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Joswig, J.

Publications and source records attributed to Joswig, J..

2 recordsLinked to original sources

Global Convergence of Plant Functional Trait Composition in the Anthropocene

Since the onset of European colonial expansion, humans have accelerated species migration across continents, reshaping plant functional composition and associated ecosystem processes. Plant functional traits-such as leaf area, plant height, or rooting depth-are structured along major axes of variation, including size and leaf economics, that reflect ecological strategies. While human-mediated changes in this trait space have been documented regionally or for specific taxa, there exists no global, grid cell-level quantification of past shifts across major axes of trait variation. Here, we link global citizen science plant occurrence data with data on 37 above- and below-ground traits, and information on native and introduced status for each occurrence. Using dimension-reduction on grid cell-level trait means and introduced species status as a proxy for anthropogenic change, we identify three major axes of functional variation: the size, leaf economics, and life-span axes. By comparing past (native-only) and present-day trait distributions in 3D trait space and geographically, we find prominent region-specific shifts along all three axes. Overall, functional composition converges toward (mostly) smaller, more acquisitive, and shorter-lived assemblages, with region-specific differences in which axis shifts are most pronounced. These results provide the first global estimate of how human-mediated plant introductions have altered ecosystem functional composition in the past centuries, highlighting the spatial patterns and trait dimensions most affected by anthropogenic pressures.

ecology↗

Bioinspired Design of Lysolytic Triterpenoid-Peptide Conjugates that Kill African Trypanosomes

Humans have evolved a natural immunity against Trypanosoma brucei infections, which is executed by two serum (lipo)protein complexes known as trypanolytic factors (TLF). Active TLF-ingredient is the primate-specific apolipoprotein L1 (ApoL1). The protein has a pore-forming activity that kills parasites by lysosomal and mitochondrial membrane fenestration. Of the many trypanosome subspecies only two are able to counteract the activity of ApoL1, which illustrates its evolutionary optimized design and trypanocidal potency. Here we ask the question whether a synthetic (syn)TLF can be synthesized using the design principles of the natural TLF-complexes but relying on different chemical building blocks. We demonstrate the stepwise development of triterpenoid-peptide conjugates, in which the triterpenoids act as a cell binding, uptake and lysosomal transport-moduls and the synthetic peptide GALA as a pH-sensitive, pore-forming lysolytic toxin. As designed, the conjugate kills infective-stage African trypanosomes through lysosomal lysis demonstrating proof-of-principle for the bioinspired, forward-design of a synTLF.

synthetic biology↗