An affinity-directed phosphatase, AdPhosphatase, system for targeted protein dephosphorylation. Issue 2 (16th February 2023)
- Record Type:
- Journal Article
- Title:
- An affinity-directed phosphatase, AdPhosphatase, system for targeted protein dephosphorylation. Issue 2 (16th February 2023)
- Main Title:
- An affinity-directed phosphatase, AdPhosphatase, system for targeted protein dephosphorylation
- Authors:
- Simpson, Luke M.
Fulcher, Luke J.
Sathe, Gajanan
Brewer, Abigail
Zhao, Jin-Feng
Squair, Daniel R.
Crooks, Jennifer
Wightman, Melanie
Wood, Nicola T.
Gourlay, Robert
Varghese, Joby
Soares, Renata F.
Sapkota, Gopal P. - Abstract:
- Summary: Reversible protein phosphorylation, catalyzed by protein kinases and phosphatases, is a fundamental process that controls protein function and intracellular signaling. Failure of phospho-control accounts for many human diseases. While a kinase phosphorylates multiple substrates, a substrate is often phosphorylated by multiple kinases. This renders phospho-control at the substrate level challenging, as it requires inhibition of multiple kinases, which would thus affect other kinase substrates. Here, we describe the development and application of the affinity-directed phosphatase (AdPhosphatase) system for targeted dephosphorylation of specific phospho-substrates. By deploying the Protein Phosphatase 1 or 2A catalytic subunits conjugated to an antigen-stabilized anti-GFP nanobody, we can promote the dephosphorylation of two independent phospho-proteins, FAM83D or ULK1, knocked in with GFP-tags using CRISPR-Cas9, with exquisite specificity. By redirecting protein phosphatases to neo-substrates through nanobody-mediated proximity, AdPhosphatase can alter the phospho-status and function of target proteins and thus, offers a new modality for potential drug discovery approaches. Graphical abstract: Highlights: Affinity-directed phosphatase (AdPhosphatase) can mediate protein dephosphorylation AdPhosphatase consists of a target binder conjugated to a phosphatase catalytic subunit Target dephosphorylation by AdPhosphatase requires phosphatase catalytic activity AdPhosphataseSummary: Reversible protein phosphorylation, catalyzed by protein kinases and phosphatases, is a fundamental process that controls protein function and intracellular signaling. Failure of phospho-control accounts for many human diseases. While a kinase phosphorylates multiple substrates, a substrate is often phosphorylated by multiple kinases. This renders phospho-control at the substrate level challenging, as it requires inhibition of multiple kinases, which would thus affect other kinase substrates. Here, we describe the development and application of the affinity-directed phosphatase (AdPhosphatase) system for targeted dephosphorylation of specific phospho-substrates. By deploying the Protein Phosphatase 1 or 2A catalytic subunits conjugated to an antigen-stabilized anti-GFP nanobody, we can promote the dephosphorylation of two independent phospho-proteins, FAM83D or ULK1, knocked in with GFP-tags using CRISPR-Cas9, with exquisite specificity. By redirecting protein phosphatases to neo-substrates through nanobody-mediated proximity, AdPhosphatase can alter the phospho-status and function of target proteins and thus, offers a new modality for potential drug discovery approaches. Graphical abstract: Highlights: Affinity-directed phosphatase (AdPhosphatase) can mediate protein dephosphorylation AdPhosphatase consists of a target binder conjugated to a phosphatase catalytic subunit Target dephosphorylation by AdPhosphatase requires phosphatase catalytic activity AdPhosphatase system can be used to study the role of target protein phosphorylation Abstract : Simpson and Fulcher et al. describe the development of an affinity-directed phosphatase (AdPhosphatase) system to promote targeted dephosphorylation of phosphorylated proteins of interest (POIs). The AdPhosphatase consists of a POI-binding nanobody conjugated to the catalytic subunit of a promiscuous phosphatase (PPP1CA/PPP2CA), which can mediate POI dephosphorylation through proximity in cells. … (more)
- Is Part Of:
- Cell chemical biology. Volume 30:Issue 2(2023)
- Journal:
- Cell chemical biology
- Issue:
- Volume 30:Issue 2(2023)
- Issue Display:
- Volume 30, Issue 2 (2023)
- Year:
- 2023
- Volume:
- 30
- Issue:
- 2
- Issue Sort Value:
- 2023-0030-0002-0000
- Page Start:
- 188
- Page End:
- 202.e6
- Publication Date:
- 2023-02-16
- Subjects:
- affinity-directed phosphatase -- AdPhosphatase -- targeted dephosphorylation -- PPP1CA -- PPP2CA -- nanobody -- ULK1 -- FAM83D
Biochemistry -- Periodicals
572.05 - Journal URLs:
- http://www.cell.com/cell-chemical-biology/home ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.chembiol.2023.01.003 ↗
- Languages:
- English
- ISSNs:
- 2451-9456
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.733000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25952.xml