WO1997016460A1

WO1997016460A1 - Casein fragments having growth promoting activity

Info

Publication number: WO1997016460A1
Application number: PCT/GB1996/002658
Authority: WO
Inventors: John Arthur Smith; Mark Charles Wilkinson; Qing-Ming Liu
Original assignee: Pepsyn Limited
Priority date: 1995-10-31
Filing date: 1996-10-31
Publication date: 1997-05-09
Also published as: JPH11515022A; DE69623803D1; ATE224403T1; EP0861265A1; EP0861265B1; GB9522302D0; DE69623803T2

Abstract

Amino acid sequences substantially identical to the C-terminal end of an α-S2 casein precursor are shown to act as growth promoters. Disclosed are sequences from Bovine α-S2 casein including the 9 C-terminal amino acids: LysValIleProTyrValArgTyrLeu. Also disclosed are foodstuffs and medicaments comprising the peptides of the invention and a method of producing same.

Description

DESCRIPTION

CASEIN FRAGMENTS HAVING GROWTH PROMOTING ACTIVITY

The present invention relates to growth

promoters.

It has long been known that milk contains growth promoting activity for cells that is additional to its nutritional content. Thus, Epidermal Growth Factor (EGF) has been identified in human (Shing and

Klagsbrun, 1984, Petrides, 1985), rat (Raaberg et al, 1990), swine (Tan et al 1990) and goat (Brown and Blakeley, 1983) milk.

Indeed the EGF present in rat milk has been shown to be significant for the normal development of pups (Oka et al 1983). EGF has not, however, been found in bovine milk (Read 1985). Instead insulin-like growth factor (IGF) I and II (Francis et al, 1986) and bovine colostrum growth factor (BCGF), which is structurally related to Platelet-derived Growth Factor (PDGF)

(Shing and Klagsbrun, 1984, Brown and Blakeley, 1984), have been identified.

The applicant has surprisingly discovered that bovine milk contains growth promoting activity for rat mammary fibroblast cell line (Rama 27), which is not significantly stimulated by IGF or PDGF.

Furthermore, they have identified peptide

sequences which elicit this growth promoting activity. The invention relates to a peptide or a salt thereof comprising an amino acid sequence

substantially identical to the C-terminal end of the α-S2 casein precursor.

According to a first aspect of the present invention there is provided the use of a peptide or a salt thereof comprising an amino acid sequence

substantially identical to the C-terminal end of an α-S2 casein precursor, for the manufacture of a

medicament or foodstuff for promoting growth.

Whilst whole casein protein shows no growth activity, the applicant has identified a number of peptides, derived from the C-terminal end of Bovine α-S2 casein, which elicit growth promoting activity.

Indeed, the applicant has shown this growth promoting activity to be present in at least peptides of 9 to 31 amino acids in length which have been derived from the C-terminal end of Bovine α-S2 casein. It is reasonable to hypothesise that the natural sequence responsible for the growth promoting activity is the sequence comprising the last 9 amino acids of the C-terminal end or an even shorter sequence from within the nine amino acid sequence, possibly an 8 or 7 amino acid sequence. Indeed, it may be as short as a 3 amino acid sequence.

The bovine α-S2 casein precursor is characterised in that it has an amino acid sequence

In three letter codes this translates to

The applicant has found that short peptide sequences incorporating the C-terminal sequence

-LysValIleProTyrValArgTyrLeu show growth promoting activity.

According to a second aspect of the present invention there is provided a growth factor comprising the amino acid sequence -LysValIleProTyrValArgTyrLeu

Furthermore, comparison of, for example, the last 20 amino acids of the C-terminal sequence for bovine α-S2 casein with those for goat, and sheep shows a high degree of homology as does to a lesser extent the C-terminal amino acid sequence of rabbit and pig α-S2 casein

The sequences for these are set out below.

In three letter code these translate to:

It will be apparent from this that the C-terminal sequence can vary from species to species and that consequently whilst the preferred sequences comprise those derived from the C-terminal end of the bovine α-S2 casein those of the other species might be used.

