VHH (variable domain heavy/heavy chain antibodies, lacking in light chains) single domain antibodies have high affinity, stability, productivity, and processability for antigens. These antibodies will highly likely offer a next-generation drug discovery modality. The storage environment may correspond to a loss of activity if the structure of a therapeutic antibody changes with temperature or freeze/thaw cycles. Therefore, it is essential to evaluate the structural stability in order to maintain quality control. Antibody based drugs are typically stored in a refrigerated or frozen state, but this may lead to denaturation from changes in temperature or repeated freezing and thawing.
FTIR spectroscopy has been widely used to evaluate the structure of proteins such as VHH antibodies. Secondary structure estimation (SSE) of α-Helices and β-Sheets can be performed quickly and easily. In this application note we discuss the results of FTIR measurements of secondary structure changes caused by the cooling process and repeated freezing and thawing of a VHH antibody that binds to the novel coronavirus (SARS-CoV-2).
Three Species of Anti SARS-CoV-2 VHH*1
No.1 (6.27 mg/mL)
No.2 (7.22 mg/mL)
No.3 (5.15 mg/mL)
Buffer: 20 mM PBS
Structural change caused by the cooling process
An FT/IR-6600 spectrometer fitted with ATR PRO ONE (cooling option) to cover a temperature range from room temperature to -10 ºC was used for the measurement (Figure 1). For sample No.1, IR spectra were measured at a range of temperatures from room temperature to just above freezing, and the secondary structure was estimated.
Figure 1. FT/IR-6600 + ATR PRO ONE with cooling option
|ATR PRO ONE with cooling option
|Band path filter (< 2000 cm-1)
Figure 2 shows the percentage of α-Helix and β-Sheet structures at each temperature. The VHH antibody (sample No.1) is considered to have high stability during cooling, because the secondary structure does not change significantly during the cooling process.
Figure 2. Changes in secondary structure of VHH antibody No. 1 during the cooling process
Structural changes during repeated freezing and thawing
Samples Nos. 1, 2 and 3 were frozen to -25 ºC, thawed, and measured at room temperature. Freeze/thawing was repeated 3 times. The freezing time was set to 2 hours for the first cycle and 90 hours for the second and third cycles. In order to measure a small amount of sample with high sensitivity, a pentagonal prism multi-reflection ATR (ATR PRO PENTA) was used (Figure 3.).
Figure 3. ATR PRO PENTA
|ATR PRO PENTA
|MCT (PV type)
Figure 4 shows the difference spectrum between the sample and the buffer before freezing. The Amide I and Amide II bands were confirmed clearly even in a small amount (a few μL) of diluted aqueous protein solution.
Figure 4. Difference spectrum between the VHH antibody and buffer
Figure 5 shows the SSE result using the ATR corrected difference spectrum. Numerical values in the figure are mean values for n = 3 and error bars are standard deviations. The secondary structures of the three VHH antibody samples used here were similar, and it was confirmed that the secondary structure of all three VHH antibodies did not change significantly after three freeze/thaw cycles.
Figure 5. Changes in secondary structure of VHH antibody by repeated freezing and thawing
New corona virus, SARS-CoV-2, COVID-19, Biopharmaceuticals, Antibody drug, BioSimilar, VHH antibody, HOS, Secondary Structure, Tertiary Structure
It was found that the VHH antibody used in this experiment does not significantly change its secondary structure during the cooling process nor freezing and thawing, demonstrating high structural stability against cooling. We believe that similar systems can be used not only for stability of antibody drugs against environmental changes but also for other evaluations, such as reactivity with other components.
*1: VHH antibody was kindly provided by RePHAGEN https://rephagen.com/