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Agglomeration: when folded proteins clump together.

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Romero-Romero,  M. Luisa
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Romero-Romero, M. L., & Garcia-Seisdedos, H. (2023). Agglomeration: when folded proteins clump together. Biophysical reviews, 15(6), 1987-2003. doi:10.1007/s12551-023-01172-4.


Cite as: https://hdl.handle.net/21.11116/0000-000E-AAA0-D
Abstract
Protein self-association is a widespread phenomenon that results in the formation of multimeric protein structures with critical roles in cellular processes. Protein self-association can lead to finite protein complexes or open-ended, and potentially, infinite structures. This review explores the concept of protein agglomeration, a process that results from the infinite self-assembly of folded proteins. We highlight its differences from other better-described processes with similar macroscopic features, such as aggregation and liquid-liquid phase separation. We review the sequence, structural, and biophysical factors influencing protein agglomeration. Lastly, we briefly discuss the implications of agglomeration in evolution, disease, and aging. Overall, this review highlights the need to study protein agglomeration for a better understanding of cellular processes.