Nβ-methylation changes the recognition pattern of aza-β3-amino acid containing peptidomimetic substrates by protein kinase A
© Kisseljova et al; licensee Springer. 2011
Received: 17 June 2011
Accepted: 8 November 2011
Published: 8 November 2011
The protein kinase A (PKA)-catalyzed phosphorylation of peptide substrate RRASVA analogs, containing Nβ-Me-aza-β3-amino acid residues in all subsequent positions, was studied. This work follows along the lines of our previous research of the phosphorylation of aza-β3-analogs of RRASVA (the shortest active substrate of PKA) and allows characterizing the influence of Nβ-methylation of aza-β3-amino acid residues on substrate recognition by PKA on substrate binding and phosphorylation steps. It was found that the effect of Nβ-methylation was dependent upon the position of the structure alteration. Moreover, the presence of a single Nβ-methylation site in the substrate changed the recognition pattern of this series of peptidomimetics, strongly affecting the phosphorylation step. Structure modeling of aza-β3- and Nβ-Me-aza-β3-containing substrates revealed that Nβ-methylation of aza-β3-moieties changed the peptide bond geometry from trans- to cis-configuration in -CO-NMe- fragments, with an exception for the N-terminally methylated Nβ-Me-aza-β3-RRRASVA (with the N-terminal amino group not participating in the peptide bond) and RRAS-Nβ-Me-aza-β3-VA. As has been shown in literature, this conformational preference of the backbone has a significant influence on the flexibility of the peptide substrate chain. Following our results, this property seems to have significant influence on the recognition of the amino acid side groups by the enzyme binding site, and in the case of PKA this structural modification was decisive for the phosphate transfer step of the catalytic process.
KeywordsPeptidomimetic Nβ-Me-aza-β3-amino acid c-AMP-dependent protein kinase A peptidomimetics recognition phosphorylation protein kinase specificity
N-Methylation is one of the most common ways of peptide backbone modification . Replacement of the amide group hydrogen atom by a bulk methyl group results in disruption of backbone hydrogen bonding, restricts the conformation of the side chains , increases hydrophobicity by reducing the number of possible intramolecular hydrogen bonds , and decreases peptide bond preference for trans-configuration [3, 4]. All these changes have made this way of backbone modification an attractive tool of peptidomimetic design.
In this study, the influence of Nβ-methylation of the same series of peptidomimetic substrates on their recognition in the enzyme binding site was investigated. Therefore, peptidomimetic RRASVA analogs with Nβ-methyl-aza-β3-mutations in five different positions were prepared and their phosphorylation by PKA was studied. It was found that Nβ-methylation significantly affects the substrate recognition pattern and the effects observed were dependent upon Nβ-aza-β3-substitution position.
Results and discussion
Phosphorylation of Nβ-methylated peptidomimetic substrates by PKA catalytic subunit at ATP concentration 100 μM, 30°C, 50 mM TRIS/HCl, pH 7
K m (μM)
102 k cat (μmole mg-1 s-1)
102 k II (L mg-1 s-1)
209 ± 24
24.4 ± 1.5
0.098 ± 0.010
79 ± 18
11.9 ± 1.0
0.11 ± 0.07
91 ± 15
5.5 ± 0.3
0.034 ± 0.005
118 ± 36
16 ± 2.0
0.12 ± 0.02
57 ± 17
5.0 ± 0.4
0.090 ± 0.015
RRASVA (from )
11.1 ± 3.5
36 ± 3
3.2 ± 0.1
It was found that all the synthesized Nβ-methylated aza-β3-peptides were phosphorylated by PKA and the results of the kinetic study of their phosphorylation are listed in Table 1. The phosphorylation reactions followed the classical Michaelis-Menten rate equation and therefore all substrates were characterized by the K m and k cat values, which correspond to the constant ATP concentration of 0.1 mM. The initial linear part of the Mihaelis-Menten plot was used for the calculation of the second order rate constants k II as described in  and these values are also listed in Table 1. Agreement between the parameters k II and values of the ratio of k cat/K m for substrates confirms the applicability of the Michelis-Menten rate equation for the description of the kinetic data .
The Δlog k II values shown in this figure represent the logarithm of the ratio of the k II values for peptidomimetics and the parent peptide RRASVA, and also include data from our previous article and are represented by white bars . Second, it should be noted that in this numbering system (Figure 2) the position of the phosphorylatable serine is denoted as zero, amino acid residues to the left and right of it--with negative and positive numerals, respectively.
It is noteworthy that the reactivities of substrates Nβ-Me-aza-β3-RRASVA and aza-β3-RRASVA were practically similar, indicating that methylation of the N-teminal amino group of these compounds had no effect on their recognition by the enzyme. Not surprisingly, the K m and k cat values of these two substrates were also similar. However, apart from the N-terminal position Nβ-methylation of aza-β3-moiety caused significant differences in reactivity of the methylated and non-methylated compounds, whereby the latter substrates were always more efficiently phosphorylated (Figure 2). In one case, if the structure of aza-β3-alanine residue in position -1 was methylated, the effect reached almost two orders of magnitude.
