4.8 Review

Biomimetic engineering of the molecular recognition and self-assembly of peptides and proteins via halogenation

Journal

COORDINATION CHEMISTRY REVIEWS
Volume 411, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2020.213242

Keywords

Halogen bonding; Supramolecular; Self-assembly; Crystal engineering; Halogenation; Iodine; Bromine; Chlorine; Fluorine; Peptide; Protein

Funding

  1. European Research Council (ERC) [ERC-2012-StG_20111012 FOLDHALO (307108), ERC-2017-PoC MINIRES (789815)]
  2. Fondazione Cariplo [2014-0746]

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Halogenation is widespread in Nature, as witnessed by the several thousands of naturally occurring halogenated compounds. This review seeks to provide an overview on the pathways and multiple roles of halogenation in Nature, as a source of inspiration to chemists. Remarkably, several halogenation pathways were recently found in humans, sparking an increasing interest into halogens as biomolecular recognition sites. A description of the molecular mechanisms underlining the role of halogenation in the biomolecular context is provided, highlighting how the strategic use of halogen-driven interactions can be exploited to tune the properties of both small compounds and macromolecules. The complexity, versatility and bio-orthogonality of halogen-driven interactions are indeed key figures of merit in promoting novel opportunities for halogenation in a range of applications, spanning from drug design to self-assembly and biomolecular engineering. Specifically, the most relevant and impactful recent contributions in the field of peptide and protein science are presented and critically discussed, with a particular emphasis on the existing opportunities to control their conformational and self-assembly properties towards novel therapeutics and functional materials. (C) 2020 Elsevier B.V. All rights reserved.

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