Furthermore, due to the similar nature of some amino acids it is possible that minor substitutions may have little effect on the functioning of the sequence.

Thus, for example, Leucine, isoleucine and valine may be interchanged. Tyrosine and phenylalanine may be interchanged, and arginine and lysine may be interchanged

The significance of the discovery is that a peptide supplement which can promote growth can be added to food or drink products, for both human or animal consumption.

According to a further aspect of the present invention there is provided a food or drink product comprising a peptide or salt thereof of the invention.

Preferably the food or drink product is an infant formula or an animal feed. It may be in liquid or powder form.

Whilst it is possible to synthetically produce peptides according to the present invention it would be desirable to produce the peptide in situ from cows milk .

According to a further aspect of the present invention milk is treated with an enzyme to break the casein in the milk into smaller fragments containing the active peptide or a salt thereof of the invention.

Preferably the enzyme is a protease and more particularly one which cleaves lysine cross-bonds.

More preferably still it is plasmin or trypsin.

The invention will be further described by way of example only with reference to the following examples:

EXAMPLE 1

The growth promoting activity of different milk types was determined by precipitating caseins and assaying the supernatants for their ability to

stimulate the incorporation of [3H] thymidine into the DNA of Rama 27 cells by known methodology (Smith et al, 1984).

The results of the tests are illustrated in Fig 1. which shows the growth-promoting activity of different milk types. Three sorts of commercial milks were acidified to precipitate the caseins and assayed for their growth promoting activity. The greatest activity was found in semi-skimmed milk. SDM (step down medium) represents the negative control and FCS (foetal calf serum) represents the positive control. EXAMPLE 2

5 litres of semi-skimmed milk was made to pH 3.0 with HCl and left for 2 hours at 4°C. It was

centrifuged in a Sorvall RC5B centrifuge at 9000 rpm in a GS3 rotor for 40 min, and the supernatant

(approximately 3.6 litres) was poured through glass wool to remove fat. Solid (NH₄)₂SO₄ was added slowly to the supernatant with stirring at 4°C to a

concentration of 22% (w/v), and was left for 2 hours at 4°C without stirring. Precipitated protein was removed by centrifugation as above. To the

supernatant was added further (NH₄)₂SO₄ to a

concentration of 35% (w/v) and the precipitate

recovered as above. The precipitate was redissolved in 1600ml distilled water and dialyzed against running tap water overnight, then against 20mM NaH₂PO₄, pH6.0, for 8 hours.

The active fractions were obtained using a series of chromatographic techniques as outlined in (i) to (iv) below:

(i) The active fraction prepared as above was

subjected to CM-Sepharose chromatography. It was added to a column of CM-Sepharose (10cm × 5cm id, Pharmacia) that had been pre-equilibrated with 20mM Sodium phosphate buffer pH6.0. After loading, the column was washed with 500ml of 50mM NaCl in the same buffer. Protein was eluted with a 1500ml linear gradient of 0.1 to 0.7M NaCl in 20mM sodium phosphate buffer pH 6.0. The bioactive fractions eluted at 0.28M NaCl and approximately 0.4M NaCl - see Fig. 2. In Fig 2 the upper panel shows the absorbance of the protein at 280nm and the lower panel shows the activity (The incorporation of ³H- thymidine into DNA). The sample was from material precipitating between 22 to 35% (NH₄)₂SO₄. After being redissolved and dialyzed it was loaded into the column (10 cm x 5 cm) with 0.05 M NaCl in 20mM NaH₂PO₄, pH 6.0. The eluting gradient was 0.1-0.7 M NaCl in 20 mM

NaH₂PO₄, pH6. The flowrate was 5ml/min, the fraction size was 25 ml each. Two activities eluted at 0.28 M NaCl and 0.34-0.45 M NaCl respectively. The high absorbance at 280 nm at the beginning of the trace indicates the amount of unbound protein. The

fraction-eluted at 0.28 M NaCl was used for further purification.

