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Scientists Reveal Intricate Mechanisms Cells Use to Build Protein Destruction Signals

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09/22/2023
phys.org
TR-EM reveals structure of APC/C–CDH1–UBE2C–UBE2SCTP during substrate polyubiquitination. a, Cartoon representation of reaction cycle carried out by the APC/C as it ubiquitinates substrates. The transition from the ‘CRL (cullin–RING) down’ inactive conformation to the ‘CRL up’ active conformation is facilitated by coactivator binding. Initiation of ubiquitination on target substrates is carried out by the recruitment of UBE2C~Ub by the APC2 WHB (winged-helix B) and APC11 RING domains. UBE2S elongates chains initiated by UBE2C. b, Overview of TR-EM approach. Two mixtures containing the reaction components are incubated at room temperature (1). The mixtures are combined to start the reaction (2). Samples are taken from the reaction at timepoints indicated and applied to a grid (3) that is then plunge frozen (4) and imaged using cryo-EM. Representative samples were taken at the time the grids were plunge frozen for SDS–PAGE (5), shown in c. c, Fluorescent monitoring of an SDS–PAGE gel showing APC/CCDH1-E2 (UBE2C or both UBE2C and UBE2S)-dependent substrate modification at each timepoint for which a grid was frozen. At least three experimental replicates were repeated to optimize conditions. Uncropped gel image available in source data. d, 3D reconstruction of particles from the filtered APC/C–CDH1–UBE2C–UBE2S dataset at 3.5 Å showing the active catalytic architecture assembled. Atomic models of key subunits and ubiquitination components fitted into the cryo-EM density, including CDH1 bound to the APC/C scaffold (i and ii), UBE2C clamped by the APC2 WHB and APC11 RING domains (iii), and the UBE2S CTP bound to the groove formed by APC2 (green) and APC4 (light pink) (iv). Credit: Nature Structural & Molecular Biology (2023). DOI: 10.1038/s41594-023-01105-5

Within the intricate molecular landscape inside of a cell, the orchestration of proteins demands precise control to avoid disease. While some proteins must be synthesized at specific times, others require timely breakdown and recycling. Protein degradation is a fundamental process that influences cellular activities such as the cell cycle, cell death, or immune response.

At the core of this process lies the proteasome, a recycling hub in the cell. The proteasome degrades proteins if they carry a molecular tag formed by a chain of ubiquitin molecules. The task of attaching this tag falls to enzymes known as ubiquitin ligases.

This process, known as polyubiquitination, has long been difficult to study due to its rapid and complex nature. To tackle this challenge, scientists at the IMP Research Institute of Molecular Biology in Vienna, the University of North Carolina School of Medicine, and collaborators employed a combination of techniques, integrating cryo-electron microscopy (cryo-EM) with cutting-edge deep learning algorithms.

David Haselbach, Ph.D., a group leader at the IMP, said, "Our aim was to capture polyubiquitination step by step through time-resolved cryo-EM studies. This method allowed us to visualize and dissect the intricate molecular interactions that take place during this process, like in a stop motion movie."

A biochemical timelapse

The study, published in the journal Nature Structural & Molecular Biology, delves into the movements of the Anaphase-Promoting Complex/Cyclosome (APC/C), a ubiquitin ligase that drives the cell cycle. The mechanics behind APC/C's attaching of a ubiquitin signal remained an unsolved puzzle. Haselbach and Nicholas Brown, Ph.D., associate professor of pharmacology at the University of North Carolina School of Medicine, are co-senior authors.

"We had a solid grasp of APC/C's fundamental structure, a prerequisite for time-resolved cryo-EM," said first author Tatyana Bodrug, Ph.D., a postdoctoral pharmacology researcher at UNC-Chapel Hill. "Now we have a much better understanding of its function, every step of the way."

Ubiquitin ligases perform many tasks, including recruiting different substrates, interacting with other enzymes, and forming different types of ubiquitin signals. The scientists visualized interactions between ubiquitin-linked proteins and APC/C and its co-enzymes. They reconstructed the movements undergone by APC/C during polyubiquitination using a form of deep learning called neural networks. This was a first in protein degradation research.

The APC/C is a part of the large family of ubiquitin ligases (more than 600 members) that have yet to be characterized in this manner. Global efforts will keep pushing the boundaries of this field.

"A key to the success of our work was collaboration with several other teams," said Brown, also a member of the UNC Lineberger Comprehensive Cancer Center. "At Princeton University, Ellen Zhong's software and programming contributions were key to uncovering new insights about the APC/C mechanism. Subsequent validation of these findings required the help of several other groups led by Drs Harrison, Steimel, Hahn, Emanuele, and Zhang. "A team effort was crucial to push our research over the finish line."

The significance of this research extends beyond its immediate impact, paving the way for future explorations into the regulation of ligases, ultimately promising deeper insights into the mechanisms underpinning protein metabolism important for human health and diseases, such as many forms of cancer.

More information: Bodrug, T. et al. Time-resolved cryo-EM (TR-EM) analysis of substrate polyubiquitination by the RING E3 anaphase-promoting complex/cyclosome (APC/C), Nature Structural & Molecular Biology (2023). DOI: 10.1038/s41594-023-01105-5. www.nature.com/articles/s41594-023-01105-5

Citation: Scientists reveal intricate mechanisms cells use to build protein destruction signals (2023, September 21) retrieved 21 September 2023 from https://phys.org/news/2023-09-scientists-reveal-intricate-mechanisms-cells.html

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