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  1. Article: Macroporous Poly(N-isopropylacrylamide) hydrogels with adjustable size "cut-off" for the efficient and reversible immobilization of biomacromolecules.

    Fänger, Christian / Wack, Holger / Ulbricht, Mathias

    Macromolecular bioscience

    2006  Volume 6, Issue 6, Page(s) 393–402

    Abstract: Poly(N-isopropylacrylamide) (PNIPA) hydrogels with varied degree of crosslinking (DC) were ...

    Abstract Poly(N-isopropylacrylamide) (PNIPA) hydrogels with varied degree of crosslinking (DC) were synthesized by using poly(ethylene glycol) (PEG) as an additive. A phase separated ("macroporous") morphology was formed when using PEG contents of > or = 20 wt.-%. Temperature-dependent degrees of swelling had been measured, and average mesh sizes of the swollen polymer network had been calculated. The loading of the hydrogels with labelled dextrans with various molar masses and bovine serum albumin (BSA)-via swelling of the shrunken gel in a cold solution-and their subsequent unloading-via immersion in hot water-were studied in detail. The loading efficiencies were close to zero for PNIPA prepared at PEG contents of < or = 10 wt.-%, and they increased sharply to about 100% for PNIPA prepared with PEG contents of > or = 20 wt.-%. A complete unloading was achieved as well. For macroporous PNIPA prepared at 40 wt.-% PEG content, the loading efficiency was a function of the DC, and the "cut-off" observed as a function of dextran or protein size correlated with the mesh size of the hydrogel. The function of these "smart" hydrogels can be explained by the temperature-induced "pumping" of the solution into the gel bulk via the permanent pores, along with an uptake into the adjacent hydrogel network. Those materials could be used as matrices for the efficient and reversible immobilization of (bio)macromolecules.
    MeSH term(s) Acrylic Resins/chemical synthesis ; Acrylic Resins/chemistry ; Cross-Linking Reagents/chemistry ; Dextrans/chemistry ; Hydrogels ; Polyethylene Glycols/chemical synthesis ; Polyethylene Glycols/chemistry ; Porosity ; Temperature
    Chemical Substances Acrylic Resins ; Cross-Linking Reagents ; Dextrans ; Hydrogels ; poly-N-isopropylacrylamide (25189-55-3) ; Polyethylene Glycols (30IQX730WE)
    Language English
    Publishing date 2006-06-16
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2039130-4
    ISSN 1616-5195 ; 1616-5187
    ISSN (online) 1616-5195
    ISSN 1616-5187
    DOI 10.1002/mabi.200600027
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Thesis ; Online: Schaltbare polymere Hydrogele für die reversible Immobilisierung von Enzymen

    Fänger, C.

    2005  

    Abstract: n der vorliegenden Arbeit sollten Hydrogele untersucht werden, die als Immobilisierungsmatrix ...

    Abstract n der vorliegenden Arbeit sollten Hydrogele untersucht werden, die als Immobilisierungsmatrix für Enzyme dienen können. Mit diesen Hydrogelen sollte es möglich sein, die Enzyme reversibel zu immobilisieren. Dazu wurden Hydrogele auf PNIPA-Basis verwendet, da sie einen thermoreversiblen Phasenübergang aufweisen. Zunächst wurden Messungen zur Synthese selber durchgeführt, auch im Hinblick auf eine weitestgehende Vereinfachung der Synthesevorschrift für eine eventuelle Umsetzung im technischen Maßstab. Bei den Vorsynthesen ergab sich, dass mindestens ein Starterverhältnis von 1:100 nötig ist, um eine größtmögliche Ausbeute an Gel zu erhalten. Eine Begasung der Reaktionslösung mit Stickstoff erzielte keinen wesentlichen Effekt, allerdings muss bei dem APS/Na2S2O5 - Startersystem ein neutraler Phosphat-Puffer als Lösungsmittel verwendet werden, um eine ausreichende Anzahl an Radikalen für die Polymerisation zu erzeugen. In Wasser funktioniert dieses Startersystem nicht. Deswegen wurde dort das APS/TEMED-Startersystem verwendet, da die Reaktion hierbei in einem rein wässrigen Medium ablaufen konnte. Für eine großtechnische Herstellung des Gels würde aber wohl das APS/Na2S2O5 - Startersystem mit Puffer verwendet werden, da dies kostengünstiger ist. Eine Vorreinigung des NIPA vor der Polymerisation ist nicht nötig, da dies auch keinen wesentlichen Einfluss auf den späteren Quellgrad besitzt.
    Keywords hydrogel ; immobilisation ; enzyme ; synthesis ; polymerisation ; 620
    Subject code 660
    Language German
    Publishing country de
    Document type Thesis ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: PTC-174, a positive allosteric modulator of NMDA receptors containing GluN2C or GluN2D subunits.

