bioRxiv Science⌕ Search

Biology subjects

Overton, M.

Publications and source records attributed to Overton, M..

2 recordsLinked to original sources

Arrayed hydrogels pair whole-cell imaging with single-cell mass spectrometry proteomics

Multimodal single-cell analysis aims to elucidate cellular-level phenotype within heterogeneous cell populations. Advancements in single-cell proteomics (SCP) seek to deepen quantitative depth, coverage, and reproducibility for a robust view of functional cell state. However, broadly accessible multimodal approaches are poised to benefit from sample-preparation advancements upstream of the mass spectrometer. Here, we introduce ProteoParcel, a multimodal SCP platform for indexing upstream widefield single-cell images to downstream label-free, bottom-up proteomics. Parcels are spatially arrayed planar polyacrylamide gels patterned with microwells. Each parcel, containing one microwell and an abutting gel region, is designed to integrate the single-cell imaging and SCP analysis modes. First, for whole-cell imaging, each microwell isolates an intact, individual breast cancer cell (MCF-7). After imaging, cells are subjected to in-microwell chemical cell lysis, electro-injection of whole-cell lysate from the microwell into the abutting gel region, in-gel chemical fixation, and finally in-gel tryptic digestion prior to peptide extraction for SCP. Location-indexed parcels are independently releasable to confer single-cell resolution to downstream mass spectrometry. To ensure SCP-suitable proteome solubilization and trypsin/Lys-C digestion, we optimize cell lysis, electrophoresis, and gel pre-equilibration conditions within the gel. Using ProteoParcel, we identify over 1,400 protein species from single, imaged MCF-7 cells. Scrutiny of the gel preparation conditions confirms that hydrogel-lysate interactions introduce predictable, physicochemically interpretable (cell membrane, hydrophobicity) detection biases, while broad functional-class composition and subcellular compartment coverage are preserved when benchmarked to in-solution digestion. ProteoParcel makes facile same-cell multimodal SCP and live-cell imaging.

bioengineering↗

Design of SARS-CoV-2 RBD Immunogens to Focus Immune Responses Towards Conserved Coronavirus Epitopes

SARS-CoV-2 continues to evolve, with new variants emerging that evade pre-existing immunity and limit the efficacy of existing vaccines. One approach towards developing superior, variant-proof vaccines is to engineer immunogens that preferentially elicit antibodies with broad cross-reactivity against SARS-CoV-2 and its variants by targeting conserved epitopes on spike. The inner and outer faces of the Receptor Binding Domain (RBD) are two such conserved regions targeted by antibodies that recognize diverse human and animal coronaviruses. To promote the elicitation of such antibodies by vaccination, we engineered "resurfaced" RBD immunogens that contained mutations at exposed RBD residues outside the target epitopes. In the context of pre-existing immunity, these vaccine candidates aim to disfavor the elicitation of strain-specific antibodies against the immunodominant Receptor Binding Motif (RBM) while boosting the induction of inner and outer face antibodies. The engineered resurfaced RBD immunogens were stable, lacked binding to monoclonal antibodies with limited breadth, and maintained strong interactions with target broadly neutralizing antibodies. When used as vaccines, they limited humoral responses against the RBM as intended. Multimerization on nanoparticles further increased the immunogenicity of the resurfaced RBDs immunogens, thus supporting resurfacing as a promising immunogen design approach to rationally shift natural immune responses to develop more protective vaccines.

immunology↗