Author: Zhang, Z.; Smith, D. L.
Description: A new method based on protein fragmentation and directly coupled microbore high-performance liquid chromatography-fast atom bombardment mass spectrometry (HPLC-FABMS) is described for determining the rates at which peptide amide hydrogens in proteins undergo isotopic exchange. Horse heart cytochrome c was incubated in D2O as a function of time and temperature to effect isotopic exchange, transferred into slow exchange conditions (pH 2-3, 0 degrees C), and fragmented with pepsin. The number of peptide amide deuterons present in the proteolytic peptides was deduced from their molecular weights, which were determined following analysis of the digest by HPLC-FABMS. The present results demonstrate that the exchange rates of amide hydrogens in cytochrome c range from very rapid (k > 140 h-1) to very slow (k < 0.002 h-1). The deuterium content of specific segments of the protein was determined as a function of incubation temperature and used to indicate participation of these segments in conformational changes associated with heating of cytochrome c. For the present HPLC-FABMS system, approximately 5 nmol of protein were used for each determination. Results of this investigation indicate that the combination of protein fragmentation and HPLC-FABMS is relatively free of constraints associated with other analytical methods used for this purpose and may be a general method for determining hydrogen exchange rates in specific segments of proteins.
Subject headings: Amides; Chromatography; High Pressure Liquid; Cytochrome c Group; Deuterium; Gas Chromatography-Mass Spectrometry; Hot Temperature; Hydrogen; Molecular Structure; Protein Conformation; Protein Denaturation; Proteins; Spectrometry, Mass; Fast Atom Bombardment; Tritium
Publication year: 1993
Journal or book title: Protein Science: A Publication of the Protein Society
Volume: 2
Issue: 4
Pages: 522-531
Find the full text: https://masspec.scripps.edu/learn/ms/pdf/1993_Zhang.pdf
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Serial number: 3433