KR101152669B1 - New fluorescent peptide sensor and detecting method of anion compositions - Google Patents

Abstract

The present invention relates to a novel fluorescent peptide sensor and a method for detecting an anion compound using the same, more particularly, a novel fluorescent peptide sensor having a high chelate enhanced fluorescence CHEF effect by reacting with a specific anion compound, By using the sensor, it is possible to effectively detect anionic compounds such as pyrophosphate (PPi) and adenosine triphosphate (ATP) in the presence of copper ions (Cu ²⁺ ), and thus research related to signal transmission and energy storage. It relates to a method for detecting anionic compounds that can be usefully applied in the field.

Fluorescent Peptides, Sensors, Copper Ions, Anionic Compounds, Pyrophosphates, Adenosine Triphosphate

Description

New fluorescent peptide sensor and method for detecting anion compounds using the same

The present invention effectively detects anion compounds in the presence of copper ions (Cu ²⁺ ) by using a novel fluorescent peptide sensor having a high chelate enhanced fluorescence CHEF effect in response to a specific anion compound and the sensor. The present invention relates to a method for detecting anionic compounds that can be usefully applied to research fields related to signal transmission and energy storage.

The design and research of new sensors for key substances and ions in vivo has been actively conducted. Recent understanding and research on supramolecule chemistry has shown great potential for the design of host compounds that can selectively bind to ions or other types of guest compounds. It is a great help in the development of a fluorescent chemosensor that can easily observe the selective binding with a guest compound using fluorescence change.

Fluorescence is a photochemical phenomenon that occurs when photons with a specific wavelength (excitation wavelength) collide with an indicator molecule and electrons are excited at high energy levels as a result of the collision. Among the various analytical methods, fluorescence has the advantage of being able to observe signals even at 10 ^-9 M concentrations due to their excellent sensitivity. Recently, studies on fluorescence chemical sensors for cations, anions and neutral organic molecules using these properties have been published (AP de Silva et al., Chem. Rev. 1997, 97, 1515).

Negative ions play an important role in a wide range of chemical and biological processes.

Thus, fluorescent sensors based on anion-induced changes are very interesting due to their high detection limits and simplicity of operation (R. Martinez-Manez and F. Sancanon, Chem. Rev. 2003 , 103 , 4419). In particular, phosphate ions and their derivatives play an important role in signal transmission and energy storage in biological systems.

In particular, pyrophosphate (PPi) may be a biologically important target as a product of ATP hydrolysis under cellular conditions. In addition, the detection of pyrophosphate release was studied as a real-time DNA sequencing method (M. Ronaghi et al. , Anal. Biochem. 1996 , 242 , 84). In recent years, the measurement of PPi has also been used for cancer research (S. Xu et al. , Anal. Biochem. 2001 , 299 , 188).

Thus, the detection and identification of anionic compounds such as pyrophosphate (PPi) has been a research goal of several research groups (R. Martinez-Manez, F. Sancanon, Chem. Rev. 2003 , 103 , 4419; D. Aldakov and P. Anzenbacher, Jr, Chem. Comm. 2003 , 1394; T. Gunnlaugsson et al. , Org. Lett. 2002 , 4 , 2449; YJ Jang et al. , J. Org.Chem . 2005 , 70, 9603; Lee, DH et al. , Angew. Chem., Int. Ed. Engl. 2004 , 43 , 4777; L. Fabbrizzi et al., Angew. Chem., Int. Ed. Engl. 2002 , 41 , 3811; S. Mizukami et al . , J. Am . Chem . Soc . 2002 , 124 , 3920 Lee, HN et al . , Org . Lett . 2007 , 9 , 243).

