Introduction

Amino acid analysis (AAA) is classic but plays an important role as quantitative method in many biological, biomedical, and food analyses. AAA has been used for determination of absolute amount of free amino acids, peptides, or proteins not just for amino acid composition of proteins. The quantitative accuracy of AAA has recently been noted again and many applications have been reported [1–6]. In proteomics, mass spectrometry (MS) has become the most informative tool and has replaced AAA as a qualitative technique and also, most recently, as a quantitative method. Quantitative MS requires an accurate amount of peptide or protein calibrants; but gravimetric method based on the weighing of solid analyte is unsuitable for the purpose since peptides or proteins often contain unknown amount of bound salts and/or hydrated water. AAA has become an important quantitative method in obtaining absolute amount of these calibrants. Another benefit is that AAA is free of bias by the amino acid sequence of proteins since the proteins are completely hydrolyzed to the constituted amino acids before AAA. Therefore, AAA is applicable to the proteins that are not easy to be analyzed by sequence-dependent enzymatic proteolysis plus MS such as Lys- and Arg-rich histones (histones are inappropriate for application of MS with enzymatic proteolysis, because histones have many modifications on Lys and Arg residues that prevent a usage of typical enzyme such as trypsin cleaving the carboxyl side of Lys or Arg) or membrane proteins that possess large hydrophobic moiety. A previously unknown histone modification, hydroxylation of Lys, was recently identified and quantified by AAA [2]. In another example, the 3D structure of a membrane protein in solution predicted by molecular dynamics simulations was experimentally confirmed from quantification of intramolecular Cys–Cys bond formation by AAA [3] (distance between two Cys residues of the membrane protein can be estimated by quantification of intramolecular Cys–Cys disulfide bond formation since the disulfide bond is formed when the two residues are positioned enough close to each other).

In the early 1950s, AAA was originally accomplished by separation of amino acids with ion-exchange chromatography, labeling of the amino acids with ninhydrin, and detection of them by visible light absorbance [7, 8]. The sensitivity of the AAA with the ninhydrin detection is not sufficient for small amount of proteins. Therefore, many sensitive methods for detection of amino acids have been developed based on chemical modifications of amino acids for fluorometry [9–12] or MS [13–15] before amino acid separation by liquid chromatography (LC), i.e., pre-column derivatization. In the pre-column derivatization, the hydrophobicity of amino acids can be enhanced, facilitating their separation by reversed-phase chromatography, which prevents dilution of peaks and enhances the sensitivity of detection. These pre-column labeling methods provide femtomole to picomole sensitivity to AAA [16, 17]. In this study, we quantified amino acids by a pre-column derivatization with 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate (AQC) for fluorescence detection because of three reasons: the reagent react with all amino acids including the secondary amino acids, the derivatized amino acid are stable at room temperature, the derivatization reaction is linear with amount of amino acids, and the excess reagent does not disturb analysis [12].

Because of development of highly sensitive AAA, quantification of free amino acids can be readily achieved in sub-picomole level, but obtaining accurate quantity of low-abundance proteins (less than 100 ng) after hydrolysis steps without or less contamination from environment is far more difficult [18, 19]. For accurate quantification of amino acids in protein samples, following three requirements must be satisfied.

First, protein samples must be purified and rendered homogeneous before hydrolysis, because the amino acids of contaminant proteins cannot be distinguished from those of the sample proteins. A favorite method for preparation of homogeneous protein samples is sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) because of its inherent high resolution and simplicity. Direct hydrolysis of proteins in polyacrylamide gels causes the liberation of large quantities of ammonia, which hinders the use of AAA because the excessive ammonia consumes the reagent used for the pre-column labeling of amino acids. To circumvent this issue, the separated proteins are electroblotted onto a polyvinylidene difluoride (PVDF) membrane and hydrolyzed on the membrane [20, 21]. If the protein to quantify is not isolated from other proteins, the amount of the protein is unknown, whereas the total amount of protein mixture can be known by sum of multiplying amino acid amount by the each residual mass. Second, protein samples should be completely and quantitatively hydrolyzed to amino acids.

