Human nerve growth factor by recombinant technology

Abstract

The .beta.-subunit of human nerve growth factor (.beta.NGF) is prepared in essentially pure form in commercially viable quantities using recombinant DNA technology. The nucleotide sequence and vectors encoding human .beta.NGF and host cells transformed with the vectors are also provided.

Description

FIELD OF THE INVENTION

This invention relates to the polypeptide hormone human Nerve Growth Factor (NGF), its preparation using recombinant technology and compositions which contain it.

BACKGROUND OF THE INVENTION

A. Nerve Growth Factor

A multi-component protein of molecular weight .about.130,000 has been isolated from mouse salivary glands, it being particularly concentrated in the glands of male mice, which is commonly referred to as "Nerve Growth Factor." The principal neural activity exhibited by the protein has been its ability to cause an increase in the size of sensory neurons, nerve cells which transmit impulses from sensory receptors to the brain, and in the size of sympathetic neurons, one of the two kinds of neurons which make up the autonomic nervous system which regulates the functional activity of the circulatory system, the glands, smooth muscles and other organs.

NGF as obtained by extraction at neutral pH from mouse salivary glands is known as 7S NGF and is made up of three subunits termed .alpha.-, .beta.-, and .gamma.-subunits. All of the neural activity of 7S NGF is exhibited by the .beta.-subunit, a dimer of two identical 118 amino acid peptides bound together by non covalent forces. This subunit is also referred to as 2.5S NGF. The .alpha.-subunit has no known biological activity. The .gamma.-subunit, however, is an arginine esteropeptidase. The initial genetic product in the synthesis of NGF is a prepro-NGF polypeptide which is cleaved by the .gamma.-subunit. The .gamma.-subunit has also been shown to accelerate wound healing in mice.

Recently, a third NGF component (M. wt. .about.116,000) has been reported to have been isolated from mouse salivary glands and to have shown to exhibit the property of being a plasminogen activator, i.e., it converts plasminogen to plasmin, suggesting its utility in the lysis of blood clots. See European Patent Application "Nerve Growth Factor and Process For Obtaining It" 78300656.2 (Publication No. 0002139Al) filed Nov. 22, 1978, published May 30, 1979.

As indicated above, the neural activity of NGF is exhibited by the .beta.-subunit (hereinafter .beta.NGF). It has been shown to stimulate markedly regenerative resprouting of transected axons of central adrenergic neurons, a property which makes it useful in the repair of damaged axons.

B. Recombinant DNA Technology

Recombinant DNA technology has reached the age of some sophistication. Molecular biologists are able to recombine various DNA sequences with some facility, creating new DNA entities capable of producing copious amounts of exogenous protein product in transformed microbes and cell cultures. The general means and methods are in hand for the in vitro ligation of various blunt ended or "sticky" ended fragments of DNA, producing potent expression vectors useful in transforming particular organisms, thus directing their efficient synthesis of desired exogenous product. However, on an individual product basis, the pathway remains tortuous and the science has not advanced to a stage where regular predictions of success can be made. Indeed, those who portend successful results without the underlying experimental basis, do so at considerable risk of inoperability.

DNA recombination of the essential elements, i.e., an origin of replication one or more phenotypic selection characteristics, an expression promoter, heterologous gene insert and remainder vector, generally is performed outside the host cell. The resulting recombinant replicable expression vector, or plasmid, is introduced into cells by transformation and large quantities of the recombinant vehicle are obtained by growing the transformant. Where the gene is properly inserted with reference to portions which govern the transcription and translation of the encoded DNA message, the resulting expression vector is useful to produce the polypeptide sequence for which the inserted gene codes, a process referred to as "expression." The resulting product may be obtained by lysis, if necessary, of the host cell and recovery of the product by appropriate purifications from other proteins.

In practice, the use of recombinant DNA technology can express entirely heterologous polypeptides--so-called direct expression--or alternatively may express a heterologous polypeptide fused to a portion of the amino acid sequence of a homologous polypeptide. In the latter cases, the intended bioactive product is sometimes rendered bioinactive within the fused, homologous/heterologous polypeptide until it is cleaved in an extracellular environment.

Similarly, the art of cell or tissue cultures for studying genetics and cell physiology is well established. Means and methods are in hand for maintaining permanent cell lines, prepared by successive serial transfers from isolated normal cells. For use in research, such cell lines are maintained on a solid support in liquid medium, or by growth in suspension containing support nutriments. Scale-up for large preparations seems to pose only mechanical problems.

