Electron paramagnetic resonance and magnetic susceptibility studies of dimanganese concanavalin A. Evidence for antiferromagnetic exchange coupling

The double Mn2+ complex of concanavalin A with bound saccharide (SMMPL) was examined by electron paramagnetic resonance (EPR) spectroscopy and magnetic susceptibility measurements. A room temperature X-band (9 GHz) EPR spectrum of SMMPL revealed a relatively weak, broad resonance in contrast to the...

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Veröffentlicht in:Biochemistry (Easton) 1987-12, Vol.26 (24), p.7932-7937
Hauptverfasser: Antanaitis, Bradley C, Brown, Rodney D, Chasteen, N. Dennis, Freedman, Jonathan H, Koenig, Seymour H, Lilienthal, Henry R, Peisach, Jack, Brewer, C. Fred
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container_end_page 7937
container_issue 24
container_start_page 7932
container_title Biochemistry (Easton)
container_volume 26
creator Antanaitis, Bradley C
Brown, Rodney D
Chasteen, N. Dennis
Freedman, Jonathan H
Koenig, Seymour H
Lilienthal, Henry R
Peisach, Jack
Brewer, C. Fred
description The double Mn2+ complex of concanavalin A with bound saccharide (SMMPL) was examined by electron paramagnetic resonance (EPR) spectroscopy and magnetic susceptibility measurements. A room temperature X-band (9 GHz) EPR spectrum of SMMPL revealed a relatively weak, broad resonance in contrast to the spectrum with a six-line hyperfine-split pattern observed for the mononuclear, high-spin Mn2+ complex found in Ca2+-Mn2+-concanavalin A with saccharide present (SCMPL). The EPR spectrum of SMMPL at 77 K, however, consisted of a series of overlapping patterns of 11 hyperfine-split lines near g = 2.0 with members of each pattern separated by 47 G, half the value of the hyperfine splitting of SCMPL. These 11-line patterns are preserved at Q-band (35 GHz), indicating that the manganese ions in SMMPL form a spin-coupled, binuclear center. As expected for an exchange-coupled system, the EPR signal of SMMPL at 77 K saturates at a higher microwave power than those for SCMPL or Mn2+ aquoion. There is also a marked loss of EPR signal intensity for SMMPL between 4.2 and 1.4 K, which supports the view that the pair of manganese ions is exchanged-coupled. The temperature dependence of both the magnetic susceptibility and the low-temperature EPR spectral intensity can be explained by a model in which the two high-spin Mn2+ ions of SMMPL are antierromagnetically exchanged-coupled with an isotropic coupling constant J = 1.8 cm-1 (for the spin Hamiltonian Hex = JS1.S2). Zero-field splitting D' was estimated to be 375 G from the EPR spectrum.
doi_str_mv 10.1021/bi00398a058
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The EPR spectrum of SMMPL at 77 K, however, consisted of a series of overlapping patterns of 11 hyperfine-split lines near g = 2.0 with members of each pattern separated by 47 G, half the value of the hyperfine splitting of SCMPL. These 11-line patterns are preserved at Q-band (35 GHz), indicating that the manganese ions in SMMPL form a spin-coupled, binuclear center. As expected for an exchange-coupled system, the EPR signal of SMMPL at 77 K saturates at a higher microwave power than those for SCMPL or Mn2+ aquoion. There is also a marked loss of EPR signal intensity for SMMPL between 4.2 and 1.4 K, which supports the view that the pair of manganese ions is exchanged-coupled. The temperature dependence of both the magnetic susceptibility and the low-temperature EPR spectral intensity can be explained by a model in which the two high-spin Mn2+ ions of SMMPL are antierromagnetically exchanged-coupled with an isotropic coupling constant J = 1.8 cm-1 (for the spin Hamiltonian Hex = JS1.S2). Zero-field splitting D' was estimated to be 375 G from the EPR spectrum.</description><identifier>ISSN: 0006-2960</identifier><identifier>EISSN: 1520-4995</identifier><identifier>DOI: 10.1021/bi00398a058</identifier><identifier>PMID: 2827763</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Biological and medical sciences ; Canavalia ensiformis ; Concanavalin A ; Electron Spin Resonance Spectroscopy ; Fundamental and applied biological sciences. 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The EPR spectrum of SMMPL at 77 K, however, consisted of a series of overlapping patterns of 11 hyperfine-split lines near g = 2.0 with members of each pattern separated by 47 G, half the value of the hyperfine splitting of SCMPL. These 11-line patterns are preserved at Q-band (35 GHz), indicating that the manganese ions in SMMPL form a spin-coupled, binuclear center. As expected for an exchange-coupled system, the EPR signal of SMMPL at 77 K saturates at a higher microwave power than those for SCMPL or Mn2+ aquoion. There is also a marked loss of EPR signal intensity for SMMPL between 4.2 and 1.4 K, which supports the view that the pair of manganese ions is exchanged-coupled. The temperature dependence of both the magnetic susceptibility and the low-temperature EPR spectral intensity can be explained by a model in which the two high-spin Mn2+ ions of SMMPL are antierromagnetically exchanged-coupled with an isotropic coupling constant J = 1.8 cm-1 (for the spin Hamiltonian Hex = JS1.S2). Zero-field splitting D' was estimated to be 375 G from the EPR spectrum.