Patent Application
20050239695
The present invention relates to a novel method for the formation of an intramolecular disulfide bond in peptide or peptidomimetic molecules.
Many biologically active peptides which are useful in the treatment of various disorders are known to contain disulfide bonds (1, 2). Many of these are already registered as pharmaceuticals, while others are still at the development stage; some significant examples of peptides with disulfide bonds arm listed below:
Octreotide:
Vapreotide:
Eptifibatide:
Somatostatin:
Oxytocin:
Methods which are conventionally used for the formation of disulfide bonds make use of linear precursors which contain cysteine or other derivatives containing —SH groups in the free form, which are subjected to oxidative processes by means of various oxidising agents. These oxidative methods have been thoroughly described in the literature (3, 4).
The main disadvantage of oxidative methods is the exposure of the peptide molecule to oxidising agents which can bring about the formation of impurities, with consequent low process yields and difficulties in purification. These treatments may furthermore result in the partial inactivation of the peptide from the standpoint of biological activity.
Other disadvantages, especially for the purposes of industrial production, arise from the fact that some of these processes, whether in the —SH group deprotection phase or in the oxidation phase, use reactants such as heavy metals, iodine, potassium ferricyanide, etc., which entail appropriate disposal methods.
A non-oxidative process for the cyclisation of peptides has been described in (5). The principle disadvantage of this method, which makes use of the presence of a preformed —S—S-alkyl group, resides in the necessity of appropriately disposing of the toxic gases (alkyl mercaptans) which are released by the reaction.
It is also known (6) that the —S-sulfonate group (Bunte salt) reacts with the —SH groups to form disulfide bonds; moreover, in those cases known in the literature, the —S-sulfonate group has been introduced into peptide molecules by oxidative sulfitolysis of cysteine residues and this strategy cannot be applied to the preparation of cyclic peptides, which requires the simultaneous presence, in the same molecule, of an —S-sulfonate group and a free —SH group.
The possibility of introducing preformed -S-sulfonate groups during the synthesis of peptide molecules has been described (8). We have now found, and this is the subject matter of the present invention, that the second —SH group in free form, which is necessary for the formation of the intramolecular disulfide bond, may be obtained, in presence of the —S-sulfonate group, by selectively removing, under suitable acidic conditions, a protective group of the trityl or at least acid-labile type.
The present invention provides a novel synthesis method, which is simple and non-oxidative, for the cyclisation of peptide or peptidomimetic molecules by means of the formation of intramolecular disulfide bonds; said method comprises:
The process of the present invention may be applied to any linear peptide or peptidomimetic compound which contains at least two cysteines or other residues with —SH groups in the side chain. The amino acid derivative containing a first —SH group (normally a cysteine) is initially protected with a protective group which may be removed selectively with regard to the S-sulfonate group; said protective groups and the associated conditions of use are well known in the art and are described, for example, in (7), which is incorporated herein by reference; preferably, they are selected from among 4-methoxytrityl (Mmt), 2,4,6-trimethoxybenzyl (Tmob), 4,4′,4″-trimethoxytrityl (TmTr), trityl (Trt), with trityl (Trt) being the particularly preferred protective group. The remaining one of the two SH groups which will then be used to form the disulfide bond is thus protected with the S-sulfonate group; such S-sulfonate groups and the associated application methods are likewise known from the art and are, for example, described in (8), which is incorporated herein by reference. In practice, the peptide to be cyclised is synthesised chemically using amino acid derivatives containing already protected —SH groups (in the case both of the acid-labile protection and of the sulfonate group), so as to avoid possible selectivity problems.
The subsequent step then involves the selective removal of the first acid-labile protective group; in this manner, a peptide is obtained which comprises a free —SH group and an —SH group protected by an S-sulfonate group. However, known prior art conditions for removing the above-stated protective group exhibit a series of disadvantages; for example, incorrect deblocking of the protective group may damage the polypeptide chain and, in particular, may also deblock the second —SH residue protected by the sulfonate group.