Likewise, protein biochemistry is a useful, indeed necessary, adjunct in biotechnology. Cells producing the desired protein also produce hundreds of other proteins, endogenous products of the cell's metabolism. These contaminating proteins, as well as other compounds, if not removed from the desired protein, could prove toxic if administered to an animal or human in the course of therapeutic treatment with desired protein. Hence, the techniques of protein biochemistry come to bear, allowing the design of separation procedures suitable for the particular system under consideration and providing a homogeneous product safe for intended use. Protein biochemistry also proves the identity of the desired product, characterizing it and ensuring that the cells have produced it faithfully with no alterations or mutations. This branch of science is also involved in the design of bioassays, stability studies and other procedures necessary to apply before successful clinical studies and marketing can take place.

SUMMARY OF THE INVENTION

The present invention provides the .beta.-subunit of human NGF, which previously had not been isolated by extraction techniques or otherwise synthesized, in essentially pure form. Further, we have discovered that, unexpectedly, .beta.-NGF can be expressed as a heterologous protein in E. Coli as a mature polypeptide, i.e., free of any fused homologous protein which might be required to afford it protection from cellular enzymes which recognize it as foreign protein. We believe the .beta.-subunit of NGF to be the smallest protein directly expressed as mature protein in E. coli.

The .beta.-NGF which the invention provides is useful in treating nerve damage or for other related purposes for which it is beneficial. Being identical with naturally secreted human .beta.-NGF, but free of other protein of mammalian origin, it is unlikely its use will result in an immunogenic response during treatment with it, unlike the case when peptide hormones of non-human origin are used to treat human illness. Furthermore, being obtained as a heterologous protein, the .beta.-NGF will be essentially free of other proteins of mammalian origin which accompany .beta.-NGF obtained as a tissue extract and which may exhibit undesirable biological activity in compositions which contain them.

The invention is further directed to replicable DNA expression vectors which contain a gene sequence which codes for the polypeptide in expressible form. The invention is also directed to recombinant host cells such as microorganism strains or cell lines transformed with such vectors, and to the cultures thereof. Still further, the invention is directed to compositions comprising the polypeptide for parenteral administration.

Accordingly an object of this invention is to acquire human .beta.-NGF essentially free of other mammalian proteins.

Another object is to obtain human .beta.-NGF in quantities in excess of those which are possible by extraction from natural sources.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the amino acid sequence of the .beta.-subunit of mouse NGF and gene sequences coding for it and the complementary DNA strands for specific segments of the gene.

FIG. 2 shows a Northern Blot Analysis of clones containing segments of .beta.NGF mRNA.

FIG. 3 is a partial restriction map of the mouse NGF gene and the approximate correspondence between the nucleotide sequences of plasmids constructed in the making of the invention with the nucleotide sequence of the mouse NGF gene.

FIG. 4 shows the physical map of the recombinant phage .lambda.hN8 and flanking regions in the human genome.

FIG. 5 is the nucleotide sequence of the human .beta.NGF chromosomal gene.

FIG. 6 shows a comparison of nucleotide sequences of human and mouse Prepro- .beta.NGF gene and amino acid sequences.

FIG. 7 shows the gene constructed for expression of human .beta.NGF.

FIG. 8 depicts a portion of the process for assembling the plasmid ph.beta.NGFtrpl for transformation of E. coli to express human .beta.NGF.

DETAILED DESCRIPTION

Host Cell Cultures and Vectors

As used in the present application, the term "expression vector" includes vectors which are capable of expressing DNA sequences contained therein, where such sequences are operably linked to other sequences capable of effecting their expression. It is implied, although not always explicitly stated, that these expression vectors must be replicable in the host organisms either as episomes or as an integral part of the chromosomal DNA. Clearly a lack of replicability would render them effectively inoperable. In sum, "expression vector" is given a functional definition, and any DNA sequence which is capable of effecting expression of a specified DNA code disposed therein is included in this term as it is applied to the specified sequence. In general, expression vectors of utility in recombinant DNA techniques are often in the form of "plasmids" which refer to circular double stranded DNA loops which, in their vector form, are not bound to the chromosome. In the present specification, "plasmid" and "vector" are used interchangeably as the plasmid is the mostcommonly used form of vector. However, the invention is intended to includesuch other forms of expression vectors which serve equivalent functions andwhich become known in the art subsequently hereto.

Further as used herein, the term "recombinant host cells" refers to cells which have been transformed with vectors constructed using recombinant DNAtechniques.

The vectors and methods disclosed herein are suitable for use in host cellsover a wide range of prokaryotic and eukaryotic organisms.