</description><subject>Biological and medical sciences</subject><subject>Canavalia ensiformis</subject><subject>Concanavalin A</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Kinetics</subject><subject>lectins</subject><subject>Magnetics</subject><subject>Manganese</subject><subject>manganese II</subject><subject>Metalloproteins</subject><subject>Molecular biophysics</subject><subject>Protein Binding</subject><subject>Protein Conformation</subject><subject>Spectroscopy : techniques and spectras</subject><subject>Thermodynamics</subject><issn>0006-2960</issn><issn>1520-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuLFDEUhYMoYzu6ci1kIbqQGvOqSmo5DO2LFgdscRlSqZs2Y3VSJlXDzO_wD5umm8KF4Cok57vn5t6D0HNKLihh9G3nCeGtMqRWD9CK1oxUom3rh2hFCGkq1jbkMXqS8025CiLFGTpjiknZ8BX6vR7ATikGPJpk9mYXYPIWJ8gxmGABm9Dj5TnP2cI4-c4PfrrHeZp7DxlHh3u_N2FnAmTANgZrgrk1gw_48gKvb30PBy8XU_GbvIOU4mIKd_ZHqT3UzWMp2T1Fj5wZMjw7nefo27v19upDtfny_uPV5aYyQpGparreKsd4J1smrCU1YbJT0naO2LaRvRI1lcZaqJmQlANl0vWqU1wCFbJ1_By9OvqOKf6aIU9678t8w1DGiHPWUraEcUH-C1LRNjVnsoBvjqBNMecETo-pLCbda0r0ISv9V1aFfnGynbs99At7CqfoL0-6ydYMLpVAfF4wKUVD1aFpdcR8nuBukU36qRvJZa2311_1p83n79dbvtVN4V8feWOzvolzCmXJ__zgH8htupA</recordid><startdate>19871201</startdate><enddate>19871201</enddate><creator>Antanaitis, Bradley C</creator><creator>Brown, Rodney D</creator><creator>Chasteen, N. 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Psychology</topic><topic>Kinetics</topic><topic>lectins</topic><topic>Magnetics</topic><topic>Manganese</topic><topic>manganese II</topic><topic>Metalloproteins</topic><topic>Molecular biophysics</topic><topic>Protein Binding</topic><topic>Protein Conformation</topic><topic>Spectroscopy : techniques and spectras</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Antanaitis, Bradley C</creatorcontrib><creatorcontrib>Brown, Rodney D</creatorcontrib><creatorcontrib>Chasteen, N. Dennis</creatorcontrib><creatorcontrib>Freedman, Jonathan H</creatorcontrib><creatorcontrib>Koenig, Seymour H</creatorcontrib><creatorcontrib>Lilienthal, Henry R</creatorcontrib><creatorcontrib>Peisach, Jack</creatorcontrib><creatorcontrib>Brewer, C. 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Fred</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electron paramagnetic resonance and magnetic susceptibility studies of dimanganese concanavalin A. Evidence for antiferromagnetic exchange coupling</atitle><jtitle>Biochemistry (Easton)</jtitle><addtitle>Biochemistry</addtitle><date>1987-12-01</date><risdate>1987</risdate><volume>26</volume><issue>24</issue><spage>7932</spage><epage>7937</epage><pages>7932-7937</pages><issn>0006-2960</issn><eissn>1520-4995</eissn><abstract>The double Mn2+ complex of concanavalin A with bound saccharide (SMMPL) was examined by electron paramagnetic resonance (EPR) spectroscopy and magnetic susceptibility measurements. A room temperature X-band (9 GHz) EPR spectrum of SMMPL revealed a relatively weak, broad resonance in contrast to the spectrum with a six-line hyperfine-split pattern observed for the mononuclear, high-spin Mn2+ complex found in Ca2+-Mn2+-concanavalin A with saccharide present (SCMPL). The EPR spectrum of SMMPL at 77 K, however, consisted of a series of overlapping patterns of 11 hyperfine-split lines near g = 2.0 with members of each pattern separated by 47 G, half the value of the hyperfine splitting of SCMPL. These 11-line patterns are preserved at Q-band (35 GHz), indicating that the manganese ions in SMMPL form a spin-coupled, binuclear center. As expected for an exchange-coupled system, the EPR signal of SMMPL at 77 K saturates at a higher microwave power than those for SCMPL or Mn2+ aquoion. There is also a marked loss of EPR signal intensity for SMMPL between 4.2 and 1.4 K, which supports the view that the pair of manganese ions is exchanged-coupled. The temperature dependence of both the magnetic susceptibility and the low-temperature EPR spectral intensity can be explained by a model in which the two high-spin Mn2+ ions of SMMPL are antierromagnetically exchanged-coupled with an isotropic coupling constant J = 1.8 cm-1 (for the spin Hamiltonian Hex = JS1.S2). Zero-field splitting D' was estimated to be 375 G from the EPR spectrum.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>2827763</pmid><doi>10.1021/bi00398a058</doi><tpages>6</tpages></addata></record>
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subjects Biological and medical sciences
Canavalia ensiformis
Concanavalin A
Electron Spin Resonance Spectroscopy
Fundamental and applied biological sciences. Psychology
Kinetics
lectins
Magnetics
Manganese
manganese II
Metalloproteins
Molecular biophysics
Protein Binding
Protein Conformation
Spectroscopy : techniques and spectras
Thermodynamics
title Electron paramagnetic resonance and magnetic susceptibility studies of dimanganese concanavalin A. Evidence for antiferromagnetic exchange coupling
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