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Efficient Total Chemical Synthesis of 13 C= 18 O Isotopomers of Human Insulin for Isotope‐Edited FTIR
Author(s) -
Dhayalan Balamurugan,
Fitzpatrick Ann,
Mandal Kalyaneswar,
Whittaker Jonathan,
Weiss Michael A.,
Tokmakoff Andrei,
Kent Stephen B. H.
Publication year - 2016
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.201500601
Subject(s) - isotopomers , isotope , radiochemistry , chemistry , fourier transform infrared spectroscopy , kinetic isotope effect , nuclear chemistry , deuterium , organic chemistry , physics , nuclear physics , molecule , quantum mechanics
Isotope‐edited two‐dimensional Fourier transform infrared spectroscopy (2 D FTIR) can potentially provide a unique probe of protein structure and dynamics. However, general methods for the site‐specific incorporation of stable 13 C= 18 O labels into the polypeptide backbone of the protein molecule have not yet been established. Here we describe, as a prototype for the incorporation of specific arrays of isotope labels, the total chemical synthesis—via a key ester insulin intermediate—of 97 % enriched [(1‐ 13 C= 18 O)Phe B24 ] human insulin: stable‐isotope labeled at a single backbone amide carbonyl. The amino acid sequence as well as the positions of the disulfide bonds and the correctly folded structure were unambiguously confirmed by the X‐ray crystal structure of the synthetic protein molecule. In vitro assays of the isotope labeled [(1‐ 13 C= 18 O)Phe B24 ] human insulin showed that it had full insulin receptor binding activity. Linear and 2 D IR spectra revealed a distinct red‐shifted amide I carbonyl band peak at 1595 cm −1 resulting from the (1‐ 13 C= 18 O)Phe B24 backbone label. This work illustrates the utility of chemical synthesis to enable the application of advanced physical methods for the elucidation of the molecular basis of protein function.