Many hydrolysis methods that utilize enzymes, strong bases, or strong acids are available, and the proper method depends on the aim of the analysis [22]. Hydrolysis using hydrochloric acid (HCl) is currently universally applied to AAA, because HCl can cleave peptide bonds completely independent of the amino acid sequence and can easily be removed from hydrolysates by evaporation. Except for labile or inert amino acids under acidic conditions, most amino acids are obtained quantitatively from proteins by hydrolysis with HCl (see details in the “Experimental section”). Furthermore, we have developed an automated hydrolysis system using a solid acid catalyst, which yielded over 70 % of the amino acids recovered after conventional hydrolysis of proteins with HCl [23]. Since the automated system cannot be used for hydrolyzing electroblotted samples, HCl was used in this study.

Third, contamination from environment during many complicated operations, SDS-PAGE, electroblotting, and hydrolysis, must be prevented or restricted. Among them, the hydrolysis of proteins is responsible for most analysis errors and a precise technique for handling small amounts of samples is necessary. Then a sufficient amount of protein, typically from one to several micrograms, has been used to overcome the contribution from potential contaminants for obtaining an accurate amino acid composition [17, 18]. In the previous work, highly sensitive AAA was reviewed, in which 0.5 μg of bovine serum albumin (BSA) in solution was hydrolyzed and a part of them, 45 and 100 ng, was quantified [16]. Cohen et al. investigated in detail the relationship between hydrolyzed protein amount of sample solution and average errors in the composition dividing the categories according to the protein amount: trace analysis (<100 ng), high sensitivity (100–500 ng), low intermediate (500–100 ng), high intermediate (1,000–2,000 ng), and high (>2,000 ng) [18]. They also showed similar investigation of dot-blotted protein solution to membranes collected from capillary electrophoresis [24]. In both cases, a steady increase in the average error as sample amount decreases was observed. At the high sensitivity range for proteins on the membrane and at the trace analysis range for protein solutions, the average errors in the composition reached around 20 % [18, 24]. The reduction of the contamination from environment is most critical for accurate quantification of low-abundant proteins. The purpose of this study is that the method to obtain meaningful results from trace analysis (the amount hydrolyzed < 100 ng of proteins both in solution and on membrane) is established by improving both handling- and equipment-dependent factors. The accuracy of AAA for less than 100 ng of proteins was evaluated by the accuracy of amino acid composition and by assessing whether analyzed proteins were correctly identified from the obtained composition using the Swiss-Prot database. Only ten or a few tens of nanograms of BSA in solution or on a blotted membrane and thyroglobulin (TG) on a blotted membrane were correctly identified and quantified. These results demonstrate that AAA is a feasible method for biological significant proteins.

Experimental section

Reagents

BSA (A7638) and TG from bovine thyroid (T1001) were purchased from Sigma (St. Louis, MO). Sample solutions of BSA or TG were prepared on the basis of the dry weight of the proteins. HCl, sodium tetraborate, Coomassie brilliant blue (CBB) R-250, and tetrabutylammonium bromide (TBA-Br) were purchased from Wako (Osaka, Japan). A type H amino acid standard containing 17 amino acids (2.5 mmol/l each) was purchased from Pierce Chemical Co. (Rockford, IL), and LC/MS-grade acetonitrile (AN, A955-212) was purchased from Thermo Fisher Scientific Inc. (Waltham, MA). The phosphate buffer for chromatography was made from sodium dihydrogen phosphate monohydrate (NaH2PO4·H2O, 106,346), and disodium hydrogen phosphate dihydrate (Na2HPO4·2H2O, 106,580) was purchased from Merck KGaA (Darmstadt, Germany). 3-cyclohexylamino-1-propanesulfonic acid (CAPS) was purchased from Nacalai Tesque, Inc. (Kyoto, Japan).

