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dc.contributor.authorLee, Yun-Tzaien_US
dc.contributor.authorSu, Tz-Hsiangen_US
dc.contributor.authorLo, Wei-Chengen_US
dc.contributor.authorLyu, Ping-Chiangen_US
dc.contributor.authorSue, Shih-Cheen_US
dc.date.accessioned2014-12-08T15:24:18Z-
dc.date.available2014-12-08T15:24:18Z-
dc.date.issued2012-08-24en_US
dc.identifier.issn1932-6203en_US
dc.identifier.urihttp://dx.doi.org/10.1371/journal.pone.0043820en_US
dc.identifier.urihttp://hdl.handle.net/11536/16898-
dc.description.abstractSplit-protein systems have emerged as a powerful tool for detecting biomolecular interactions and reporting biological reactions. However, reliable methods for identifying viable split sites are still unavailable. In this study, we demonstrated the feasibility that valid circular permutation (CP) sites in proteins have the potential to act as split sites and that CP prediction can be used to search for internal permissive sites for creating new split proteins. Using a protein ligase, intein, as a model, CP predictor facilitated the creation of circular permutants in which backbone opening imposes the least detrimental effects on intein folding. We screened a series of predicted intein CPs and identified stable and native-fold CPs. When the valid CP sites were introduced as split sites, there was a reduction in folding enthalpy caused by the new backbone opening; however, the coincident loss in entropy was sufficient to be compensated, yielding a favorable free energy for self-association. Since split intein is exploited in protein semi-synthesis, we tested the related protein trans-splicing (PTS) activities of the corresponding split inteins. Notably, a novel functional split intein composed of the N-terminal 36 residues combined with the remaining C-terminal fragment was identified. Its PTS activity was shown to be better than current reported two-piece intein with a short N-terminal segment. Thus, the incorporation of in silico CP prediction facilitated the design of split intein as well as circular permutants.en_US
dc.language.isoen_USen_US
dc.titleCircular Permutation Prediction Reveals a Viable Backbone Disconnection for Split Proteins: An Approach in Identifying a New Functional Split Inteinen_US
dc.typeArticleen_US
dc.identifier.doi10.1371/journal.pone.0043820en_US
dc.identifier.journalPLOS ONEen_US
dc.citation.volume7en_US
dc.citation.issue8en_US
dc.citation.epageen_US
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.identifier.wosnumberWOS:000308225500105-
dc.citation.woscount6-
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