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Royal Society of Chemistry, Chemical Communications, 76(50), p. 11097-11100, 2014

DOI: 10.1039/c4cc03606a

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Programmed stereoselective assembly of DNA-binding helical metallopeptides

This paper is available in a repository.
This paper is available in a repository.

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Abstract

We have applied solid phase peptide synthesis methods for the construction of peptide ligands that coordinate Fe(ii) ions and fold into chiral peptide helicates that show great affinity and chiral selectivity for three-way DNA junctions and promising cell-internalization properties.