Amino acids were analyzed after pre-column derivatization with a fluorophore. The derivatization regent, AQC, was synthesized as described in previous reports [12, 23], and purified to avoid unnecessary peaks that are due to side reaction with impurities of the synthesized AQC. The reagent is also commercially available from Waters (Waters corp., Milford, MA). For derivatization, the AQC powder was dissolved in dry acetonitrile to provide a 3 mg/ml solution (about 10 mM).

Materials

Small glass tubes (6 × 32 mm, Crimp Top Vials, P/N: 03-CVG, Chromacol, UK) for samples and glass vials (27.75 × 70 mm, P/N: 224832, Wheaton, NJ) as hydrolysis vessels were pyrolyzed before use at 550 °C for 3 h to remove organic substances. Mininert valves (No. SC-24, P/N: 10130, Pierce, IL) were used for vacuum sealing of the glass vials before hydrolysis. The sample vials were heated by a heat block bath (Thermo Alumi bath ALB-121, Scinics Corporation, Tokyo, Japan) at hydrolysis.

Sample preparations

One-dimensional SDS-PAGE and electroblotting

One-dimensional SDS-PAGE was performed on commercial pre-cast gels (8 × 8 × 0.1 cm, 12 wells, 5–20 % gradient; Bio Craft Co., Ltd., Tokyo, Japan). The BSA or TG solution was mixed with an equal volume of sample buffer (125 mM Tris–HCl, pH 6.8; 4 % SDS; 20 % glycerol; 0.2 M DTT; and 0.0125 % bromophenol blue). Aliquots of the mixed solutions were loaded onto individual lanes of polyacrylamide gels and separated by electrophoresis at 10 mA for 3 h at room temperature.

Electroblotting onto a PVDF membrane (ProBlott, Applied Biosystems, Life Technologies Co., Carlsbad, CA) was carried out using a tank blotting procedure (KS-8451, System Instruments Co. Ltd., Tokyo, Japan). Before electroblotting, the PVDF membrane was wetted in methanol and was equilibrated in CAPS transfer buffer (10 mM CAPS and 10 % methanol at pH 11.0) [25]. Blotting in CAPS transfer buffer is useful in reducing the level of Tris and glycine contamination from the polyacrylamide gel. The membrane was handled with gloves and forceps to avoid contamination from skin proteins. After electrophoresis, the gel and the membrane were sandwiched between gel blot papers (GB-003; Whatman, GE Healthcare) and were placed in the blotting cassette in an ice box. Electroblotting was carried out for 15 min at 0.5 A (constant current) in the CAPS transfer buffer. Then, the membrane was rinsed in Milli-Q water, stained with 0.2 % CBB for 1 min, and destained in the mixture of 50 % methanol and 7.5 % acetic acid at room temperature. The membrane was finally rinsed in Milli-Q water, air-dried in a glove box, and stored in doubled-over plastic bags in a refrigerator. In the glove box, the electroblotted bands of BSA or TG on PVDF membranes were excised over the inner plastic bag and rinsed with 50 % acetonitrile in water before treatment with 20 mM HCl. Each piece of the membrane was placed in the hydrolysis tube containing 50 pmol of norvaline as an internal standard.

Solution samples

In the glove box, aliquot of BSA solution was placed in the hydrolysis tube containing 50 pmol of norvaline as an internal standard.

Gas-phase hydrolysis

The hydrolysis tubes containing the sample on the PVDF membrane or in solution were set to a container with a cover and brought into an oxygen-free chamber for hydrolysis that we constructed. The chamber is under positive pressure of nitrogen to prevent oxidation of samples and to prevent contamination from the environment. After the sample container was brought in it, hydrolysis procedures were started when oxygen level in the chamber reached less than 0.1 % detected by an oxygen monitor (JKO-O2LD II, JIKCO Ltd., Tokyo, Japan). The chamber is an appropriate glove box that includes stuff needed for hydrolysis: a vacuum line, a centrifugal concentrator, the heat block bath, and reagents for hydrolysis. The samples in the hydrolysis tubes were dried by the centrifugal concentrator with the vacuum line. The dried tubes were placed in the glass vial containing 200 μl of constant-boiling HCl and a piece of phenol crystal. Then the vial was sealed under vacuum using the Mininert valve and heated at 110 °C for 20 h by the heat block bath [16, 23]. After hydrolysis, the sample tubes were dried under vacuum.

