From 2011.igem.org

Revision as of 17:58, 20 September 2011

S-layer

Molecular nanotechnology, especially nanobiotechnology starts to use and modify functionalized surfaces. Especially the immobilization of self-assembling biomolecules draws an increasing attention. The advantages of using immobilized enzymes in well-defined positions on nano-structured surfaces may even be greater. Self-assembly is an organization of molecules into defined structures, lowering the free energy of the system. Interaction between the molecules is non-covalent (e.g. hydrophobic-hydrophobic, van der Waals forces, molecular stacking) ([http://onlinelibrary.wiley.com/doi/10.1002/smll.200700200/abstract Schäffer et al., 2007]).

Many biomolecules such as protein, polysaccharides and lipid have the ability to self-assemble into different shapes (e.g. spherical, rod- or sheet-like shapes), allowing several specific functions as virus capsids, cytoskeleton components or extracellular surface layer protein. The so-called paracrystalline cell surface-layer (S-layer) are build up on S-layer proteins and are one of the most common surface structures in bacteria and archaea. They are regarded as the outmost cell envelope of prokaryotic organisms ([http://onlinelibrary.wiley.com/doi/10.1111/j.1574-6968.2006.00573.x/full Sleytr et al., 2007]).

S-layer in general

S-layer proteins fulfill various functions as molecular sieves, ion traps and protective coats ([http://onlinelibrary.wiley.com/doi/10.1002/3527600035.bpol7011/abstract Sleytr et al., 2005]). They build up periodic structures, posses pores of identical size and morphology and show equal physicochemical properties on each molecular unit. Isolated they have the special ability to reassemble into two-dimensional crystals equal to structures found on intact bacterial cells. S-layers have the ability to form self-assembly products in solution and to recrystallize into monomolecular layers on solid supports, at air-water interface and on lipid films. They can cover liposomes and nanocapsules als well as small beads completely. S-layer are mainly composed of a single (glyco)protein species, assembled into a layer completely covering the cell. In organisms the may represent up to 20% of the total protein content of a bacterial cell. Most S-layer proteins are weak acidic (pI 4-6) and contain a high proportion of hydrophobic amino acids as well as few or no sulphur-containing amino acids, their molecular mass varies between 40 – 200 kDa and is often strain-specific. The assembled S-layer lattices are generally 5 – 20 nm thick, in archaea lattices are up to 70 nm thick. The protein subunits of S-layer are arranged in lattices with different symmetry; olique (p1, p2), square (p4) or hexagonal (p3, p6) with a center-to-center spacing of the subunits of 3 – 35 nm. S-layer are highly porous with a porosity of 30 – 70% ([http://onlinelibrary.wiley.com/doi/10.1111/j.1742-4658.2006.05606.x/abstract Sleytr et al., 2007]).

Various S-layer proteins from archaea and eubacteria are glycosylated, with strain-specific modifications. S-layer proteins were the first prokaryotic proteins that were shown to exhibit this remarkable characteristic. Up until now glycosylation has been proven for several archaeal S-layer proteins. Among the bacterial species glycosylation was demonstrated only for S-layer proteins of Bacillaceae ([http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2958.1997.d01-1868.x/abstract Chami et al., 1997], [http://onlinelibrary.wiley.com/doi/10.1002/smll.200700200/abstract Schäffer et al., 2007]).

In gram-negative archaea, S-layer are the exclusive cell wall component. In gram-positive bacteria and archaea, S-layer assemble on the outmost part of a firm wall matrix, which is composed mostly of peptidoglycan, pseudomurein. In gram-negative bacteria, S-layer are linked to specific lipopolysaccharides (LPS) ([http://onlinelibrary.wiley.com/doi/10.1002/3527600035.bpol7011/abstract Sleytr et al., 2005]). For gram-positive bacteria a cell-wall-targeting domain could be identified at the N-terminal end of many S-layer proteins. The domain facilitates binding to a specific secondary cell wall polymer (SCWP) by a lectin-type binding ([http://onlinelibrary.wiley.com/doi/10.1111/j.1742-4658.2006.05606.x/abstract Sleytr et al., 2007]). It was found that some S-layer proteins consist of two distinct domains with different functions. One domain ist involved in the assembly with other S-layer protein monomers and the other domain mediates the interaction with the cell wall. Several SLH domains have been identified at the amino-terminal region of different S-layer proteins and at the carboxy-terminal region of cell-assiociated exoroteins. The domain may be repeated within the sequence and is involved in anchoring the S-layer proteins to the cell surface ([http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2958.1997.d01-1868.x/abstract Chami et al., 1997], [http://www.sciencedirect.com/science/article/pii/S0966842X99015139 Sleytr & Beveridge, 1999]). In various S-layer proteins from bacillacaea the deletion of significant parts of the carboxy-terminal or amino-terminal did not affect self-assembly and the capability of the S-layer proteins to form lattices ([http://onlinelibrary.wiley.com/doi/10.1111/j.1742-4658.2006.05606.x/abstract Sleytr et al., 2007]).

