Site of linkage (new turn between b1 and b6) and at

Site of linkage (new turn between b1 and b6) and at the sites of the new N and 125-65-5 biological activity C-termini (loop between b1 and b2). In other words, these structural elements have not started to form native contacts in the rate limiting transition state for folding. Furthermore, the rate constant for formation of the intermediate (Dcis-P to I in Figure 5) was decreased upon circular permutation resulting in a lower maximum concentration of intermediate during the folding reaction. Thus, the result of the circular permutation is very different for the structurally very similar domains, PTP-BL PDZ2 and SAP97 PDZ2, and the basis for the difference is found in their early folding events.Folding of a Circularly Permuted PDZ KDM5A-IN-1 DomainTo sum up, our results show how a circular permutation neither alters the structure (Figure 1) nor significantly affects the function (Figure 2) of the protein, SAP97 PDZ2. We further demonstrate that the canonical protein and the circular permutant fold via a similar mechanism (Figure 5), and that the rate of formation of the low energy intermediate has decreased in the circular permutant. These data illustrate the general feasibility of circular permutation as a mechanism for molecular evolution and, as suggested earlier [9], show that such events are most likely to be successful in regions of the protein that are not part of a folding nucleus.Materials and Methods Cloning, Expression and PurificationCloning. The cDNA for the circular permutant of human SAP97 PDZ2, residues 327?05 connected to residues 315?26 via a GSG linker (see Figure 1A), was ordered from Geneart. Two additional mutations as compared to wild type SAP97 PDZ2 were present in the circularly permuted construct: I342W, as a probe for fluorescence, and C378A, to avoid formation of disulfide bridges. Both mutations have been shown to only have minimal effects on the wild type SAP97 PDZ2 [23]. The cDNA construct was cloned into the EcoRI/BamHI sites of a modified pRSET vector (Invitrogen), which added an N- terminal MHHHHHLVPRGS tag to the expressed protein. This His tag has previously been shown not to affect the stability nor binding of PDZ domains [23,43,44]. The expressed product is hereafter referred to as cpSAP97 PDZ2. The canonical variant, pwtSAP97 PDZ2, refers to amino acids 311?07 of the same protein and with the same mutations (I342W, C378A) as used in previous studies [21,23]. Expression. The vector was transformed into Escherichia coli BL21-DE3 pLyS cells that grew on LB- agar plates under selection of ampicillin (100 mg/ml) and chloramphenicol (35 mg/ml) at 37uC overnight. From the plates colonies where transferred to liquid LB culture at 37uC under selection of 50 mg/ml ampicillin. At an A600 of ,0.6, protein expression was induced with 1 mM isopropyl-b-D-1-thiogalactopyranoside (IPTG) and grown for 3 more hours before harvesting by centrifugation. Purification for kinetic experiments. The cell pellet was resuspended and frozen in 50 mM potassium phosphate, pH 7.0. After thawing, the cells were disrupted by ultrasonication followed by centrifugation (35 000 g) for 1 hour. The resulting supernatant was filtered through a 0.2 mm filter and incubated with Ni-NTA agarose, Qiagen, for 30 minutes. The agarose was then washed with 50 mM potassium phosphate, 25 mM imidazole, pH 7.5, until the A280 was close to 0. The protein was eluted with 50 mM potassium phosphate, 250 mM imidazole at pH 7.5. 1662274 The eluate was dialysed against 50 mM potassium phosphate pH 7.0 an.Site of linkage (new turn between b1 and b6) and at the sites of the new N and C-termini (loop between b1 and b2). In other words, these structural elements have not started to form native contacts in the rate limiting transition state for folding. Furthermore, the rate constant for formation of the intermediate (Dcis-P to I in Figure 5) was decreased upon circular permutation resulting in a lower maximum concentration of intermediate during the folding reaction. Thus, the result of the circular permutation is very different for the structurally very similar domains, PTP-BL PDZ2 and SAP97 PDZ2, and the basis for the difference is found in their early folding events.Folding of a Circularly Permuted PDZ DomainTo sum up, our results show how a circular permutation neither alters the structure (Figure 1) nor significantly affects the function (Figure 2) of the protein, SAP97 PDZ2. We further demonstrate that the canonical protein and the circular permutant fold via a similar mechanism (Figure 5), and that the rate of formation of the low energy intermediate has decreased in the circular permutant. These data illustrate the general feasibility of circular permutation as a mechanism for molecular evolution and, as suggested earlier [9], show that such events are most likely to be successful in regions of the protein that are not part of a folding nucleus.Materials and Methods Cloning, Expression and PurificationCloning. The cDNA for the circular permutant of human SAP97 PDZ2, residues 327?05 connected to residues 315?26 via a GSG linker (see Figure 1A), was ordered from Geneart. Two additional mutations as compared to wild type SAP97 PDZ2 were present in the circularly permuted construct: I342W, as a probe for fluorescence, and C378A, to avoid formation of disulfide bridges. Both mutations have been shown to only have minimal effects on the wild type SAP97 PDZ2 [23]. The cDNA construct was cloned into the EcoRI/BamHI sites of a modified pRSET vector (Invitrogen), which added an N- terminal MHHHHHLVPRGS tag to the expressed protein. This His tag has previously been shown not to affect the stability nor binding of PDZ domains [23,43,44]. The expressed product is hereafter referred to as cpSAP97 PDZ2. The canonical variant, pwtSAP97 PDZ2, refers to amino acids 311?07 of the same protein and with the same mutations (I342W, C378A) as used in previous studies [21,23]. Expression. The vector was transformed into Escherichia coli BL21-DE3 pLyS cells that grew on LB- agar plates under selection of ampicillin (100 mg/ml) and chloramphenicol (35 mg/ml) at 37uC overnight. From the plates colonies where transferred to liquid LB culture at 37uC under selection of 50 mg/ml ampicillin. At an A600 of ,0.6, protein expression was induced with 1 mM isopropyl-b-D-1-thiogalactopyranoside (IPTG) and grown for 3 more hours before harvesting by centrifugation. Purification for kinetic experiments. The cell pellet was resuspended and frozen in 50 mM potassium phosphate, pH 7.0. After thawing, the cells were disrupted by ultrasonication followed by centrifugation (35 000 g) for 1 hour. The resulting supernatant was filtered through a 0.2 mm filter and incubated with Ni-NTA agarose, Qiagen, for 30 minutes. The agarose was then washed with 50 mM potassium phosphate, 25 mM imidazole, pH 7.5, until the A280 was close to 0. The protein was eluted with 50 mM potassium phosphate, 250 mM imidazole at pH 7.5. 1662274 The eluate was dialysed against 50 mM potassium phosphate pH 7.0 an.