Derivatization of amino acids

A standard solution containing a mixture of 50 pmol of standard amino acids and norvaline, and the hydrolysate of the BSA solution were derivatized by AQC as previously described [16, 23]. The hydrolysate of BSA or TG from the blotted band was derivatized by adding the AQC solution directly into the hydrolysis tubes containing the PVDF membrane, as follows: The membrane was wetted with 5 μl of acetonitrile, and then, 10 μl of 20 mM HCl was added and vigorously stirred to extract the hydrolysate. Borate buffer (25 μl and 0.2 M at pH 8.8) was added, mixed, and finally 10 μl of the AQC solution was added. The reaction mixtures were stirred immediately. After the mixtures were left to stand for 1 min at room temperature, they were heated at 55 °C for 10 min. The derivatized solution was transferred to a new tube before chromatographic analysis to avoid adsorption of amino acids onto the membrane and piercing of the membrane by a needle of the autosampler. A tenth of the derivatized solution was analyzed by high-performance liquid chromatography (HPLC) as described in the next section.

Analytical procedures

Chromatography

AQC-amino acids of the hydrolysates and the standard solution of amino acids were separated by ion-pair chromatography using a reversed-phase column [16, 26]. An Agilent HPLC system for ultra-high-pressure use (1200 SL series, pressure resistance = 600 bar) equipped with binary pumps, a column oven, an autosampler, and a fluorescence detector (excitation at 250 nm and emission at 395 nm) was used. In this system, fluorescence signal can be amplified by increasing the voltage applied to the photomultiplier of the fluorescence detector. We used middle-range voltage, except for obtaining the chromatogram of the 5-fmol amino acid standard solution, in which signals were amplified by approximately a factor of 10 against other measurements. The column used was an InertSustain C18HP column suitable for ultra-high pressure (pressure resistance = 500 bar), 3 μm, 3.0 × 250 mm (GL Sciences Inc, Tokyo, Japan). Elution buffer A was 95 % of 30 mM phosphate buffer (pH 7.3) containing 5 mM TBA-Br as the ion-pair reagent and 5 % acetonitrile, whereas elution buffer B was 50 % of 30 mM phosphate buffer (pH 7.3) with 50 % acetonitrile. The different two elution programs were used based on column condition: linear increases from 2 % B at time 0 to 7.3 % B at 2.7 min, and then to 72.3 % B at 26 min or to 72.3 % B at 35.4 min, followed by a wash with 99 % B for 1.8 min and re-equilibration with 2 % B for 12.4 min. The column was kept at 42 °C, the flow rate was 0.4 ml/min, and the injected volume of the solution of AQC-derivatized amino acids was 5 μl.

Quantification

Under the conditions of conventional acidic hydrolysis, Asn and Gln are completely hydrolyzed to Asp and Glu, respectively, and Trp, Cys, and cystine are partially destroyed [27]. We quantified Asp as the sum of Asp and Asn and Glu as the sum of Glu and Gln. For quantitative analysis, 50 pmol of the standard solution containing 17 amino acids (other than Trp, Asn, and Gln) was derivatized by the same procedure used with the hydrolyzed samples. A tenth of the total hydrolysate of the standard solution was injected onto the column. We evaluated the amounts of 17 amino acids in the samples by calculating the ratio of the peak height of an amino acid in the sample to that of the same amino acid in the standard. Total weight of amino acids was calculated by sum of multiplying the obtained amounts of amino acids by each residual mass. In all experiments for protein quantification, each sample was hydrolyzed and analyzed three times, and the standard deviation of the means was calculated as (Σ(experimental value − average value)2/2)1/2.

