4.8 Article

Multicompartment Lipid Cubic Nanoparticles with High Protein Upload: Millisecond Dynamics of Formation

期刊

ACS NANO
卷 8, 期 5, 页码 5216-5226

出版社

AMER CHEMICAL SOC
DOI: 10.1021/nn5012946

关键词

lipid-protein nanoassembly; dynamic membrane curvature; amphiphile nanoarchitectonics; multicompartment lipid nanoparticle; morphological transition pathway; millisecond time-resolved SAXS; cryo-TEM; BDNF-loaded cubosome

资金

  1. Czech Science Foundation [P208/10/1600]
  2. ANR SIMI10 Nanosciences
  3. LabEx LERMIT
  4. BIMF (Bayreuth Institute of Macromolecular Research)
  5. BZKG (Bayreuth Center for Colloids and Interfaces)
  6. [SC-3358]

向作者/读者索取更多资源

Membrane shapes, produced by dynamically assembled lipid/protein architectures, are crucial for both physiological functions and the design of therapeutic nanotechnologies. Here we Investigate the dynamics of lipid membrane-neurotrophic BDNF protein complexes formation and ordering In nanoparticles, with the purpose of innovation in nanostructure-based neuroprotection and biomimetic nanoarchitectonics. The kinetic pathway of membrane states associated with rapidly occurring nonequilibrium self-assembled lipid/protein nanoarchitectures was determined by millisecond time-resolved small-angle X-ray scattering (SAXS) at high resolution. The neurotrophin binding and millisecond trafficking along the flexible membranes induced an unusual overlay of channel-network architectures including two coexisting cubic lattices epitaxially connected to lamellar membrane stacks. These time-resolved membrane processes, involving intercalation of discrete stiff proteins in continuous soft membranes, evidence stepwise curvature control mechanisms. The obtained three-phase liquid-crystalline nanoparticles of neurotrophic composition put forward important advancements in multicompartment soft-matter nanostructure design.

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