Stochastic ordering of complexoform protein assembly by genetic circuits.
Ontology highlight
ABSTRACT: Top-down proteomics has enabled the elucidation of heterogeneous protein complexes with different cofactors, post-translational modifications, and protein membership. This heterogeneity is believed to play a previously unknown role in cellular processes. The different molecular forms of a protein complex have come to be called "complex isoform" or "complexoform". Despite the elucidation of the complexoform, it remains unclear how and whether cellular circuits control the distribution of a complexoform. To help address this issue, we first simulate a generic three-protein complexoform to reveal the control of its distribution by the timing of gene transcription, mRNA translation, and protein transport. Overall, we ran 265 computational experiments: each averaged over 1,000 stochastic simula
SUBMITTER: Jensen MH
PROVIDER: S-EPMC7351240 | biostudies-literature | 2020 Jun
REPOSITORIES: biostudies-literature
ACCESS DATA