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Biology subjects

Con, P.

Publications and source records attributed to Con, P..

2 recordsLinked to original sources

Single-molecule FRET with a minimalistic 3D-printed setup and dyes in the blue-green spectral region

Forster Resonance Energy Transfer (FRET) is a powerful technique for the detection and characterization of biomolecular interactions and conformational changes with sub-nanometer spatial resolution and a temporal resolution down to the timescale of fluorescence. While the technique is widely adopted in structural biology and biophysics, the evolution of single-molecule FRET has led to experimental setups with sophisticated optical layouts, multi-laser excitation schemes and time-resolved detection electronics. We here present an accessible alternative towards single-molecule FRET based on Brick-MIC, a recently introduced 3D-printed micro-spectroscopy platform. The FRET-Brick uses continuous-wave excitation at 488 nm with a minimal set of opto-mechanical components and photomultiplier detectors (PMTs). With this we were able to significantly reduce the setup complexity retaining single-molecule sensitivity with dyes matching the sensitivity of PMTs. To maximize the photon output of Alexa488, ATTO488 (donors), Alexa555, ATTO542 and Cy3B (acceptors), we introduce ferrocene-derivatives as photostabilizers that increase both dye brightness and remove dark-states. We benchmark the performance of the FRET-Brick with fluorophore-labelled oligonucleotide reference structures also in comparison to accessible volume simulations, and by detecting conformational changes in bacterial substrate binding proteins. Our work demonstrates that qualitative and quantitative smFRET measurements are possible with the minimalistic and cost-effective FRET-Brick.

biophysics↗

Specialized cells and transporters mediate integument-absorption of environmental peptides in cichlids larvae.

Nutrient absorption through the skin and gills into the organisms tissues has been documented in several aquatic invertebrates from different phyla. However, the actual absorption mechanism is still unknown. In teleost fish, as in all jawed vertebrates, intestinal absorption is considered as the sole source of nutrients. The proton-dependent peptide transporters (PepT) of the slc15a gene family are the only known mechanism for cellular absorption of di- and tri-peptides within the animal kingdom. In this study, we explored the expression and localization of PepT2 in Mozambique tilapia (Oreochromis mossambicus) larvae. Transcript levels of PepT2 in dissected yolk-sacs from larvae showed significant expression during the larval developmental period. Immunofluorescence staining of PepT2 with Na/K-ATPase (NKA) and Na+/K+/2Cl- co-transporter (NKCC) on the yolk-sac membrane revealed co-staining with NKA and differential-staining with NKCC. While NKA staining was observed on the ionocytes basolateral membrane, PepT2 staining was restricted to the apical pit of the ionocytes, facing the surrounding water. In this study, we identified a nutrient transporter located on integument-specific cells, facing the outside aquatic environment. This is the first indication of environmental nutrients absorption in teleosts, and the first evidence of a possible absorption mechanism through PepT2, in specialized yolk-sac ionocytes.

physiology↗