(ii) The active fractions from the above separation were subjected to hydrophobic interaction

chromatography. It was made 3.7M with NaCl in 20mM NaH₂PO₄, pH6.5, and applied to a butyl Sepharose column (8.6 cm × 2.5 cm id) that had been pre-equilibrated with 4M NaCl in 20mM NaH₂PO₄, pH6.5. Protein was eluted with a decreasing gradient of NaCl as indicated in Fig 3. In Fig. 3 the upper panel shows the absorbance of the protein at 280 nm and the lower panel shows the activity (The incorporation of ³H-thymidine into DNA). The sample was from the early activity after CM-Sepharose chromatography. The column (2.5 cm × 8.6 cm, butyl bonded Sepharose) had been equilibrated with 4 M NaCl in 20 mM NaH₂PO₄, pH 6.5. The flowrate was 3.5 ml/min and fraction size was 3.5 ml. The activity eluted at 1.6 M NaCl, just before the major protein peak.

(iii) The active fractions from the

hydrophobic interaction column were subjected to

Reversed Phased HPLC-1 chromatography. It was applied in 8 batches to a butyl reversed phase column

(Brownlee, 300A pore size, 7μm particle size, 25cm × 4.6mm id) that had been pre-equilibrated with 0.1% TFA. After washing the column with 0.1% TFA, protein was eluted with a gradient of acetonitrile (far uv grade, Rathburns, Walkerburn, Scotland) as indicated in Fig 4. In Fig. 4 the upper panel shows the

absorbance of the protein at 214 nm and the lower panel shows the activity (The incorporation of ³H-thymidine into DNA). The sample was from the activity after hydrophobic interaction chromatography. The column (250 cm × 4.6 mm, C4) had been equilibrated with 0.1% TFA. The flow rate was 0.7 ml/min and fraction size was 0.7 ml. The eluting gradient was 10 to 30% acetonitrile in 0.1% TFA in 30 min. The activity eluted at 23% acetonitrile.

(iv) The active fractions were then subjected to reversed phase HPLC-2 chromatography. The mitogenic fractions from all 8 batches of the above reversed phase chromatograms were pooled and concentrated on a centrifugal drier to a total volume of 100μl. This concentrated material was loaded onto a C18 reversed phase column (ODS ultrasphere, Beckman) which had been pre-equilibrated with 0.1% TFA, and was eluted with a shallow gradient of 20 to 40% acetonitrile, 0.1% TFA over 45 min, at a flow rate of 0.2ml/min. Absorbance was monitored at 214nm, and material from each peak of absorbance was collected separately by hand - see Fig 5. In Fig. 5 the upper panel shows the absorbance of the protein at 214 nm and the lower panel shows the activity (The incorporation of ³H-thymidine into DNA). The sample was from the activity after reversed phase HPLC-1. The column (ODS) had been equilibrated with 0.1% TFA. The flowrate was 0.2 ml/min. Each

absorption peak at 214 nm was collected manually. The eluting gradient was 20 to 40% acetonitrile in 0.1% TFA in 45 min. The peaks A,B,C (arrows) were all active. The purified proteins (peaks A,B,C) obtained in step (iv) were then analysed.

Protein content was measured by the binding of Coomassie Blue according to the Bio-Rad protocol, using bovine gamma globulin as standard. Peptide quantification of fractions separated by HPLC was by their absorbance at 214nm, using cytochrome c and lysozyme as standards.

The protein fractions A,B,C, of the casein digest where assayed for their ability to stimulate the incorporation of [3H] thymidine into the DNA of Rama 27 cells exactly as described previously.

The results are illustrated in Table 1 which shows the growth promoting activity of progressively purified fractions of α-S2 casein.

The peptides from the peaks B and C of reversed phase HPLC-2 were then sequenced. They were found to be a nested series of sequences of 5 peptides. They corresponded to the C-terminus of bovine α-S2 casein. The peak C was solely ThrLysValIleProTyrValArgTyrLeu, the other sequences were from peak B.

The sequences of the peaks are identified below:

To ascertain that the activity was not due to impurities identical peptide sequences were

synthesized on a Milligen/Biosearch 9050 peptide synthesizer (Millipore, Watford) using Fmoc chemistry and pentafluorophenyl esters according to the standard protocol.

