Structure-based mutation analysis (Phenylketonuria)

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Summary

In Task 8 the sequence of PAH was used for finding mutational effects, now the structure will be taken for these analysis. But how to find out, if a mutation changes the structure? Therefore, one calculates the energy of all atoms for the wildtype and the mutated structure and compares the results for changes. There are two different methods for this calculations given: Quantum Mechanics (QM) and Molecular Mechanics (MM). In QM the energy of all electrons in a protein is calculated. It is one of the most accurated methods, but it is very time consuming. In MM the energy of a system is calculated as a function of nuclear positions. It is very fast and easy to calculate, but it ignores electronic motions and is not as accurate as QM. Since QM is too time intensive and the results of MM are nearly as good as the ones calculated with QM, we use MM for the further analysis. Molecular Mechanics uses force fields for the energy calculation, which is defined as a sum of terms. The terms are non-bonded (electrostatic and Van-der-Waals) and bonded (Bond stretching, Angle stretching, bond rotation) interactions. <ref name="molmech"> Andrew R. Leach (2001): "Molecular Modelling: Principles and Applications (Second Edition)". Prentice Hall, ISBN: 9780582382107. </ref> For the structure based mutation analysis the tools SCWRL and FoldX were used.

Structure selection

Lab journal

In some Tasks before, we used the protein structure of 2PAH as reference, but now we have to check some more constraints for the protein structure selection:

  • Structure with the highest resolution (small Å value),
  • smallest R-factor,
  • highest coverage,
  • pH-value ideally near physiological pH of 7.4 and
  • no gaps (missing residues) included in the structure, so a consecutive numbering of residues should be given.

To check which protein structure to use for further analysis, we compared the constraint data for all sequences given in the PAH (P00439) Uniprot entry. <figtable id="pro-struc">

Protein Method Resolution(Å) R-factor pH Gaps Chain Positions Coverage %
1DMW X-ray 2.00 0.20 6.80 - A 118-424 67,92
1J8T X-ray 1.70 0.20 6.80 - A 103-427 71.90
1J8U X-ray 1.50 0.16 6.80 - A 103-427 71.90
1KW0 X-ray 2.50 0.22 6.80 - A 103-427 71.90
1LRM X-ray 2.10 0.21 6.80 - A 103-427 71.90
1MMK X-ray 2.00 0.20 6.80 - A 103-427 71.90
1MMT X-ray 2.00 0.21 6.80 - A 103-427 71.90
1PAH X-ray 2.00 0.18 6.80 - A 117-424 68.14
1TDW X-ray 2.10 0.21 6.80 - A 117-424 68.14
1TG2 X-ray 2.20 0.21 6.80 - A 117-424 68.14
2PAH X-ray 3.10 0.25 7.00 136LEU-143ASP A/B 118-452 74.12
3PAH X-ray 2.00 0.18 6.80 - A 117-424 68.14
1ANP X-ray 2.11 0.20 6.80 - A 104-427 71.68
4PAH X-ray 2.00 0.17 6.80 - A 117-424 68.14
5PAH X-ray 2.10 0.16 6.80 - A 117-424 68.14
6PAH X-ray 2.15 0.17 6.80 - A 117-424 68.14

Comparison of all pdb structures of P00439 in the used method, Resolution (in Å), R-factor, pH, included Gaps and chain/s, positions in P00439 (PAH) and the coverage to this sequence. </figtable> All structures do not cover the whole PAH protein (coverage = 100%) and were found with the X-ray diffraction method. In <xr id="pro-struc"/> we can see, that the structure of 1J8U has a better resolution value as well as R-factor than the other structures. Although 2PAH has a better pH-value, a higher coverage and even two chains, however, the structure includes one gap. For this reason as well as the better R-factor and higher resolution value, we have chosen the structure of 1J8U for further analysis. 1J8U is the catalytic domain of human phenylalanine hydroxylase Fe(II) and does not contain any gaps. Moreover, the structure includes the second highest coverage and also a very good pH-value.

The 3D structure of 1J8U as well as its ligands are shown in the <xr id="1j8u"/> below. The binding site for the ligand FE(II) consists of the residues His285, His290 and Glu330 and the one for ligand H4B consists of Val245, Gly247, Leu249 and Ser251. Both were taken from the pdb entry of 1J8U. These binding sites are shown in detail in <xr id="bindingsite"/>.

</figure> </figure>
<figure id="1j8u">
 3D-structure of 1J8U (green) in cartoon style with its two ligands H4B - C9H15N5O3 (blue sticks) and FE(II) (grey sphere). The binding site of FE(II) is shown in orange and the one of H4B in pink. Both are illustrated in sticks with surrounding surfaces.
<figure id="bindingsite">
3D-structure of 1J8U (green) in cartoon style with zoom to the ligands H4B - C9H15N5O3 (blue) with corresponding binding site (pink) and FE(II) (grey) with corresponding binding site (orange). The binding sites are shown in sticks and their belonging surface structures.

