Literature DB >> 23363440

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

Eun-Kyoung Bang1, Giulio Gasparini1, Guillaume Molinard1, Aurélien Roux1, Naomi Sakai1, Stefan Matile1.   

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.

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Year:  2013        PMID: 23363440      PMCID: PMC4601153          DOI: 10.1021/ja311961k

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  40 in total

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9.  Fifteen years of cell-penetrating, guanidinium-rich molecular transporters: basic science, research tools, and clinical applications.

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10.  Synthesis of functional 1,2-dithiolanes from 1,3-bis-tert-butyl thioethers.

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