TY - JOUR
T1 - Electrical currents generated by a partially purified Na/Ca exchanger from lobster muscle reconstituted into liposomes and adsorbed on black lipid membranes
T2 - Activation by photolysis of caged Ca2+
AU - Eisenrauch, A.
AU - Juhaszova, M.
AU - Ellis-Davies, G. C.R.
AU - Kaplan, J. H.
AU - Bamberg, E.
AU - Blaustein, M. P.
PY - 1995/5
Y1 - 1995/5
N2 - The Na/Ca exchanger from lobster muscle crossreacts specifically with antibodies raised against the dog heart Na/Ca exchanger. Immunoblots of the lobster muscle and mammalian heart exchangers, following SDS-PAGE, indicate that the invertebrate and mammalian exchangers have similar molecular weights: about 120 kDa. The exchanger from lobster muscle was partially purified and functionally reconstituted into asolectin vesicles which were loaded with 160 m m NaCl. 45Ca uptake by these proteoliposomes was promoted by replacing 160 m m NaCl in the external medium with 160 m m KCl to produce an outwardly-directed Na+ concentration gradient. When the proteoliposomes were adsorbed onto black lipid membranes (BLM), and DMNitrophen-Ca2+ ("caged Ca2+") was added to the KCl medium, photolytically-evoked Ca2+ concentration jumps elicited transient electric currents. These currents corresponded to positive charge exiting from the proteoliposomes, and were consistent with the Na/Ca exchanger-mediated exit of 3 Na+ in exchange for 1 entering Ca2+. The current was dependent upon the Ca2+ concentration jump, the protein integrity, and the outwardly directed Na+ gradient. KCl-loaded proteoliposomes did not produce any current. Low external Na+ concentrations augmented the current, whereas Na+ concentrations >25 mM reduced the current. The dependence of the current on free Ca2+ was Michaelis-Menten-like, with halfmaximal activation (KM(Ca)) at <10 μm Ca2+. Caged Sr2+ and Ba2+, but not Mg2+, also supported photolysisevoked outward current, as did Ni2+, but not Mn2+. However, Mg2+ and Mn2+ augmented the Cadependent current, perhaps by facilitating the adsorption of proteoliposomes to the BLM. The Ca-dependent current was irreversibly blocked by La3+ (added as 200 μm DMN-La3+). The results indicate that the properties of the Na/Ca exchanger can be studied with these electrophysiological methods.
AB - The Na/Ca exchanger from lobster muscle crossreacts specifically with antibodies raised against the dog heart Na/Ca exchanger. Immunoblots of the lobster muscle and mammalian heart exchangers, following SDS-PAGE, indicate that the invertebrate and mammalian exchangers have similar molecular weights: about 120 kDa. The exchanger from lobster muscle was partially purified and functionally reconstituted into asolectin vesicles which were loaded with 160 m m NaCl. 45Ca uptake by these proteoliposomes was promoted by replacing 160 m m NaCl in the external medium with 160 m m KCl to produce an outwardly-directed Na+ concentration gradient. When the proteoliposomes were adsorbed onto black lipid membranes (BLM), and DMNitrophen-Ca2+ ("caged Ca2+") was added to the KCl medium, photolytically-evoked Ca2+ concentration jumps elicited transient electric currents. These currents corresponded to positive charge exiting from the proteoliposomes, and were consistent with the Na/Ca exchanger-mediated exit of 3 Na+ in exchange for 1 entering Ca2+. The current was dependent upon the Ca2+ concentration jump, the protein integrity, and the outwardly directed Na+ gradient. KCl-loaded proteoliposomes did not produce any current. Low external Na+ concentrations augmented the current, whereas Na+ concentrations >25 mM reduced the current. The dependence of the current on free Ca2+ was Michaelis-Menten-like, with halfmaximal activation (KM(Ca)) at <10 μm Ca2+. Caged Sr2+ and Ba2+, but not Mg2+, also supported photolysisevoked outward current, as did Ni2+, but not Mn2+. However, Mg2+ and Mn2+ augmented the Cadependent current, perhaps by facilitating the adsorption of proteoliposomes to the BLM. The Ca-dependent current was irreversibly blocked by La3+ (added as 200 μm DMN-La3+). The results indicate that the properties of the Na/Ca exchanger can be studied with these electrophysiological methods.
KW - Caged Ca
KW - Capacitive coupling
KW - Lobster muscle
KW - Na/Ca exchanger
KW - Planar lipid bilayers
KW - Proteoliposomes
UR - https://www.scopus.com/pages/publications/0029062482
U2 - 10.1007/BF00237373
DO - 10.1007/BF00237373
M3 - Article
C2 - 7563017
AN - SCOPUS:0029062482
SN - 0022-2631
VL - 145
SP - 151
EP - 164
JO - Journal of Membrane Biology
JF - Journal of Membrane Biology
IS - 2
ER -