Molecular Sensing and Manipulation of Protein Oligomerization in Membrane Nanotubes with Bolaamphiphilic Foldamers.


Journal

Journal of the American Chemical Society
ISSN: 1520-5126
Titre abrégé: J Am Chem Soc
Pays: United States
ID NLM: 7503056

Informations de publication

Date de publication:
22 Nov 2023
Historique:
medline: 23 11 2023
pubmed: 10 11 2023
entrez: 10 11 2023
Statut: ppublish

Résumé

Adaptive and reversible self-assembly of supramolecular protein structures is a fundamental characteristic of dynamic living matter. However, the quantitative detection and assessment of the emergence of mesoscale protein complexes from small and dynamic oligomeric precursors remains highly challenging. Here, we present a novel approach utilizing a short membrane nanotube (sNT) pulled from a planar membrane reservoir as nanotemplates for molecular reconstruction, manipulation, and sensing of protein oligomerization and self-assembly at the mesoscale. The sNT reports changes in membrane shape and rigidity caused by membrane-bound proteins as variations of the ionic conductivity of the sNT lumen. To confine oligomerization to the sNT, we have designed and synthesized rigid oligoamide foldamer tapes (ROFTs). Charged ROFTs incorporate into the planar and sNT membranes, mediate protein binding to the membranes, and, driven by the luminal electric field, shuttle the bound proteins between the sNT and planar membranes. Using Annexin-V (AnV) as a prototype, we show that the sNT detects AnV oligomers shuttled into the nanotube by ROFTs. Accumulation of AnV on the sNT induces its self-assembly into a curved lattice, restricting the sNT geometry and inhibiting the material uptake from the reservoir during the sNT extension, leading to the sNT fission. By comparing the spontaneous and ROFT-mediated entry of AnV into the sNT, we reveal how intricate membrane curvature sensing by small AnV oligomers controls the lattice self-assembly. These results establish sNT-ROFT as a powerful tool for molecular reconstruction and functional analyses of protein oligomerization and self-assembly, with broad application to various membrane processes.

Identifiants

pubmed: 37948300
doi: 10.1021/jacs.3c05753
pmc: PMC10682987
doi:

Substances chimiques

Membrane Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

25150-25159

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM121725
Pays : United States

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Auteurs

Kathrin Aftahy (K)

Department of Pharmacy, Ludwig-Maximilians-Universität München, Munich 81377, Germany.

Pedro Arrasate (P)

Biofisika Institute (CSIC, UPV/EHU), University of the Basque Country, Leioa 48940, Spain.
Department of Biochemistry and Molecular Biology, University of the Basque Country, Leioa 48940, Spain.

Pavel V Bashkirov (PV)

Research Institute for Systems Biology and Medicine, Moscow 117246, Russia.

Petr I Kuzmin (PI)

A.N. Frumkin Institute of Physical Chemistry and Electrochemistry, Moscow 119071, Russia.

Victor Maurizot (V)

Univ. Bordeaux, CNRS, Bordeaux Institut National Polytechnique, CBMN (UMR 5248), Pessac 33600, France.

Ivan Huc (I)

Department of Pharmacy, Ludwig-Maximilians-Universität München, Munich 81377, Germany.

Vadim A Frolov (VA)

Biofisika Institute (CSIC, UPV/EHU), University of the Basque Country, Leioa 48940, Spain.
Department of Biochemistry and Molecular Biology, University of the Basque Country, Leioa 48940, Spain.
Ikerbasque, Basque Foundation for Science, Bilbao 48009, Spain.

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Classifications MeSH