Molecular Relay Stations in Membrane Nanotubes: IRSp53 Involved in Actin-Based Force Generation

被引:3
作者
Madarasz, Tamas [1 ]
Brunner, Brigitta [2 ]
Halasz, Henriett [1 ]
Telek, Elek [1 ]
Matko, Janos [3 ]
Nyitrai, Miklos [1 ]
Szabo-Meleg, Edina [1 ]
机构
[1] Univ Pecs, Med Sch, Dept Biophys, H-7624 Pecs, Hungary
[2] Univ Pecs, Inst Biol, Fac Sci, H-7624 Pecs, Hungary
[3] Eotvos Lorand Univ, Fac Sci, Dept Immunol, H-1117 Budapest, Hungary
关键词
actin; fluorescence microscopy; IRSp53; membrane nanotube; protein-protein interactions; TUNNELING NANOTUBES; LIPID-COMPOSITION; STRUCTURAL BASIS; HOMOLOGY DOMAIN; CDC42; FILOPODIA; PROTEINS; BINDING; RAC; COMPLEX;
D O I
10.3390/ijms241713112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane nanotubes are cell protrusions that grow to tens of micrometres and functionally connect cells. Actin filaments are semi-flexible polymers, and their polymerisation provides force for the formation and growth of membrane nanotubes. The molecular bases for the provision of appropriate force through such long distances are not yet clear. Actin filament bundles are likely involved in these processes; however, even actin bundles weaken when growing over long distances, and there must be a mechanism for their regeneration along the nanotubes. We investigated the possibility of the formation of periodic molecular relay stations along membrane nanotubes by describing the interactions of actin with full-length IRSp53 protein and its N-terminal I-BAR domain. We concluded that I-BAR is involved in the early phase of the formation of cell projections, while IRSp53 is also important for the elongation of protrusions. Considering that IRSp53 binds to the membrane along the nanotubes and nucleates actin polymerisation, we propose that, in membrane nanotubes, IRSp53 establishes molecular relay stations for actin polymerisation and, as a result, supports the generation of force required for the growth of nanotubes.
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页数:24
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