PPi (YJ Jang et al . , J. Org . Chem . 2005 , 70, 9603; Lee, DH et al ., Angew . Chem ., Int . Ed . Engl . 2004 , 43 , 4777; Fabbrizzi et al. , Angew. Chem., Int. Ed. Engl. 2002 , 41 , 3811; S. Mizukami et al. , J. Am. Chem. Soc. 2002 , 124 , 3920). In particular, fluorescence sensors that exhibit PPi selectivity for ATP and Pi in aqueous solutions (Hong, J.-I. et al., Angew. Chem., Int. Ed. Engl. 2004 , 43 , 4777) are even rarer. . In addition, fluorescent peptide sensors showing selective fluorescence increase for anionic compounds, in particular pyrophosphate, have not been reported.

It is an object of the present invention to provide a fluorescent chemical sensor for the detection and identification of anionic compounds such as pyrophosphate (PPi) and ATP.

Another object of the present invention is to provide a method for selectively detecting anionic compounds using the fluorescence chemical sensor.

The present invention solves the above problems by providing a fluorescent peptide sensor represented by the following formula (1).

In Formula 1, l and m are each an integer of 1 ≦ l ≦ 2, 1 ≦ m ≦ 3,

R is NH ₂ , NHR ₁ (R ₁ is an alkyl group having 1 to 18 carbon atoms), OH, OR ₁ (R ₁ is an alkyl group having 1 to 18 carbon atoms), (OCH ₂ CH ₂ ) _n -COOH (n is 2 Or (OCH ₂ CH ₂ ) _n -polystyrene (n is an integer from 2 to 5000) or an amino acid.

In addition, the present invention relates to a method for detecting an anion compound using the fluorescent peptide sensor, wherein the detection is performed by providing a method for detecting an anion compound, wherein the detection is performed in the presence of copper ions (Cu ²⁺ ). Solve the problem.

The novel fluorescent peptide sensor according to the present invention exhibits a high fluorescence amplification effect with certain anionic compounds such as pyrophosphate (PPi) and ATP in the presence of copper [II] ions, and thus can be usefully applied as a fluorescent chemical sensor. .

In addition, while the anion compound can be detected only in the presence of an organic solvent, the novel fluorescent peptide sensor according to the present invention can detect anion compounds pyrophosphate (PPi) and ATP in the presence of copper ions even under 100% aqueous solution. It can be effective.

In addition, the present invention provides a method for detecting anionic compounds in the presence of copper ions using a fluorescent peptide sensor, which can be usefully applied to research fields related to signal transmission and energy storage in vivo.

The present invention has the greatest technical features to provide a novel fluorescent peptide sensor having a high chelate enhanced fluorescence CHEF effect by reacting with anionic compounds such as pyrophosphate (PPi) and ATP.

Hereinafter, the present invention will be described in detail.

It is generally known that fluorescent chemistry or peptide sensors, including the Dansyl group and the imidazole group of histidine, have a high binding force with copper due to the imidazole group of histidine. [Shults MD, Pearce DA, Imperiali B: J Am Chem Soc 2003 , 125 : 10591-10597.] Accordingly, the fluorescent peptide represented by Chemical Formula 1 has a Dansyl group, glycine (Gly) and histidine, which are fluorescence substituents. As a compound consisting of a combination of amino acids consisting of (His), the present invention provides the aforementioned novel fluorescent peptide sensor capable of detecting a specific anionic compound in the presence of copper ions [II].

As a more preferable example of the fluorescent peptide sensor according to the present invention, l and m are each 1 in Formula 1, and R is NH ₂ .

Moreover, as a more preferable example of the fluorescent peptide sensor which concerns on this invention, in Formula 1, l is 1 and m is 1, for example.

On the other hand, the fluorescent peptide sensor according to the present invention has a high binding force with copper due to the imidazole group of histidine (His), and due to the structural change due to the bonding with copper, the group of Dansil (Dansyl) group which is a fluorescence substituent It is characterized by quenching fluorescence.

Accordingly, the present invention has a high chelate enhanced fluorescence CHEF effect when the fluorescent peptide sensor fluorescence quenched reacts with a specific anionic compound in the presence of copper ions [II], thereby exciting it at a wavelength of 300 to 360 nm. In this case, it was found that the fluorescence of the wavelength of 500 to 600 nm was emitted and led to the present invention.

