PEDS Advance Access originally published online on April 22, 2005
Protein Engineering Design and Selection 2005 18(4):181-189; doi:10.1093/protein/gzi019
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A theoretical model of restriction endonuclease NlaIV in complex with DNA, predicted by fold recognition and validated by site-directed mutagenesis and circular dichroism spectroscopy
1Laboratory of Bioinformatics and Protein Engineering, International Institute of Molecular and Cell Biology, ul. ks. Trojdena 4, 02-109 Warsaw, 2Institute of Microbiology, Warsaw University, ul. Miecznikowa 1, 02-093 Warsaw, and 3Institute of Biochemistry and Molecular Biology, University of Wroc
aw, ul. Tamka 2, 50-137 Wrocaw, Poland
4 To whom correspondence should be addressed. E-mail: iamb{at}genesilico.pl
Restriction enzymes (REases) are commercial reagents commonly used in DNA manipulations and mapping. They are regarded as very attractive models for studying protein–DNA interactions and valuable targets for protein engineering. Their amino acid sequences usually show no similarities to other proteins, with rare exceptions of other REases that recognize identical or very similar sequences. Hence, they are extremely hard targets for structure prediction and modeling. NlaIV is a Type II REase, which recognizes the interrupted palindromic sequence GGNNCC (where N indicates any base) and cleaves it in the middle, leaving blunt ends. NlaIV shows no sequence similarity to other proteins and virtually nothing is known about its sequence–structure–function relationships. Using protein fold recognition, we identified a remote relationship between NlaIV and EcoRV, an extensively studied REase, which recognizes the GATATC sequence and whose crystal structure has been determined. Using the ‘FRankenstein's monster’ approach we constructed a comparative model of NlaIV based on the EcoRV template and used it to predict the catalytic and DNA-binding residues. The model was validated by site-directed mutagenesis and analysis of the activity of the mutants in vivo and in vitro as well as structural characterization of the wild-type enzyme and two mutants by circular dichroism spectroscopy. The structural model of the NlaIV–DNA complex suggests regions of the protein sequence that may interact with the ‘non-specific’ bases of the target and thus it provides insight into the evolution of sequence specificity in restriction enzymes and may help engineer REases with novel specificities. Before this analysis was carried out, neither the three-dimensional fold of NlaIV, its evolutionary relationships or its catalytic or DNA-binding residues were known. Hence our analysis may be regarded as a paradigm for studies aiming at reducing ‘white spaces’ on the evolutionary landscape of sequence–function relationships by combining bioinformatics with simple experimental assays.
Keywords: extreme divergence/fold recognition/molecular evolution/restriction modification/structural model validation/structure prediction
Received December 8, 2004; revised March 5, 2005; accepted March 9, 2005.
Edited by Lynne Regan
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