Enhancing response of a protein conformational switch by using two disordered ligand binding domains
Introduction: Protein conformational switches are often constructed by fusing an input domain, which recognizes a target ligand, to an output domain that establishes a biological response. Prior designs have employed binding-induced folding of the input domain to drive a conformational change in the...
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| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2023-03-01
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| Series: | Frontiers in Molecular Biosciences |
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fmolb.2023.1114756/full |
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| author | Harsimranjit Sekhon Jeung-Hoi Ha Stewart N. Loh |
| author_facet | Harsimranjit Sekhon Jeung-Hoi Ha Stewart N. Loh |
| author_sort | Harsimranjit Sekhon |
| collection | DOAJ |
| description | Introduction: Protein conformational switches are often constructed by fusing an input domain, which recognizes a target ligand, to an output domain that establishes a biological response. Prior designs have employed binding-induced folding of the input domain to drive a conformational change in the output domain. Adding a second input domain can in principle harvest additional binding energy for performing useful work. It is not obvious, however, how to fuse two binding domains to a single output domain such that folding of both binding domains combine to effect conformational change in the output domain.Methods: Here, we converted the ribonuclease barnase (Bn) to a switchable enzyme by duplicating a C-terminal portion of its sequence and appending it to its N-terminus, thereby establishing a native fold (OFF state) and a circularly permuted fold (ON state) that competed for the shared core in a mutually exclusive fashion. Two copies of FK506 binding protein (FKBP), both made unstable by the V24A mutation and one that had been circularly permuted, were inserted into the engineered barnase at the junctions between the shared and duplicated sequences.Results: Rapamycin-induced folding of FK506 binding protein stretched and unfolded the native fold of barnase via the mutually exclusive folding effect, and rapamycin-induced folding of permuted FK506 binding protein stabilized the permuted fold of barnase by the loop-closure entropy principle. These folding events complemented each other to turn on RNase function. The cytotoxic switching mechanism was validated in yeast and human cells, and in vitro with purified protein.Discussion: Thermodynamic modeling and experimental results revealed that the dual action of loop-closure entropy and mutually exclusive folding is analogous to an engine transmission in which loop-closure entropy acts as the low gear, providing efficient switching at low ligand concentrations, and mutually exclusive folding acts as the high gear to allow the switch to reach its maximum response at high ligand concentrations. |
| first_indexed | 2024-04-10T06:13:47Z |
| format | Article |
| id | doaj.art-35e72e9ba6864d34b5f29038a32f3c6c |
| institution | Directory Open Access Journal |
| issn | 2296-889X |
| language | English |
| last_indexed | 2024-04-10T06:13:47Z |
| publishDate | 2023-03-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Molecular Biosciences |
| spelling | doaj.art-35e72e9ba6864d34b5f29038a32f3c6c2023-03-02T10:18:54ZengFrontiers Media S.A.Frontiers in Molecular Biosciences2296-889X2023-03-011010.3389/fmolb.2023.11147561114756Enhancing response of a protein conformational switch by using two disordered ligand binding domainsHarsimranjit SekhonJeung-Hoi HaStewart N. LohIntroduction: Protein conformational switches are often constructed by fusing an input domain, which recognizes a target ligand, to an output domain that establishes a biological response. Prior designs have employed binding-induced folding of the input domain to drive a conformational change in the output domain. Adding a second input domain can in principle harvest additional binding energy for performing useful work. It is not obvious, however, how to fuse two binding domains to a single output domain such that folding of both binding domains combine to effect conformational change in the output domain.Methods: Here, we converted the ribonuclease barnase (Bn) to a switchable enzyme by duplicating a C-terminal portion of its sequence and appending it to its N-terminus, thereby establishing a native fold (OFF state) and a circularly permuted fold (ON state) that competed for the shared core in a mutually exclusive fashion. Two copies of FK506 binding protein (FKBP), both made unstable by the V24A mutation and one that had been circularly permuted, were inserted into the engineered barnase at the junctions between the shared and duplicated sequences.Results: Rapamycin-induced folding of FK506 binding protein stretched and unfolded the native fold of barnase via the mutually exclusive folding effect, and rapamycin-induced folding of permuted FK506 binding protein stabilized the permuted fold of barnase by the loop-closure entropy principle. These folding events complemented each other to turn on RNase function. The cytotoxic switching mechanism was validated in yeast and human cells, and in vitro with purified protein.Discussion: Thermodynamic modeling and experimental results revealed that the dual action of loop-closure entropy and mutually exclusive folding is analogous to an engine transmission in which loop-closure entropy acts as the low gear, providing efficient switching at low ligand concentrations, and mutually exclusive folding acts as the high gear to allow the switch to reach its maximum response at high ligand concentrations.https://www.frontiersin.org/articles/10.3389/fmolb.2023.1114756/fullalternate frame foldingmutually exclusive foldingloop closure entropyallosteryprotein engineering |
| spellingShingle | Harsimranjit Sekhon Jeung-Hoi Ha Stewart N. Loh Enhancing response of a protein conformational switch by using two disordered ligand binding domains Frontiers in Molecular Biosciences alternate frame folding mutually exclusive folding loop closure entropy allostery protein engineering |
| title | Enhancing response of a protein conformational switch by using two disordered ligand binding domains |
| title_full | Enhancing response of a protein conformational switch by using two disordered ligand binding domains |
| title_fullStr | Enhancing response of a protein conformational switch by using two disordered ligand binding domains |
| title_full_unstemmed | Enhancing response of a protein conformational switch by using two disordered ligand binding domains |
| title_short | Enhancing response of a protein conformational switch by using two disordered ligand binding domains |
| title_sort | enhancing response of a protein conformational switch by using two disordered ligand binding domains |
| topic | alternate frame folding mutually exclusive folding loop closure entropy allostery protein engineering |
| url | https://www.frontiersin.org/articles/10.3389/fmolb.2023.1114756/full |
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