One of the characterising aspects of the present invention is thus that of having found specific reaction conditions which permit selective deblocking of the first —SH group with regard to the —SH group protected by the sulfonate group. In a preferred aspect of the present invention, selective liberation of the —SH group is performed in an anhydrous aprotic non-polar organic solvent in the presence of anhydrous trifluoroacetic acid and a suitable carbocation scavenger, such as for example triisopropylsilane. Preferably, the protective group is trityl and the deblocking reaction is performed in the presence of a mixture of trifluoroacetic acid and triisopropylsilane in ratios by volume of between 90:10 and 99:1, still more preferably in a ratio of approx. 95:5.
The reaction conditions are compatible with the presence of further scavengers capable of scavenging carbocations, such as for example anisole, derivatives of tryptophan, such as tryptophan methyl ester (H-Trp-OMe) and/or phenol; said scavengers are used in quantities of between 1 and 3, preferably approx. 2, equivalents relative to the peptide to be cyclised; phenol has proved to be the best of these.
Finally, the anhydrous aprotic non-polar solvent is preferably selected from among dichloromethane, chloroform, dichloroethane, trichloroethylene and/or tetrachloroethylene, with dichloromethane being particularly preferred. This solvent is preferably used in a quantity of between 25 and 10 litres, preferably between 20 and 15 litres, per mole of peptide to be cyclised. The preferred ratio between the solvent and trifluoroacetic acid is approx. 2.2:1 by volume.
Simply dissolving the peptide comprising a free —SH group and an —SH group protected by an S-sulfonate group at a pH of between 5 and 9 spontaneously gives rise, without the necessity for other reactants, to the formation of the disulfide bond by displacement of the S-sulfonate group.
As shown in Tables 1 and 2, the percentage conversions over time, reaction times and purity at different pH values were evaluated in order to define the pH range within which to perform the cyclisation. The optimum pH has proved to be between 5 and 9, and in particular the pH used is pH 8.3.
In the Table, 8SH indicates the linear intermediate, while octreotide is the example of a cyclised peptide with a disulfide bridge.
Using a pH of less than 5 results in slow reaction times, an incomplete reaction and poor purity. Using a pH of greater than 9 should be avoided due to possible racemisation reactions with the formation of difficult to identify diastereomers, which are typical of peptides with a basic pH (9, 10). Using a pH of greater than 9 should also be avoided due to possible disproportionation reactions which would cause the disulfide bridge to break with the possible formation of dimers or oligomers (11).
Formation of the disulfide bond is thus preferably performed at a pH of between 7 and 9, still more preferably of between 8 and 8.5.
The reaction solvent is preferably a mixture of buffer solution/aprotic polar organic solvent at a suitable pH: the buffer will be prepared using salts such as sodium or potassium phosphates or ammonium acetates, preferably sodium phosphate; the aprotic polar organic solvent will be selected from among acetonitrile, tetrahydrofuran, dimethylformamide, more preferably acetonitrile.
Said aprotic polar organic solvent is preferably present in a quantity of 0.5-1.5 volumes per volume of said aqueous buffer, still more preferably in quantity of 0.8-1.2 volumes per volume of said aqueous buffer.
The reaction is moreover preferably performed at a temperature of between 0 and 50° C., still more preferably at a temperature of between 15 and 30° C.; the time required to perform cyclisation is usually between 5 minutes and 24 hours, preferably between 5 and 60 minutes.
The resultant peptide may then be isolated and/or subjected to further purification with the methods normally used for the purification of peptides (phase inversion, ion exchange, etc.); in particular, it may be isolated by precipitation, for example by addition of methyl tert.-butyl ether (MTBE), ethyl ether, n-hexane or n-heptane to the aqueous buffer, with methyl tert.-butyl ether being particularly preferred.
The linear precursor may be prepared in solution or in the solid phase, by sequential attachment of the amino acid derivatives or by fragments, using methods which are well known in peptide synthesis, which provide protection for the side chains, and subsequent protection and deprotection of the terminal amino group. Carboxyl activation makes it possible to use active esters, EDC, DCC or other typical peptide synthesis methods (10).