In particular, the chelate amplification fluorescence effect may occur better at the conditions of pH 7.0 ~ 8.0.

The manufacturing method of the fluorescent peptide sensor according to the present invention described above is not particularly limited to a manufacturing method generally used in the art, for example, by using a solid phase synthesis method in a manual or automatic peptide synthesizer, it can be more preferably manufactured. .

Preferred examples of the fluorescent peptide sensor manufacturing method as described in more detail as follows.

The method for preparing a fluorescent peptide sensor comprises the steps of: 1) synthesizing a peptide in which the carboxy terminus is bound to the resin by an amino acid whose side chain is reactive with a protecting group by a protecting group; 2) reacting the peptide bound with the resin with piperidine to remove the protecting group at the amino terminal, and then reacting with 5-dimethylamino-1-naphtharensulfonyl (Dansyl) chloride; And 3) reacting the reaction product with a side chain protecting group and a resin removal solution. In this case, the peptides are each independently Gly, (L) -His, (D) -His or two or more peptides thereof.

In addition, the protecting group may be commonly used in the art, and is not particularly limited. Specifically, as a protecting group for protecting the amino terminal, 9-fluorenylmethyloxycarbonyl group may be more preferably used, and a reactive side chain may be used. As a protecting group for protecting the amine, any one residue selected from triphenylmethyl, butyloxycarbonyl, and t-butyl ester can be used more preferably. In addition, the resin may be commonly used in the art, and is not particularly limited. For example, linked amide methylbenzhydryl amine (rinked amide MBHA) resin or Wang resin may be more preferably used. .

In addition, in the step of synthesizing the peptide bonded to the resin by a solid phase synthesis method, it is preferable to use the resin and the peptide is combined in a molar ratio of 1: 2 to 10. More preferably, in consideration of economics, it is preferable to use a resin and a peptide formed by combining in a molar ratio of 1: 3 to 7.

Fluorescent peptide sensor can be prepared in the above manner.

The method for detecting an anion compound using the fluorescent peptide sensor according to the present invention has the biggest technical feature in that it is necessarily performed in the presence of copper ions (Cu ²⁺ ). In this case, the anion compound may be more preferably detected when the compound selected from pyrophosphate (PPi) and ATP.

The synthesized fluorescent peptide of Formula 1 has a high hydrophilic property, copper ions (Cu ²⁺ ) is the third highest amount of heavy metal ions present in the human body, when the fluorescent peptide is injected into the living body, It naturally binds to the copper ions (Cu ²⁺ ) present in it and can detect specific anionic compounds.

On the other hand, in the case of a sample in which no copper ions (Cu ²⁺ ) are present, copper ions (Cu ²⁺ ) may be introduced by a method of introducing copper ions (Cu ²⁺ ) generally used in the art. For example, by mixing the fluorescent peptide sensor and the copper precursor according to the present invention with a solvent in the same equivalent, the copper precursor can be commonly used in the art, but is not particularly limited, for example For example, copper perchlorate [II] can be used more preferably. In addition, the solvent may be commonly used in the art, and is not particularly limited, but a conventional organic solvent may be used, but a 10 mM HEPES buffer solution similar to in vivo conditions may be more preferably used.

As an example of a more specific method of detecting an anion compound using the fluorescent peptide sensor, in the presence of a fluorescent peptide sensor and copper ions (Cu ²⁺ ), a sample containing anion compounds such as pyrophosphate (PPi) and ATP is prepared. It can be detected by a method comprising the steps of mixing, irradiating light of a predetermined wavelength to the mixture and confirming the fluorescence amplification effect.

