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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.

Recent publications by network


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Andreis, L., Bassetti, F. & Hirsch, C. (2026). LDP for the covariance process in fully connected Gaussian neural networks. Electronic Journal of Probability, 31, Article 22. https://doi.org/10.1214/26-EJP1477
Nielsen, K. H. (2026). Markovnikovs regel. Weekendavisen, Sektion 4 (Ideer), 5.
Adam, L., Molenkamp, W. H., Nowak, J. S., Farzadfard, A., Gaarthuis, K., Kumar, R., Nielsen, J., Otzen, D. E., Johansson, J. & Abelein, A. (2026). Mechanism-selective inhibition of α-synuclein aggregation by the chaperone-like BRICHOS domain. The Journal of Biological Chemistry, 302(6), 113117. Article 113117. https://doi.org/10.1016/j.jbc.2026.113117
Hoetzel, J., Walbrun, A., Schäfer, M., Wang, T., Jørgensen, A. G., Becker, O., Stamatakis, K., Gunawan, V., Reichardt, L., Boettger, L., Bruckhoff, R. W., Kjems, J., Wachtveitl, J., Rief, M. & Suess, B. (2026). Mechanism underlying the high regulatory performance of the doxycycline riboswitch G12. Nature Communications, 17(1), Article 7697. https://doi.org/10.1038/s41467-026-76256-2