Improving iPSC reprogramming and CRISPR gene editing workflows and efficacy using CellRaft technology - Project Summary
Induced pluripotent stem cells (iPSCs) have become a commonly used tool to generate multiple cell types from
a given individual patient. Reprogramming non-invasively harvested cells, such as dermal fibroblasts, into
iPSCs, allows investigators to generate any cell type from a patient with known genetic and clinical backgrounds.
This method has been particularly powerful for cases in which a disease condition manifests in a tissue where
acquiring patient-derived primary cells is challenging, or there are genetic mutations. However, the workflows
associated with reprogramming, CRISPR gene editing, and differentiating iPSCs are low-throughput, costly,
time-consuming, and not supported by commercially available automated instrumentation. Customized
automation systems have been published and generally require considerable capital investment, multiple types
of equipment, custom programming, and commitment to a single reprogramming method. There is an unmet
need in academia and industry for technology that can improve the efficiency and success rates of a)
reprogramming, b) iPSC viability, and c) the ability to generate clonally derived CRISPR edited cell lines in an
automated fashion. The development of streamlined workflows on a single platform that can deliver higher
efficiencies in iPSC reprogramming and cell line development is likely to dramatically enhance the utility and
throughput of the technology, thereby accelerating the use of iPSCs in personalized medicine and drug
discovery. Cell Microsystems proposes the use of the CellRaft Technology, comprising the automated AIR
System and CytoSort Array cell culture consumable as a cost-effective, automated, and gentle solution that can
solve many of the pain points that plague these critical workflows. In this Phase I program, we will develop
protocols for the culture, reprogramming, and editing of iPSCs using our proprietary consumable and
instrumentation and demonstrate that our technology provides faster, more cost effective, and more efficient
workflows for iPSC cloning. Commercially, there is a tremendous potential market in laboratories across all
industries that perform these workflows, and our company has a proven successful track record in developing
tools for the drug discovery market.
