High-resolution profiling of homing endonuclease binding and catalytic specificity using yeast surface display.
High-resolution profiling of homing endonuclease binding and catalytic specificity using yeast surface display.
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DOI:
10.1093/nar/gkp726
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发表时间:
2009-11
影响因子:
14.9
通讯作者:
Scharenberg AM
中科院分区:
文献类型:
--
作者:
Jarjour J;West-Foyle H;Certo MT;Hubert CG;Doyle L;Getz MM;Stoddard BL;Scharenberg AM
Experimental analysis and manipulation of protein–DNA interactions pose unique biophysical challenges arising from the structural and chemical homogeneity of DNA polymers. We report the use of yeast surface display for analytical and selection-based applications for the interaction between a LAGLIDADG homing endonuclease and its DNA target. Quantitative flow cytometry using oligonucleotide substrates facilitated a complete profiling of specificity, both for DNA-binding and catalysis, with single base pair resolution. These analyses revealed a comprehensive segregation of binding specificity and affinity to one half of the pseudo-dimeric interaction, while the entire interface contributed specificity at the level of catalysis. A single round of targeted mutagenesis with tandem affinity and catalytic selection steps provided mechanistic insights to the origins of binding and catalytic specificity. These methods represent a dynamic new approach for interrogating specificity in protein–DNA interactions.
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