    Yi, Feng / Rouzbeh, Nirvan / Hansen, Kasper B / Xu, Yuelian / Fanger, Christopher M / Gordon, Earl / Paschetto, Kathy / Menniti, Frank S / Volkmann, Robert A

    Neuropharmacology

    2020  Volume 173, Page(s) 107971

    Abstract: NMDA receptors are ionotropic glutamate receptors that mediate excitatory neurotransmission. The diverse functions of these receptors are tuned by deploying different combinations of GluN1 and GluN2 subunits (GluN2A-D) to form either diheteromeric NMDA ... ...

    Abstract NMDA receptors are ionotropic glutamate receptors that mediate excitatory neurotransmission. The diverse functions of these receptors are tuned by deploying different combinations of GluN1 and GluN2 subunits (GluN2A-D) to form either diheteromeric NMDA receptors, which contain two GluN1 and two identical GluN2 subunits, or triheteromeric NMDA receptors, which contain two GluN1 and two distinct GluN2 subunits. Here, we characterize PTC-174, a novel positive allosteric modulator (PAM) of receptors containing GluN2C or GluN2D subunits. PTC-174 potentiates maximal current amplitudes by 1.8-fold for diheteromeric GluN1/2B receptors and by > 10-fold for GluN1/2C and GluN1/2D receptors. PTC-174 also potentiates responses from triheteromeric GluN1/2B/2D and GluN1/2A/2C receptors by 4.5-fold and 1.7-fold, respectively. By contrast, PTC-174 produces partial inhibition of responses from diheteromeric GluN1/2A and triheteromeric GluN1/2A/2B receptors. PTC-174 increases potencies of co-agonists glutamate and glycine by 2- to 5-fold at GluN1/2C and GluN1/2D receptors, and NMDA receptor activation facilitates allosteric modulation by PTC-174. At native NMDA receptors in GluN2D-expressing subthalamic nucleus neurons, PTC-174 increases the amplitude of responses to NMDA application and slows the decay of excitatory postsynaptic currents (EPSCs) evoked by internal capsule stimulation. Furthermore, PTC-174 increases the amplitude and slows the decay of EPSCs in hippocampal interneurons, but has not effect on the amplitudes of NMDA receptor-mediated EPSCs in hippocampal CA1 pyramidal neurons. Thus, PTC-174 provides a useful new pharmacological tool to investigate the molecular pharmacology and physiology of GluN2C- and GluN2D-containing NMDA receptors.
    MeSH term(s) Allosteric Regulation/drug effects ; Allosteric Regulation/physiology ; Animals ; Excitatory Amino Acid Agonists/pharmacology ; Female ; Glycine/pharmacology ; Hippocampus/drug effects ; Hippocampus/physiology ; Interneurons/drug effects ; Interneurons/physiology ; Male ; Mice ; Mice, Inbred C57BL ; Pyramidal Cells/drug effects ; Pyramidal Cells/physiology ; Receptors, N-Methyl-D-Aspartate/metabolism ; Subthalamic Nucleus/drug effects ; Subthalamic Nucleus/physiology ; Xenopus
    Chemical Substances Excitatory Amino Acid Agonists ; NR2C NMDA receptor ; NR2D NMDA receptor ; Receptors, N-Methyl-D-Aspartate ; Glycine (TE7660XO1C)
    Language English
    Publishing date 2020-01-25
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 218272-5
    ISSN 1873-7064 ; 0028-3908
    ISSN (online) 1873-7064
    ISSN 0028-3908
    DOI 10.1016/j.neuropharm.2020.107971
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Enterococcus

    Griffin, Matthew E / Espinosa, Juliel / Becker, Jessica L / Luo, Ji-Dung / Carroll, Thomas S / Jha, Jyoti K / Fanger, Gary R / Hang, Howard C

    Science (New York, N.Y.)

