The Society for Laboratory Automation and Screening (SLAS)
Innovation Award is an annual cash prize (US$ 10,000) given out at the SLAS
International Conference and Exhibition. The award goes to one exceptional
podium presentation that showcases the most innovative research for improving
laboratory technology.
This year’s 10 finalists include
- S.
Tori Ellison, NCATS, has developed a 3D bioprinted skin tissue model that
mimics the dermis and epidermis to study HSV infection pathways and test
new therapeutics. Using fluorescent biosensors and a high-throughput
format, over 700 compounds were screened, demonstrating that the potency
of antiviral treatments depends on the cell type and mechanism of action,
offering a scalable solution for advancing HSV drug discovery. “A 3D
Bioprinted Skin Assay Platform to Perform High-Throughout Screens and
Identify Potent HSV Anitvirals.”
- Keisuke
Goda, University of Tokyo, has overcome the limitation of traditional cell
sorting methods like FACS with image-activated cell sorting (IACS). IACS
uses real-time, AI-powered imaging
to sort live cells based on visual and functional attributes, with
applications in fields ranging from cancer biology to food science. “Intelligent
Image-Activated Cell Sorting & Beyond.”
- Sunghoon
Kwon, Seoul National University, explores the role of spatial technologies
in oncology, highlights recent discoveries, and offers perspectives on
therapeutic applications and future innovations in their recent work.
“AI-Driven ‘Smart Laser Gun’ for Spatial Omics as an Innovative Biomarker
Discovery Tool: From Lab Bench to Real-world.”
- Nitin
Joshi, Brigham and Women’s Hospital—Harvard Medical School, has developed
BraiN-TNGS, a high-throughput in vivo screening method using DNA
barcodes to track and quantify nanoparticle
(NP) formulations in the brain. This innovative approach enables the
identification of NPs with high brain accumulation and precise cell-type
targeting, optimizing therapeutic delivery while minimizing animal use and
improving efficiency. “Unlocking
Nano-Bio Interactions in the Brain for Precision Delivery of Gene
Therapies.”
- Justin
Langerman, UCLA, has developed a method called Secretion Encoded
single-Cell sequencing (SEC-seq) using hydrogel particles (nanovials) to
capture and analyze single
cells and their secretions alongside transcriptomic data. This
technique uncovered a unique population of mesenchymal stromal cells with
high regenerative capacity, revealed insights into early cell-cell
communication during embryonic development, and demonstrated the potential
for investigating intricate cellular interactions. “Utilizing
Nanovials to Associate Secretions and Transcriptomes of Single Cells with
SEC-seq and to Capture the Discrete Effects of Cell-Cell Interaction”
- Maria
Bueno Alvez Lim, KTH Royal Institute of Technology Stockholm, conducted a
pilot pan-cancer study that compared cancer types against one another,
analyzing 1,463 proteins from over 1,400 patients, uncovering a biomarker
signature distinguishing specific cancers. Expanding this approach to 59
diseases, researchers created a Human Disease Blood Atlas, paving the way
for more precise biomarker discovery and improved disease monitoring
across various conditions. “Comprehensive
Blood Proteome Profiling for Pan-Cancer and Pan-Disease Biomarker
Discovery.”
- Babak
Mahjour, MIT, whose study introduces an automated cheminformatic workflow
that leverages expert-encoded reaction templates to systematically invent
and optimize chemical reactions. Using a mechanistic network, the method
predicts reaction pathways, demonstrated through both the regeneration of
known multicomponent reactions and the discovery of novel transformations
validated experimentally. The approach highlights its utility in exploring
chemical space efficiently, with robotics-assisted experimentation
providing insights into reaction kinetics and conditions. “Ideation and
Evaluation of Novel Multicomponent Reactions via Mechanistic Network
Analysis and Automation.”
- Caitlin
Mills, Harvard Medical School, has developed a Dye Drop microscopy
assay method for staining and fixing cells in culture with kinome-wide
affinity data, allowing for the identification of drug targets in cancer
and neurodegeneration, advancing cost-effective and robust drug
development workflows. “Drug Response
Phenotyping and Target Deconvolution Using Dye Drop Multiplexed Imaging.”
- Taci
Pereira, Systemic Bio, is addressing challenges in generating scalable,
human-relevant data, as traditional animal models and simplistic in
vitro systems often fail to accurately mimic human biology. The
h-VIOS™ platform addresses these issues by integrating bioprinted
organ-chips with endothelialized vasculatures, enabling complex,
human-like tissue models and multimodal data generation to assess
therapeutic safety and efficacy in applications like drug-induced liver
and vascular injuries. “h-VIOS: A
Human-Relevant Drug Discovery and Development Platform Using Bioprinted
Human Tissues.”
- Ritu
Raman, MIT, who has found that current drug discovery often measures
biomarkers instead of functional muscle force, leading to limited success
in restoring mobility. The Raman Lab addresses this gap with engineered
neuromuscular tissues and a patented flexure platform to quantify muscle
function, enabling high-throughput screening for therapies aimed at
improving muscle health and patient outcomes. “Tissue
Engineering High-Throughput Models of the Neuromuscular System”
The winner will be announced at 4:15pm on January 29th
during the 2025 SLAS Conference.