Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4983438 | Colloids and Surfaces B: Biointerfaces | 2017 | 10 Pages |
â¢Self-assembly regulation of an artificial microsystem mediated by ATP.â¢Structural characterization of artificial erythrocyte cytoskeletons.â¢Quantitative nanomechanical mapping of lipid-protein surfaces in liquid media.
Erythrocyte membranes have been particularly useful as a model for studies of membrane structure and mechanics. Native erythroid membranes can be electroformed as giant unilamellar vesicles (eGUVs). In the presence of ATP, the erythroid membrane proteins of eGUVs rearrange into protein networks at the microscale. Here, we present a detailed nanomechanical study of individual protein microfilaments forming the protein networks of eGUVs when spread on supporting surfaces. Using Peak Force tapping Atomic Force Microscopy (PF-AFM) in liquid environment we have obtained the mechanical maps of the composite lipid-protein networks supported on solid surface. In the absence of ATP, the protein pool was characterized by a Young's Modulus Epool â 5-15 MPa whereas the complex filaments were found softer after protein supramolecular rearrangement; Efil â 0.4 MPa. The observed protein softening and reassembling could be relevant for understanding the mechanisms of cytoskeleton reorganization found in pathological erythrocytes or erythrocytes that are affected by biological agents.
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