In general, of course, prokaryotes are preferred for cloning of DNA sequences in constructing the vectors useful in the invention. For example, E. coli K12 strain 294 (ATTC No. 31446) is particularly useful. Other microbial strains which may be used include E. coli strains such as E. coli B, and E. coli X1776 (ATTC No. 31537). These examples are, of course, intended to be illustrative rather than limiting.

Prokaryotes may also be used for expression. The aforementioned strains, aswell as E. coli W3110 (F.sup.-, .lambda..sup.-, prototrophic, ATTC No. 27325), bacilli such as Bacillus subtilus, and other enterobacteriaceae such as Salmonella typhimurium or Serratia marcescens, and various Pseudomonas species may be used.

In general, plasmid vectors containing replicon and control sequences whichare derived from species compatible with the host cell are used in connection with these hosts. The vector ordinarily carries a replication site, as well as marking sequences which are capable of providing phenotypic selection in transformed cells. For example, E. coli is typically transformed using pBR322, a plasmid derived from an E. coli species (Bolivar, et al., Gene 2:95 (1977)). pBR322 contains genes for ampicillin and tetracycline resistance and thus provides easy means for identifying transformed cells. The pBR322 plasmid, or other microbial plasmid, must also contain, or be modified to contain, promoters which canbe used by the microbial organism for expression of its own proteins. Thosepromoters most commonly used in recombinant DNA construction include the .beta.-lactamase (penicillinase) and lactose promoter systems (Chang et al, Nature, 275:615 (1978); Itakura, et al., Science, 198: 1056 (1977); Goeddel, et al, Nature,281: 544 (1979)) and a tryptophan (trp) promoter system (Goeddel, et al, Nucleic Acids Res., 8: 4057 (1980); EPO Appl. Publ. No.. 0036776). While these are the most commonly used, other microbial promoters have been discovered and utilized, and details concerning their nucleotide sequences have been published, enabling a skilled worker to ligate them functionally with plasmid vectors (Siebenlist, et al, Cell 20: 269 (1980)).

In addition to prokaryotes, eukaryotic microbes, such as yeast cultures, may also be used. Saccharomyces cerevisiae, or common baker's yeast, is the most commonly used among eukaryotic microorganisms, although a number of other strains are commonly available. For expression in Saccharomyces, the plasmid YRp7, for example, (Stinchcomb, et al, Nature, 282: 39 (1979);Kingsman, et al, Gene, 7: 141 (1979); Tschemper, et al, Gene, 10: 157 (1980)) is commonly used. This plasmid already contains the trpl gene which provides a selection marker for a mutant strain of yeast lacking theability to grow in tryptophan, for example ATCC No. 44076 or PEP4-1 (Jones,Genetics, 85: 12 (1977)). The presence of the trpl lesion as a characteristic of the yeast host cell genome then provides an effective environment for detecting transformation by growth in the absence of tryptophan.

Suitable promoting sequences in yeast vectors include the promoters for 3-phosphoglycerate kinase (Hitzeman, et al., J. Biol. Chem., 255: 2073 (1980)) or other glycolytic enzymes (Hess, et al, J. Adv. Enzyme Reg., 7: 149 (1968); Holland, et al, Biochemistry, 17: 4900 (1978)), such as enolase, glyceraldehyde-3-phosphate dehydrogenase, hexokinase, pyruvate decarboxylase, phosphofructokinase, glucose-6-phosphate isomerase, 3-phosphoglycerate mutase, pyruvate kinase, triosephosphate isomerase, phosphoglucose isomerase, and glucokinase. In constructing suitable expression plasmids, the termination sequences associated with these genesare also ligated into the expression vector 3' of the sequence desired to be expressed to provide polyadenylation of the mRNA and termination. Otherpromoters, which have the additional advantage of transcription controlled by growth conditions, are the promoter regions for alcohol dehydrogenase 2, isocytochrome C, acid phosphatase, degradative enzymes associated with nitrogen metabolism, and the aforementioned glyceraldehyde-3-phosphate dehydrogenase, and enzymes responsible for maltose and galactose utilization (Holland, ibid.). Any plasmid vector containing yeast-compatible promoter, origin of replication and termination sequencesis suitable.

