4.7 Article

Noncovalent Protein-Pseudorotaxane Assembly Incorporating an Extended Arm Calix[8]arene with α-Helical Recognition Properties

期刊

CRYSTAL GROWTH & DESIGN
卷 21, 期 3, 页码 1424-1427

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.cgd.0c01717

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资金

  1. NUI Galway (College of Science and Engineering postgraduate scholarship)
  2. Royal Society of Chemistry
  3. NUI
  4. Irish Research Council [GOIPD/2019/513]
  5. Australian Research Council [DP1092810]
  6. Science Foundation Ireland [13/CDA/2168, 12/RC/2275_P2]
  7. Australian Research Council [DP1092810] Funding Source: Australian Research Council

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A new extended arm calixarene with increased protein masking capacity was discovered, forming a hydrogen-bonded stacking structure. The four hydrophobic grooves of this receptor bind to proteins through a new recognition mode, suggesting new possibilities in supramolecular protein chemistry.
Water-soluble, anionic calix[n]arenes are useful receptors for protein recognition and assembly. For example, sulfonato-calix[8]arene (sclx(8)) can encapsulate proteins and direct their assembly into porous frameworks. In this work, we turned our attention to an extended arm calixarene with 16 phenyl rings. We hypothesized that this larger receptor would have increased capacity for protein masking/encapsulation. A cocrystal structure of p-benzyl-sulfonato-calix[S]arene (b-sclx(8)) and cytochrome c (cyt c) revealed a surprising assembly. A pseudorotaxane comprising a stack of three b-sclx(8) molecules threaded by polyethylene glycol (PEG) was bound to the protein. The trimeric b-sclx(8) stack, a tubelike structure with a highly charged surface, mediated assembly via a new mode of protein recognition. The calixarene stack presents four hydrophobic grooves, each of which binds to one cyt c by accommodating the N-terminal alpha-helix. This unprecedented binding mode suggests new possibilities for supramolecular protein chemistry.

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