JPH11152298A - Specific inhibitor for phosphorylase ii dependent to calmodulin - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an inhibitor having a strong and specific inhibiting action against calmodulin-dependent phosphorylase II and capable of being used as a tool useful for elucidating physiological functions related to the enzyme. SOLUTION: A peptide having an amino acid sequence of the formula: Lys- Lys-X-Leu-Arg-Arg-Glu-Glu-Ala-Phe-Asp-Ala-Tyr (X is Ala or Lys). The inhibitor against calmodulin-dependent phosphorylase II contains the peptide.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

TECHNICAL FIELD The present invention relates to a peptide showing a selective and potent inhibitory activity on calmodulin-dependent kinase II. Furthermore, the present invention relates to an excellent specific inhibitor for calmodulin-dependent kinase II. The inhibitor of the present invention is expected to be very useful for elucidating various physiological functions mediated by the calmodulin-dependent kinase II.

[0002]

BACKGROUND OF THE INVENTION Calmodulin-dependent kinase II
(CaM kinase II: CaMKII) was discovered in 1980 as a new type of calmodulin-dependent kinase that activates tryptophan hydroxylase, the rate-limiting enzyme of serotonin biosynthesis, in the rat brain. The enzyme was used. With the progress of recent research, it has been revealed that this enzyme plays an important role in the control of higher nerve functions such as memory and the regulation of various cell functions. This enzyme is 1) abundant in the brain, 2) soluble and granule-bound, 3) has broad substrate specificity, 4) has organ-specific isoforms, 5) autophosphorylates It has outstanding features such as controlling the activity by. In particular, it is suggested that the enzyme is involved in the biosynthesis of neurotransmitters, release of neurotransmitters, long-term potentiation that is considered to be the basic principle of memory, memory, especially spatial memory, etc. ing.

[0003] Therefore, in order to further elucidate the function of calmodulin-dependent kinase II in vivo, a selective and potent inhibitor of calmodulin-dependent kinase II is extremely useful. It is considered to be a powerful tool for elucidating functions.

[0004] Representative inhibitors of calmodulin-dependent kinase II currently being developed from such a viewpoint include non-peptide KN62 and KN93 and the N-region of calmodulin-dependent kinase II. Numerous synthetic peptides derived from certain autoinhibitory domains (e.g.,
CaMK (281-302Ala286) (amino acid sequence: MHRQE
AVDCLKKFNARRKLKGA)].
However, since KN62 and KN93 exert their inhibitory activity by inhibiting the calmodulin binding site, they also inhibit other calmodulin-dependent kinases, resulting in a lack of specificity. There is a disadvantage that the inhibitory activity is reduced depending on the concentration of the. In addition, although synthetic peptides derived from an autoinhibitory domain such as CaMK (281-302Ala286) have been used in various physiological experiments, they have recently been reported to have low inhibitory power and a problem in specificity. (Proc. Natl. Acad. Sci. USA vo
1.91 (1994) 4761-4765).

[0005]

DISCLOSURE OF THE INVENTION The present invention provides a powerful and highly specific inhibitor of calmodulin-dependent kinase, which is a useful tool for elucidating physiological functions involving the enzyme. With the goal.

[0006]

Means for Solving the Problems In view of the conventional circumstances, the present inventors have developed an inhibitor which has a stronger inhibitory activity on calmodulin-dependent kinase II than known inhibitors and which has excellent specificity. While conducting day and night research for the purpose of development, we found that a peptide obtained by substituting 3 to 4 amino acids at a specific site of autocamtide-2 with another amino acid was an inhibitor suitable for the above purpose. The invention has been developed.

The present inventors have already proposed autocamtide-2.
Autocamtide-2 related inh prepared by substituting the 9th amino acid (threonine) with alanine
It has been found that the ibitory peptide (hereinafter referred to as AIP; amino acid sequence: KKALRRQEAVDAL) has a potent and highly specific inhibitory activity against calmodulin-dependent kinase II (Biochemical).
and Biophysical Research Communication vo1.212, N
o.3 (1995) 806-812), the inhibitor of the present invention is more excellent in inhibitory activity than the AIP.

That is, the present invention relates to the following formula: Lys-Lys-X-Leu-Arg-Arg-Gln-Glu-Ala-Phe-Asp-Ala-Tyr (1) wherein X is Ala or Lys. )).

