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21/11/2024 | News release | Distributed by Public on 21/11/2024 14:31

Mapping Protein Interactions to Fight Lung Cancer: Coskun Pioneering New Field of Research

Mapping Protein Interactions to Fight Lung Cancer: Coskun Pioneering New Field of Research

Spatial Interactomics: Mapping Protein Interactions to Fight Lung Cancer Coskun pioneering new research area and building a company around iseqPLA technology
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Ahmet Coskun's lab has developed iseqPLA to map protein interactions.

Nov 21, 2024

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 - with the study's lead author Shuangyi Cai and co-author Thomas Hu - wants 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.

"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."

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.

CITATION: Shuangyi Cai, Thomas Hu, Abhijeet Venkataraman, Felix G. Rivera Moctezuma, Efe Ozturk, Nicholas Zhang, Mingshuang Wang, Tatenda Zvidzai, Sandip Das, Adithya Pillai, Frank Schneider, Suresh S. Ramalingam, YouTake Oh, Shi-Yong Sun, and Ahmet F. Coskun. "Spatially resolved subcellular protein-protein interactomics in drug-perturbed lung-cancer cultures and tissues." Nature Biomedical Engineering.

https://doi.org/10.1038/s41551-024-01271-x

FUNDING: This research was supported by the National Institutes of Health, grant Nos. P50CA217691, P30CA138292, and R33CA291197; and the National Science Foundation, grant No. R35GM151028. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of any funding agency.

COMPETING INTERESTS: Coskun, Cai, and Hu declare a patent application related to the spatial-signaling interactomics assay (U.S. Provisional 63/399,427 and U.S. Application No. 18/452,178).

Additional Media

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An artistic rendering of sub-cellular activity: The cell membrane is seen at the top, nucleus on the bottom/right. Protein pairs are being targeted by antibodies (sets of two). Then antibodies are linked to DNA pieces that glow when proteins were found to be closely interacting with each other. The glowing fluorescence DNA signal is then imaged by a microscope indicating the spatial locations of protein interactions as dots, which researchers use to generate graph models. The straight lines connecting the antibody and protein pairs indicate their graph wiring that gets altered in drug resistance.