glnl8 contacts base pair 7 of lacO. This proposal is consistent with the contact predicted in Ebright, R. in Protein Structure, Folding, and Design. D. Oxender ed., Alan R. Liss, New York (1985), in press.
AB - A procedure to identify which base pair of lac operator (lacO) a suspected contacting amino acid of Lac repressor (LacR) interacts with is presented. The procedure is to eliminate the ability of the amino acid under study to contact DNA, and then to determine at which base pair-if any-specificity is eliminated. To implement this procedure, four sets of Escherichia coli K-12 strains have been constructed. These strains permit: (i) the substitution of a selected amino acid of LacR by, respectively, Gly, Ser, Leu, or Gin, and (ii) the analysis of the specificity of the resulting substituted LacR with respect to base pairs 5, 6, 7, 8, 9, and 10 of lacO. This procedure has been applied to Glnl8 of LacR. The preliminary data indicate that LacR(Glnl8=“Gly) is unable to distinguish between the 0+ base pair G: C and the 0° base pair T:A at position 7 of lacO (KDOc/KDO+ = 0.93). In contrast, LacR(Glnl8=>Gly) discriminates 0+ from Oc by a factor of 13 to 23 at each other position. The same qualitative ‘ pattern of results was obtained with LacR(Glnl8=>Ser) and LacR(Glnl8=“Leu). Therefore, I propose that Glnl8 contacts base pair 7 of lacO. This proposal is consistent with the contact predicted in Ebright, R. in Protein Structure, Folding, and Design. D. Oxender ed., Alan R. Liss, New York (1985), in press.
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U2 - 10.1080/07391102.1985.10508417
DO - 10.1080/07391102.1985.10508417
M3 - Article
C2 - 3917212
AN - SCOPUS:0022351389
SN - 0739-1102
VL - 3
SP - 281
EP - 296
JO - Journal of Biomolecular Structure and Dynamics
JF - Journal of Biomolecular Structure and Dynamics
IS - 2
ER -