Biological buffer solution, a mixture of weak acid and its conjugate base, is used to maintain pH when a moderate amount of acid and base is added to it. Tris-HCl buffer is one of the most widely used buffers in biochemistry and molecular biology because of its high stability and compatibility [1]. In particular, Tris-HCl buffer in the range of pH 7.0-9.0 has been used as a neutralizing buffer to maintain optimum pH for various biological processes such as unzipping and hybridization of DNA [2], conformational dynamics of DNA including bending, cleavage and breathing processes of enzymatic proteins [3-5]. For biomedical applications, Tris-HCl buffer has also been used in sequence-specific DNA biosensors and protein biochips for disease screening and diagnosis [6-11].
THz dielectric spectroscopy (THz-TDS) has recently been used to study spectroscopic information of various biomolecules and biomedical tissues since it can probe molecular vibration and hydration dynamics of biomolecules such as RNA, DNA, and proteins [12-15]. Almost all of these THz measurements have been performed in biological buffers, not in pure water. However, in spite of the physiological importance of pH environment, there have been only a few studies on biological buffers at THz frequencies [16-18], and the THz dielectric property of Tris-HCl buffer has not been reported so far. The biochemical change of solute molecules in a buffer solution usually yields only a small difference in the THz dielectric property of an aqueous solution. For example, with commonly encountered dilute DNA solutions, it is very challenging to probe the conformational changes of DNAs and proteins by THz-TDS. The THz permittivity is usually obtained from THz transmission coefficient using a theoretical model based on effective medium approximation where biomolecules with hydration layers (inclusions) are randomly distributed in a buffer solution (background medium) [19-21]. Therefore, it is necessary to precisely characterize the THz dielectric properties of the buffer solution, especially for a low concentration of biomolecules. In this work, we performed high-precision THz-TDS to obtain THz complex dielectric functions of Tris-HCl buffer and pure water.
II. EXPERIMENTAL RESULTS AND DISCUSSION
We used purified water (DEPC-treated and sterile filtered, Sigma Aldrich) to prepare 10 mM Tris-HCl buffer solution with a pH of 7.4 at 25℃. THz pulses were generated using an InAs wafer pumped by a Ti:sapphire laser with a pulse width of 100 fs, and detected by a photoconductive antenna fabricated on a low-temperature-grown GaAs substrate. A quartz liquid cell was placed at the focal point of the THz beam between two off-axis parabolic mirrors in a transmission geometry. To prevent the absorption of THz radiation by atmospheric water vapor, the entire THz-TDS system was enclosed in a chamber that was continuously purged with dry air during the measurements.
The liquid cell consists of two fused quartz plates with a small gap. The THz absorption of water has a strong absorption coefficient (~200 cm−1 at 1 THz), and the gap thickness should be chosen carefully to ensure high sensitivity of THz-TDS. In this work, we used a 50 μm gap for the optimum sensitivity of THz-TDS. As a calibration procedure, we first measured THz transmission coefficient of the liquid cell with an air gap to obtain the THz complex dielectric functions of the fused quartz by using transfer matrix analyses [22]. The thicknesses of the fused quartz and air gap were simultaneously determined in a self-consistent manner using a least-square method based on the Levenberg-Marquardt algorithm [23]. From these calibration data, we measured the THz complex dielectric functions of Tris-HCl buffer and pure water. We used an extended double Debye model, including conductivity of ionic species (Tris-H+ and Cl−), to obtain the slow and fast relaxation times of water molecules in the buffer and pure water.
Figure 1(a) shows the THz pulse signals transmitted through the liquid cell with water and Tris-HCl buffer. The THz pulse for Tris-HCl buffer is delayed by ~70 fs and the positive peak is reduced by 0.3 nA, compared with that for water, which means that the Tris-HCl buffer has slightly higher refractive index and absorption coefficient. The fast Fourier transformed (FFT) amplitude and phase spectra in Fig. 1(b) and 1(c) also show very small differences between the two liquids, demonstrating the high precision of our measurements.
We obtained the complex dielectric functions using a doubleDebye model with slow and fast relaxation processes [24], including conductivity of solute ions such as Tris-H+ and Cl−:
with the real (
where
As shown in Figs. 2(a) and 2(b), the measured complex dielectric functions are in good agreement with the best-fit curves for both water and Tris-HCl buffer. At 1 THz, the real and imaginary parts (
[TABLE 1.] Dielectric relaxation parameters of water and Tris-HCl buffer
Dielectric relaxation parameters of water and Tris-HCl buffer
We have performed high-precision THz time-domain spectroscopy of 10 mM Tris-HCl buffer and water. The measured and best-fit complex dielectric functions have shown the difference between the two liquids very clearly even with a dilute Tris-HCl buffer solution. These findings suggest that the high-precision THz-TDS is a powerful spectroscopic tool for probing various biochemical processes even in physiological buffer solutions.