As a more specific detection method, 1) preparing a buffer solution in which the fluorescent peptide sensor and copper ions (Cu ²⁺ ) of the present invention are dissolved, and then mixing them, and 2) the mixed buffer solution and anion Mixing a sample comprising a compound, 3) irradiating an excitation wavelength of 300 to 360 nm to the mixture, and 4) detecting an fluorescence amplification signal by the excitation wavelength, thereby reacting with the peptide sensor. It can be detected by a method comprising the step of detecting the presence.

In the fluorescent peptide sensor according to the present invention, a fluorescent peptide in which a Dansyl group having excellent fluorescence properties is bound to a peptide forms a complex with copper [II] ions in an environment in which copper [II] ions are present. It reduces the fluorescence of the phosphor. The fluorescent peptide sensor coupled to the copper [II] ion weakens the binding of the copper ion to the single thread by the selective binding to a specific anion compound, thereby exhibiting the amplified fluorescence effect of the single thread phosphor.

The amplification fluorescence effect is better in the aqueous environment conditions of pH 7.0 ~ 8.0, more preferably can detect anionic compounds such as pyrophosphate (PPi) and ATP. In this case, when the excitation wavelength for chelate amplification of the fluorescent peptide sensor is in the range of 300 to 360 nm, it is possible to more preferably detect the anion compound by emitting fluorescence with a wavelength of 500 to 600 nm.

Accordingly, the novel fluorescent peptide according to the present invention exhibits high fluorescence increase by reacting with anionic compounds such as pyrophosphate (PPi) and ATP in the presence of copper [II] ions, which can be usefully applied as a fluorescent chemical sensor. It works. In addition, while the anion can be detected only in the presence of an organic solvent, the novel fluorescent peptide sensor according to the present invention has the effect of detecting an anion compound even under 100% aqueous solution. In addition, the present invention has an effect that can be usefully applied to the field of research related to signal transmission and energy storage in vivo by providing a method for detecting anion compounds using the peptide sensor.

Hereinafter, the present invention will be described in more detail with reference to the following examples, which are not intended to limit the present invention.

Example 1

Fluorescent Peptide Sensor (Dansyl-Gly-His-CONH ₂ Manufacturing

Link amide methylbenzhydryl amine resin (147 mg, 0.1 mmol) was added to 3 ml of dimethylformamide (DMF) anhydrous organic solvent and swollen for about 30 minutes. Separately, 0.3 mmol of 9-fluorenylmethyloxycarbonyl (Fmoc) -L-Histidine acid (158 mg) in 1.5 mL of DMF anhydrous organic solvent, carboxyl activator N, N-Diisopropyl carbodiimde (DIC, 48 μl) , And an adjuvant N-Hydrobenzotriazole (HOBt, 40 mg) was added and mixed to activate for about 20 minutes. After the activated solution and the resin was stirred for 2 hours to react, the reaction solution was filtered, the resin was washed several times with DMF and methanol, and then a kaiser test was performed. If the kaiser test is positive, recreate and add the activation solution. If negative, mix with 3 ml of piperidine solution dissolved in 50% by weight of DMF solvent and react for about 15 minutes, remove the N-terminal Fmoc group, and then activate the amino acids in the following procedure React with amino acids attached to sieve resin.

After the synthesis of the peptide moiety was completed, the N-terminal Fmoc group was removed using 50% by weight piperidine / DMF, 0.3 mmol of Dansyl Cholride and diisopropylethylamine (DIPEA) 0.6 in anhydrous DMF solvent. The mixed solution of mmol was mixed with the resin, followed by stirring at an appropriate speed for 3 hours at room temperature.

Fluorescent peptides attached to the resin are reacted with cleavage solution (trifluoroacetic acid (90%), trimethylsilane (5%), Water (5%)) at room temperature (4hr) to the side chain protection group of amino acids. Removal and separation of the peptide from the resin.