Of these initially only

LysValIleProTyrValArgTyrLeu showed bioactivity, but after storage in PBS all the peptides acquired a low level of mitogenicity. The activity of

LysValIleProTyrValArgTyrLeu was substantially

increased when maintained at alkaline pH. By way of contrast alpha-casein was inactive in the mitogenic assay. On digestion with trypsin, activity in the assay was generated, which was separable by reversed phase HPLC from that due to trypsin itself.

The example described herein demonstrates that the growth factor activity of milk is largely due to C-terminal fragments of α-S2 casein.

Given the activity of the peptide it is expected that the addition of from 0.1μg to 10μg, more

particularly about 1 μg of peptide to 250g of feed or drink will provide good growth promotion activity.

However, in order to maintain the activity the synthetic peptides should be stored in alkaline conditions, preferably at about pH 13.

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Claims

1. Use of a peptide or a salt thereof comprising an amino acid sequence substantially identical to the C-terminal end of an α-S2 casein precursor, for the manufacture of a medicament or foodstuff for promoting growth.

2. Use of a peptide as claimed in claim 1, wherein the peptide is derived from bovine, goat, sheep, rabbit or pig α-S2 casein or is a synthesised equivalent or homologue thereof.

3. Use of a peptide as claimed in claim 2, wherein the peptide is derived from bovine α-S2 casein or is a synthesised equivalent or homologue thereof.

4. Use of a peptide as claimed in any of the preceding claims, in which the peptide comprises from 9 to 31 amino acids.

5. Use of a peptide as claimed in any of the preceding claims, in which the peptide comprises 9 amino acids.

6. Use of a peptide as claimed in any of the preceding claims comprising the amino acid sequence:

LysValIleProTyrValArgTyrLeu or a homologue thereof.

7. Use of a peptide as claimed in any of claims 2 to 6, in which the homologues comprise peptides in which :

i) one or more of the amino acids Leu, Ile and

Val are replaced by one another;

ii) one or more of the amino acids Tyr and Phe are replaced by one another; and/or

iii) one or more of the amino acids Arg and Lys are replaced by one another.

8. Use of a peptide as claimed in any of claims

1 to 7, in which the peptide has the sequence:

LysValIleProTyrValArgTyrLeu.

9. Use of a peptide as claimed in any of claims

1 to 7 in which the peptide has the sequence:

ThrLysValIleProTyrValArgTyrLeu.

10. Use of a peptide as claimed in any of claims 1 to 7 in which the peptide has the sequence:

LysThrLysValIleProTyrValArgTyrLeu.

11. Use of a peptide as claimed in any of

claims 1 to 7 in which the peptide has the sequence:

AlaMetLysProTrpIleGlnProLysThrLysValIleProTyrValArgTyrLeu.

12. Use of a peptide as claimed in any of claims 1 to 7 in which the peptide have the sequence:

ProGlnTyrLeuLysThrValTyrGlnHisGlnLysAlaMetLysProTrpIleGlnPro LysThrLysValIleProTyrValArgTyrLeu.

13. Use of a peptide as claimed in any of the

preceding claims in which foodstuff is an infant

formula or an animal feed.

14. Use of a peptide as claimed in any of the preceding claims in which the medicament or foodstuff is a liquid or powder.

15. Use of a peptide as claimed in any of the preceding claims, in which the medicament or foodstuff comprises whole milk or semi-skimmed milk.

16. Use of a peptide as claimed in any of the preceding claims, in which the medicament or foodstuff has an alkaline pH.

17. Use of a peptide as claimed in any of the preceding claims, in which the peptide is present in an effective amount.

18. Use of a peptide as claimed in claim 17, wherein the effective amount is 0.1 to 10μg to 250g of medicament or foodstuff.

19. A food or drink product comprising a peptide or a salt thereof comprising an amino acid sequence substantially identical to the C-terminal end of an α-S2 casein precursor.

20. A method of producing a medicament or foodstuff comprising a growth promoting peptide comprises treating milk with an enzyme to break milk casein present in the milk into one or more peptides comprising an amino acid sequence substantially identical to the C-terminal end of the α-S2 casein precursor.