In addition to microorganisms, cultures of cells derived from multicellularorganisms may also be used as hosts. In principle, any such cell culture isworkable, whether from vertebrate or invertebrate culture. However, interest has been greatest in vertebrate cells, and propagation of vertebrate cells in culture (tissue culture) has become a routine procedure in recent years [Tissue Culture, Academic Press, Kruse and Patterson, editors (1973)]. Examples of such useful host cell lines are VERO and HeLa cells, Chinese hamster ovary (CHO) cell lines, and W138, BHK, COS-7 and MDCK cell lines. Expression vectors for such cells ordinarily include (if necessary) an origin of replication, a promoter located in front of the gene to be expressed, along with any necessary ribosome binding sites, RNA splice sites, polyadenylation site, and transcriptional terminator sequences. It will be understood that this invention, although described herein in terms of a preferred embodiment, should not be construed as limited to those sequences exemplified.

For use in mammalian cells, the control functions on the expression vectorsare often provided by viral material. For example, commonly used promoters are derived from polyoma, Adenovirus 2, and most frequently Simian Virus 40 (SV40). The early and late promoters of SV40 virus are particularly useful because both are obtained easily from the virus as a fragment whichalso contains the SV40 viral origin of replication (Fiers, et al, Nature, 273: 113 (1978) incorporated herein by reference). Smaller or larger SV40 fragments may also be used, provided there is included the approximately 250 bp sequence extending from the Hind III site toward the Bgl I site located in the viral origin of replication. Further, it is also possible, and often desirable, to utilize promoter or control sequences normally associated with the desired gene sequence, provided such control sequencesare compatible with the host cell systems.

An origin of replication may be provided either by construction of the vector to include an exogenous origin, such as may be derived from SV40 orother viral (e.g. Polyoma, Adeno, VSV, BPV, etc.) source, or may be provided by the host cell chromosomal replication mechanism. If the vectoris integrated into the host cell chromosome, the latter is often sufficient.

Methods Employed

If cells without formidable cell wall barriers are used as host cells, transfection is carried out by the calcium phosphate precipitation method as described by Graham and Van der Eb, Virology, 52: 546 (1978). However, other methods for introducing DNA into cells such as by nuclear injection or by protoplast fusion may also be used.

If prokaryotic cells or cells which contain substantial cell wall constructions are used, the preferred method of transfection is calcium treatment using calcium chloride as described by Cohen, F.N., et al, Proc.Natl. Acad. Sci. (USA), 69: 2110 (1972).

Construction of suitable vectors containing the desired coding and control sequences employs standard ligation techniques. Isolated plasmids or DNA fragments are cleaved, tailored, and religated in the form desired to formthe plasmids required.

Cleavage is performed by treating with restriction enzyme (or enzymes) in suitable buffer. In general, about 1 .mu.g plasmid or DNA fragments is used with about 1 unit of enzyme in about 20.mu.l of buffer solution. (Appropriate buffers and substrate amounts for particular restriction enzymes are specified by the manufacturer.) Incubation times of about 1 hour at 37.degree. C. are workable. After incubations, protein is removed by extraction with phenol and chloroform, and the nucleic acid is recovered from the aqueous fraction by precipitation with ethanol.

If blunt ends are required, the preparation is treated for 15 minutes at 15.degree. with 10 units of E. coli DNA Polymerase I (Klenow), phenol-chloroform extracted, and ethanol precipitated.

Size separation of the cleaved fragments is performed using 6 percent polyacrylamide gel described by Goeddel, D., et al, Nucleic Acids Res., 8:4057 (1980), incorporated herein by reference.

For ligation, approximately equimolar amounts of the desired components, suitably end tailored to provide correct matching, are treated with about 10 units T4 DNA ligase per 0.5 .mu.g DNA. (When cleaved vectors are used as components, it may be useful to prevent religation of the cleaved vector by pretreatment with bacterial alkaline phosphatase.)

The ligation mixture was used to transform E. coli K12 strain 294 (ATLC 31446), and successful transformants were selected by ampicillin resistance. Plasmids from the transformants were prepared, analyzed by restriction and/or sequenced by the method of Messing, et al, Nucleic Acids Res., 9: 309 (1981) or by the method of Maxam, et al, Methods in Enzymology, 65: 499 (1980).

Preferred Embodiments

The following description of preferred embodiments involving polypeptide expression in E. coli is intended to illustrate but not to limit the invention.

Isolation of cDNA clones coding for mouse pro-.beta.NGF

In order to obtain a gene coding for the .beta.-subunit of human NGF, it was determined to use cloned cDNA coding for mouse .beta.NGF as a hybridization probe.

The cDNA cloning approach took advantage of the known amino acid sequence of the mouse .beta.NGF subunit which is shown in FIG. 1, employing synthetic oligonucleotide primers; the difference in NGF levels found in male and female mouse salivary glands was used as an additional means of identification. Three small portions of the mouse .beta.NGF amino acid sequence were chosen, and oligonucleotide pools complementary to all possible sequences coding for them were synthesized by the method of Crea,et al, Nucleic Acids Res., 8: 2331 (1980). The nucleotide sequences for thecoding and complementary strands are shown in FIG. 1.

