Cholesterol-directed nanoparticle assemblies based on single amino acid peptide mutations activate cellular uptake and decrease tumor volume† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc02616a Click here for additional data file.

نویسندگان

  • Shang Li
  • Rongfeng Zou
  • Yaoquan Tu
  • Junchen Wu
  • Markita P. Landry
چکیده

Key Laboratory for Advanced Materials & Chemistry and Molecular Engineering, E Technology, Shanghai 200237, China. E-ma Department of Chemical and Bio-molecul Berkeley, 476 Stanley Hall, Berkeley, Ca berkeley.edu California Institute for Quantitative Bios Berkeley, Berkeley, CA 94720, USA Division of Theoretical Chemistry and Biol Institute of Technology, SE-10691 Stockholm † Electronic supplementary informa 10.1039/c7sc02616a ‡ These authors contributed equally to th Cite this: Chem. Sci., 2017, 8, 7552

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Cholesterol-directed nanoparticle assemblies based on single amino acid peptide mutations activate cellular uptake and decrease tumor volume.

Peptide drugs have been difficult to translate into effective therapies due to their low in vivo stability. Here, we report a strategy to develop peptide-based therapeutic nanoparticles by screening a peptide library differing by single-site amino acid mutations of lysine-modified cholesterol. Certain cholesterol-modified peptides are found to promote and stabilize peptide α-helix formation, re...

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This work describes how a small-molecule chemical trigger, reacting through the mediatory of an inverse electron demand Diels-Alder reaction, results in enhanced cellular uptake and selective nanoparticle disintegration and cargo liberation, via gross polymeric morphological alterations. The power of these responsive nanoparticles is demonstrated through encapsulation of the anti-cancer agent d...

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2017