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Recent research news on Artificial Biology


Distinct Network Morphologies from In Situ Polymerization of Microtubules in Giant Polymer-Lipid Hybrid Vesicles

Creating artificial cells with a dynamic cytoskeleton, akin to those in living cells, is a major goal in bottom-up synthetic biology. In this study, we demonstrate the in situ polymerization of microtubules encapsulated in giant polymer-lipid hybrid vesicles (GHVs) composed of 1,2-dioleoyl-sn-glycero-3-phosphocholine and an amphiphilic block copolymer. The block copolymer is comprised of poly(cholesteryl methacrylate-co-butyl methacrylate) as the hydrophobic block and either poly(6-O-methacryloyl-D-galactopyranose) or poly(carboxyethyl acrylate) as the hydrophilic extension. Depending on the concentrations of guanosine triphosphate (GTP) or its slowly hydrolyzable analog, guanosine-5′-[(α,β)-methyleno]triphosphate (GMPCPP), different microtubule morphologies are observed, including encapsulated microtubule networks, spike protrusions, as well as membrane-associated or aggregated microtubules. Overall, this work represents a step forward in mimicking the cellular cytoskeletons and uncovering the influence of membrane composition on microtubule morphologies.

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Sitte, J., Pollok, K., Finster, K., Löffler, S., Burkhardt, E.-M., Langenhorst, F., Büchel, G. & Küsel, K. (2010). Nickel sulfide formation by a sulfate-reducing consortium originated from heavy metal polluted creek soil. Poster session presented at Goldschmidt conference, Knoxville, Tennessee, United States.
Sitte, J., Pollok, K., Finster, K., Langenhorst, F. & Küsel, K. (2010). Nickel sulfide precipitation of a sulfate-reducing consortium originated from a metal contaminated creek soil in the former uranium-mining district Ronneburg. Poster session presented at VAAM conference 2010, Hannover, Germany.
Hosta-Rigau, L., Chandrawati, R., Saveriades, E., Odermatt, P. D., Postma, A., Ercole, F., Breheney, K., Wark, K. L., Stadler, B. & Caruso, F. (2010). Noncovalent Liposome Linkage and Miniaturization of Capsosomes for Drug Delivery. Biomacromolecules, 11, 3548-3555.
Triano, I., Barrera, F. N., Renart, M. L., Molina, M. L., Fernández-Ballester, G., Poveda, J. A., Fernández, A. M., Encinar, J. A., Ferrer-Montiel, A. V., Otzen, D. & González-Ros, J. M. (2010). Occupancy of nonannular lipid binding sites on KcsA greatly increases the stability of the tetrameric protein. Biochemistry, 49(25), 5397-5404. https://doi.org/10.1021/bi1003712