Initial attempts to identify or isolate mouse .beta.NGF cDNA clones from anoligo dT-primed, cDNA bank from male mouse salivary glands failed, using the synthetic oligonucleotides as hybridization probes. This result indicated that while .beta.NGF comprised 0.1 percent of the protein in themale salivary glands, its mRNA was not of equal abundance. Therefore, the primer pool representing sequences closest to the carboxyl terminus of theprotein (FIG. 1, 1) was used to specifically prime reverse transcription ofpolyA-containing (A+) RNA, from male salivary glands, in order to first enrich for .beta.NGF-specific nucleotide sequences. Molecules of cDNA greater than 200 bp in length were cloned into the well known plasmid pBR322. A total of 10,000 clones was screened using the 5'-.sup.32 P-labeled NGF primer pool originally used in the cDNA priming as a hybridization probe and 0.8 percent of the clones gave a positive signal under high stringency hybridization conditions. It is likely that the remaining 99.2 percent of the "primed" cDNA bank resulted from self-priming as well as from priming by trace amounts of oligo dT eluted during preparation of polyA.sup.+ MSG RNA. S1 nuclease treatment during the cloning procedure may also have damaged some of the terminal primer sequence, resulting in fewer detected positive clones.

Clones scored as positive in the first screen were rescreened using radiolabeled primer pools 2 and 3 derived from DNA sequences upstream fromoligonucleotide pool 1 as shown in FIG. 1, as hybridization probes. In addition, .sup.32 P-cDNA primed with pool 1 from polyA.sup.+ RNA from either male or female mouse salivary glands were used as probes on duplicate filters. A total of 10 male-specific clones, again in pBR322, which hybridized with oligonucleotide pools 2 and 3 were identified. Restriction enzyme analyses demonstrated that all 10 had common HaeIII andHinfI fragments. The clone containing a plasmid which we designated pm.beta.N-9G1 and which expressed the longest DNA insert (.about.700 bp) was sequenced in its entirety. The amino acid sequence deduced from the nucleotide sequence contained the expected NGF sequence in one translational frame in addition to an NH.sub.2 -terminal pro-sequence. SeeFIG. 4. Further details of the construction and identification of bacterialclones containing mouse NGF cDNA sequences are given hereinafter.

In order to determine the size of the complete NGF mRNA, northern blot hybridization as well as primer extension analysis was employed. A 470 bp long .sup.32 P-labeled DNA fragment (RsaI-RsaI 789, FIG. 3) that included NGF as well as propeptide sequences hybridized to an RNA species about 1300 nucleotides long which was male mouse salivary gland specific. A primer extension experiment using 2 short, double stranded, 5' end-labeledrestriction fragments (see legend, FIG. 3) localized the 5' end of the .beta.NGF mRNA to about 230 bases upstream from the 5' end of the pm.beta.N-9Gl cDNA fragment, leaving approximately 370 bases downstream from the 3' end of our clone. All but .about.30 nucleotides of the missing5' sequences are contained in clones we designated pm.beta.N-16F7 and pm.beta.N-21B5, which overlap each other and clone pm.beta.N-9G1 as shown in FIG. 3 and which were isolated as described in the more detailed discussion hereinafter concerning the use of restriction fragments to prime cDNA synthesis.

In order to obtain cloned cDNA which included the sequences from the 3' endof the primer sequence downstream to the 3' polyA sequence, we first enriched for .beta.NGF mRNA by fractionating total polyA.sup.+ male mouse salivary gland RNA on a preparative urea agarose gel. The largest size fraction, containing sequences hybridizing to a .beta.NGF cDNA probe, was used for oligo dT-primed cDNA synthesis and cloning. The screening of 3,700 clones resulted in 4 positive hybridization signals. Nucleotide sequence analysis of clones we designated pm.beta. N-12E4, and pm.beta.N-8B3 added 239 nucleotides to the 3' coding and untranslated sequences. Although oligo dT primed, none of our clones contained the entire 3' untranslated region of .beta.NGF mRNA due to incomplete synthesis of the second DNA strand or to extensive Sl nuclease treatment. Northern blot analysis (FIG. 2) indicated that the polyA sequence was not far beyond the sequences we cloned. Further details of the preparation of oligo dT primed cDNA clones from enriched mRNA are provided hereinafter.

Isolation and characterization of the human chromosomal .beta.NGF gene.

