Contents 1 CEST Based Marker Proteins 1.1 Scanning for Candidates 1.2 Molecular Dynamics 1.3 References

CEST Based Marker Proteins

To create bacteria with the ability to generate contrast on a CEST MRI scan, polypeptides that have that ability had to be found. Various solutions based on short Lysine, Arganine, Threonine or Serine rich sequences were proposed.McMahonDIACESTM.T. McMahon, New "Multicolor" Polypeptide Diamagnetic Chemical Exchange Saturation Transfer (DIACEST) Contrast Agents for MRI. Magnetic Resonance in Medicine 60, 803-812 (2008) However, it is hard to predict how well these sequences will express in bacteria and whether they are sufficiently stable in vivo. To avoid these problems a new approach was taken. The suitability as a CEST based marker was estimated for proteins of which the structure is already clarified.

Scanning for Candidates

For good CEST contrast a protein should have a high Lysine or Arganine content.McMahonDIACESTGiladArtificialGeneA.A. Gilad, Artificial reporter gene providing MRI contrast based on proton exchange.. Nature biotechnology 25.2, 217-219 (2007) To find these suitable proteins the [http://www.pdb.org RCSB Protein Data Bank] was queried for all entries containing proteins. This was done using the SEARCH Web Service of PDB.org, for the XML query used see query.xml. A Python program was written to analyse the obtained amino acid sequences and calculate the ratio of Lysine or Arginine to the total chain length (see PDB.py and queryPDB.py). The results are visualized in and .

Using this data a selection of interesting proteins was made for further analysis. The protein list was also filtered by chain length and general practicality of the sequences. The selection is shown below:

PDB ID	Frequent Amino Acid	Amount of Frequent Amino Acids (#)	Chain Length (#)	Ratio (-)
1ETF	Arginine	11	23	0.48
1IWQ	Lysine	7	19	0.37
1PJN	Lysine	8	21	0.38
2IGR	Lysine	15	34	0.44
2KLW	Lysine	10	32	0.31
2PCO	Lysine	8	26	0.30
1G70	Arginine	10	22	0.46
1BY0	Lysine	8	27	0.30
1NWD	Lysine	8	28	0.29
1PEH	Lysine	10	35	0.29
2L9A	Lysine	8	24	0.33
2L96	Lysine	8	24	0.33
2L99	Lysine	8	24	0.33
1LYP	Lysine	9	32	0.28
1LQ7	Lysine	17	67	0.25

Molecular Dynamics

To refine the selection the accessibility of the various exchangable hydrogen atoms of the Lysines and Arginines was taken into account. Hereto Molecular Dynamics simulations of the proteins in water were carried out. Gromacs was used to run the sequence of simulations. For every protein a in vacuo energy minimization was carried out to stabilize the protein. Subsequently an energy minimization in water with ions (0.15 M KCl) was executed to stabilize the whole system. Further stabilization was done by running a NVT and NPT simulation with position restraints followed by a NPT simulation without the restraints. Then the final run, of which the data was used for further analysis, was carried out.

For the analysis of the data the g_dist utility provided with Gromacs was used in combination with self-made Matlab scripts. Using g_dist the number of water molecules within a 5 nm radius of certain characteristic groups was calculated for each protein. This value was divided by the runtime of the simulation, resulting in an indication of the accessibility of the characteristic group by water molecules. The results are shown in the table below, numbers should be interpreted as an index value.

PDB ID	Backbone Secondary Amine	Arginine Guanidine	Arginine Secondary Amine	Secondary Amine	Lysine Primary Amine
1ETF	0.9935	1.0525	0.7954	0.8028	X
1IWQ	5.2279	5.6850	4.6562	5.3046	5.1866
1PJN	8.1621	4.2782	4.5149	8.5247	7.6893
2IGR	4.7848	X	X	4.7848	3.2901
2KLW
2PCO
1G70	2.9608	2.2858	2.2338	2.7171	X
1BY0	5.5306	7.1884	6.7331	5.7483	1.9289
1NWD	2.7855	X	X	2.7855	3.6024
1PEH
2L9A	3.0711	X	X	3.0711	3.4460
2L96
2L99
1LYP
1LQ7	0.0814	0.7923	0.3797	0.0810	1.7040

In this case a higher value is expected to give a better CEST contrast. Taking this into account a selection was made. For the contrast Guanidine (of Arginine) based contrast 1G70 and 1ETF were selected. Based on the simulations it is expected that 1G70 will give better contrast. 1PJN was also tested to see the result of a protein that is expected to give high contrast with saturation pulses at the chemical shifts of both characteristic groups (Guadine of Arginine and the primary Amide of Lysine).

References