ORCID Profile
0000-0001-9033-5522
Current Organisation
Tierärztliche Hochschule Hannover
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Publisher: Wiley
Date: 05-12-2011
Abstract: A series of well-defined polymer-drug conjugates were prepared in order to modify the physical properties of a known cytotoxic drug, 7-ethyl-10-hydroxyc tothecin (SN-38), the active metabolite of irinotecan (CPT-11). Reversible addition-fragmentation chain transfer (RAFT) polymerisation was used to covalently and site-specifically append a defined N-(2-hydroxypropyl)methacrylamide (HPMA) polymer to SN-38 using a graft-from process. These poly-HPMA-SN-38 conjugates displayed excellent aqueous solubility and stability, whilst retaining the cytotoxic activity of the parent SN-38. In vitro co-culture assays containing both cancer and noncancer cell lines demonstrated the specificity of RAFT-derived poly-HPMA-SN-38 conjugates for cancerous cells. The concept of post-optimisation modification of small-molecule drugs through a graft-from polymer conjugation method is introduced.
Publisher: Elsevier BV
Date: 06-2014
Publisher: Proceedings of the National Academy of Sciences
Date: 23-10-2018
Abstract: Group A Streptococcus (GAS) causes invasive streptococcal infections in humans, resulting in high mortality. Thus, GAS is also known as “killer bacteria” or “flesh-eating bacteria.” The mechanism by which the immune system recognizes this potent pathogen remains elusive. In this study, we showed that the innate immune receptor Mincle (macrophage inducible C-type lectin) plays pivotal roles against invasive GAS infection through the recognition of monoglucosyldiacylglycerol (MGDG), a component of the lipoteichoic acid anchor. MGDG induced proinflammatory cytokines, ROS, and NO production in a Mincle-dependent manner. In an invasive GAS infection model, Mincle-deficient mice exhibited severe bacteremia and rapid lethality. These results indicate that Mincle plays a central role in protective immunity against acute GAS infection.
Publisher: Elsevier BV
Date: 04-2012
DOI: 10.1016/J.CBPA.2011.12.006
Abstract: Glycomics and glycoproteomics have become indispensible tools in the study of glycoconjugates. Mass spectrometry based methods are standardly used to study the proteome and/or glycome and these approaches are capable of providing both, qualitative and quantitative information using top down techniques. The human immune system marks a particular area of interest for glycomics and glycoproteomics research since a large number of key proteins in innate and adaptive immunity are glycoproteins. In numerous ex les, the crucial influence of glycosylation on critical steps such as receptor interaction and binding has been demonstrated. In this review, we focus on different glycomics and glycoproteomics approaches and their application for studying protein glycosylation in the immune system.
No related grants have been discovered for Bernd Lepenies.