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  FICD activity and AMPylation remodelling modulate human neurogenesis

Kielkowski, P., Buchsbaum, I. Y., Kirsch, V. C., Bach, N. C., Drukker, M., Cappello, S., et al. (2020). FICD activity and AMPylation remodelling modulate human neurogenesis. NATURE COMMUNICATIONS, 11(1): 517. doi:10.1038/s41467-019-14235-6.

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 Creators:
Kielkowski, Pavel, Author
Buchsbaum, Isabel Y.1, Author           
Kirsch, Volker C., Author
Bach, Nina C., Author
Drukker, Micha, Author
Cappello, Silvia1, Author           
Sieber, Stephan A., Author
Affiliations:
1Max Planck Research Group Developmental Neurobiology (Silvia Cappello), Max Planck Institute of Psychiatry, Max Planck Society, ou_2173645              

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Free keywords: POSTTRANSLATIONAL MODIFICATIONS; ENDOPLASMIC-RETICULUM; PROTEIN; MECHANISM; PROTEOMICS; DIVERSITY; DISCOVERY; REVEALS; GTPASES; ENZYMEScience & Technology - Other Topics;
 Abstract: Posttranslational modification (PTM) of proteins represents an important cellular mechanism for controlling diverse functions such as signalling, localisation or protein-protein interactions. AMPylation (also termed adenylylation) has recently been discovered as a prevalent PTM for regulating protein activity. In human cells AMPylation has been exclusively studied with the FICD protein. Here we investigate the role of AMPylation in human neurogenesis by introducing a cell-permeable propargyl adenosine pronucleotide probe to infiltrate cellular AMPylation pathways and report distinct modifications in intact cancer cell lines, human-derived stem cells, neural progenitor cells (NPCs), neurons and cerebral organoids (COs) via LC-MS/MS as well as imaging methods. A total of 162 AMP modified proteins were identified. FICD-dependent AMPylation remodelling accelerates differentiation of neural progenitor cells into mature neurons in COs, demonstrating a so far unknown trigger of human neurogenesis.

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Language(s): eng - English
 Dates: 2020
 Publication Status: Published online
 Pages: 13
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Degree: -

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Title: NATURE COMMUNICATIONS
Source Genre: Journal
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Publ. Info: MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND : NATURE PUBLISHING GROUP
Pages: - Volume / Issue: 11 (1) Sequence Number: 517 Start / End Page: - Identifier: ISSN: 2041-1723