Further, the present invention is an inhibitor for calmodulin-dependent kinase II containing a peptide having the amino acid sequence represented by the above formula (1).

[0010] In the present specification, abbreviations of amino acids, peptides, and the like are used to refer to IUPAC and IUB regulations,
The guidelines shall be in accordance with “Guidelines for Preparing Specifications and the Like Containing Base Sequence or Amino Acid Sequence” (edited by the Patent Office) and conventional symbols in the relevant field.

[0011]

BEST MODE FOR CARRYING OUT THE INVENTION The peptide of the present invention has a specific amino acid sequence represented by the formula Lys-Lys-X-Leu-Arg-Arg-Gln-Glu-Ala-Phe-Asp-Ala-Tyr (1). It is characterized by having. Here, X may be either Ala or Lys. In the present invention, a peptide having Ala is referred to as V10F-AIP,
The peptide having Lys is referred to as A3K / V10F-AIP. Calmodulin-dependent kinase II (CaMK
From the viewpoint of high inhibitory activity against II), A3K / V10F-AIP having Lys as X is preferable. The peptide of the present invention may have one to several amino acids at least at one of the C-terminus and the N-terminus as long as the peptide has the specific amino acid sequence.

The peptide of the present invention is a calmodulin-dependent kinase II belonging to a group of enzymes called Ca ²⁺ / CaM-dependent protein kinase (CaM kinase).
Have the property of activating the strong inhibition of: (CaM kinase II CaMKII), its an IC ₅₀ value, the conditions detailed in Example 1, V10F-AIP is about 8 nM, A3K
/ V10F-AIP is about 4.1 nM.

As will be described later, the peptide of the present invention is a calmodulin-dependent kinase IV (CaKMI) belonging to a multifunctional CaM kinase like CaMKII.
V), cyclic AMP-dependent kinase (catalytic subunit) (PKA) and protein kinase C (PK
The activity of C) has no effect even at a concentration of 1 μM, which is about 10 times the concentration that almost completely inhibits the activity of CaMKII, and has a selective and specific inhibitory activity on CaMKII. ing.

For this reason, the peptide of the present invention comprises CaMK
It is an excellent inhibitor of II and is useful as an extremely useful tool for elucidating the physiological function of CaMKII. That is, the present invention also provides use of the above peptide as an inhibitor having a strong and high selectivity for CaMKII.

[0015]

DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in more detail with reference to embodiments. However, the examples do not limit the technical scope of the present invention in any way, and those skilled in the art can easily modify or change the present invention based on the description of the present specification, and any of them can Included in the technical scope of the invention.

Example 1 Inhibitory activity on calmodulin-dependent kinase II Two kinds of peptides of the present invention (Lys-Lys-Ala-Leu-Arg-Arg-
Gln-Glu-Ala-Phe-Asp-Ala-Tyr: V10F-AIP; Lys-Ly
s-Lys-Leu-Arg-Arg-Gln-Glu-Ala-Phe-Asp-Ala-Tyr: A3
The inhibitory activity of each peptide on CaMKII was determined by measuring the activity of calmodulin-dependent kinase II (CaMKII) in the presence of K / V10F-AIP). In addition, both peptides were synthesized by the fmoc peptide synthesis method using a peptide solid phase synthesizer PSSM8 (manufactured by Shimadzu Corporation) and purified by reversed-phase high performance liquid chromatography according to a conventional method.

The measurement of the enzymatic activity of CaMKII was performed using [γ- ³²
[P] In the presence of ATP, the enzyme was synthesized with the synthetic peptide syntide-2.
(American Peptide Company) at 30 ° C., and measuring the amount of [ ³² P] phosphoric acid incorporated into syntide-2 per minute. In this reaction system, the above peptide (V10F-AIP , A3K / V10F-AI
The inhibitory activity of the peptide was evaluated from the decrease in enzyme activity caused by the presence of P). In addition, syntide-
[ ³² P] phosphate incorporation into Roskoski's method using phosphocellulose paper (Methods. Enzymo
l. 99, 3-6 (1983)).