Visualisation of used mutations

Following five mutations from the previously selected mutations in Task8 are mapped to the crystal structure:

Substitution Prediction Database
Gln172His neutral dbSNP
Ala259Val non-neutral HGMD
Thr266Ala non-neutral dbSNP
Phe392Ser non-neutral dbSNP
Pro416Gln non-neutral HGMD

For the conversion of the residues, which include a mutation, we used the Mutagenesis tool in PyMOL. A little overview of the mutations is located in the next subsections with associated figures.

Gln172His

<figure id="Q172H">

Mutation of glutamine (yellow) to histidine (purple) with their polar contacts located at position 172 of 1J8U (green). The ligands and binding sites are shown in the same colors and representations as given in Figure 1 and 2.

</figure> This mutation is located far away from any of the two binding sites, so one would not expect a huge effect on the protein. The mutation contains only two of the three polar contacts of the wildtype residue. (some changes???)

Ala259Val

<figure id="A259V">

Mutation of alanine (yellow) to valine (purple) at position 259 of 1J8U (green). The ligands and binding sites are shown in the same colors and representations as given in Figure 1 and 2.

</figure> ... (beide polar contacts bleiben bestehen, jedoch verschiebt sich eines nur um eine sehr geringe Menge)

Thr266Ala

<figure id="T266A">

Mutation of threonine (yellow) to alanine (purple) at position 266 of 1J8U (green). The ligands and binding sites are shown in the same colors and representations as given in Figure 1 and 2.

</figure> In <xr id="T266A"/> we can see, that this residue is not located directly to the binding sites, but it lies between both ones. So, we would expect, that this mutation is disease causing. The mutation has only two of the three polar contacts of the wildtype residue included. (changes???)

Phe392Ser

<figure id="F392S">

Mutation of phenylalanine (yellow) to serine (purple) at position 392 of 1J8U (green). The ligands and binding sites are shown in the same colors and representations as given in Figure 1 and 2.

</figure> Since this mutations lies far away from both binding sites, we would expect only a small effect on the protein.

Pro416Gln

<figure id="P416Q">

Mutation of proline (yellow) to glutamine (purple) at position 416 of 1J8U (green). The ligands and binding sites are shown in the same colors and representations as given in Figure 1 and 2.

</figure> This mutation is as far away as the mutation before, so we think it has not a huge effect on the protein as well.

Mutated structure creation

SCWRL4

SCWRL4 (Side-chain Conformation Prediction With Rotamer Library) predicts protein side-chain conformations. Therefore, it uses a backbone-dependent rotamer library. The tool is based on graph theory, easy to use, accurate and very fast. The output includes a 3D structure of the prediction. <ref name="scwrl4"> Georgii G. Krivov1, Maxim V. Shapovalov1 and Roland L. Dunbrack Jr. (2009): "Improved prediction of protein side-chain conformations with SCWRL4". Proteins Vol.77(4):778-95. doi:10.1002/prot.22488</ref> There is also an online SCWRL Server available.

After generating the mutated structures with SCWRL, we compared the results to the wildtype structure in Pymol and checked if only the mutated side chain or another one has been changed. In the observation, only the mutated side chain was changed.

  • Q172H: ... (ein polar contact ist nicht mehr vorhanden!)

  • A259V: ... (man sieht nur die mutation, da diese den wildtype residue komplett überdeckt. polar contacts exakt gleich)

  • T266A: ... (wildtype überdeckt mutation komplett. zwei polar contacts gehen verloren)

  • F392S: ... (wildtype überdeckt mutation fast komplett. polar contacts exakt gleich)

  • P416Q: ... ()

FoldX

FoldX is an empirical force field to provide a fast and accurate estimation of mutational free energy changes (effect of SNPs) on the protein stability<ref name="foldef"> Raphael Guerois, Jens Erik Nielsen and Luis Serrano (2002): "The FoldX web server: an online force field". Nucleic Acids Research Vol.33: W382–W388. doi:10.1093/nar/gki387</ref>,<ref name="foldx"> Georgii G. Krivov1, Maxim V. Shapovalov1 and Roland L. Dunbrack Jr. (2002): "Predicting Changes in the Stability of Proteins and Protein Complexes: A Study of More Than 1000 Mutations". J. Mol. Biol. Vol.320: 369–387. doi:10.1002/prot.22488</ref>. In the output many different