The supramolecular structure as well as the mechanism of binding the outmost cell wall vary between S-layers of different species, leading to the development different isolation procedures. S-layers normally are attached to the cell wall through non-covalent binding, and can therefore be isolated and completely disintegrated in dissociating agents (e.g. lithium chloride), metal-chelating agents (e.g. ethylendiaminetetraacetic acid EDTA), chaotropic denaturants such as urea or guanidine hydrochloride and by raising or lowering pH. After removal of the disrupting agent reassembly takes place. ([http://onlinelibrary.wiley.com/doi/10.1002/3527600035.bpol7011/abstract Sleytr et al., 2005]).

The S-layer protein PS2 of Corynbacterium glutamicum

The S-layer of the Gram-positive bacterium Corynebacterium glutamicum ATCC 17965 is formed by the PS2 protein. The protein is encoded by the cspB gene. The mature protein has a molecular mass of 52.5 kDa. It is devoid of any sulfur-containing amino acids, whereas its nature is due to a high content of hydrophobic amino acids. Although there exist a lot of different S-layer proteins, PS2 has no similarities to any other protein in the EMBL database. The S-layer of C. glutamicum is characterized by a hexagonal lattice symmetry. Attachment between S-layer and cell wall was found to be due to the hydrophobic carboxy-terminus of the PS2 protein. It was found that peptidoglycan is probably not involved in interaction between the PS2 S-layer and the cell because the interaction between PS2 and the cell is disrupted by adding detergents. Also the S-layer protein from C. glutamicum does not contain a SLH domain, which is characteristic for several S-layer proteins and other enzymes bound to the peptidoglycan. Besides some other S-layer proteins show a carboxy-terminal hydrophobic sequence of 20 – 24 amino acids. (e.g. Halobacterium halobium, Haloferax volcanii, Rickettsia rickettsii)([http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2958.1997.d01-1868.x/abstract Chami et al., 1997], [http://www.sciencedirect.com/science/article/pii/S016816560400241X Hansmeier et al., 2004]).

The S-layer protein SgsE of

Further applications of S-layer proteins

The ability of self-assembly and forming defined nanostructures makes the S-layer proteins to some sort of building blocks in a biomolecular construction kit for generating a universal matrix. By using the matrix as a nano pinboard for further components or just the nanostructure itself, a great variety of applications in modular nanobiotechnology, biomimetics, bioanalytics and medical diagnostic are imaginable. One current research theme is the design of more sensitive and improved optical and electrochemical sensors. As example could be mentioned the luminescence lifetime based oxygen sensor, described from Schleicher et al. (2009). Therefore metalloporphyrin dyes which change luminescence properties in presence and absence of oxygen were bond to S-layer proteins. These proteins were used to form monolayer coatings on optical fiber surfaces allowing evanescent field fluorescence excitation of the linked fluorophores. The key benefits of using S-layer proteins for this type of sensor are the imparted anti-fouling properties and the good biocompatibility. This is especially valuable for sensing applications in complex biological fluids or implantable sensors.

Concentrating on the repetitive features of S-layer proteins to form a well defined nanolattice, the use as filtration units become reasonable. Sára and Sleytr (2000) described a so-called isoporous S-layer ultrafiltration membrane (SUM). This filtration system bases on a nylon microfiltration membrane as recrystallization surface for S-layer fragments of Bacillus sphaericus CCM 2120, to build up a constant lattice with a well-defined pore size of 12.5 nm. Another advantage of this membrane is the presence of functional groups in defined positions and orientations. These functional groups could be used for highly reproducible chemical modifications to optimize molecular sieving properties and nonspecific adsorption (antifouling) characteristics.

