The Crystal Structure of a Sodium Galactose Transporter Reveals Mechanistic Insights into Na <sup>+</sup> /Sugar SymportMembrane transporters that use energy stored in sodium gradients to drive nutrients into cells constitute a major class of proteins. We report the crystal structure of a member of the solute sodium symporters (SSS), the Vibrio parahaemolyticus sodium/galactose symporter (vSGLT). The approximately 3.0 angstrom structure contains 14 transmembrane (TM) helices in an inward-facing conformation with a core structure of inverted repeats of 5 TM helices (TM2 to TM6 and TM7 to TM11). Galactose is bound in the center of the core, occluded from the outside solutions by hydrophobic residues. Surprisingly, the architecture of the core is similar to that of the leucine transporter (LeuT) from a different gene family. Modeling the outward-facing conformation based on the LeuT structure, in conjunction with biophysical data, provides insight into structural rearrangements for active transport.
Changes in fluorescence, turbidity, and birefringence associated with nerve excitation.Ichiji Tasaki, Akira Watanabe, Rebecca D. Sandlin et al.|Proceedings of the National Academy of Sciences|1968 Proceedings of the National Academy of Sciences (PNAS), a peer reviewed journal of the National Academy of Sciences (NAS) - an authoritative source of high-impact, original research that broadly spans the biological, physical, and social sciences.
The mechanism of sodium and substrate release from the binding pocket of vSGLTImpulse Propagation at the Septal and Commissural Junctions of Crayfish Lateral Giant AxonsAkira Watanabe, Harry Grundfest|The Journal of General Physiology|1961 Transmission across the septal junctions of the segmented giant axons of crayfish is accounted for quantitatively by a simple equivalent circuit. The septal membranes are passive, resistive components and transmission is ephaptic, by the electrotonic spread of the action current of the pre-septal spike. The electrotonic spread appears as a septal potential, considerably smaller than the pre-septal spike, but usually still large enough to initiate a new spike in the post-septal segments. The septal membranes do not exhibit rectification, at least over a range of +/- 25 mv polarization and this accounts for their capacity for bidirectional transmission. The commissural branches, which are put forth by each lateral axon, make functional connections between the two axons. Transmission across these junctions can also be bidirectional and is probably also ephaptic. Under various conditions, the ladder-like network of cross-connections formed by the commissural junctions can give rise to circus propagation of impulses from one axon to the other. This can give rise to reverberatory activity of both axons at frequencies as high as 400/sec.
The Change of Discharge Frequency by A.C. Stimulus in A Weak Electric FishAkira Watanabe, Kimihisa Takeda|Journal of Experimental Biology|1963 ABSTRACT A South American gymnotid Eigenmannia, changes the discharge frequency of its electric organ when a weak electric signal is applied to it with a frequency very close to that of its own discharge. Otherwise, the discharge frequency is extremely constant at a fixed temperature. When the frequency of the applied signal is higher or lower than that of the fish discharge, the response is a decrease or increase of the discharge frequency, respectively. When the two frequencies are exactly the same, the response fails to occur. The threshold of this response is very low. In one fish it was about 3 μV./cm.