SARS-CoV-2 nsp3 macrodomain Time-Resolved FRET peptide displacement assay

Haim Barr, Noa Lahav

Published: 2024-04-25 DOI: 10.17504/protocols.io.eq2ly7r2mlx9/v3

Disclaimer

The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Abstract

This protocol details the Time-Resolved FRET (TR-FRET) assay for SARS-CoV-2 nsp3 macrodomain (Mac1) binding of adenosine diphosphate (ADP)–ribosylated (ADPr) peptide. This method is intended to measure the activity of Mac1 by using a specific ADPr-modified peptide that allows the detection of binding. When bound, the biotinylated-peptide and the HIS-tagged Mac1 form a proximity complex that is detected by TR-FRET using Streptavidin-Eu Cryptate and anti-HIS-XL665 as a donor/acceptor pair. Excitation of the Eu Cryptate complex at 325 nm emits a resonant energy of 625 nm which in turn excites the XL665 to emit fluorescence at 665 nm. This energy transfer occurs only when ADPr modified peptide is in sufficient proximity to Mac1 and inhibitors which displace the peptide will prevent energy transfer. Binding activity is reported as the ratio of Acceptor/Donor (Em/Em) X 10,000.


Experiment Concentrations (From Stock to Assay)

ABCDE
ReagentStockLoaded into CombiFinal in assay plateUnits
His-SARS CoV-2 MAC11830005012.5nM
Substrate (Biotin-ADPr)100000001600400nM
Detection solution
Streptavidin-XL665 (SA-XL)10.250.125%
MAb Anti-6HIS-Eu cryptate Gold1000.250.125%
Assay buffer
HEPES pH=7.02502525mM
NaCl2002020mM
BSA0.50.050.05mg/ml
Tween 200.50.050.05%
HTRF PPI Europium Detection Buffer1001010%

For more information, please check out the "Materials" Section

Compound Plate Design for Dose Response:

Total Assay Volume: 16 µL

 **Compounds Top Assay Concentration:** 100 µM



 **Dilution Factor:**  3



 **Dose Response Points:** 10



**Number of Replicates:**  2

Backfill with DMSO: Yes

Compounds Plate Design for 2-Point Assay:

Total Assay Volume: 16 µL

 **Compounds Assay Concentration:** 100 µM and 50 µM



 **Dilution Factor:**  2



 **Dose Response Points:** 2



**Number of Replicates:**  2

Backfill with DMSO: Yes

Before start

Note: Inhibitor compounds stock concentration is 20millimolar (mM). Compounds are pre-dispensed into 384 plates and stored at -20˚C until use.

Steps

Prepare Reagents

1.

PREPARE all of the reagents/buffers required for this experiment.

Assay Buffer

ABCDE
ReagentStockLoaded into CombiFinal in assay plateUnits
HEPES pH=7.02502525mM
NaCl2002020mM
BSA0.50.050.05mg/ml
Tween 200.50.050.05%
HTRF PPI Europium detection buffer1001010%

Reagents (dilute reagents in assay buffer for required volume)

ABCDE
ReagentStockLoaded into CombiFinal in assay plateUnits
His-SARS-CoV-2 MAC11830005012.5nM
Substrate (Biotin-ADPr)100000001600400nM

Detection Solution (dilute reagents in assay buffer for required volume)

ABCDE
ReagentStockLoaded into CombiFinal in assay plateUnits
Streptavidin-XL665 (SA-XL)10.250.125%
MAb Anti-6HIS-Eu cryptate Gold1000.250.125%

Prepare 384-well Plate

2.

PRIME Multi-Drop Combi Tube Dispensing Cassette with Assay Buffer by selecting the PRIME button on the Combi Dispenser until the tubes are filled completely.

  • Note: Be sure to cycle dispensing several times on a a clean plate lid (This confirms there are no bubbles in the Dispensing Cassette).
2.1.

DISPENSE 4µL to Columns 1 and 23 of assay plate

  • Note: These will represent the inhibitor control columns
2.2.

EMPTY Multi-Drop Combi Tube Dispensing Cassette (by selecting the EMPTY button on the Combi Dispenser until the tubes of the cassette are emptied). Discard the Assay Buffer discharged from the cassette.

3.

PRIME Multi-Drop Combi Tube Dispensing Cassette with His-SARS COV2 MAC1 Enzyme by selecting the PRIME button on the Combi Dispenser until the tubes are filled completely.

  • Note: Be sure to cycle dispensing several times on a a clean plate lid (This confirms there are no bubbles in the Dispensing Cassette).
3.1.

DISPENSE 4µL 50nanomolar (nM) to Columns 2-22 and 24 of assay plate

Note:

  • 50nanomolar (nM) is four times the final concentration for the assay. It will be diluted to be a final concentration of 12.5nanomolar (nM)
  • Column 2 and Column 24 are neutral control columns (Contain: Enzyme, Substrate, DMSO; no experimental compounds )
3.2.