The novel cyclisation method has been used in the synthesis of various cyclic peptides with a disulfide bond such vapreotide, eptifibatide and octreotide. Scheme 1 shows, purely by way of example, the application of the method to the preparation of the peptide octreotide: the peptide is obtained by cyclisation of the linear precursor H-DPbe-Cys(SO3Na)-Phe-DTrp-Lys-Thz-Cys-T-ol (8SH).
The following Examples are given purely by way of example and do not limit the invention.
The stability of the sulfonate protective group under trityl removal conditions was evaluated, using Fmoc-Cys(SO3Na)—ONa and Fmoc-Cys(Trt)-OH as model products. The two products (100 mg of each) were suspended separately in dichloromethane (1 ml) and trifluoroacetic acid (0.5 ml) and triisopropylsilane (0.05 ml) were added. The formation of Fmoc-Cys-OH (the product obtained by removal of the protective groups) was evaluated by HPLC.
The formation of Fmoc-Cys-OH was evaluated using a Vydac C18 (5 μm) (4.6×250) mm column.
Fmoc-Cys-OH was identified by means of LC-MS; [M+H]+=344
After 15 minutes, removal of the trityl from Fmoc-Cys(Trt)-OH was practically complete, while no removal of the protective group from Fmoc-Cys(SO3Na)—ONa was observed, apart from a tiny percentage and that only starting from 30 minutes.
The protected octapeptide [Boc-DPhe-Cys(SO3Na)-Phe-DTrp-Lys(Boc)-Thr-Cys(Trt)-Thr-ol] (0.27 moles; 420 g) and methylene chloride (4.9 l) were introduced into a 50 litre reactor. Phenol (0.54 moles; 50 g) and trifluoroacetic acid [TFA] (2.19 l), were added and the mixture was stirred for 10 minutes at 23° C. Triisopropylsilane [TIS] (1.2 moles; 247 ml) was added to the solution and the mixture was stirred for 5 minutes. Finally, methyl tert.-butyl ether [MTBE] (19.7 l) was added and the mixture stirred for at least 60 minutes. The solid was filtered out, washed with MTBE (10.4 l) and dried under a vacuum at 30 ° C. for at least 15 hours.
The solid obtained [2TFA.H-DPhe-Cys(SO3Na)-Phe-DTrp-Lys-Thr-Cys-Thr-ol] was introduced into a 100 litre reactor together with acetonitrile (39.1 l) and the mixture was stirred at 23° C. for at least 5 minutes.
A phosphate buffer solution which had previously been flushed with nitrogen (39.1 l of 0.2 molar buffer prepared with 1394 g of Na2HPO4*2H2O, 39.1 l of H2O and adjusted to pH=8.3 by addition of H3PO4) was added to the reaction mixture, and the mixture was stirred under nitrogen at 23° C. until the disulfide bond formed. The reaction mixture was acidified with trifluoroacetic acid (0.731 l) to pH =3.
The volatile fraction was removed under a vacuum, then the NaCl (5.7 kg) and tetrahydrofuran (12.6 l) were introduced. The mixture was stirred, allowed to separate out and the phases were separated. The aqueous phase was reintroduced into the reactor with tetrahydrofuran (12.6 l). The mixture was stirred, allowed to separate out and the phases were separated. The combined organic phases were concentrated under a vacuum until a stirrable residue was obtained. The residue was resuspended three times with isopropanol (29.7 l), then isopropanol (3.5 l) was added. Once the complete removal of the water had been verified by Karl Fischer analysis, the salts were filtered out and washed with isopropanol (1.5 l). The alcoholic solution (8.1 l) was added dropwise to a mixture of n-hexane (60 l) and MTBE (19.9 l) at 0° C. The precipitate was stirred for at least 15 minutes. The product was filtered out, washed with n-hexane (7.5 l) and dried under a vacuum at 30° C. for at least 15 hours.
The product was identified by means of LC-MS: [M+H]+=1019 and HPLC (identification relative to standard).
HPLC method used:
| Number | Date | Country | Kind |
|---|---|---|---|
| MI2004A000812 | Apr 2004 | IT | national |
