Autor: |
Üclü S; Department for Organic Chemistry and Macromolecular Chemistry, Heinrich Heine University Düsseldorf, Universitätsstraße 1, Düsseldorf 40225, Germany., Marschelke C; Leibniz Institute of Polymer Research Dresden, Hohe Str. 6, Dresden 01069, Germany., Drees F; Department for Organic Chemistry and Macromolecular Chemistry, Heinrich Heine University Düsseldorf, Universitätsstraße 1, Düsseldorf 40225, Germany.; Institute for Macromolecular Chemistry, University Freiburg, Stefan-Meier-Str. 31, Freiburg Im Breisgau 79104, Germany., Giesler M; Department for Organic Chemistry and Macromolecular Chemistry, Heinrich Heine University Düsseldorf, Universitätsstraße 1, Düsseldorf 40225, Germany., Wilms D; Department for Organic Chemistry and Macromolecular Chemistry, Heinrich Heine University Düsseldorf, Universitätsstraße 1, Düsseldorf 40225, Germany., Köhler T; Department for Organic Chemistry and Macromolecular Chemistry, Heinrich Heine University Düsseldorf, Universitätsstraße 1, Düsseldorf 40225, Germany., Schmidt S; Department for Organic Chemistry and Macromolecular Chemistry, Heinrich Heine University Düsseldorf, Universitätsstraße 1, Düsseldorf 40225, Germany.; Institute for Macromolecular Chemistry, University Freiburg, Stefan-Meier-Str. 31, Freiburg Im Breisgau 79104, Germany., Synytska A; Leibniz Institute of Polymer Research Dresden, Hohe Str. 6, Dresden 01069, Germany.; Bavarian Polymer Institute, Research Group Functional Polymer Interfaces, University of Bayreuth, Ludwig-Thoma Str. 36a, Bayreuth 95447, Germany., Hartmann L; Department for Organic Chemistry and Macromolecular Chemistry, Heinrich Heine University Düsseldorf, Universitätsstraße 1, Düsseldorf 40225, Germany.; Institute for Macromolecular Chemistry, University Freiburg, Stefan-Meier-Str. 31, Freiburg Im Breisgau 79104, Germany. |
Abstrakt: |
Escherichia coli and other bacteria use adhesion receptors, such as FimH, to attach to carbohydrates on the cell surface as the first step of colonization and infection. Efficient inhibitors that block these interactions for infection treatment are multivalent carbohydrate-functionalized scaffolds. However, these multivalent systems often lead to the formation of large clusters of bacteria, which may pose problems for clearing bacteria from the infected site. Here, we present Man-containing Janus particles (JPs) decorated on one side with glycomacromolecules to target Man-specific adhesion receptors of E. coli . On the other side, poly( N -isopropylacrylamide) is attached to the particle hemisphere, providing temperature-dependent sterical shielding against binding and cluster formation. While homogeneously functionalized particles cluster with multiple bacteria to form large aggregates, glycofunctionalized JPs are able to form aggregates only with individual bacteria. The formation of large aggregates from the JP-decorated single bacteria can still be induced in a second step by increasing the temperature and making use of the collapse of the PNIPAM hemisphere. This is the first time that carbohydrate-functionalized JPs have been derived and used as inhibitors of bacterial adhesion. Furthermore, the developed JPs offer well-controlled single bacterial inhibition in combination with cluster formation upon an external stimulus, which is not achievable with conventional carbohydrate-functionalized particles. |