Substrate-initiated synthesis of cell-penetrating poly(disulfide)s

J Am Chem Soc. 2013 Feb 13;135(6):2088-2091. doi: 10.1021/ja311961k. Epub 2013 Feb 4.

Abstract

Lessons from surface-initiated polymerization are applied to grow cell-penetrating poly(disulfide)s directly on substrates of free choice. Reductive depolymerization after cellular uptake should then release the native substrates and minimize toxicity. In the presence of thiolated substrates, propagators containing a strained disulfide from asparagusic or, preferably, lipoic acid and a guanidinium cation polymerize into poly(disulfide)s in less than 5 min at room temperature at pH 7. Substrate-initiated polymerization of cationic poly(disulfide)s and their depolymerization with dithiothreitol causes the appearance and disappearance of transport activity in fluorogenic vesicles. The same process is further characterized by gel-permeation chromatography and fluorescence resonance energy transfer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Disulfides / chemical synthesis*
  • Disulfides / chemistry
  • Fluorescence Resonance Energy Transfer
  • Hydrogen-Ion Concentration
  • Molecular Structure
  • Polymerization
  • Polymers / chemical synthesis*
  • Polymers / chemistry
  • Temperature

Substances

  • Disulfides
  • Polymers