The trifluoroacetic acid of the filtered fluorescent peptide solution was removed by passing through nitrogen gas, and after adding diethyl ether cooled to -20 ° C, the precipitated peptide was centrifuged (3,000 rpm, 20 min). The fluorescent peptide thus obtained was purified using reversed phase HPLC (C-18 column delta pak C18-300A, 1.9 * 30cm). (Eluent: water / acetonitrile in 0.1% TFA (gradient): Flow Rate 2.5mL / min). As shown in FIG. 1, the fluorescent peptide was able to identify Dans-Gly-His-NH ₂ sensor material having a molecular weight of 444.34 using an ESI-Mass mass spectrometer.

Example 2

Preparation of Fluorescent Peptide Sensor (Dansyl-Gly-Gly-His-COOH)

A wang resin was used in place of the link amide methylbenzhydryl amine resin used in Example 1, and the fluorescent peptide manufacturing method was performed in the same manner as in Example 1. As shown in FIG. 2, the fluorescent peptide was able to identify a Dans-Gly-Gly-His-NH ₂ sensor material having a molecular weight of 501.11 using an ESI-Mass mass spectrometer.

Experimental Example 1: Fluorescence Experiment

Copper ions (Cu ²⁺ ) Dansyl-Gly-His-CONH of Example 1 ₂ Fluorescence Experiments for the Analysis of the Binding of Phosphorus and Several Anions

Example under the copper ions of the fluorescent peptide prepared in 1 pyrophosphate (PPi) or various anions (ATP, ADP, AMP, Pi , HSO 4 -, CH 3 COO -, I -, Br -, Cl - , and , experiments were performed as described below to evaluate the binding properties between) ^- F.

The anion (TP, ADP, AMP, Pi , HSO 4 -, CH 3 COO -, I -, Br -, Cl - and F ^-) tetrabutyl ammonium salt stock solutions (10mM) and peroxide having a copper ion of chlorine with Stock solutions of salts (1 mM) were prepared using 10 mM HEPES (pH 7.4) buffer. The stock solution (1 mM) of the fluorescent peptide of Example 1 ( Dansyl-Gly-His-CONH ₂ ) was prepared using deionized water distilled _twice . The stock solutions were used on the day of preparation.

The test solution was added 20 μl into a test tube so that the final concentration of the probe storage solution (compound stock solution of formula 1 of the present invention) was 10 μM in 2 ml solution with 10 mM HEPES (pH 7.4) buffer, and the final copper ion be the concentration of 10 μM put 20μl after 10 minutes, PPi and each anion in the above test solution (ATP, ADP, AMP, Pi , HSO 4 -, CH 3 COO -, I -, Br -, Cl - and F ^- ) 40 μl of the aliquot of the stock solution was added to 20 equivalents (200 μM), and all fluorescence changes were carried out using a ParkinElmer LS 55 Luminescence Spectrometer, with an excitation wavelength of 330 nm and excitation and emission slit width of 3 It measured by nm and the result is shown in FIG.

 As shown in FIG. 3, at pH 7.4, in the presence of copper ions (1 equivalent), when the final concentration of the compound of formula 1 according to the invention is 10 μΜ, the emission spectrum of the compound of formula 1 according to the invention is PPi. It showed selective fluorescence amplification effect for the addition of 20 equivalents and slight fluorescence increase for the addition of 20 equivalents of ATP, while no change was shown for the addition of 20 equivalents of other anions.

Copper ions (Cu ²⁺ ) Dansyl-Gly-His-CONH of Example 1 ₂ Fluorescence Titration Experiments for the Analysis of Binding Properties of PP and PPi

In the presence of copper ions, the following experiment was carried out to investigate the binding properties between the compound of Example 1 Dansyl-Gly-His-CONH ₂ and PPi. Stock solution of tetrabutyl ammonium salt with PPi (10 mM) was prepared using 10 mM HEPES (pH 7.4) buffer. In addition, the stock solution (1 mM) of the compound of Formula 1 prepared in Example 1 and the stock solution (1 mM) having copper ions (Cu ²⁺ ) were prepared by using distilled deionized water. The stock solutions were used on the day of preparation.