EMPTY Multi-Drop Combi Tube Dispensing Cassette (by selecting the EMPTY button on the Combi Dispenser until the tubes of the cassette are emptied). Discard the 50nanomolar (nM) discharged from the cassette.

4.

PRIME Multi-Drop Combi Tube Dispensing Cassette with Assay Buffer by selecting the PRIME button on the Combi Dispenser until the tubes are filled completely. Then, EMPTY the Multi-Drop Combi Tube Dispensing Cassette (by selecting the EMPTY button on the Combi Dispenser until the tubes of the cassette are emptied). Discard the Assay Buffer discharged from the cassette.

5.

CENTRIFUGE plate 1500rpm to remove bubbles

6.

INCUBATE plate for 0h 15m 0s atRoom temperature

7.

PRIME Multi-Drop Combi Tube Dispensing Cassette with1600nanomolar (nM) by selecting the PRIME button on the Combi Dispenser until the tubes are filled completely.

  • Note: Be sure to cycle dispensing several times on a a clean plate lid (This confirms there are no bubbles in the Dispensing Cassette).
7.1.

DISPENSE 4µL 1600nanomolar (nM) into Columns 1-24 (full plate)

Note:

  • 1600nanomolar (nM) is four times the final concentration for the assay. It will be diluted to be a final concentration of400nanomolar (nM)
7.2.

EMPTY Multi-Drop Combi Tube Dispensing Cassette (by selecting the EMPTY button on the Combi Dispenser until the tubes of the cassette are emptied). Discard the 1600nanomolar (nM) discharged from the cassette.

8.

CENTRIFUGE plate 1500rpm to remove bubbles

9.

PRIME Multi-Drop Combi Tube Dispensing Cassette with Assay Buffer by selecting the PRIME button on the Combi Dispenser until the tubes are filled completely. Then, EMPTY the Multi-Drop Combi Tube Dispensing Cassette (by selecting the EMPTY button on the Combi Dispenser until the tubes of the cassette are emptied). Discard the Assay Buffer discharged from the cassette.

10.

PRIME Multi-Drop Combi Tube Dispensing Cassette with 0.25% volume by selecting the PRIME button on the Combi Dispenser until the tubes are filled completely.

  • Note: Be sure to cycle dispensing several times on a a clean plate lid (This confirms there are no bubbles in the Dispensing Cassette).
10.1.

DISPENSE 8µL 0.25% volume into full plate

Note:

  • 0.25% volume is two times the final concentration for the assay. It will be diluted to be a final concentration of 0.125% volume
10.2.

EMPTY Multi-Drop Combi Tube Dispensing Cassette (by selecting the EMPTY button on the Combi Dispenser until the tubes of the cassette are emptied). Discard the 1600nanomolar (nM) discharged from the cassette.

11.

CENTRIFUGE 1500rpm plate to remove bubbles

12.

INCUBATE plate for 1h 0m 0s at Room temperature

Recommended: Clean/Empty the Multi-Drop Combi Reagent Dispenser and Dispensing Cassette during this incubation step

Read Plate Fluorescence

13.

READ and RECORD the plate Relative fluorescence units (RFU) via the " Mac1 Protocol " on the PHERAstar FS Control Software.

Equipment

ValueLabel
PHERAstar FSNAME
Microplate readerTYPE
BMG LABTECHBRAND
0471B0001ASKU

Citation
Donor 325/620 ex/em should be ~ 5000 . Acceptor ~ 3000

Diagram of assay

14.

Figure 1 graphical depiction of assay principal and its use in screening campaign

Principal of ADPr peptide displacement assayA - Binding of ADPr-modified peptide to Mac1 protein B- Detection reagents added to protein+peptide complex C- TR-FRET detects binding of peptide to Mac1 if proximity of donor and acceptor detection reagents is sufficient to enable resonant energy transfer D- Inhibitor compounds are detected by reduced TR-FRET signal when inhibitor displaces/prevents binding of ADPr-peptide to Mac1
Principal of ADPr peptide displacement assayA - Binding of ADPr-modified peptide to Mac1 protein B- Detection reagents added to protein+peptide complex C- TR-FRET detects binding of peptide to Mac1 if proximity of donor and acceptor detection reagents is sufficient to enable resonant energy transfer D- Inhibitor compounds are detected by reduced TR-FRET signal when inhibitor displaces/prevents binding of ADPr-peptide to Mac1

Experimental Design

15.
384 plate layout
384 plate layout

Keywords

16.

Mac1, Nsp3, TR-FRET, HTRF, ADPr, Displacement, Screening, Assay, Inhibitor, Fragment, Binding, Macrodomain

推荐阅读

Nature Protocols
Protocols IO
Current Protocols
扫码咨询