<figtable id="foldx">

Type Total energy Backbone Hbond Sidechain Hbond Van der Waals Electrostatics Solvation Polar Solvation Hydrophobic Van der Waals clashes Entropy sidechain Entropy mainchain Sloop entropy Mloop entropy Cis bond Torsional clash Backbone clash Helix dipole Water bridge Disulfide Electrostatic kon Partial covalent bonds Energy Ionisation Entropy Complex
WT x x x x x x x x x x x x x x x x x x x x x x
Q172H 13.84 -196.19 -56.45 -378.50 -19.95 492.48 -495.07 33.39 193.60 453.85 0.00 0.00 0.00 11.68 227.36 -14.78 -11.79 0.00 0.00 0.00 1.55 0.00
A259V 14.08 -198.14 -59.00 -379.98 -19.12 495.02 -497.16 34.93 194.60 454.17 0.00 0.00 0.00 13.19 227.82 -15.57 -10.30 0.00 0.00 0.00 1.45 0.00
T266A 15.08 -196.56 -56.37 -378.45 -19.86 493.23 -494.94 32.68 193.42 453.13 0.00 0.00 0.00 11.94 227.53 -15.13 -9.46 0.00 0.00 0.00 1.45 0.00
F392S 24.59 -195.99 -57.60 -377.49 -19.29 495.41 -492.28 34.80 193.85 453.89 0.00 0.00 0.00 11.71 227.42 -15.39 -8.47 0.00 0.00 0.00 1.45 0.00
P416Q 21.20 -196.09 -57.10 -379.58 -19.53 496.13 -495.90 34.25 195.06 454.65 0.00 0.00 0.00 11.44 228.58 -15.11 -8.47 0.00 0.00 0.00 1.45 0.00

... </figtable>

Comparison

Now, we want to compare the results of SCWRL and FoldX. Therefore, we loaded the pdb structures into PyMOL and looked after differences between the two results. There was only one change in the 3D structure of the two programs, which can be seen in <xr id="comparison_all"/> and <xr id="comparison_part"/>.

</figure> </figure>
<figure id="comparison_all">
 Comparison of the structures predicted with SCWRL (purple) and FoldX (teal). The only change is one beta strand.
<figure id="comparison_part">
Zoom into the region of the only changed beta strand.

We also compared the two structures with the wildtype 1J8U structure and there are some little changes, but the interesting part was the change between SCWRL and FoldX. FoldX has the beta strand on the position of the wildtype structure whereas the one of SCWRL has changed. Since it is only a small difference in the structures, we do not think, that it has a huge consequence for the protein.

It is also very interesting, which changes the SCWRL and FoldX outputs show in each mutation. Hence, we want to analyse every mutation on its own.

  • Q172H: Comparison of the mutation Gln172His generated with SCWRL (purple) and FoldX (teal) in stick form. The only difference is a slight change in the angle of the two residues. Furthermore, the SCWRL mutation does include H-atoms which the FoldX mutation does not.

  • A259V: Comparison of the mutation Ala172Val generated with SCWRL (purple) and FoldX (teal) in stick form. The only difference is ...

  • T266A: Comparison of the mutation Thr172Ala generated with SCWRL (purple) and FoldX (teal) in stick form. The only difference is ...

  • F392S: Comparison of the mutation Phe172Ser generated with SCWRL (purple) and FoldX (teal) in stick form. The only difference is ...

  • P416Q: Comparison of the mutation Pro172Gln generated with SCWRL (purple) and FoldX (teal) in stick form. The only difference is ...

All in all one can see, that SCWRL has hydrogen atoms in the structures included, which FoldX does not. Furthermore, do all mutations got a slight twisting. But in the whole, there are only small changes between the two tools.

Energy comparisons

<figtable id="scwrl">

SCWRL results FoldX results
Type Energy Energy Mutation /
Energy Wildtype 		Prediction Energy Energy Mutation /
Energy Wildtype 		Prediction
WT 164.210 1.00 - x x x
Q172H 169.699 1.03 x x x x
A259V 197.235 1.20 x x x x
T266A 167.116 1.02 x x x x
F392S 171.409 1.04 x x x x
P416Q 169.007 1.03 x x x x

Comparison of the SCWRL results between the wildtype and the mutant structures. In the first column the type (mutation or wildtype) is given, then the resulting total minimal energy of the graph from the SCWRL results. In the third column this energy is divided through the wildtype resulting energy, to check the difference between this two types, and in the last column the prediction of the SCWRL results is represented. </figtable> ...

Minimise

In the table below, the energy for all five runs of minimise are given. Since the SCWRL output could not be minimised, we only can see the difference between the wildtype (WT) and the five mutation structures constructed with foldX. <figtable id="minimise">

minimise run
Type 1 2 3 4 5
WT -7516.27 -7524.20 -7291.36 -7133.71 -6996.34
Q172H -7514.27 -7504.92 -7281.60 -7131.31 -7023.56
A259V -7469.61 -7462.48 -7221.58 -7065.94 -6951.32
T266A -7536.77 -7523.38 -7298.14 -7165.29 -7084.60
F392S -7511.51 -7528.61 -7290.01 -7132.75 -7010.52
P416Q -7556.57 -7542.79 -7299.39 -7151.21 -7040.37
...

</figtable> The energies of the wildtype and the mutated structures is very similar and is per run increasing slightly. Only for the structures of the wildtype and the mutation F392S has the second run a small decreased value.

References

<references/>

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