The test solution contains 20 μl of the probe stock solution (compound of formula 1 of the present invention) to a final concentration of 10 μM into the test tube, and 20 μl of the aliquot of the copper ion (Cu ²⁺ ) stock solution to 1 equivalent. After forming the complex, add 20-160 μl of aliquots of the PPi stock solution to 1-8 equivalents. The solution was diluted to 2 ml with 10 mM HEPES (pH 7.4) buffer, and all fluorescence changes were measured at an excitation wavelength of 330 nm and an excitation and emission slit width of 3 nm. The results are shown in FIG. 4.

As shown in FIG. 4, in the presence of copper ions at pH 7.4, the compound of formula 1 (final concentration: 10 μM) of the present invention showed a gradual fluorescence amplification effect as the amount of PPi added increased from 1 to 20 equivalents. As a result of titration with PPi, it was found that the binding constant of the compound Dansyl - Gly - His - CONH ₂ , copper (II) ion and PPi of Example 1 of the present invention was 2.8 × 10 ⁴ M ⁻¹ .

Copper ions (Cu ²⁺ Fluorescence experiment for binding analysis of Dansyl-Gly-Gly-His-COOH and various anions in Example 2)

Example 2 under the copper ions of the fluorescent peptide produced in the pyrophosphate salt (PPi) or various anions (ATP, ADP, AMP, Pi , HSO 4 -, CH 3 COO -, I -, Br -, Cl - , experiments were performed as described below) to investigate the binding properties between the ^- and F.

The anion (ATP, ADP, AMP, Pi , HSO 4 -, CH 3 COO -, I -, Br -, Cl - and F ^-) tetrabutyl ammonium salt stock solutions (10mM) and peroxide having a copper ion of chlorine with A stock solution of salt (1 mM) was prepared using 10 mM HEPES (pH 7.4) buffer. A stock solution (1 mM) of the fluorescent peptide of Formula 1 ( Dansyl-Gly-Gly-His-COOH ) was prepared using double distilled demineralized water. The stock solutions were used on the day of preparation.

The test solution was added 20 μl into a test tube so that the final concentration of the probe storage solution (compound stock solution of formula 1 of the present invention) was 10 μM in 2 ml solution with 10 mM HEPES (pH 7.4) buffer, and the final copper ion be the concentration of 10 μM put 20μl after 10 minutes, PPi and each anion in the above test solution (ATP, ADP, AMP, Pi , HSO 4 -, CH 3 COO -, I -, Br -, Cl - and F ^- ) 40 μl of the aliquot of the stock solution was added to 20 equivalents (200 μM), and all fluorescence changes were carried out using a ParkinElmer LS 55 Luminescence Spectrometer, with an excitation wavelength of 330 nm and excitation and emission slit width of 3 The results were measured in nm and shown in FIG. 5.

 As shown in FIG. 5, at pH 7.4, in the presence of copper ions (1 equivalent), when the final concentration of the compound of formula 1 according to the invention is 10 μΜ, the emission spectrum of the compound of formula 1 according to the invention is A strong fluorescence amplification effect was observed for the addition of 20 equivalents of PPi and a slight increase in fluorescence for the addition of 20 equivalents of ATP and ADP, but no change was found for the addition of 20 equivalents of other anions.

Copper ions (Cu ²⁺ Fluorescence titration experiments for the analysis of the binding properties of Dansyl-Gly-Gly-His-COOH and PPi in Example 2)

In the presence of copper ions, the following experiment was conducted to investigate the binding properties between the compound of Example 2 of the present invention Dansyl-Gly-Gly-His-COOH and PPi. Stock solution of tetrabutyl ammonium salt with PPi (10 mM) was prepared using 10 mM HEPES (pH 7.4) buffer. In addition, the stock solution (1 mM) of the compound prepared in Example 2 and the stock solution (1 mM) having copper ions (Mn ²⁺ ) were prepared by using distilled deionized water. The stock solutions were used on the day of preparation.