    2021  Volume 373, Issue 6558, Page(s) 1040–1046

    Abstract: The antitumor efficacy of cancer immunotherapy can correlate with the presence of certain bacterial species within the gut microbiome. However, many of the molecular mechanisms that influence host response to immunotherapy remain elusive. In this study, ... ...

    Abstract The antitumor efficacy of cancer immunotherapy can correlate with the presence of certain bacterial species within the gut microbiome. However, many of the molecular mechanisms that influence host response to immunotherapy remain elusive. In this study, we show that members of the bacterial genus
    MeSH term(s) Animals ; B7-H1 Antigen/antagonists & inhibitors ; Bacterial Load ; Bacterial Proteins/metabolism ; Enterococcus/enzymology ; Enterococcus/metabolism ; Enterococcus faecalis/metabolism ; Enterococcus faecium/metabolism ; Gastrointestinal Microbiome ; Immune Checkpoint Inhibitors/therapeutic use ; Immunotherapy ; Melanoma, Experimental/immunology ; Melanoma, Experimental/therapy ; Mice ; Mice, Inbred C57BL ; N-Acetylmuramoyl-L-alanine Amidase/metabolism ; Nod2 Signaling Adaptor Protein/metabolism ; Peptide Fragments/metabolism ; Peptidoglycan/metabolism ; Probiotics ; Signal Transduction
    Chemical Substances B7-H1 Antigen ; Bacterial Proteins ; Cd274 protein, mouse ; Immune Checkpoint Inhibitors ; Nod2 Signaling Adaptor Protein ; Nod2 protein, mouse ; Peptide Fragments ; Peptidoglycan ; N-Acetylmuramoyl-L-alanine Amidase (EC 3.5.1.28)
    Language English
    Publishing date 2021-08-17
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 128410-1
    ISSN 1095-9203 ; 0036-8075
    ISSN (online) 1095-9203
    ISSN 0036-8075
    DOI 10.1126/science.abc9113
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Book: The excited states of 62Ni studied by the (n, [gamma]) reaction

    Fanger, Ulrich

    Nuclear physics : A ; 146

    (KfK ; 1232)

    1970  

    Author's details U. Fanger
    Series title KfK ; 1232
    Language English
    Size S. 549 - 576, graph. Darst
    Publisher Gesellschaft für Kernforschung mbh
    Publishing place Karlsruhe
    Document type Book
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  6. Book: Bestimmung des Wolframgehalts von natürlichen Gesteinsproben aus Scheelitlagerstätten mit Hilfe der prompten n,g-Analyse

    Fanger, Ulrich

    (KfK ; 1404 ; PACT-Bericht Projekt Actiniden ; Nr. 3)

    1971  

    Institution Institut für Angewandte Kernphysik
    Author's details Institut für Angewandte Kernphysik ... von U. Fanger
    Series title KfK ; 1404
    PACT-Bericht Projekt Actiniden ; Nr. 3
    Language German
    Size 14 S, graph. Darst, 30 cm
    Edition Als Ms. vervielfältigt
    Publisher Gesellschaft für Kernforschung mbH
    Publishing place Karlsruhe
    Document type Book
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  7. Article: Monoclonal antibodies PMN 6, PMN 29, and PM-81 bind differently to glycolipids containing a sugar sequence occurring in lacto-N-fucopentaose III.

    Magnani, J L / Ball, E D / Fanger, M W / Hakomori, S I / Ginsburg, V

    Archives of biochemistry and biophysics

    1984  Volume 233, Issue 2, Page(s) 501–506

    Abstract: ... these differences, the binding of all three antibodies to cells was inhibited by the oligosaccharide, lacto-N ... using purified glycolipids containing sugar sequences found in lacto-N-fucopentaose III demonstrated ... Ball, R. F. Graziano, L. Shen, and M. W. Fanger (1982) Proc. Natl. Acad. Sci. USA 79, 5374-5378 ...

