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Structure and substrate-induced conformational changes of the secondary citrate/sodium symporter CitS revealed by electron crystallography.

Type of publication Peer-reviewed
Publikationsform Original article (peer-reviewed)
Publication date 2013
Author Kebbel Fabian, Kurz Mareike, Arheit Marcel, Grütter Markus G, Stahlberg Henning,
Project Software for Electron Microscopy of Membrane Proteins
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Original article (peer-reviewed)

Journal Structure (London, England : 1993)
Volume (Issue) 21(7)
Page(s) 1243 - 50
Title of proceedings Structure (London, England : 1993)
DOI 10.1016/j.str.2013.05.011


The secondary Na+/citrate symporter CitS of Klebsiella pneumoniae is the best-characterized member of the 2-hydroxycarboxylate transporter family. The recent projection structure gave insight into its overall structural organization. Here, we present the three-dimensional map of dimeric CitS obtained with electron crystallography. Each monomer has 13 a-helical transmembrane segments; six are organized in a distal helix cluster and seven in the central dimer interface domain. Based on structural analyses and comparison to VcINDY, we propose a molecular model for CitS, assign the helices, and demonstrate the internal structural symmetry. We also present projections of CitS in several conformational states induced by the presence and absence of sodium and citrate as substrates. Citrate binding induces a defined movement of a helices within the distal helical cluster. Based on this, we propose a substrate translocation site and conformational changes that are in agreement with the transport model of ‘‘alternating access’’.