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Biology subjects

Lane, Z. M.

Publications and source records attributed to Lane, Z. M..

2 recordsLinked to original sources

Cell-Based Sensor for Extracellular DNA

Detection of molecules with cell-based sensors allows for conversion of binding events into gene expression outputs. Here, we present a cell-based sensor that can detect extracellular double-stranded DNA. This sensor is based on an engineered receptor which we call Luminescent Ultrasensitive Nucleic Acid Reporter, or LUNAR. LUNAR is based on a recently developed Programmable Antigen-gated G-protein-coupled Engineered Receptor (PAGER). PAGERs are a genetic fusion of an auto-inhibitory peptide, a protein-binding domain, and a modified kappa opioid receptor. PAGERs are gated by two binding events. First, a protein ligand displaces an intramolecular inhibitor, Arodyn, then a second ligand activates the receptor. By replacing the protein-binding domain with a DNA binding zinc finger protein (ZFP) we could detect extracellular DNA in a dose-dependent fashion. Here, we show that first-generation LUNAR constructs can detect both oligonucleotides and plasmid double-stranded DNA with nanomolar sensitivity in mammalian cells. Future work will focus on improving sensitivity, fold-change, and multiplexing capabilities for sequence-specific DNA detection.

synthetic biology↗

A gene-agnostic FACS technique to isolate stem cells in Hydractinia symbiolongicarpus validated with cytology

Hydractinia symbiolongicarpus is a powerful model for stem cell research and maintains a population of pluripotent adult stem cells throughout its lifetime. Here we describe a gene expression-agnostic FACS technique to isolate a live cell population from Hydractinia feeding polyps that appear to be stem cells. This technique utilizes only the general cellular component stains DAPI, DRAQ5, Calcein AM, and Pyronin Y. The stem cell population was identified via subtractive gating based on samples whose stem cell populations had been selectively depleted with the DNA-alkylating agent Mitomycin C. To validate the identity of the isolated population, a colorimetric cytological assay capable of simultaneously discriminating between all major Hydractinia cell types in a live-dissociated cell solution was developed using May-Grunwald and Giemsa stains. The isolated cell population was significantly depleted by Mitomycin C administration, had a high RNA content, was proliferative, had a cytological profile that matched that of Piwi1+ stem cells, and was [~]10x enriched with Piwi1+ stem cells compared to whole cell suspension, all of which support the conclusion that the isolated population is indeed comprised of stem cells. This gene-agnostic FACS technique will serve future research into Hydractinia stem cell biology by enabling the use of isolated populations of live stem cells in transplantation, cell culture, and spheroid experimentation, and may serve as a reference for the development of new methods in other cnidarian species.

cell biology↗