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Biology subjects

Ouassil, N.

Publications and source records attributed to Ouassil, N..

2 recordsLinked to original sources

Near Infrared Nanosensors Enable Optical Imaging of Oxytocin with Selectivity over Vasopressin in Acute Mouse Brain Slices

Oxytocin plays a critical role in regulating social behaviors, yet our understanding of its role in both neurological health and disease remains incomplete. Real-time oxytocin imaging probes with the spatiotemporal resolution relevant to its endogenous signaling are required to fully elucidate oxytocin function in the brain. Herein we describe a near-infrared oxytocin nanosensor (nIROx), a synthetic probe capable of imaging oxytocin in the brain without interference from its structural analogue, vasopressin. nIROx leverages the inherent tissue-transparent fluorescence of single-walled carbon nanotubes (SWCNT) and the molecular recognition capacity of an oxytocin receptor peptide fragment (OXTp) to selectively and reversibly image oxytocin. We employ these nanosensors to monitor electrically stimulated oxytocin release in brain tissue, revealing oxytocin release sites with a median size of 3 m which putatively represents the spatial diffusion of oxytocin from its point of release. These data demonstrate that covalent SWCNT constructs such as nIROx are powerful optical tools that can be leveraged to measure neuropeptide release in brain tissue.

bioengineering↗

Supervised Learning Model Predicts Protein Adsorption to Nanotubes

Engineered nanoparticles are advantageous for numerous biotechnology applications, including biomolecular sensing and delivery. However, testing the compatibility and function of nanotechnologies in biological systems requires a heuristic approach, where unpredictable biofouling via protein corona formation often prevents effective implementation. Moreover, rational design of biomolecule-nanoparticle conjugates requires prior knowledge of such interactions or extensive experimental testing. Toward better applying engineered nanoparticles in biological systems, herein, we develop a random forest classifier (RFC) trained with proteomic mass spectrometry data that identifies proteins that adsorb to nanoparticles, based solely on the proteins amino acid sequence. We model proteins that populate the corona of a single-walled carbon nanotube (SWCNT)-based optical nanosensor and study whether there is a relationship between the proteins amino acid-based properties and the proteins adsorption to SWCNTs. We optimize the classifier and characterize the classifier performance against other models. To evaluate the predictive power of our model, we apply the classifier to rapidly identify proteins with high binding affinity to SWCNTs, followed by experimental validation. We further determine protein features associated with increased likelihood of SWCNT binding: high content of solvent-exposed glycine residues and non-secondary structure-associated amino acids. Conversely, proteins with high content of leucine residues and beta-sheet-associated amino acids are less likely to form the SWCNT protein corona. The classifier presented herein provides a step toward undertaking the otherwise intractable problem of predicting protein-nanoparticle interactions, which is needed for more rapid and effective translation of nanobiotechnologies from in vitro synthesis to in vivo use. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=66 SRC="FIGDIR/small/449132v2_ufig1.gif" ALT="Figure 1"> View larger version (22K): org.highwire.dtl.DTLVardef@bbc175org.highwire.dtl.DTLVardef@9a0b94org.highwire.dtl.DTLVardef@16e22e1org.highwire.dtl.DTLVardef@1b40a84_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioengineering↗