A human gene library (consisting of 15-20 kb, partial HaeIII/AluI human fetal liver DNA fragments inserted into .lambda.Charon 4A vectors) was screened using the 470 bp mouse NGF cloned cDNA fragment (pm.beta.N-9G1 RsaI fragment) described above as radioactive hybridization probe. A totalof 27 recombinant phage were plaque purified and partially characterized byEcoRI digestion; the 27 phage displayed 6 different types of restriction pattern. Each patterns category shared restriction fragments and thus appeared to overlap the same genomic region. The phage designated .gamma.h.beta.N8 was further characterized by physical mapping and nucleotide sequencing; FIG. 4 shows a physical map of clone .gamma.h.beta.N8 and regions flanking its sequences in the human genome, generated by phage mapping, sequencing and genomic Southern blotting experiments. A portion of a 12,000 bp nucleotide sequence derived from subcloned, overlapping EcoRI and HindIII fragments is shown in FIG. 5.

Comparison of the sequences of mouse .beta.NGF cDNA with the human .beta.NGF gene.

The mouse .beta.NGF cDNA sequence contains a reading frame with the potential to code for mature .beta.NGF, and the predicted amino acid sequence corresponds to the known sequence of mouse .beta.NGF. Angeletti, et al, Biochemistry, 12: 90 (1973) and 12: 100 (1973). Unexpectedly, the cDNA sequence predicts a C-terminal, arginine-glycine dipeptide extension,linked onto the end of the reported sequence for mouse .beta.NGF.

The human .beta.NGF gene contains a region predicting an amino acid sequence approximately 90 percent homologous with the mature mouse .beta.NGF amino acid sequence, which, therefore, must be the gene for human .beta.NGF. The human .beta.NGF protein also has a C-terminal dipeptide extension.

When one aligns the human and mouse .beta.NGF sequences (FIG. 6) it becomesclear that extensive homology extends a significant distance upstream from the known sequence of the mature mouse protein. Evidence has been presented for the existence of a 22,000 dalton biosynthetic pro- .beta.NGFprecursor. Berger and Shooter, Proc. Nat. Acad. Sci. (USA), 74: 3647, (1977), which may extend upstream from the mature protein to a potential arginine-arginine cleavage site at nucleotide positions 419 and 420 in FIG. 6. The nucleotide sequence-predicted precursor is longer than that previously detected; as will be described below, the entire prepro-.beta.-NGF sequence is predicted to have a molecular weight of 27,000, the pro-sequence is predicted to be 25,000 daltons, and considering the presence of specific pairs of arginine residues, processing intermediates of 21,500 and 18,000 daltons exist within the cell.

Localization of the Initiation Methionine Codon and Signal Sequence.

Three methionine residues are candidates for designation as the protein synthesis initiation codon (amino acids -187, -121 and -119 in FIG. 6); however several factors strongly implicate amino acid -121 of our sequenceas the actual initiation codon employed. Since .beta.NGF is a secreted protein, the initiation codon is likely to be followed by a signal sequence for cotranslational transfer of this polypeptide into the lumen of the endoplasmic reticulum. Amino acids -121 to -104 represent an excellent candidate signal sequence. These 18 amino acids are of the correct length and include a stretch of six completely hydrophobic amino acids (ala-phe-leu-ile-gly-val). Cleavage by signal peptidase could occur between the small amino acid ala-104 and the glu residue at position -103.It is known that signal peptidase cleaves after an identical gln-ala sequence to leave an identical N-terminal glu residue in the case of pre-alpha lactalbumin. The stretch of amino acids following the met residue at position -187 contains a high percentage of polar and charged amino acids and bears no resemblance to any previously described signal sequence.

Therefore, it seems most likely that methionine -121 is used for translation initiation of mouse and human prepro-.beta.NGF which would result in a 27,000 dalton preprohormone and a 25,000 dalton pro-.beta.NGF if signal peptide processing occurs at residue -104.

Direct expression of human .beta.NGF in E. coli.

EcoRI fragments from .lambda.h.beta.N8 were subcloned in pBR322. A subcloneplasmid we designated ph.beta.N8-B9 contained a 2 kb human DNA insert, including most of the sequences coding for the human .beta.NGF subunit. Sequencing determined that only the 10 NH.sub.2 -terminal amino acids wereexcluded from this sequence. Our approach for expression of the .beta.NGF coding sequence in E. coli was to excise the largest possible fragment from the .beta.NGF coding portion of ph.beta.N8-B9, to subsequently fill in missing codons, and to modify the 5' and 3' ends of the sequence to make it suitable for insertion into an E. coli expression plasmid. The expression system employed was the Trp promoter system of pHGH207-1, H. deBoer et al., "P.N.A.S."80: 21-25 (Jan., 1983).

