Difference between revisions of "Part:BBa K3470014"

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'''HlyB''' acts as an ATP-binding cassette and recognizes the substrate via its secretion signal peptide (HlyA). It exports any protein (like IL-10) fused to the secretion signal, produced inside the bacteria that must act on targets outside and is responsible for the specificity of the secretion system process(Bravo et al., 2008, Delepelaire, 2004).
 
'''HlyB''' acts as an ATP-binding cassette and recognizes the substrate via its secretion signal peptide (HlyA). It exports any protein (like IL-10) fused to the secretion signal, produced inside the bacteria that must act on targets outside and is responsible for the specificity of the secretion system process(Bravo et al., 2008, Delepelaire, 2004).
 
   
 
   
'''HlyD''' consists of a short cytoplasmic domain at the N-terminus, a membrane anchor and a large periplasmic domain. It acts as a membrane fusion or adaptor protein by linking the HlyB and TolC domains of the Hemolysin transport system and helps in the transportation of proteins. TolC is a specific outer membrane protein that forms a long channel throughout the periplasm and the outer membrane, largely open towards the extracellular matrix for export of required components to targets outside the bacteria(Gentschev et al., 2002, Schmitt et al., 2003).  
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'''HlyD''' consists of a short cytoplasmic domain at the N-terminus, a membrane anchor and a large periplasmic domain. It acts as a membrane fusion or adaptor protein by linking the HlyB and '''TolC''' domains of the Hemolysin transport system and helps in the transportation of proteins. TolC is a specific outer membrane protein that forms a long channel throughout the periplasm and the outer membrane, largely open towards the extracellular matrix for export of required components to targets outside the bacteria(Gentschev et al., 2002, Schmitt et al., 2003).  
  
'''HlyA''' is a signal sequence that interacts with the cytoplasmic region of the pre-formed HlyB–D complex. After the binding of the HlyA secretion signal by the HlyB–D complex, HlyD induces the interaction with TolC which then transports it out of the cell (Hess et al., 1990).   
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'''HlyA''' is a signal sequence that interacts with the cytoplasmic region of the pre-formed HlyB–D complex. After the binding of the HlyA secretion signal by the HlyB–D complex, HlyD induces the interaction with '''TolC''' which then transports it out of the cell (Hess et al., 1990).   
  
 
==Proposed experimentation==
 
==Proposed experimentation==

Revision as of 12:01, 20 October 2020

Circuit

Constitutive Promoter – RBS – HlyB – RBS – HlyD – RBS – TolC – RBS - GFP+HlyA - Double Terminator

Usage and Biology

HlyB acts as an ATP-binding cassette and recognizes the substrate via its secretion signal peptide (HlyA). It exports any protein (like IL-10) fused to the secretion signal, produced inside the bacteria that must act on targets outside and is responsible for the specificity of the secretion system process(Bravo et al., 2008, Delepelaire, 2004).

HlyD consists of a short cytoplasmic domain at the N-terminus, a membrane anchor and a large periplasmic domain. It acts as a membrane fusion or adaptor protein by linking the HlyB and TolC domains of the Hemolysin transport system and helps in the transportation of proteins. TolC is a specific outer membrane protein that forms a long channel throughout the periplasm and the outer membrane, largely open towards the extracellular matrix for export of required components to targets outside the bacteria(Gentschev et al., 2002, Schmitt et al., 2003).

HlyA is a signal sequence that interacts with the cytoplasmic region of the pre-formed HlyB–D complex. After the binding of the HlyA secretion signal by the HlyB–D complex, HlyD induces the interaction with TolC which then transports it out of the cell (Hess et al., 1990).

Proposed experimentation

The efficiency of the control system consisting of HlyB, HlyD, TolC, and HlyA against control with HlyB, HlyD and TolC absent must be tested. The HlyA + GFP transported outside the cells, HlyA + GFP remaining inside the cells and the total HlyA + GFP produced must be mapped with absorbance vs time graphs to show to efficiency in getting the anti-inflammatory cytokines outside the cell to the target site. The plot should determine the amount of HlyA+GFP transported outside. Hence it should be ideally equal to the plot of control showing that the transport system is extremely efficient in getting the anti-inflammatory cytokines outside the cell to the target site.


References

Bavro, V. N., Pietras, Z., Furnham, N., Pérez-Cano, L., Fernández-Recio, J., Pei, X. Y., Misra, R., & Luisi, B. (2008). Assembly and Channel Opening in a Bacterial Drug Efflux Machine. Molecular Cell, 30(1), 114–121. https://doi.org/10.1016/j.molcel.2008.02.015

Delepelaire, P. (2004). Type I secretion in gram-negative bacteria. Biochimica et Biophysica Acta - Molecular Cell Research, 1694(1-3 SPEC.ISS.), 149–161. https://doi.org/10.1016/j.bbamcr.2004.05.001

Hess, J., Gentschev, I., Goebel, W., & Jarchau, T. (1990). Analysis of the haemolysin secretion system by PhoA-HlyA fusion proteins. MGG Molecular & General Genetics, 224(2), 201–208. https://doi.org/10.1007/BF00271553

Schmitt, L., Benabdelhak, H., Blight, M. A., Holland, I. B., & Stubbs, M. T. (2003). Crystal structure of the nucleotide-binding domain of the ABCtransporter haemolysin B: Identification of a variable region within ABC helical domains. Journal of Molecular Biology, 330(2), 333–342. https://doi.org/10.1016/S0022-2836(03)00592-8