Automated Protein Quantification with the Biomek-FX Liquid Handler System

Yan Chen, Nurgul Kaplan Lease, Jennifer Gin, Tad Ogorzalek, Christopher J Petzold

Published: 2021-10-12 DOI: 10.17504/protocols.io.bsyynfxw

Abstract

This protocol details steps to perform the protein quantification (Lowry-based) assay by using a Biomek FX liquid handler system. It is optimized to assay a full 96-well plate of protein samples in duplicate with a separate (control) plate for BSA standards. You will need a plate reader to measure the samples and standards.

This protocol works best as part of a full proteomic sample preparation workflow with:

Automated Chloroform-Methanol Protein Extraction on the Biomek-FX Liquid Handler System

and

Automated Protein Normalization and Tryptic Digestion on a Biomek-FX Liquid Handler System

Before start

Prepare BSA Standards Plate (1st 4 rows from A to D):

  1. Add 40 uL of H2O into wells A1 to D1.

  2. Add 40 uL of BSA Standards 1 (125 ug/mL) to 7 (2000 ug/mL) into columns 2 to 8. For this protocol you will need:

  3. Beckman-Coulter Biomek FX liquid handler system with a 96-pod head.

  4. Upload the attached method file and modify it to fit your deck and system configuration. Modular Protein Quantitation method.bmf

Steps

Deck Setup

1.

Open Biomek Software that controls Biomek-FX liquid handler system. Under "File" drop down click "Open" to select the automation method "Modular Protein Quantitation method"

Note
Because different deck orientations and system components are possible, you will need to modify the method file (attached in the 'Before start' section) for your specific Biomek liquid handler system.

2.

Click on "Instrument Setup" under the "Setup" group node to get visual instruction of how to set up the deck.

3.

Set up the deck (refer to the deck setup picture below):

ABC
Deck LabelLabwareReagent
proteinPCR96 plate (BIO-RAD, Cat.#HSP9601)unknown amount of protein to quantify
titratePCR96 plate (BIO-RAD, Cat.#HSP9601)
BSA standardsPCR96 plateBSA Standards (Thermo Fisher, Cat.#23208)
tips1,220 µl pipet tips (Molecular Bioproducts BioRobotix, Cat.#918-262 )
tips 3,5200 uL pipet tips (Molecular Bioproducts BioRobotix, Cat.#919-262 )
control read, prot read 1, prot read 2Black Microplate (Fisher Scientific, Cat.#07-200-567)
Buffer AReservoir Microplate (Agilent, Cat.#201254-100)DC Protein Assay Reagent A (Bio-rad Laboratories, Cat.#500-0113)
waterReservoir Microplate (Agilent, Cat.#201254-100)LC-MS grade Water (VWR Scientific, Cat.#BJLC365-2.5)
Buffer B96 Deep Well Reagent Reservoir (VWR, Cat.#101100-962)DC Protein Assay Reagent B (Bio-rad Laboratories, Cat.#500-0114)

Materials for Deck setup

Deck setup
Deck setup
Labware for Deck setup
Labware for Deck setup
4.

MANUAL STEP: Use a multichannel pipette to mix protein samples right before starting.

5.

Click the "Run" button (green arrow) to start.

DC protein assay

6.

Transfer 25 µl of Buffer A to Protein Read Plate 1, Protein Read Plate 2, and Control Read Plate.

7.

Transfer 20 µl of H2O into Titrate Plate. Then transfer 5 µl from protein plate to titrate plate and mix on deck.

Note
Note: The dilution factor could be altered as needed by changing the volumes of water and proteins transferred to the titration plate. Be sure to multiply the protein quant results by the dilution factor before you do your normalization calculation.

8.

Transfer 5 µl of protein from Titrate Plate to Protein Read Plate 1 and Protein Read Plate 2.

9.

Transfer 5 µl from BSA Standard plate to Control Read Plate.

Note
Prepare BSA Standards Plate (1st 4 rows from A to D):Add 40 µl of H2O into wells A1 to D1.Add 40 µl of BSA Standards 1 (125 µg/ml) to 7 (2000 µg/ml) into columns 2 to 8.

10.

Method will pause until user resume it again. Set a timer for 5 minutes.

11.

After 5 min., click OK to resume method

12.

Transfer 200 µl from Buffer B to the 3 Read Plates and incubate for 0h 10m 0s .

The method will pause until user resume it again. Set up a 10 minutes timer and click OK afterwards to finish.

Spectrophotometer reading for protein Quantification

13.

Transfer plates to the microplate reader (MD Spectramax 250) to read absorbance at 750 nm and calculate protein concentration.

14.

Read "control read" plate.

ABC
SampleConcentrationMean OD Value (Absorbance)
St011250.024
St022500.042
St035000.090
St047500.138
St0510000.165
St0615000.239
St0720000.281

Standards (µg/ml)

Example Standard Curve
Example Standard Curve
15.

Read "prot read 1" and "prot read 2" plates.

AB
SampleConcentration
Un88585.249
Un89785.257
Un90670.135
Un91718.864
Un92868.962
Un93679.907
Un94743.064
Un95994.173
Un961115.072

Data concentrations example

Note
Remember to multiply the protein concentrations by five (5) to account for the five-fold dilution in Step #3.

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