    Abstract Three monoclonal antibodies, PMN 6, PMN 29, and PM-81, bind myeloid cells. Antibodies PMN 6 and PMN 29 bind specifically to granulocytes but differ in their ability to bind some other cell lines [E. D. Ball, R. F. Graziano, L. Shen, and M. W. Fanger (1982) Proc. Natl. Acad. Sci. USA 79, 5374-5378]. Antibody PM-81, in addition to granulocytes, also binds to eosinophils, monocytes, and most acute myelocytic leukemia cells [E. D. Ball, R. F. Graziano, and M. W. Fanger (1983) J. Immunol. 130, 2937-2941]. Despite these differences, the binding of all three antibodies to cells was inhibited by the oligosaccharide, lacto-N-fucopentaose III [Gal beta 1-4(Fuc alpha 1-3)GlcNAc beta 1-3Gal beta 1-4Glc]. Solid-phase radioimmunoassays using purified glycolipids containing sugar sequences found in lacto-N-fucopentaose III demonstrated different binding characteristics for each antibody. PM-81 bound lower concentrations of glycolipids than PMN 29, while PMN 6 required the highest concentration of glycolipids for binding. Autoradiography of thin-layer chromatograms of glycolipid antigens supported these results. The binding of these monoclonal antibodies to cells probably depends on the density of antigens on the cell surface, each antibody requiring a different density. Thus, cells containing antigen below a certain threshold concentration may not bind low-affinity antibodies.
    MeSH term(s) Antibodies, Monoclonal/immunology ; Antibody Affinity ; Antibody Specificity ; Autoradiography ; Binding Sites, Antibody ; Carbohydrate Sequence ; Glycolipids/immunology ; Humans ; Lewis X Antigen/immunology ; Neutrophils/immunology ; Oligosaccharides/immunology ; Radioimmunoassay
    Chemical Substances Antibodies, Monoclonal ; Glycolipids ; Lewis X Antigen ; Oligosaccharides
    Language English
    Publishing date 1984-09
    Publishing country United States
    Document type Journal Article
    ZDB-ID 523-x
    ISSN 1096-0384 ; 0003-9861
    ISSN (online) 1096-0384
    ISSN 0003-9861
    DOI 10.1016/0003-9861(84)90473-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Book: Activation-analysis prospects by using a concentric 5 x 10 n/s sealed neutron tube combined with a fast rabbit system

    Fanger, Hans-Ulrich / Michaelis, W / Pepelnik, R

    (GKSS : E ; 80,38)

    1980  

    Author's details H.-U. Fanger; R. Pepelnik; W. Michaelis
    Series title GKSS : E ; 80,38
    Size 14 S, graph. Darst
    Publisher GKSS
    Publishing place Geesthacht
    Document type Book
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  9. Book: Cross-section determination for the 50Ti(n,p) 50Sc reaction in the 14MeV neutron energy region

    Barreira Filho, J. L / Fanger, Hans-Ulrich

    (GKSS : E ; 81,53)

    1981  

    Author's details J. L. Barreira Filho; H.-U. Fanger
    Series title GKSS : E ; 81,53
    Language German ; English
    Size 16 S
    Publisher GKSS
    Publishing place Geesthacht
    Document type Book
    Note Mit dt. Zsfassung
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  10. Book: Winkelverteilungsmessungen an [gamma]-Kaskaden aus der Reaktion 57Fe(n, [gamma])58Fe

    Schmidt, Harald / Fanger, Ulrich / Michaelis, Walfried

    Nuclear physics : A ; 136

    (KfK ; 1113)

    1969  

    Author's details H. Schmidt; W. Michaelis; U. Fanger
    Series title KfK ; 1113
    Language German
    Size S. 122 - 144, graph. Darst
    Publisher Gesellschaft für Kernforschung mbh
    Publishing place Karlsruhe
    Document type Book
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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