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Semisynthetic Nanoreactor for Reversible Single-Molecule Covalent Chemistry
Author(s) -
Joongoo Lee,
Arnold J. Boersma,
Marc A. Boudreau,
Stephen Cheley,
Oliver Daltrop,
Jianwei Li,
Hiroko Tamagaki,
Hagan Bayley
Publication year - 2016
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/acsnano.6b04663
Subject(s) - nanoreactor , covalent bond , chemistry , molecule , side chain , monomer , dynamic covalent chemistry , combinatorial chemistry , cysteine , amino acid , organic chemistry , polymer , biochemistry , supramolecular chemistry , catalysis , enzyme
Protein engineering has been used to remodel pores for applications in biotechnology. For example, the heptameric α-hemolysin pore (αHL) has been engineered to form a nanoreactor to study covalent chemistry at the single-molecule level. Previous work has been confined largely to the chemistry of cysteine side chains or, in one instance, to an irreversible reaction of an unnatural amino acid side chain bearing a terminal alkyne. Here, we present four different αHL pores obtained by coupling either two or three fragments by native chemical ligation (NCL). The synthetic αHL monomers were folded and incorporated into heptameric pores. The functionality of the pores was validated by hemolysis assays and by single-channel current recording. By using NCL to introduce a ketone amino acid, the nanoreactor approach was extended to an investigation of reversible covalent chemistry on an unnatural side chain at the single-molecule level.

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