G

Günter Vogel

University of Wuppertal

Publishes on Cellular transport and secretion, Protein Kinase Regulation and GTPase Signaling, Cellular Mechanics and Interactions. 34 papers and 879 citations.

34Publications
879Total Citations

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Structural Analysis and Detection of Biological Inositol Pyrophosphates Reveal That the Family of VIP/Diphosphoinositol Pentakisphosphate Kinases Are 1/3-Kinases
Hongying Lin, Peter C. Fridy, Anthony A. Ribeiro et al.|Journal of Biological Chemistry|2008
Cited by 135Open Access

We have characterized the positional specificity of the mammalian and yeast VIP/diphosphoinositol pentakisphosphate kinase (PPIP5K) family of inositol phosphate kinases. We deployed a microscale metal dye detection protocol coupled to a high performance liquid chromatography system that was calibrated with synthetic and biologically synthesized standards of inositol pyrophosphates. In addition, we have directly analyzed the structures of biological inositol pyrophosphates using two-dimensional 1H-1H and 1H-31P nuclear magnetic resonance spectroscopy. Using these tools, we have determined that the mammalian and yeast VIP/PPIP5K family phosphorylates the 1/3-position of the inositol ring in vitro and in vivo. For example, the VIP/PPIP5K enzymes convert inositol hexakisphosphate to 1/3-diphosphoinositol pentakisphosphate. The latter compound has in We have determined that the of the that synthesized and a the inositol hexakisphosphate kinase and VIP/PPIP5K the in the structures of inositol pyrophosphates. For example, in the the and to the of the that specificity in the and biological of inositol pyrophosphates. We have characterized the positional specificity of the mammalian and yeast VIP/diphosphoinositol pentakisphosphate kinase (PPIP5K) family of inositol phosphate kinases. We deployed a microscale metal dye detection protocol coupled to a high performance liquid chromatography system that was calibrated with synthetic and biologically synthesized standards of inositol pyrophosphates. In addition, we have directly analyzed the structures of biological inositol pyrophosphates using two-dimensional 1H-1H and 1H-31P nuclear magnetic resonance spectroscopy. Using these tools, we have determined that the mammalian and yeast VIP/PPIP5K family phosphorylates the 1/3-position of the inositol ring in vitro and in vivo. For example, the VIP/PPIP5K enzymes convert inositol hexakisphosphate to 1/3-diphosphoinositol pentakisphosphate. The latter compound has in We have determined that the of the that synthesized and a the inositol hexakisphosphate kinase and VIP/PPIP5K the in the structures of inositol pyrophosphates. 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and to and the and The of the the and in the The of the and the and that the has the and to these was the of that a was of detection of the VIP/PPIP5K family and the in that the latter convert to a of the in vitro of in have to the of in mammalian to the specificity of the VIP/PPIP5K family that we have characterized in to inositol pyrophosphates in of of mammalian we of in inositol with of and We a to of inositol pyrophosphates to we with the that the inositol pyrophosphates the of with the of of was to the of of that with of of has in vivo. 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with the the the to to the has the and of the the inositol ring of and two-dimensional and the the and the The latter to the to and The in a with the two-dimensional 1H-31P to the to the the to the and the and to the the to a with the that the the The a to the to The to the and these the The a to the to The to the a the and with to the and that the the and The a to the to The to the and these the The to the a 1H-31P of and that the two-dimensional in the two-dimensional and of the In the and and of the of and the and the to a with and the to a and with and of the the and a with of the the of a with of the of the and the to a with The of the and of a in the of the of the the and a with of and of the and and the of and with of the the to a with of the the a with and the with and The and of the the and the to a with in the The of the and of a in of the of the and the and and to of the the to a of the the to a of the the to a The and in in in in in in a in in in in in in a in in in in in in a The of the in the of the the and to and the and The of the the and in the The of the and the and that the has the and to these was the of that a was of detection of the VIP/PPIP5K family and the in that the latter convert to a of the in vitro of in have to the of in mammalian to the specificity of the VIP/PPIP5K family that we have characterized in to inositol pyrophosphates in of of mammalian we of in inositol with of and We a to of inositol pyrophosphates to we with the that the inositol pyrophosphates the of with the of of was to the of of that with of of has in vivo. 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In the a to with with the in of the that we have to in vitro the VIP/PPIP5K of inositol phosphate kinases. and of to the of that synthesized of the that the inositol In the we a of the of the VIP/PPIP5K We that the yeast and mammalian VIP/PPIP5K to the of and in vivo. a of we that yeast and the of in of and the of in of The of in and that in mammalian and In the of the of in that of the mammalian inositol and inositol in has the in the that and that of a system of of inositol pyrophosphates to mammalian the in a of the in yeast and mammalian with a that directly in vitro the of the of and to of For example, of the the positional specificity of the and in The of the structures of inositol pyrophosphates in the the the VIP/PPIP5K The that the VIP/PPIP5K enzymes and the that to the of specificity the of the of a kinase that phosphate a to the of the of of inositol pyrophosphates and the of of the and of of to a of that the inositol pyrophosphates to We and the of and with with

Diphospho-myo-inositol phosphates from Dictyostelium identified as d-6-diphospho-myo-inositol pentakisphosphate and d-5,6-bisdiphospho-myo-inositol tetrakisphosphate
Tim Laußmann, Komandla Malla Reddy, K. Kishta Reddy et al.|Biochemical Journal|1997
Cited by 59Open Access

Two diphospho-myo-inositol phosphates from Dictyostelium were recently investigated by two-dimensional 1H/31P NMR analysis and assigned to be either D-4-diphospho-myo-inositol pentakisphosphate (D-4-PP-InsP5) and D-4,5-bisdiphospho-myo-inositol tetrakisphosphate (D-4,5-bis-PP-InsP4) or their corresponding enantiomers D-6-PP-InsP5 and D-5,6-bis-PP-InsP4. In the present study the naturally occurring enantiomers were identified by using defined synthetic PP-InsP5 isomers as substrates for a partially purified PP-InsP5 5-kinase from Dictyostelium. This enzyme specifically phosphorylates the naturally occurring PP-InsP5 and the synthetic D-6-PP-InsP5, leading to D-5,6-bis-PP-InsP4. In contrast, neither D-4-PP-InsP5 nor D-1-PP-InsP5 or D-3-PP-InsP5 are converted by the enzyme.

Structures of diphospho-<i>myo</i>-inositol pentakisphosphate and bisdiphospho-<i>myo</i>-inositol tetrakisphosphate from <i>Dictyostelium</i> resolved by NMR analysis
Tim Laußmann, R. Eujen, C. M. WEISSHUHN et al.|Biochemical Journal|1996
Cited by 57Open Access

Diphospho-myo-inositol phosphates (PP-InsP5 and bis-PP-InsP4) were isolated from Dictyostelium in order to clarify the precise positional isomerism by two-dimensional 1H/31P-NMR analysis. The diphosphorylated inositol phosphates are 4-PP-Ins(1,2,3,5,6)P5 and 4,5-bis-PP-Ins(1,2,3,6)P4 or their corresponding enantiomers. The vicinal arrangement of the diphospho groups with its steric and electrostatic constraints possibly qualifies bis-PP-InsP4 as a metabolite with high phosphate-group-transfer potential in phosphotransferase reactions.