The composition of the reaction solution for measuring the enzyme activity used was 40
mM HEPES-NaOH (pH 8.0), 5 mM
Magnesium acetate, 40 μM syntide-2, 50 μM
[Γ- ³² P] ATP, 0.01% Tween40, 0.3
mM CaCl ₂ , 1 μM calmodulin, 0.1 m
M EGTA, various concentrations of peptide (V10F-AIP or A3
K / V10F-AIP), and CaMKII was added to this reaction solution at 0.3.
The reaction was started by adding 054 μg / ml. Note that C
aMKII used was isolated and purified from rat cerebral cortex as described in J. Biochem. 115, 1075-1082 (1994).

FIG. 1 shows the results for V10F-AIP.
Alternatively, FIG. 2 shows A3K / V10F-AIP. As can be seen from the results, the peptide of the present invention (V10F-A
IP and A3K / V10F-AIP) inhibited CaMKII in a concentration-dependent manner. The peptide concentration (IC ₅₀ value) required to inhibit the activity of the enzyme by 50% was V10F-AI
It was 8 nM for P and 4.1 nM for A3K / V10F-AIP.

From these IC ₅₀ values, the peptide of the present invention can be identified as CaMK (281-302Ala286), a known inhibitor.
(IC ₅₀ value = 2 μM) and KN93 (IC ₅₀ value = 20 μM)
It can be seen that the inhibitory activity on CaMKII is 500 to 5000 times higher than that of M).

Further, the inhibitory activity is 5 to 10 times higher than that of AIP (IC ₅₀ value = 40 nM), indicating that the peptide of the present invention has extremely high inhibitory activity on calmodulin-dependent kinase II. It was revealed.

Example 2 Reaction specificity In the same manner as in Example 1, the peptide of the present invention (V10F-
In the presence of AIP, A3K / V10F-AIP), in addition to calmodulin-dependent kinase II (CaMKII), calmodulin-dependent kinase IV (CaMKIV), cyclic
AMP-dependent kinase (catalytic subunit) (PK
By measuring the enzymatic activity of each of the multifunctional kinases via various second messengers such as A) and protein kinase C (PKC), it was determined whether the inhibition of the activity by the peptide of the present invention was selective for CaMKII. Examined.

The composition of the reaction solution for measuring the enzyme activity used is as follows.

(1) CaMKII: same as in Example 1 (2) CaMKIV: 40 mM HEPES-NaOH (p
H8.0), 5 mM magnesium acetate, 100 μM
syntide-2, 50 μM [γ- ³² P] ATP, 2 mM D
TT, 0.2 mM CaCl ₂ , 0.84 μM calmodulin, 0.1 mM EGTA, various concentrations of peptide (V10F-AIP or A3K / V10F-AIP), 3.46 μg / ml
Calmodulin-dependent phosphorylase IV (CaMKIV) (3) PKA: 40 mM Mes-NaOH (pH 7.
0) 5 mM magnesium acetate, 100 μM syntid
e-2, 50 μM [γ- ³² P] ATP, 0.01% Tw
een20, various concentrations of peptide (V10F-AIP or A3K / V1
0F-AIP), 0.8 μg / ml cyclic AMP-dependent kinase (catalytic subunit) (PKA) (4) PKC: 40 mM HEPES-NaOH (pH
8.0) 10 mM magnesium acetate, 100 μM
syntide-2, 50 μM [γ- ³² P] ATP, 0.35 m
M CaCl ₂ , 0.01% Tween 20, ₂ μg /
ml 1,2-dioleoyl-rac-glycerol, 20.2 μg / m
l phosphatidylserine, 0.1 mM EGTA, various concentrations of peptide (V10F-AIP or A3K / V10F-AIP),
0.328 μg / ml protein kinase C (PK
C) The results for V10F-AIP are shown in FIG.
The results for V10F-AIP are shown in FIG. As can be seen from these results, calmodulin-dependent kinase
IV, cyclic AMP-dependent kinase (PKA) and protein kinase C (PKC) were hardly affected by the presence of the peptide of the present invention (1 μM). The peptide of the present invention is almost completely CaM at a concentration of 0.1 μM corresponding to 1/10 of the above concentration.
The inhibition of KII activity (FIGS. 3 and 4) indicates that the peptide is an inhibitor with extremely high selectivity for CaMKII.

