Multifunctional activity-based chemical probes for sirtuins. Issue 17 (14th April 2023)
- Record Type:
- Journal Article
- Title:
- Multifunctional activity-based chemical probes for sirtuins. Issue 17 (14th April 2023)
- Main Title:
- Multifunctional activity-based chemical probes for sirtuins
- Authors:
- Sharma, Chiranjeev
Donu, Dickson
Curry, Alyson M.
Barton, Elizabeth
Cen, Yana - Abstract:
- Abstract : Multifunctional activity-based chemical probes enable sirtuin labeling, affinity capture, PROTAC construction, and inhibitor discovery. Abstract : The sirtuin family of NAD + -dependent protein deacylases has gained significant attention during the last two decades, owing to their unique enzymatic activities as well as their critical roles in a broad array of cellular events. Innovative chemical probes are heavily pursued for the functional annotation and pharmacological perturbation of this group of "eraser" enzymes. We have developed several series of activity-based chemical probes (ABPs) to interrogate the functional state of active sirtuins in complex biological samples. They feature a simple Ala–Ala–Lys tripeptide backbone with a thioacyl "warhead", a photoaffinity group (benzophenone or diazirine), and a bioorthogonal group (terminal alkyne or azido) for conjugation to reporters. When applied in a comparative fashion, these probes reveal the changes of active sirtuin contents under different physiological conditions. Additionally, they can also be utilized in a competitive manner for inhibitor discovery. The Nobel-winning "click" conjugation to a fluorophore allows the visualization of the active enzymes, while the covalent adduct to a biotin leads to the affinity capture of the protein of interest. Furthermore, the "clickable" tag enables the easy access to proteolysis targeting chimeras (PROTACs) that effectively degrade human SIRT2 in HEK293 cells, albeitAbstract : Multifunctional activity-based chemical probes enable sirtuin labeling, affinity capture, PROTAC construction, and inhibitor discovery. Abstract : The sirtuin family of NAD + -dependent protein deacylases has gained significant attention during the last two decades, owing to their unique enzymatic activities as well as their critical roles in a broad array of cellular events. Innovative chemical probes are heavily pursued for the functional annotation and pharmacological perturbation of this group of "eraser" enzymes. We have developed several series of activity-based chemical probes (ABPs) to interrogate the functional state of active sirtuins in complex biological samples. They feature a simple Ala–Ala–Lys tripeptide backbone with a thioacyl "warhead", a photoaffinity group (benzophenone or diazirine), and a bioorthogonal group (terminal alkyne or azido) for conjugation to reporters. When applied in a comparative fashion, these probes reveal the changes of active sirtuin contents under different physiological conditions. Additionally, they can also be utilized in a competitive manner for inhibitor discovery. The Nobel-winning "click" conjugation to a fluorophore allows the visualization of the active enzymes, while the covalent adduct to a biotin leads to the affinity capture of the protein of interest. Furthermore, the "clickable" tag enables the easy access to proteolysis targeting chimeras (PROTACs) that effectively degrade human SIRT2 in HEK293 cells, albeit at micromolar concentrations. These small molecule probes offer unprecedented opportunities to investigate the biological functions and physiological relevance of the sirtuin family. … (more)
- Is Part Of:
- RSC advances. Volume 13:Issue 17(2023)
- Journal:
- RSC advances
- Issue:
- Volume 13:Issue 17(2023)
- Issue Display:
- Volume 13, Issue 17 (2023)
- Year:
- 2023
- Volume:
- 13
- Issue:
- 17
- Issue Sort Value:
- 2023-0013-0017-0000
- Page Start:
- 11771
- Page End:
- 11781
- Publication Date:
- 2023-04-14
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d3ra02133e ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 27104.xml