Method validation

We derivatized 150 pmol of the amino acid standard, and the derivatized solution was diluted to make a dilution series of the standard. By plotting the quantified amount of AQC-Arg against the injected amount of AQC-Arg, we ascertained the linear range and the LOD (limit of detection) of the fluorescence detector. We defined the minimum amount that maintained the linear response as the LOQ (limit of quantification).

We validated the quantitative accuracy of AAA by protein identification using the amino acid compositions derived from the analyses and a search program of a protein database. For the Swiss-Prot database search, the ExPASy AACompIdent tool was used (http://web.expasy.org/aacompident/) with constellation 2 (Asp + Asn = Asx, Gln + Glu = Glx, and Cys and Trp are not considered) chosen without any limit of species, isoelectric point, or molecular weight of the proteins. Proteins, at amounts ranging from a few nanograms to several tens of nanograms, were quantified and validated. We defined the minimum quantity of protein that was identified correctly by the database search as the LOH (limit of handling).

Results and discussion

Chromatographic analysis of amino acids

Pre-column derivatization with fluorescent molecules enhances the hydrophobicity of amino acids and enables separation of amino acids by reversed-phase liquid chromatography (RPLC), resulting in faster analysis and higher sensitivity than that of conventional ion-exchange chromatography. In the case of RPLC, hydrophilic molecules elute earlier, and hydrophobic molecules are eluted later, with progressive elution at increasing ratios of organic solvents. In general, the fluorescence intensity of eluted compounds is stronger in hydrophobic circumstances. Therefore, in the case of fluorescence detection of eluted samples of RPLC, the fluorescence intensity of samples that are eluted later is stronger. The solvent effect leads to a different response factor for each amino acid, and the peak-areas of amino acids that are eluted earlier are almost one fifth smaller than the later one [12]. It is more difficult to quantify the amino acids with small response factors rather than those with large response factors especially in extremely small amount of samples. To circumvent this issue, we used an ion-pair reagent to enhance the hydrophobicity of the AQC-derivatives of hydrophilic amino acids and to reduce the solvent effect [26]. By application of the latest ultra-high-pressure LC, we were able to use a long column with small internal diameter and to improve theoretical plate-number and signal-to-noise ratio of chromatograms resulting in high sensitivity with excellent resolution. Figure 1 represents the typical chromatogram of 5 fmol of the AQC-amino acid standard (after subtraction of the chromatogram of the blank/water).

Fig. 1
figure 1

Typical chromatogram of AQC-amino acid standards of 5 fmol that subtracted a blank chromatogram of injection of water (gradient condition, 2–7.3–72.3 % B/0–2.7–26 min)

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Quantification of small amounts of amino acids

The sensitivity and linear response range of the detector need to be adequate enough to quantify small amounts of proteins. These requirements depend on the two kinds of limitations dependent on the performance of the fluorescence detector, LOD and LOQ. Usual photomultipliers, including those in fluorescence detectors, have a linear response range of two to four orders of sample quantities against the intensity of incident light. Because the response is not linear at both ends of the intensity plot, at the lowest and highest intensities of incident light, the amounts of amino acids cannot be quantified accurately even if the signals are detectable. We defined the sample limit at which the linear response is maintained as the LOQ and the lower limit at which the signal from the amino acids is still detectable as the LOD. We evaluated LOQ and LOD by measuring the detector response to a dilution series of AQC-Arg standards. The amounts of the AQC-Arg quantified are plotted against the injected amounts of AQC-Arg in Fig. 2. For our chromatographic condition and detection system, almost four-order linearity from 0.6 fmol to 5 pmol was observed, which means that the LOQ was 0.6 fmol. In contrast, the LOD was 50 amol, as shown in Fig. 2.