The self-assembly and immobilization properties of S-layer fusion proteins open also new innovative perspectives in clinical applications like immune therapy, blood purification and drug targeting. Bohle et al. (2011) showed that a genetic fusion of an allergen to SbsC S-layer proteins from Geobacillus stearothermophilus combine reduced allergenicity with immunomodulatory capacity. These qualities makes them to an ideal allergen carrier/adjuvants in specific immunotherapy, which is the only causative treatment for type I allergy. Fusion proteins of a synthetic analogue of the immunoglobulin G (IgG)-binding B-domain of protein A of Staphylococcus aureus and SbpA S-layer proteins from Bacillus sphaericus CCM 2177 are proposed as a microsphere-based extracorporeal blood detoxification system to remove IgG from human plasma from patients suffering from autoimmune disease. The use of microparticles to detoxify the plasma allows rapid removal of the pathogenic substances and leads to higher binding capacities then commercially available immunoadsorbents (Völlenkle et al., (2003)). The natural/original ability of crystallization on lipid membranes/liposomes for heightening the mechanical and thermal stability of S-liposomes and the possibility for immobilizing biologically active molecules can be cross-linked and exploited as a matrix for the covalent attachment of functional molecules to built up a biocompatible drugtargeting or gene therapy system.

But the main advantage of S-layer proteins is their application as universal matrix for the immobilization. This versatility could be upgraded by fusing the S-layers with minimum-sized core-streptavidin to build up a universal affinity matrix any kind of biotinylated molecule. This concept fits exactly in the primary aim of constructing a biomolecular construction kit. Huber et al. (2006) used the streptavidin matrix for building up functional sensor surface by recrystallization these heterotetramers on gold chips. This could be exploited for the development of cheaper DNA or protein chips.

In conclusion the S-layer proteins are one of the most innovative and promising discoversies for combining biology with engineering in the new field of system biology.

References

Bohle B, Breitwieser A, Zwölfer B, Jahn-Schmid B, S´ara M, Sleytr UB & Ebner C (2004) A novel approach to specific allergy treatment: the recombinant fusion protein of a bacterial cell surface (S-layer) protein and the major birch pollen allergen Bet v 1 (rSbsC-Bet v 1) combines reduced allergenicity with immunomodulating capacity, [http://www.jimmunol.org/content/172/11/6642.full J Immunol 172: 6642–6648].

Chami M, Bayan N, Peyret JL, Gulik-Krzywicki T, Leblon G, Shechter E (1997) The S-layer protein of Corynebacterium glutamicum is anchored to the cell wall by its C-terminal hydrophobic domain, [http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2958.1997.d01-1868.x/abstract Mol Microbiol. 23(3):483-92.]

Hansmeier N, Bartels FW, Ros R, Anselmetti D, Tauch A, Pühler A, Kalinowski J (2004) Classification of hyper-variable Corynebacterium glutamicum surface-layer proteins by sequence analyses and atomic force microscopy [http://www.sciencedirect.com/science/article/pii/S016816560400241X J Biotechnol. 26;112(1-2):177-93.]

Schäffer C, Novotny R, Küpcü S, Zayni S, Scheberl A, Friedmann J, Sleytr UB, Messner P (2007) Novel biocatalysts based on S-layer self-assembly of Geobacillus stearothermophilus NRS 2004/3a: a nanobiotechnological approach, [http://onlinelibrary.wiley.com/doi/10.1002/smll.200700200/abstract Small 3(9):1549-59.]

Sleytr UB, Beveridge TJ (1999) Bacterial S-layers. [http://www.sciencedirect.com/science/article/pii/S0966842X99015139 Trends Microbiol. 7(6):253-60.]

Sleytr UB, Sára M, Pum D, Schuster B, Messner P, Schäffer C (2005) Self-assembling protein systems: microbial S-layers, in: [http://onlinelibrary.wiley.com/doi/10.1002/3527600035.bpol7011/abstract Steinbüchel A, Fahnestock SR (Eds.), Polyamides 34 and complex proteinaceous materials, Wiley-VCH, Weinheim, pp. 285-338.]

Sleytr UB, Egelseer EM, Ilk N, Pum D, Schuster B (2007) S-Layers as a basic building block in a molecular construction kit, [http://onlinelibrary.wiley.com/doi/10.1111/j.1574-6968.2006.00573.x/full FEBS J 274(2):323-34]

Sleytr UB, Huber C, Ilk N, Pum D, Schuster B, Egelseer EM (2007) S-layers as a tool kit for nanobiotechnological applications, [http://onlinelibrary.wiley.com/doi/10.1111/j.1574-6968.2006.00573.x/full FEMS Microbiol Lett. 267(2):131-44.]

Völlenkle C, Weigert S, Ilk N et al. (2004) Construction of a functional S-layer fusion protein comprising an immunoglobulin G-binding domain for development of specific adsorbents for extracorporeal blood purification. [http://aem.asm.org/cgi/content/short/70/3/1514 Appl Environ Microbiol 70: 1514–1521].