For several other positions, the decrease in reactivity was not so significant; however, the Nβ-methylated peptidomimetics were phosphorylated at about 30 times lower rate when compared to RRASVA. In Nβ-Me-aza-β3-RRASVA, the trans-geometry of the -CO-NMe- bond was observed in computer models, which was not the surprising result as the N-terminal nitrogen atom was methylated. Indeed, reactivity of this substrate differed much less from its non-methylated counterpart aza-β3-RRASVA. Therefore, the amide group cis- and trans- configurations seem to play a crucial role in the determination of substrate reactivity. Structure calculations have also shown trans-configuration of -CO-NMe- bond for RRAS-Nβ-Me-aza-β3-VA analog. It can be observed in Figure 2 that the difference in reactivity of this substrate (in terms of Δlog k II) is less than that of between other members of the reaction series and their non-methylated aza-β3-counterparts. The compound (Nβ-Me-aza-β3-RRRASVA) was an understandable exception, as the N-terminal amino group does not participate in peptide bond formation.
For simplification, the k cat value for RRASVA phosphorylation was used for the normalization of kinetic data and the calculation of the Δlog k cat values as shown in Figure 4. However, Nβ-methylation of the aza-β3-group essentially changed this regularity, as the Δlog k cat values for these compounds varied significantly within the reaction series.
It is noteworthy that the Δlog k cat versus pK m plot for Nβ-methylated peptidomimetics had a negative slope and the phosphorylation rate of these compounds decreased if the pK m values increased (Figure 4). This change in the specificity pattern of Nβ-methyl-aza-β3-derivatives, when compared to that of aza-β3-derivatives and common peptides, was surprising, as structures of these peptidomimetics were not very different from each other, and changes in substrate backbone occurred at a distance from the phosphorylatable serine residue. On the other hand, this change in specificity pattern confirmed the significant role of peptide or peptidomimetic backbone flexibility that seems to be a crucial factor for matching ligand side-chains with its binding sites. Nβ-methylation obviously limits this kind of flexibility .
The comparison of kinetic data of the PKA catalyzed phosphorylation of RRASVA analogs with Nβ-Me-aza-β3- and aza-β3-mutations of all subsequent positions revealed that Nβ-methylation changed the pattern of substrate recognition by this enzyme. This change manifested itself in the different relationships between the binding effectiveness of substrates and the catalytic activity of the enzyme, characterized in terms of the log k cat versus pK m relationship (Figure 4). It was shown that recognition of Nβ-methylated substrates occurred on both binding and catalytic steps, while peptides and their aza-β3-derivatives were recognized primarily in their non-covalent binding step. This can be explained by the increase of backbone rigidity called forward by Nβ-methylation and the reduced ability of Nβ-methyl-aza-β3 peptidomimetics to adopt conformations favorable for the phosphate transfer step in the protein binding site. In other words, N-methylation changed the orientation of the side-chains, thus hampering the substrates recognition by the protein. This conclusion was supported by the structure calculations of peptidomimetic substrates, which showed the preferred cis-configuration of -CO-NMe- peptide bond in three out of four Nβ-Me-aza-β3-amino acid-containing RRASVA derivatives, except Nβ-Me-aza-β3-RRASVA, where the methylated N-terminal amino group did not participated in peptide bond formation. This means that Nβ-methylation can be used as an efficient tool for tuning both peptidomimetics reactivity and selectivity for the target site, while for the non-methylated compounds only reactivity seems to be mostly affected.
Nβ-Fmoc-Nβ-Me-aza-β3-amino acids were synthesized as described in . Peptide analogs were prepared by solid-phase peptide synthesis using Fmoc/tBu methodology. Nβ-aza-β3-amino acid analogs were coupled as reported previously , using TBTU/HOBT as activators. For coupling of the amino acid following the Nβ-aza-β3 residue, stronger activation was required and thus HATU/HOBT was used as activators.
The method of kinetic measurements was described in our previous article  and was based on utilizing the radioactive ATP with [32P]phosphate in γ-position. The phosphorylated substrates were bound onto Whatman phosphocellulose paper and the paper-bound radioactivity was counted. Linear plots between filter-bound radioactivity and time were used for calculating the initial velocity values of the phosphorylation reaction, which were thereafter processed by the classical Michaelis-Menten rate equation. Kinetic experiments were made at constant ATP concentration (100 μM) and the K m and k cat values were calculated for peptidomimetic substrates, concentrations of which were varied in the reaction mixture.
Peptidomimetic structure modeling was made using the Spartan 4.0 software suite (Wavefunction, Inc., USA) and the minimum energy conformations of compounds were obtained. Conformational searches were made using molecular mechanics with the additional condition of the aqueous medium for finding optimal geometry. All compounds were represented as zwitterions for these calculations.
2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate
O-(Benzotriazol-1-yl)-N, N, N',N'-tetramethyluronium tetrafluoroborate.
This study was supported by the Estonian Ministry of Education and Research Grant sf0180064s08 and by the Kristjan Jaak travel scholarship for KK.
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