The plasmid ph.beta.N8-B9 was digested with EcoRI and HgiAI and a .about.300 bp fragment was isolated from the digestion mixture. This fragment is shown in FIG. 7, with the sticky end termini resulting from the two step digestion indicated. In order to construct the 5' end of the human .beta.NGF sequence for expression, the codons for the 10 missing amino acids, the initiator methionine codon (ATG), and nucleotides preceding the ATG which are part of a ribosome binding site and include the cleavage site for the restriction endonuclease XbaI were added; four oligonucleotides were chemically synthesized for this purpose and are shown in FIG. 7 as oligonucleotides I-IV.

The 3' end of the .beta.NGF coding region was modified as follows: the nucleotide sequence of both DNA strands downstream from the single HgiAI site shown in FIG. 7 (at amino acid position Val 111 and Leu 112 of the mature human .beta.NGF) was chemically synthesized, including a termination codon (TAG) following Arg 118 and a SaII sticky end. These oligonucleotides are fragments V and VI in FIG. 7.

Synthetic oligonucleotides I-VI were radioactively labeled with T4 polynucleotide kinase and .beta.-.sup.32 P-ATP, and the radioactive oligonucleotides were mixed with the .about.300 bp h.beta.NGF DNA fragmentin T4 DNA ligase buffer. Ligation was carried out with 10 units of T4 DNA ligase at 12.degree. C. for 12 hrs. The mixture was phenol extracted and the DNA was precipitated in 70 percent ethanol. The precipitate was dried,dissolved in restriction endonuclease buffer, and the enzymes XbaI and SaIIwere added. Digestion was carried out for 2 hrs.

Preparative gel electrophoresis of the DNA mixture and autoradiography demonstrated the presence of a radioactive doublet at .about.370 bp. The bands were cut out separately and electrophoretically eluted. The eluted DNA fragments were then ligated (T4 DNA ligase) to a HGH-Trp expression plasmid designated pHGH207-1 that had been treated with bacterial alkalinephosphatase after digestion with XbaI and SalI. (The alkaline phosphatase treatment was used to prevent reinsertion of the HGH fragment into the Trpexpression vector.) The ligation mixture was used to transform E. coli K12/294 (ATCC 31446). Ampicillin resistant and tetracycline sensitive colonies were selected on agar plates; two hundred colonies were screened for the presence of human .beta.GF sequences by hybridization with a radioactive 300 bp EcoRI/HgiAI probe. Twelve positive colonies were analyzed for the presence of immunoreactive .beta.NGF molecules in their cell extracts using rabbit anti-mouse .beta.NGF antibodies on a Western blot. All but one clone showed a positive signal of the expected molecularweight, compared with a negative control extract. DNA sequence analysis of one of the clones verified that the final plasmid, designated by us as Ph.beta.NGFtrpl, which resulted in human .beta.NGF expression had the originally planned construction.

The sequence of operations from digestion of plasmid ph.beta.N8-B9 with EcoRI and HgiAI to assembly of plasmid ph.beta.NGFtrpl is shown in FIG. 8.The plasmid pHGH207-1 was obtained (H. de Boer et al., op cit.) from plasmid pHGH207, by digestion with BamHI followed by partial digestion with EcoRI. The largest fragment which contained the trp promoter was isolated. The largest EcoRI-BamHI fragment from pBR322 was also isolated and the two fragments were ligated and used to transform E. coli K12/294 (ATCC 31446). Clones resistant to both ampicillin and tetracycline contained pHGH207-1.

Construction and identification of bacterial clones containing mNGF cDNA sequences.

