Structure of the transmembrane cysteine residues in phospholamban

I. T. Arkin, P. D. Adams, A. T. Brünger, S. Aimoto, D. M. Engelman, S. O. Smith*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

25 Scopus citations


Phospholamban, a 52-residue membrane protein, associates to form a pentameric complex of five long α-helices traversing the sarcoplasmic reticulum membrane of cardiac muscle cells. The transmembrane domain of the protein is largely hydrophobic, with only three cysteine residues having polar side chains, yet it functions as a Ca2+-selective ion channel. In this report, infrared spectroscopy is used to probe the conformation of the three cysteine side chains and to establish whether the free S-H groups form intrahelical hydrogen bonds in the pentameric complex. Vibrational spectra of a transmembrane peptide were obtained which corresponded to the transmembrane domain of wild-type phospholamban and three peptides each containing a cysteine → alanine substitution. The observed S-H frequencies argue that each of the sulfhydryl groups is hydrogen-bonded to an i-4 backbone carbonyl oxygen. Electrostatic calculations on a model of phospholamban based on molecular dynamics and mutagenesis studies, show that the sulfhydryl groups may significantly contribute to the electrostatic potential field of the protein.

Original languageAmerican English
Pages (from-to)199-206
Number of pages8
JournalJournal of Membrane Biology
Issue number3
StatePublished - 1997
Externally publishedYes


  • Hydrogen-bonding
  • Infrared spectroscopy
  • Membrane protein
  • Sulfhydryl


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