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7ABV

Structure of the S1-cleaved mouse Notch1 Negative Regulatory Region (NRR)

Summary for 7ABV
Entry DOI10.2210/pdb7abv/pdb
DescriptorNeurogenic locus notch homolog protein 1, CALCIUM ION, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
Functional Keywordssignaling protein, type i transmembrane protein, developmental protein, calcium binding
Biological sourceMus musculus (Mouse)
Total number of polymer chains1
Total formula weight32060.59
Authors
Zeronian, M.R.,Janssen, B.J.C. (deposition date: 2020-09-08, release date: 2021-07-07, Last modification date: 2024-11-20)
Primary citationZeronian, M.R.,Klykov, O.,Portell I de Montserrat, J.,Konijnenberg, M.J.,Gaur, A.,Scheltema, R.A.,Janssen, B.J.C.
Notch-Jagged signaling complex defined by an interaction mosaic.
Proc.Natl.Acad.Sci.USA, 118:-, 2021
Cited by
PubMed Abstract: The Notch signaling system links cellular fate to that of its neighbors, driving proliferation, apoptosis, and cell differentiation in metazoans, whereas dysfunction leads to debilitating developmental disorders and cancers. Other than a five-by-five domain complex, it is unclear how the 40 extracellular domains of the Notch1 receptor collectively engage the 19 domains of its canonical ligand, Jagged1, to activate Notch1 signaling. Here, using cross-linking mass spectrometry (XL-MS), biophysical, and structural techniques on the full extracellular complex and targeted sites, we identify five distinct regions, two on Notch1 and three on Jagged1, that form an interaction network. The Notch1 membrane-proximal regulatory region individually binds to the established Notch1 epidermal growth factor (EGF) 8-EGF13 and Jagged1 C2-EGF3 activation sites as well as to two additional Jagged1 regions, EGF8-EGF11 and cysteine-rich domain. XL-MS and quantitative interaction experiments show that the three Notch1-binding sites on Jagged1 also engage intramolecularly. These interactions, together with Notch1 and Jagged1 ectodomain dimensions and flexibility, determined by small-angle X-ray scattering, support the formation of nonlinear architectures. Combined, the data suggest that critical Notch1 and Jagged1 regions are not distal but engage directly to control Notch1 signaling, thereby redefining the Notch1-Jagged1 activation mechanism and indicating routes for therapeutic applications.
PubMed: 34301900
DOI: 10.1073/pnas.2102502118
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.065 Å)
Structure validation

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