D-peptide
A D-peptide is a small sequence of D-amino acids. Since ribosomes are specific to L-amino acids, D-peptides rarely occur naturally in organisms and are not easily digested or degraded. D-peptide peptidomimetics are D-peptides designed to mimic natural L-peptides that commonly have therapeutic properties. A peptide with secondary structure cannot be mimicked by its retro-inverse, as linking in the reverse order breaks many backbone interactions essential for the secondary structure.[1] An approach to mimicking these peptides is by searching for similar (sidechain) structures in a mirrored copy of the Protein Data Bank for the structured elements, and then linking the sections by retro-inversed versions of the loops found in the original protein.[2]
![L-Peptide Asp-Val-Ser and its mirror image.](http://upload.wikimedia.org/wikipedia/commons/thumb/1/15/L-Peptide-D-PeptideMirrorImages.png/300px-L-Peptide-D-PeptideMirrorImages.png)
When placed in a nonchiral solvent like water, D-peptides, as well as the larger polypeptide D-proteins, have similar but mirrored properties to the L-peptides and L-proteins with identical sequences. If an L-protein does not require a chaperone or a structural cofactor to fold, its D-enantiomer protein should have a mirror image conformation with respect to the L-protein (Figure 2). A D-enzyme should act on substrates of reverse chirality compared to the L-enzyme with the same sequence. Similarly, if an L-peptide binds to an L-protein, their D-peptide and D-protein counterparts should bind together in a mirrored way.[3]
D-peptides also have properties that make them attractive as drugs. D-peptides are less susceptible to be degraded in the stomach or inside cells by proteolysis. D-peptide drugs can, therefore, be taken orally and are effective for a longer period of time. D-peptides are easy to synthesize when compared to many other drugs. In some cases, D-peptides can have a low immunogenic response.[4]
Ret design
[edit]An L-peptide has three analogue sequences (Figure 3) built from L and D amino acids: the D-enantiomer or inverso-peptide with the same sequence, but composed of D-amino acids and a mirror conformation; the retro-peptide, consisting of the same sequence of L amino acids but in reverse order; and the retro-inverso or D-retro-enantiomer peptide, consisting of D-amino acids in the reversed sequence.[5][6]
While the L-peptide and its D-enantiomer are mirror structures of each other, the L-retro-peptide is the mirror image of the D-retro-inverso-peptide. On the other hand, the L-peptide and the D-retro-inverso-peptide share a similar arrangement of side-chains, although their carboxyl and amino groups point in opposing directions. For small peptides that do not depend on a secondary structure for binding, an L-peptide and its D-retro-inverso-peptide is likely to have a similar binding affinity with a target L-protein.
![A fragment sequence and its analogues.](http://upload.wikimedia.org/wikipedia/commons/thumb/d/d6/L-peptideD-peptideAnalogues.png/300px-L-peptideD-peptideAnalogues.png)
Mirror-image phage display
[edit]Phage display is a technique to screen large libraries of peptides for binding to a target protein. In phage display, the DNA sequence that codes the potential drug-peptide is fused to the gene of the protein coat of bacteriophages and introduced into a vector. Diversity can be introduced to the peptide by mutagenesis. The protein coats peptides are then expressed and purified, and applied to a surface of immobilized protein targets. The surface is then washed away to remove non-binding peptides, while the remaining binding peptides are eluted.[7]
Mirror-image phage display is a similar method that can be used to screen large libraries of D-peptides that bind to target L-proteins. More precisely, since D-peptides can not be expressed in bacteriophages, mirror-image phage display screens L-peptides that bind to immobilized D-proteins that are previously chemically synthesized. Because of the mirror properties of D-peptides, the D-enantiomer of an L-peptide that binds to a D-protein will bind to the L-protein.
Mirror-image phage display, however, has two disadvantages when compared to phage display. Target D-proteins must be chemically synthesized, which is normally an expensive and time-consuming process. Also, the target protein must not require a cofactor or a chaperone to fold, otherwise the chemically synthesized D-protein will not fold to the target, mirror structure.
![](http://upload.wikimedia.org/wikipedia/commons/thumb/5/59/MirrorImagePhageDisplay.png/500px-MirrorImagePhageDisplay.png)
References
[edit]- ^ Lacroix E, Viguera AR, Serrano L (April 1998). "Reading protein sequences backwards". Folding & Design. 3 (2): 79–85. doi:10.1016/S1359-0278(98)00013-3. PMID 9565752.
- ^ Garton M, Nim S, Stone TA, Wang KE, Deber CM, Kim PM (February 2018). "Method to generate highly stable D-amino acid analogs of bioactive helical peptides using a mirror image of the entire PDB". Proceedings of the National Academy of Sciences of the United States of America. 115 (7): 1505–1510. Bibcode:2018PNAS..115.1505G. doi:10.1073/pnas.1711837115. PMC 5816147. PMID 29378946.
- ^ Milton RC, Milton SC, Kent SB (1992). "Total chemical synthesis of a D-enzyme: the enantiomers of HIV-1 protease show demonstration of reciprocal chiral substrate specificity". Science. 256 (5062): 1445–1448. doi:10.1126/science.1604320. PMID 1604320.
- ^ Welch BD, VanDemark AP, Heroux A, Hill CP, Kay MS (October 2007). "Potent D-peptide inhibitors of HIV-1 entry". Proceedings of the National Academy of Sciences of the United States of America. 104 (43): 16828–33. Bibcode:2007PNAS..10416828W. doi:10.1073/pnas.0708109104. PMC 2040420. PMID 17942675.
- ^ Guichard G, Benkirane N, Zeder-Lutz G, van Regenmortel MH, Briand JP, Muller S (October 1994). "Antigenic mimicry of natural L-peptides with retro-inverso-peptidomimetics". Proceedings of the National Academy of Sciences of the United States of America. 91 (21): 9765–9. Bibcode:1994PNAS...91.9765G. doi:10.1073/pnas.91.21.9765. PMC 44897. PMID 7937888.
- ^ Cardó-Vila M, Giordano RJ, Sidman RL, Bronk LF, Fan Z, Mendelsohn J, Arap W, Pasqualini R (March 2010). "From combinatorial peptide selection to drug prototype (II): targeting the epidermal growth factor receptor pathway". Proceedings of the National Academy of Sciences of the United States of America. 107 (11): 5118–23. Bibcode:2010PNAS..107.5118C. doi:10.1073/pnas.0915146107. PMC 2841862. PMID 20190183.
- ^ Wiesehan K, Willbold D (September 2003). "Mirror-image Phage Display: Aiming at the Mirror". ChemBioChem. 4 (9): 811–5. doi:10.1002/cbic.200300570. PMID 12964153. S2CID 34014107.