|Title||Cryo-EM structures demonstrate human IMPDH2 filament assembly tunes allosteric regulation.|
|Journal, issue, pages||Elife, Vol. 9, Year 2020|
|Publish date||Jan 30, 2020|
|Authors||Matthew C Johnson / Justin M Kollman /|
|PubMed Abstract||Inosine monophosphate dehydrogenase (IMPDH) mediates the first committed step in guanine nucleotide biosynthesis and plays important roles in cellular proliferation and the immune response. IMPDH ...Inosine monophosphate dehydrogenase (IMPDH) mediates the first committed step in guanine nucleotide biosynthesis and plays important roles in cellular proliferation and the immune response. IMPDH reversibly polymerizes in cells and tissues in response to changes in metabolic demand. Self-assembly of metabolic enzymes is increasingly recognized as a general mechanism for regulating activity, typically by stabilizing specific conformations of an enzyme, but the regulatory role of IMPDH filaments has remained unclear. Here, we report a series of human IMPDH2 cryo-EM structures in both active and inactive conformations. The structures define the mechanism of filament assembly, and reveal how filament-dependent allosteric regulation of IMPDH2 makes the enzyme less sensitive to feedback inhibition, explaining why assembly occurs under physiological conditions that require expansion of guanine nucleotide pools. Tuning sensitivity to an allosteric inhibitor distinguishes IMPDH from other metabolic filaments, and highlights the diversity of regulatory outcomes that can emerge from self-assembly.|
|External links||Elife / PubMed:31999252 / PubMed Central|
|Methods||EM (single particle)|
|Resolution||2.95 - 7.13 Å|
|Keywords||BIOSYNTHETIC PROTEIN / metabolism / filament / allostery / adenine / guanine|
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