Modular protein nanostructures.html
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+ | <td><b>DNA</b></td> | ||
+ | <td><b>POLYPEPTIDES</b></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>contains 4 nucleotides with similar properties<br><b>-</b></td> | ||
+ | <td>contains 20 AA with different chemical properties<br><b>+</b></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>can fold into defined 3D structures<br><b>+/-</b></td> | ||
+ | <td>can fold into defined 3D structures<br><b>+</b></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>used to store information in nature<br><b>-</b></td> | ||
+ | <td>builds structures and functional devices in nature<br><b>+</b></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>easy to program (Watson-Creek base pairs)<br><b>++</b></td> | ||
+ | <td>structure-encoding information (folding) is complex<br><b>-</b></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>prepared by chemical synthesis or amplification in vitro or in cells<br><b>+</b></td> | ||
+ | <td>prepared by transcription/translation machinery encoded through nucleic acids<br><b>+/-</b></td> | ||
+ | </tr> | ||
+ | </table> | ||
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Table 2: Comparison of suitability of DNA and polypeptides as nanostructure building material. | Table 2: Comparison of suitability of DNA and polypeptides as nanostructure building material. |
Revision as of 22:33, 21 October 2009
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Modular protein nanostructures
DNA shows the way
Table 2: Comparison of suitability of DNA and polypeptides as nanostructure building material. It is clear that nucleic acids surpass polypeptides only in two categories. Namely nucleic acids can by directly synthesized by chemical synthesis or easily replicated either in vitro (PCR) or by cell replication machinery, while for polypeptides the chemical synthesis is currently limited to few tens of aminoacids. Polypeptides larger than 50 residues are mainly produced by the transcription/translation machinery of cells and their isolation may be demanding. The second argument in favor of nucleic acids is that Watson-Crick base pairing is relatively easy to design to encode folding of nucleic acids in a DNA origami-like fashion. Prediction of tertiary structures by polypeptides is currently still a challenging problem and there are only a handful of proteins designed “from scratch”. On the other hand the rewards of using polypeptides for nanostructures are extremely high. In nature most of the dynamic structural assemblies as well as cellular nanomachines are made of polypeptides. Proteins can perform a wide range of functions. They can bind proteins, nucleic acids, metal ions and an enormous range of other atomically precise structures, both biological and non-biological. Protein molecules can represent effective scaffold structures: they can have the strength and stiffness like those of epoxies, polycarbonates and other engineered polymers that are also used in nanotechnology applications. On the other hand they can be extremely elastic and their absorption of energy makes them superior to many organic or inorganic materials such as steel or Kevlar. Up to now for technological applications we have used natural polypeptide polymers, such as silk, wool, keratin or collagen. Useful properties of polypeptides have been offset by a demanding design, fabrication, and testing cycle (several months) and by the small size of individual proteins (a few nanometers [http://nanoengineer-1.com/content/#dna_structures_link DNA structures]). Based on DNA encoded information polypeptides can be produced in cellular factories from simple materials and with low energy consumption and in a sustainable way. We believe that the problems hindering wider application of polypeptides as building blocks of nanostructures can be partially overcome (patent application: Self-assembled structures composed of single polypeptide comprising at least three coiled-coil forming elements). In the results section we present a technology for design and manufacturing polypeptide-based functional nanomaterials with promising applications. Approach to creation of modular protein nanostructures
Coiled-coils
![]() Figure 1: A) Helical wheel diagram showing interacting residues (a-d' and a'-d interactions between hydrophobic residues and e-e' and g-g' interactions between hydrophilic residues) in an antiparallel coiled-coil, B) 3-D structure of antiparallel coiled-coil determined by X-ray crystallography. Coiled coils can assemble either in a parallel or antiparallel orientation, with respect to the orientation of polypeptide backbone. They can form either heterodimers or homodimers and all of those combinations have already been designed and verified experimentally for pairs of coiled-coil forming segments. Stability of coiled-coil is determined by the interactions between heptads, orientation and length of the segment. Coiled-coil interactions are probably some of the most well understood types of protein-protein interactions and we can predict the stability of interacting helices with relatively good accuracy (more detailed description in the modeling section) (Mason et al., 2007). We come to the idea that coiled-coil segments could be used to assemble complex structures in a similar way as DNA assemblies by using coiled-coil segment specificity to govern pairing of the assembly. Coiled-coil segments would represent rigid rods that can form the edges between vertices of polyhedra or network connections of the lattice. All that is required is to prepare a set of coiled-coil forming segments that interact only with the designated coiled-coil forming partners (orthogonal set of coiled-coils). Coiled coil segments are delimited by flexible hinges, made of short peptide linkers between them to allow flexibility required for the assembly. At least three coiled-coil forming segments have to be present within a single polypeptide chain in order to form a 2D or 3D structure. As an illustration, a tetrahedron (Figure 2) can be formed from a single type of polypeptide containing three coiled-coils which form antiparallel homodimers. ![]() Figure 2: Tetrahedron formed from three antiparallel cioled-coil-forming segments We developed this idea and discovered its exciting potentials as the complex structures can be formed already with very simple combinations. We have explored this idea in more detail in the Modeling section and proof of the principle of one specific design was experimentally confirmed, creating the first report of a coiled-coil based polypeptide lattice. The idea of combining modular protein domain and/or coiled-coil forming segments into nanostructures was the background of our project to develop modular nanoBricks as the library that will allow to expand the universe of possible combinations of building nanostructures. In order to move beyond a mere proof of the principle we also developed a real world application based on formation of polypeptide membrane, which has been demonstrated to function for ultrafiltration of molecules and viruses. Application of the underlying idea of this project could be further developed by manufacturing numerous structures such as nano-cages, nano-networks and nano-wires. Additional advantage of such nanostructures built from polypeptide-forming coiled-coils are optionally added functional groups which can be introduced at solvent exposed residues b, c and f (e.g. cysteines for covalent modification of SH group or histidines for use as chelators of metal ions). These nanostructures can be used for diverse purposes such as drug delivery, chemical catalysis, metal binding, formation of conducting circuits and much, much more. |