Biology subjects

Osterholz, H.

Publications and source records attributed to Osterholz, H..

5 recordsLinked to original sources

bioRxiv2026

Single-molecule mass measurements uncover shifting RNA interactions during condensate phase transitions

RNA interactions are a key contributor to the formation and disassembly of intracellular protein condensates. Although some proteins utilize specific RNA-binding domains, these processes can also be mediated by charge interactions with intrinsically disordered regions. Due to the dynamic nature of these systems, investigating the underlying specificity and stoichiometry remains challenging. Here, we demonstrate that single-molecule mass measurements with mass photometry can capture RNA-protein interactions in phase-separated protein systems. Using the approach to investigate RNA-mediated phase shifts of tau condensates, we find that increasing the RNA concentration, which promotes phase re-entry, results in RNA-mediated tau multimerization, where each tau monomer binds a linear RNA sequence of approximately 30 nucleotides. Solution NMR and native mass spectrometry confirm the formation of stable complexes between RNA and the basic proline-rich and repeat domains of tau, which have a net charge of -29. Our findings demonstrate that mass photometry can distinguish between charge neutralization, which drives coacervation, and complex formation, which mediates phase re-entry, making it a highly complementary tool for the study of RNA-mediated phase separation.

biophysics↗

bioRxiv2026

Liquid-liquid phase separation of tau regulates client binding via a conformational relay

Intrinsically disordered proteins (IDPs) achieve functional specificity through dynamic, multivalent interactions that are often reorganized during liquid-liquid phase separation (LLPS). How LLPS reshapes IDP conformational landscapes and binding preferences remains poorly understood. Here, we combine native ion mobility mass spectrometry, mass photometry, fluorescence microscopy, and computational modeling to dissect how conditions that promote LLPS of the intrinsically disordered human tau protein regulate its interactions with tubulin and the neuronal anti-amyloid chaperone domain BRICHOS from Bri2. We show that electrostatically driven compaction and transient oligomerization of tau during LLPS promote BRICHOS binding to a specific Tau segment. Within tau condensates, BRICHOS can compete with tubulin for tau interactions by blocking its adjacent binding site, thereby modulating LLPS-dependent microtubule assembly. Using a generalizable experimental strategy, we provide a proof of concept for detecting conformational selectivity in a dynamic condensate.

biophysics↗

bioRxiv2025

Biogeochemical function of slicks in coastal surface waters of the Baltic Sea

The sea-surface microlayer (SML) is a crucial ocean-atmosphere interface involved in gas exchange and nutrient cycling. Slicks, i.e., viscous surface layers, common in coastal regions serve as microbial hotspots. We studied microbial abundance, surfactants, dissolved organic carbon (DOC), and net community production (NCP) of O2 in slick and non-slick SMLs and underlying water (ULW) in the coastal Baltic Sea. Slicks often showed higher surfactant levels compared to the ULW. Microbial respiration often exceeded production, resulting in net O2 consumption, although some ULW sites exhibited net O2 production. The SML was enriched with pico- and nanophytoplankton, with cyanobacteria being negatively correlated with total dissolved nitrogen. In contrast, microphytoplankton accumulated in the ULW, indicating niche separation with depth. Microscopy revealed ciliates and juvenile sporophytes dominating a slicks >100 {micro}m fraction. In eutrophic coastal systems, slicks influence plankton communities and O2 dynamics, supporting their role in surface biogeochemical cycling and climate-driven changes.

microbiology↗

bioRxiv2024

Photochemical processes drive thermal responses of dissolved organic matter in the dark ocean

How dissolved organic matter (DOM) responds to climate warming is critical for understanding its role in future ocean carbon cycling. Here, we use a highly resolved dataset of over 800 DOM samples covering the surface waters to the deep Atlantic, Southern, and Pacific oceans to examine the changes in DOM molecular composition in response to warming water temperatures, referred to as DOM thermal responses. Towards the deep waters, the strength (i.e., overall magnitude) and diversity (i.e., variation among molecules) of these thermal responses both decline. However, these responses show opposite trends with the concentration of more recalcitrant molecules, decreasing and increasing, respectively. These contrasting trends concur with the observation that, compared to the strength of thermal responses, their diversity is more strongly explained by photochemical processes of DOM. By projecting global ocean thermal responses from 1950 to 2020 using environmental temperature, salinity and radiation, we predict that increases in the diversity of thermal responses are unexpectedly largest at deeper depths (> 1,000 m). Such increases could elevate the recalcitrant deep-ocean carbon sink by approximately 10 Tg C yr-1, which accounts for > 5% of the carbon flux reaching and persisting in the deep ocean. Our findings highlight the role of photochemical processes in imprinting DOM thermal responses, offering new insights into the future capacity of the oceanic carbon sink under global climate change.

ecology↗

bioRxiv2024

Controlling Drug Partitioning in Individual Protein Condensates through Laser-Induced Microscale Phase Transitions.

Gelation of protein condensates formed by liquid-liquid phase separation (LLPS) occurs in a wide range of biological contexts, from the assembly of biomaterials to the formation of fibrillar aggregates and is therefore of interest for biomedical applications. Soluble-to-gel (sol-gel) transitions are controlled through macroscopic processes such as changes in temperature or buffer composition, resulting in bulk conversion of liquid droplets into microgels within minutes to hours. Using microscopy and mass spectrometry, we show that condensates of an engineered mini-spidroin (NT2repCTYF) undergo a spontaneous sol-gel transition resulting in the loss of exchange of proteins between the soluble and the condensed phase. We find that liquid spidroin condensates absorb visible light, which enables us to control sol-gel transitions of individual droplets through laser pulses. Fluorescence microscopy reveals that laser-induced gelation significantly alters the interactions between droplet proteins and small molecules, which allows us to load single droplets with an anticancer drug. In summary, our findings demonstrate direct control of phase transitions in individual condensates opening new avenues for functional and structural characterization. SYNOPSIS TOCThe liquid-to-solid transitions of phase-separated protein condensates are challenging to control. Leppert et al. show that condensates of engineered mini-spidroins gelate at slightly elevated temperatures. Using high-energy laser pulses at wavelengths that are absorbed by the droplets, the authors induce sol-gel transitions in single droplets. These gelated droplets are chemically stable and exhibit an increased ability to sequester drug molecules. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=177 SRC="FIGDIR/small/584573v1_ufig1.gif" ALT="Figure 1"> View larger version (48K): org.highwire.dtl.DTLVardef@a7186corg.highwire.dtl.DTLVardef@345bd0org.highwire.dtl.DTLVardef@177c94forg.highwire.dtl.DTLVardef@1416456_HPS_FORMAT_FIGEXP M_FIG C_FIG

biophysics↗