Fig. 2
figure 2

Quantified amount of AQC-Arg was plotted against injected amount. Linearity of detector response confined the limit of quantification to 0.6 fmol, whereas limit of detection was 0.05 fmol

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Recent developments in MS have enabled highly sensitive detection of free amino acids, and MS has also been used for AAA. There are basically two main methods to detect amino acids by MS. One of them is a non-labeling method, in which the amino acids are detected without derivatization. Miyano et al. [28] reported that the LOD of the non-labeling-based MS detection was 10–90 fmol. Another MS method is the pre-label method in which the amino acids are derivatized with reagents that are selectively cleaved during ionization and generate the same fragment for selective reaction monitoring (SRM). The pre-label method achieved an LOD of femtomoles to several tens of attomoles [14, 15]. Since the advantages of SRM-MS are high selectivity and short analysis time, SRM-MS is suitable for metabolomics. To use these MS methods for quantification of amino acids, however, expensive equipment and stable isotope-labeled amino acids are needed, resulting in a high cost. Moreover, detection range for each amino acid is relatively narrow: two to four orders in concentration of amino acids [14].

The quantification of amino acids in proteins is more complicated than that of free amino acids because of the requirement for hydrolysis. The LOQ of amino acids in proteins depends on the quantitative recovery of amino acids via protein hydrolysis.

Actual limit for quantification of small amounts of proteins

For the quantification of small amounts of proteins, not only the LOQ but also the LOH dominates the quantitative results because one more process, hydrolysis, is needed before quantification of the released amino acids. Hydrolysis contains complicated operational steps that create a risk of contamination from the environment to the samples. Appropriate equipment, such as the oxygen-free chamber for hydrolysis, gloves, and forceps, as well as a proper technique for handling small amounts of samples, can prevent the contamination. Generally, a blank sample tube is simultaneously hydrolyzed with protein samples for background correction. Then the contributions from the contamination that are the background peaks of the blank sample are subtracted from the chromatogram of protein sample. However, the contamination to protein samples is not necessarily the same as that to the hydrolysis blank. Furthermore, there is so far no guideline how extent of contamination makes the quantification of proteins end in failure. As a new guideline, we defined the limit of handling accuracy, LOH, and adopted the protein identification by the obtained amino acid compositions and the Swiss-Prot database for evaluation of the LOH.

We prepared three concentrations of BSA in solution, containing 2.6, 16, and 54 ng of BSA, hydrolyzed the samples, and quantified the constituted amino acids. The amount of amino acids in picomoles and calculated total amount of amino acids in nanograms by the sum of multiplying the obtained amounts of amino acids by each residual mass are listed in Table 1. The calculated residue numbers from the amount of amino acids and molecular weight of BSA were also listed in Table 1. The residue number of the sample with 54 ng of BSA matched the theoretical values, whereas a slight increase was observed in Ser and Gly values for the sample with 16 ng of BSA. We assessed whether analyzed proteins were correctly identified by the Swiss-Prot protein database search without the restriction of species using these obtained composition and the ExPASY AACompIdent program. The results of the database search for 54 and 16 ng of BSA (shown in Table 2) indicated that both the samples were identified as BSA. However, the residue number of 2.6 ng of BSA (listed in Table 1) deviated from the theoretical values, especially for Ser and Gly, and BSA was not hit until a rank of 10. From the results, the LOH was 16 ng, or 240 fmol, of BSA in solution.

Table 1 Amino acid contents of BSA
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Table 2 The closest Swiss-Prot entries from the ExPASy AACompIdent program without the restriction of species, isoelectric point (pI), and molecular weight (Mw)
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The LOQ of amino acids, 0.6 fmol, was one order lower than the obtained LOH. However, the increase of Ser and Gly prevented identification of the much smaller amount of protein such as 2.6 ng for BSA solution. If the database search was performed using the calculated compositions of Ser and Gly derived from the theoretical residue numbers and the observed compositions of other amino acids, 2.6 ng of BSA was successfully identified with a rank of 1. Since the increase of Ser and Gly may be caused from a slight contamination from the environment, the contamination should be excluded or further minimized to accomplish the quantification of 1 ng of protein, such as that achieved effectively by automation of sample preparation and/or sample hydrolysis [23].