Test solution 20 ㎕ so that one equivalent of the tracer stock solution Final concentration containing 20 ㎕ to 10 μM (Compound stock solutions of Example 2 of the present invention), a copper ion (Cu ^{2 +)} Ally quart of the stock solution into the test tube, After the formation of the complex, add 20-160 μl of aliquots of the PPi stock solution to 1-8 equivalents. The solution was diluted to 2 ml with 10 mM HEPES (pH 7.4) buffer, and all fluorescence changes were measured at 330 nm of excitation wavelength and 3 nm of excitation and emission slit widths and the results are shown in FIG. 6.

As shown in FIG. 6, in the presence of copper ions at pH 7.4, the compound of Formula 1 (final concentration of 10 μM) of the present invention showed a gradual fluorescence amplification effect as the amount of PPi added increased from 1 to 20 equivalents. . Titration with PPi, the compound of Example 2 of the present invention Dansyl - Gly - Gly - His - COOH , copper (II) ions and the binding constant of PPi was found to be 5.2 × 10 ⁴ M ^-1 .

Figure 1 is a fluorescent peptide sensor in accordance with the first embodiment of the present invention shows the mass analysis results of _{(Dansyl - His -CONH 2 - Gly} ).

Figure 2 shows the results of the mass spectrometry of the fluorescent peptide sensor ( Dansyl-Gly-Gly-His-COOH) according to Example 1 of the present invention.

FIG. 3 shows 20 equivalents of PPi and anions [CH _{3 in} Dansyl-Gly-His-CONH ₂ (10 μM) in accordance with Example 1 of the present invention at pH 7.4 (10 mM HEPES buffer) in the presence of 1 equivalent of Cu ^2+. CO ₂ ⁻ , HSO ₄ ⁻ , and H ₂ PO ₄ ⁻ ] show the change in fluorescence.

FIG. 4 shows the addition of PPi (1 to 7 equivalents) to Dansyl - Gly - His - CONH ₂ (10 μM) according to Example 1 of the present invention at pH 7.4 (10 mM HEPES buffer) in the presence of Cu ^{2 +} 1 equivalent. It shows the fluorescence change when doing.

FIG. 5 shows 20 equivalents of PPi and anion [CH in Dansyl-Gly-Gly-His-COOH (10 μM) in accordance with Example 2 of the present invention, at pH 7.4 (10 mM HEPES buffer), in the presence of 1 equivalent of Cu ^{2+. _{3 CO 2 -, HSO 4 -}} , H 2 PO 4 -] shows a change in fluorescence when the a.

FIG. 6 shows PPi (1-8 equivalents) in Dansyl-Gly-Gly-His-COOH (10 μΜ) according to Example 2 of the present invention at pH 7.4 (10 mM HEPES buffer) in the presence of 1 equivalent of Cu ²⁺ . Fluorescence change when added.

Claims (5)

Fluorescent peptide sensor for detecting pyrophosphate (PPi) and ATP represented by the following formula 1 showing selective fluorescence amplification effect on pyrophosphate (PPi) and adenosine triphosphate (ATP) in the presence of copper ions (Cu ²⁺ ) . [Formula 1]

In Formula 1, when l is 1, R is NH ₂ or OH, and when l is 2, R is OH. The fluorescent peptide sensor of claim 1, wherein the fluorescent peptide sensor is 1 and R is NH ₂ . The method of claim 1, wherein the fluorescent peptide sensor is a fluorescent peptide sensor, characterized in that l is 1 or 2, R is OH. A method for detecting an anion compound using the fluorescent peptide sensor of any one of claims 1 to 3, wherein the detection is carried out in the presence of copper ions (Cu ²⁺ ). The method of claim 4, wherein the anionic compound is a compound selected from pyrophosphate (PPi) and adenosine triphosphate (ATP).

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