Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2011Responsive hybrid block co-polymer conjugates of proteins–controlled architecture to modulate substrate specificity and solution behaviour53citations
  • 2007Immunological and structural properties of a pectic polymer from Glinus oppositifolius79citations

Places of action

Chart of shared publication
Schweins, Ralf
1 / 39 shared
Griffiths, Peter C.
1 / 2 shared
Jangher, Abdulhakim
1 / 1 shared
Thurecht, Kristofer J.
1 / 2 shared
Magnusson, Johannes P.
1 / 1 shared
Saeed, Aram
1 / 2 shared
Paul, Alison
1 / 2 shared
King, Stephen M.
1 / 16 shared
Yaşayan, Gökçen
1 / 1 shared
Davies, Martyn C.
1 / 5 shared
Fernández-Trillo, Francisco
1 / 1 shared
Alexander, Cameron
1 / 14 shared
Michaelsen, Terje E.
1 / 1 shared
Chen, Xinyong
1 / 2 shared
Paulsen, Berit S.
1 / 1 shared
Morris, Gordon
1 / 6 shared
Yamada, Haruki
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Inngjerdingen, Marit
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Diallo, Drissa
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Harding, Stephen E.
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Matsumoto, Tsukasa
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Kenne, Lennart
1 / 1 shared
Patel, Trushar R.
1 / 1 shared
Inngjerdingen, Kari T.
1 / 1 shared
Chart of publication period
2011
2007

Co-Authors (by relevance)

  • Schweins, Ralf
  • Griffiths, Peter C.
  • Jangher, Abdulhakim
  • Thurecht, Kristofer J.
  • Magnusson, Johannes P.
  • Saeed, Aram
  • Paul, Alison
  • King, Stephen M.
  • Yaşayan, Gökçen
  • Davies, Martyn C.
  • Fernández-Trillo, Francisco
  • Alexander, Cameron
  • Michaelsen, Terje E.
  • Chen, Xinyong
  • Paulsen, Berit S.
  • Morris, Gordon
  • Yamada, Haruki
  • Inngjerdingen, Marit
  • Diallo, Drissa
  • Harding, Stephen E.
  • Matsumoto, Tsukasa
  • Kenne, Lennart
  • Patel, Trushar R.
  • Inngjerdingen, Kari T.
OrganizationsLocationPeople

article

Responsive hybrid block co-polymer conjugates of proteins–controlled architecture to modulate substrate specificity and solution behaviour

  • Schweins, Ralf
  • Griffiths, Peter C.
  • Jangher, Abdulhakim
  • Thurecht, Kristofer J.
  • Magnusson, Johannes P.
  • Saeed, Aram
  • Paul, Alison
  • King, Stephen M.
  • Yaşayan, Gökçen
  • Davies, Martyn C.
  • Fernández-Trillo, Francisco
  • Allen, Stephanie
  • Alexander, Cameron
Abstract

Responsive co-polymers based on polyethyleneglycol methacrylate (PEGMA) monomers have been grown by aqueous phase ATRP from a model protein, trypsin, to generate hybrid polymer-protein block conjugates. The conjugates (Hybrids I and II) both contained the same segment of grafted responsive co-polymer to afford a phase transition at 37 °C, Hybrid II however differed from Hybrid I by having a second block of hydrophilic pPEGMA monomer grown from the end of the responsive block. The resultant ‘diblock’ and ‘triblock’ hybrids were characterised in terms of their temperature-dependent behaviour in solution by dynamic light scattering, small-angle neutron scattering and pulsed-gradient spin-echo NMR, and their structures at surfaces examined by aqueous phase atomic force microscopy and cryo transmission electron microscopy. These data showed that Hybrids I and II differed in their solution behaviour with temperature, dependent on the arrangement of their grafted polymer blocks. Hybrid I self-assembled into higher-order structures above 37 °C before precipitating reversibly, whereas Hybrid II remained essentially constant in size across a similar temperature range even when its attached intermediate polymer block underwent a phase transition. The differences in polymer-protein hybrid behaviour were also manifest in enzyme activity assays with temperature-dependent hydrolysis of both peptide and protein substrates varying with hybrid architecture. Overall the data show that it is possible to grow responsive polymer-protein block co-polymers of varied structures, architectures and solution behaviour and that these can be used to control bioconjugate activity.

Topics
  • impedance spectroscopy
  • surface
  • polymer
  • phase
  • atomic force microscopy
  • phase transition
  • transmission electron microscopy
  • Nuclear Magnetic Resonance spectroscopy
  • small-angle neutron scattering
  • dynamic light scattering