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Macromolecular assembly depends on tightly regulated pairwise binding interactions that are selectively favored at assembly sites while being disfavored in the soluble phase. This selective control can arise due to molecular density-enhanced binding, as recently found for the kinetochore scaffold protein CENP-T. When clustered, CENP-T recruits markedly more Ndc80 complexes than its monomeric counterpart, but the underlying molecular basis remains elusive. Here, we use quantitative
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Ekaterina V. Tarasovetc
University of Pennsylvania
Gunter B. Sissoko
Whitehead Institute for Biomedical Research
Anna S. Mukhina
University of Pennsylvania
Massachusetts Institute of Technology
University of Pennsylvania
Whitehead Institute for Biomedical Research
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Tarasovetc et al. (Mon,) studied this question.
synapsesocial.com/papers/68e778e0b6db6435876ede1c — DOI: https://doi.org/10.1101/2024.02.25.581584
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