← Resources / Application notes
App note
Checking the Activity of Protein Reference Materials
A concentration measurement tells you how much protein is in the vial. SPR tells you whether it still binds its partner, and how strongly.
The need
Serology tests from different makers use different antigens and antibodies, so their results are hard to compare. Shared reference materials fix that, but only if each vial holds a protein that is pure, at a known concentration, stable in storage, and still able to bind. The first three can be measured by chromatography, mass spectrometry and UV absorbance. The last one needs a binding measurement.
The same question comes up in every lab that buys or makes proteins: a new lot of antigen, an antibody from a new supplier, a protein after six months in the freezer. Is it still active?
How it works
The ACE2 protein carries one biotin at a single site. On a biotin sensor with a streptavidin layer, every ACE2 molecule is captured the same way, with its binding site facing out. The spike protein then flows over the surface at increasing concentrations, and the sensorgrams give the rates of binding and release, and from them the affinity (KD) (Figure 1).
What the study showed
| Result | |
|---|---|
| Omicron BA.4/5 spike reference material on ACE2 | KD ≈ 4.4 nM, consistent with published values: the material is active |
| Compared with the original (ancestral) spike reference material | About 4 times tighter binding |
| Where the difference comes from | Mostly a slower release from ACE2, not a faster binding |
That last point is why kinetics matter for QC. Two proteins can look similar in an end-point assay and still behave differently: here the Omicron spike stays bound more than twice as long (Figure 2).
Full method and data: Stocks et al., Analytical and Bioanalytical Chemistry 2024 (reference below).
Why Affinité SPR fits protein QC
| What a QC lab needs | What Affinité SPR brings |
|---|---|
| Proof of activity, not just quantity | Direct binding to the protein's real partner, label-free |
| A number to compare lots | Rates and KD, so a change in binding or release shows up even when an end-point signal does not |
| The same surface every time | Biotin Sensor and Streptavidin Kit for oriented, single-point capture of biotinylated proteins |
| Measurements in your own lab | Benchtop flow system: the P4PRO with the AffiPump |
| A reference in every run | Several sensing channels, so a reference channel runs alongside the sample |
Beyond reference materials
The same check works for any protein with a known partner: antigen lots for an immunoassay, antibodies from a new supplier, in-house recombinant proteins after purification or storage. For antibodies, see also our note on rapid quality control of antibodies. For planning the experiment itself, see TN-07, designing a binding experiment.
What you need
| Item | Source |
|---|---|
| P4PRO with AffiPump | Affinité Instruments |
| Biotin Sensor (SAMBT-01) and Streptavidin Kit (STRP-KIT) | Affinité Instruments |
| Biotinylated ligand (here: ACE2, biotinylated at one site) | Your protein, or a commercial biotinylated version |
| Analyte in a dilution series | The protein lot you want to check |
| Running buffer with surfactant; BSA to block the surface | Standard reagents |
Reference
- B. B. Stocks, M.-P. Thibeault, D. L'Abbé, M. Umer, Y. Liu, M. Stuible, Y. Durocher, J. E. Melanson, "Characterization of biotinylated human ACE2 and SARS-CoV-2 Omicron BA.4/5 spike protein reference materials," Analytical and Bioanalytical Chemistry, vol. 416, pp. 4861–4872, 2024. doi:10.1007/s00216-024-05413-7 (open access, CC BY 4.0).
Illustrations by Affinité Instruments. Figure 2 is simulated from the rate constants in the reference above, not measured data.