As shown in Examples 1 and 2, the peptides of the present invention (V10F-AIP, A3K / V10F-AIP)
It has a much stronger inhibitory activity on calmodulin-dependent kinase II than conventionally known inhibitors, and is excellent in selectivity. In particular, the high inhibitory activity of the peptide of the present invention contributes not only to the economic advantage that the amount of the inhibitor in the experimental system can be reduced, but also to the improvement in the selectivity for calmodulin-dependent kinase II. That is, the fact that the concentration of the effective inhibitor can be reduced means that in a system involving protein kinase C, the possibility of inhibiting other enzymes, that is, the risk of inhibiting the pathway involving protein kinase C can be avoided or reduced. This is useful in that respect.

From these, the peptide of the present invention is
It is an excellent inhibitor of calmodulin-dependent kinase II. Recently, calmodulin-dependent kinase
Biological functions and their mechanisms are being explored and proved using AIP, which is a specific inhibitor of II (Molecular
Brain Research 46 (1997) 338-342; THE JOURNAL OFBI
OLOGICAL CHEMISTRY Vol.270, No.51, pp.30257-30259
(1995); The Journal of Neuroscience, 1997, 17 (14) p
p.5357-5365; J. Neurochem. 68, pp169-175 (1997)),
According to the present invention, it is expected that the present invention will greatly contribute to elucidation of various physiological functions mediated by the enzyme over AIP.

[0027]

[Sequence list]

 SEQ ID NO: 1 Sequence length: 13 amino acid Sequence type: amino acid Topology: linear Sequence: Lys Lys Ala Leu Arg Arg Gln Glu Ala Phe Asp Ala Tyr 5 10 SEQ ID NO: 2 Sequence length: 13 amino acid Sequence type: amino acid Topology: linear Sequence: Lys Lys Lys Leu Arg Arg Gln Glu Ala Phe Asp Ala Tyr 5 10

[Brief description of the drawings]

FIG. 1 shows the results of Example 1, which shows that the peptide of the present invention (V10F-AIP) inhibits the activity of calmodulin-dependent kinase II (CaMKII) in a concentration-dependent manner.

FIG. 2 shows the results of Example 1, and shows that the peptide of the present invention (A3K / V10F-AIP) inhibits the activity of calmodulin-dependent kinase II (CaMKII) in a concentration-dependent manner.

FIG. 3 is a view showing the results of Example 2; V10F-A
IP (0.1 μM) is calmodulin-dependent kinase IV (CaMKIV) (（), protein kinase C (P
KC) (□), cyclic AMP-dependent kinase (PK
A) (■) has no effect on its activity and shows that it specifically inhibits its activity on calmodulin-dependent kinase II (CaMKII).

FIG. 4 is a diagram showing the results of Example 2, where A3K / V1
0F-AIP (0.1 μM) is a potent inhibitor of calmodulin-dependent kinase IV (CaMKIV) (○), protein kinase C (PKC) (□), and cyclic AMP-dependent kinase (PKA) (■). Calmodulin-dependent kinase II (CaMKI
It shows that it specifically inhibits its activity against I).

 ──────────────────────────────────────────────────続 き Continued on the front page (72) Inventor Noboru Yumoto 1-3-131 Midorigaoka, Ikeda-shi, Osaka Inside the Industrial Technology Research Institute Osaka Industrial Research Institute (72) Inventor Atsuhiko Ishida No. 5 Nishi-Kagura 4 Asahikawa-shi, Hokkaido Asahikawa Medical University campus (72) Inventor Isamu Kashita, Hokkaido No.5, Nishi-Kagura 4 Asahikawa City, Hokkaido Asahikawa Medical University campus (72) Inventor Sachiko Okuno, Hokkaido No.5, Nishi-Kagura 4 Asahikawa City, Hokkaido Asahikawa Medical University campus (72) (72) Inventor Jin Fujisawa Nishi-Kagura 4 Line 5, Asahikawa Medical University, Asahikawa Medical University

Claims (2)

[Claims] 1. The following formula: Lys-Lys-X-Leu-Arg-Arg-Gln-Glu-Ala-Phe-Asp-Ala-Tyr (1) (wherein X is Ala or Lys). A peptide having the amino acid sequence shown. 2. An inhibitor of calmodulin-dependent kinase II, which comprises the peptide of claim 1.