2008
DOI: 10.1002/anie.200802834
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Cryo Electron Tomography Reveals Confined Complex Morphologies of Tripeptide‐Containing Amphiphilic Double‐Comb Diblock Copolymers

Abstract: Sequence sets structure: Amphiphilic norbornene‐based double‐comb diblock polymers with peptide and oligo(ethylene oxide) side chains aggregate in water to form unprecedented complex morphologies depending on the amino acid sequence of the peptide. The internal structures of the aggregates observed by cryo electron tomography show densely folded and highly branched wormlike micelles (left) and spherical aggregates with a bicontinuous architecture (right).

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Cited by 102 publications
(83 citation statements)
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“…The block copolymerization of a norbornene derivative having a short peptide with a norbornene having a PEG substituent gives block copolymer 20, consisting of a segment with hydrophilic PEG side chains and a segment with more hydrophobic peptide side chains (Scheme 14). 56,57 The copolymer forms aggregates upon dispersion in water.…”
Section: Synthesis Of Amino Acid-and Peptide-based Polymers By Rompmentioning
confidence: 99%
“…The block copolymerization of a norbornene derivative having a short peptide with a norbornene having a PEG substituent gives block copolymer 20, consisting of a segment with hydrophilic PEG side chains and a segment with more hydrophobic peptide side chains (Scheme 14). 56,57 The copolymer forms aggregates upon dispersion in water.…”
Section: Synthesis Of Amino Acid-and Peptide-based Polymers By Rompmentioning
confidence: 99%
“…Furthermore, cryoelectron microscopy (cryo-TEM) and three-dimensional (3D) image reconstruction were used to confirm the spherical micellar morphology and uniformity of the particles and to determine their radial density profile. 11 …”
mentioning
confidence: 99%
“…Although Moor and Mühlethaler (4) and Dubochet and McDowall (5) followed different postprocessing and imaging routines (freeze-etching versus direct imaging, respectively), the basic principle of both preparation procedures is the same: the physical arresting of the sample in a frozen-hydrated state, which is achieved by the vitrification of the sample within milliseconds, resulting in a sample embedded in amorphous ice, thereby avoiding structural changes due to ice crystal growth. The convincing structural preservation achieved in the case of isolated cell organelles (6,7), viruses (8), bacteria (9,10), eukaryotic cells (11) and other softmatter applications (12), and the technical improvements in sample preparation and handling (13)(14)(15)(16)(17)(18)(19), caused this approach to spread out into other fields of microscopy like soft x-ray (20) and light microscopy (21,22), and enabled new hybrid approaches like correlative cryo-light and electron microscopy (23).…”
Section: Introductionmentioning
confidence: 99%