Spatial interactomics tool maps protein interactions to fight lung cancer

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PPI networks, co-expression analysis and predictive models of 16-plex profiling for 5 PPIs and 6 signaling and organelle markers in HCC827 cells. Credit: Nature Biomedical Engineering (2024). DOI: 10.1038/s41551-024-01271-x

As Ahmet F. Coskun and his team of researchers continue their mission to create a 3D atlas of the human body, mapping cells and tissues, they're making discoveries that could lead to better treatments for the most common type of lung cancer.

While they're at it, they're pioneering new fields of research, and possibly spinning the work into a new commercial venture.

Last year, Coskun and his team introduced a new study in "single cell spatial metabolomics," which explores the distribution of small molecules—metabolites—within tissues and organs. Now they're spearheading "spatial interactomics," a research area concerned with interactions between various biomolecules inside of individual cells.

To study these interactions, they've developed an innovative technique, or tool, to better understand why non-small cell lung cancer, or NSCLC, resists treatment in so many patients. They call it the "intelligent sequential proximity ligation assay," or iseqPLA.

"It's a smart test that can look at proteins and how they interact with each other in space," said Coskun, Bernie Marcus Early Career Professor in the Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech and Emory University.

"Basically, we're the first to create a new research area on spatial protein-protein interactions, which can tell us more about cell types and their functions," said Coskun. "With spatial interactomics, we can validate how cells physically touch, sense, and regulate nearby cells through the interaction of pairs of proteins."

So, the immediate goal of spatial interactomics is to investigate how protein-protein interactions drive drug resistance in NSCLC. And iseqPLA allows researchers to visualize how it's all happening at the subcellular level. Coskun's team described its work recently in the journal Nature Biomedical Engineering. He's also forming a company to commercialize the technology.

Smarter tools

Drugs called tyrosine kinase inhibitors (TKIs, like Osimertinib) have been successful in treating people with NSCLC. But many patients who initially respond well to the regimen, eventually develop a resistance. Protein interactions, a molecular kind of crosstalk, are a prime suspect in causing this resistance.

Proteins interact with each other all the time, and this mingling controls how cells grow, divide, or survive. Coskun and his team want to see how these interactions change in response to cancer treatment, and iseqPLA shows them, essentially attaching glowing tags to proteins, lighting up their locations and interactions under a microscope.

Evaluation of drug perturbing PPIs using VP drug in HCC827 cells. Credit: Nature Biomedical Engineering (2024). DOI: 10.1038/s41551-024-01271-x

"Think of it like a super detailed map showing how different proteins in a cell are connected," Coskun said.

The iseqPLA can examine 47 protein interactions in a single sample, which saves a lot of time (and resources) when compared to older methods, which look at two to three interactions at a time.

The researchers also created a computer model to analyze the spatial data they collected from iseqPLA, identifying patterns in protein interactions to help predict whether a cell was responding to a treatment or developing resistance.

"We showed that the test works not only in lab-grown cells but also in tissues from mice and humans," Coskun said. "It can really help us understand how patients respond to certain treatments."

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Building a spatial omics market

Going forward, Coskun aims to enhance iseqPLA to study interactions among RNA, proteins, and metabolites, as well as the RNA, proteins, metabolites, etc., and other subcellular dynamics. He also hopes to get the technology into the hands of other researchers.

"We believe it will be a groundbreaking tool," he said.

With that in mind, Coskun is planning to form a startup company called SpatAllize. He's working with VentureLab, the nonprofit organization at Georgia Tech that provides entrepreneurship programs for students and faculty.

"We are currently performing customer interviews and forming a strategy for a viable plan towards the marketplace," he said.

He also plans to expand iseqPLA's utility into other areas of research, focusing on how protein interactions influence the immune system, the heart, and brain health. His team is also developing a spatial interactomics robot that integrates iseqPLA with advanced imaging and automated deep learning.

"This will allow us to map all molecules within cells and tissues for an even better understanding of drug-cell interactions, particularly in cancer treatment planning," Coskun said.

More information: Shuangyi Cai et al, Spatially resolved subcellular protein–protein interactomics in drug-perturbed lung-cancer cultures and tissues, Nature Biomedical Engineering (2024). DOI: 10.1038/s41551-024-01271-x

Journal information: Nature Biomedical Engineering

Provided by Georgia Institute of Technology