Quantification of proteins electroblotted to PVDF membranes

The blotted protein bands are detected by staining with CBB, with a detection limit around 50 ng that sets the least value of LOH. We cut off the protein bands containing 33 ng of BSA or 44 ng of TG, and the proteins were hydrolyzed on the membrane. The obtained amounts and calculated residue numbers of amino acids of the blotted BSA are listed in Table 1. In Fig. 3, the chromatogram of the hydrolysate of the blotted TG is shown. The injected amount of TG was one-tenth of the hydrolysate, i.e., 4.4 ng (14.5 fmol). We verified the quantitative accuracy by performing the database search using the obtained amino acid composition. The composition matched the theoretical value, and the database search identified the protein bands as BSA or TG with a rank of 1 as shown in Table 2. The results mean the least value of LOH that is determined by the CBB detection limit was achieved in this study. The obtained LOH value for the electroblotted samples was the same extent as solution samples.

Fig. 3
figure 3

Chromatogram of hydrolysate of blotted TG. A blotted band that contains 44 ng (145 fmol) of TG was hydrolyzed and a tenth of them were injected. AMQ abbreviates 6-aminoquinoline that is formed by hydrolysis of AQC. The asterisk-marked peak is an internal standard, norvaline (gradient condition, 2–7.3–72.3 % B/0–2.7–35.4 min)

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In a previous report, Murayama et al. [17] analyzed a part of the hydrolysate of a protein electroblotted onto PVDF, which was 2.4 fmol of multidrug-resistant protein 1 (MDR1, 160 kDa), and successfully identified it. However, they hydrolyzed an amount of MDR1 1,000 times larger than the injected amount to eliminate the influence of contamination. In other words, the LOH was 2.4 pmol in their case, although 2.4 fmol of MDR1 was identified. In another report, Cohen et al. collected purified proteins by capillary electrophoresis onto PVDF membranes and hydrolyzed 100–700 ng of the collected proteins on the PVDF membranes. They reported that amino acid compositions of 100–700 ng of proteins were obtained with average errors 9.9–21.3 % [24]. They also pointed the average errors rose rapidly (30–60 %) for 60 ng hydrolyzed samples. In our method, accurate AAA was accomplished for an order of small amount of proteins by accumulating small improvements in handling. For hydrolysate of 33 ng of BSA or 44 ng of TG on PVDF membrane, the average errors in the amino acid composition observed was 12 %. Since percent recovery of blotted BSA from amount on SDS-PAGE gel were reported as 35 % [29], 94 ng of BSA is needed as starting amount for SDS-PAGE.

Conclusions

We improved the sensitivity of AAA to the following specifications; an LOD of 50 amol, an LOQ of 0.6 fmol, and four orders of linearity. Critical manipulation before hydrolysis was done in the oxygen-free chamber under positive pressure of nitrogen to prevent oxidation of samples and to keep out dust.

In order to evaluate the LOH of proteins the protein identification was performed with the Swiss-Prot database search using the obtained compositions of amino acids and the ExPASy AACompIdent tool. As a result, hydrolysates from solution containing 16 ng (240 fmol) of BSA, a PVDF membrane with 33 ng (500 fmol) of electroblotted BSA, and a PVDF membrane with 44 ng (145 fmol) of electroblotted TG were successfully identified. The LOH was less than one-tenth of that reported previously [17]. This method was practical for the quantification of proteins, at less than 100 ng either in solution or on PVDF membranes. In the case of 2.6 ng of BSA, the increase in Ser and Gly prevented identification of the protein. Thus a limitation of manual hydrolysis, namely the LOH, was likely a result of contamination with Ser and Gly from the environment. For further highly sensitive analysis, automation of sample preparation and/or sample hydrolysis will be effective in suppressing contamination and facilitating the quantification of 1 ng of proteins.