Two pools of 8 primers each (14 bases) were chemically synthesized. Each primer was complementary to a potential mRNA sequence for amino acids 93-96 and a portion of 97. A mixture of the 16 oligonucleotides was used to specifically prime the synthesis of cDNA on poly(A.sup.+)RNA. 220 pmoles (1 .mu.g) of each pool of 8 primers (440 pmoles total, 2 .mu.g) were annealed with 40.mu.g poly(A.sup.+) RNA in 50 .mu.l of 100 mmole KCl by incubating for 4 minutes each at 90.degree. C., 68.degree. C., 42.degree. C., and 37.degree. C. .sup.32 P-labeled cDNA was synthesized ina 100 .mu.l reaction in 50 mM Tris pH 8.3, 10 MM MgCl.sub.2, 10 mM DTT, 50 mM KCl. The reaction contained, in addition to annealed mixture, 500 .mu.MdATP, TTP, dGTP, 100 .mu.M dCTP, 20 .mu.Ci [.alpha.-.sup.32 P]dCTP (2000 Ci/mmole, Amersham), 0.5 units/.mu.l RNAsin, and 90 units reverse transcriptase. First strand synthesis was for 60 minutes at 37.degree. C. The reaction was boiled for 3 minutes, quenched on ice for 1 minute, and spun in a microfuge. The supernatant was diluted with an equal volume ddH.sub.2 O and ds cDNA was synthesized with the addition of 15 units of Klenow PolI for 18 hours at 12.degree. C. After phenol-chloroform extraction and ethanol-precipitation, the preparation was digested with 103 units of Sl nuclease in 150.mu.l for 1 hr at 37 .degree. C. After phenol-chloroform extraction and ethanol-precipitation the cDNA was fractionated by electrophoresis on a 5 percent polyacrylamide gel. Two size ranges of cDNA were electroeluted. 132 ngm were recovered .about.550 bp (upper) in length and 182 ngm were recovered 200-550 bp (lower) in length. A total of 20 ngm of each fraction was extended at the 3'-termini with 20-40 d(C) residues using terminal nucleotidyl transferase. The d(C)-tailed cDNA was annealed with 150 ngm of pBR322 which had been similarly extended with d(G) residues at the PstI site. Annealings were in50 .mu.l 100 mM NaCl, 10 mM Tris pH 7.5, 250 mM EDTA. Mixtures were heated to 70.degree. C., allowed to cool slowly to 37.degree. C. (16 hrs), then to 4.degree. C. (6 hrs). One-half of the annealed mixture was used to transform E. coli K-12 strain 294. 500 colonies from each size fraction (upper and lower) were screened by filter hybridization. .sup.32 P-labeledprobe was prepared from a mixture of the 16 primers (1 .mu.g total) by phosphorylation with 200.mu.Ci [.alpha.-.sup.32 P]ATP (5000 Ci/mmole, Amersham) and polynucleotide kinase (P-L Biochemicals) by a published procedure. The filters containing the 10,000 clones were hybridized with .about.1.times.10.sup.8 cpm of the .sup.32 P-labeled probe at room temperature for 18 hours in a primer hybridization mix (100 mM Tris pH 7.5, 0.9 M NaCl, 6 mM EDTA, 1X Denhardt's solution, 100.mu.M rATP, 1 mM NaH.sub.2 PO.sub.4 -Na pyrophosphate, 0.5 percent Nonidet P-40, 0.1 mg/ml yeast RNA (Sigma R-6750)). Filters were washed 30 minutes (3 times) in 6X SSC at 42.degree. C. and exposed to X-ray film for 16 hrs at -70.degree. C. with an intensifying screen (Dupont). Approximately 0.7-0.9 percent (370 upper, 460 lower) of the colonies were selected for a second round ofscreening with 2 additional synthetic primers which are 5' to the original priming site. 12-mers complementary to all potential mRNA sequences for amino acids 74-77 were synthesized in 2 pools of 4 primers each. Two poolsof 8 14-mers each were similarly synthesized, complementary to potential mRNA sequences for amino acids 52-58 and a portion of 56. Three sets of identical filters were prepared from the "upper" and "lower" colonies selected in the first round of screening. .sup.32 P-labeled probes were prepared as before from the 4 synthetic oligonucleotides. Filters were hybridized with 0.5.times.10.sup.8 cpm in primer hybridization mix, washed, and exposed to X-ray film. There were nine positives (3 from "lower", 6 from "upper") which hybridized with all of the 5' oligonucleotides. Plasmid DNA was isolated by a miniscreen procedure and the clone with the largest insert determined by restriction analysis. The plasmid designated pm.beta.N-9Gl was completely sequenced by the Maxam-Gilbert method. The cDNA insert contained the 14 base primer sequence (FIG. 1, pool 1) and a total of 716 bp.

Oligo dT-primed cDNA clones prepared from mRNA enriched for.mu.NGF message.

200 .mu.g of poly(A.sup.+) RNA was fractionated by electrophoresis through a denaturing agarose gel composed of 2 percent agarose in 0.025 M sodium citrate pH 3.8 and 6M urea. The ribosomal bands were visualized by staining a thin vertical slice with ethidium bromide. The gel was cut into0.5 cm slices, melted at 70.degree. C., extracted vigorously twice with phenol and once with chloroform. After 2 ethanol precipitations the pelletwas dissolved in 30 .mu.l ddH.sub.2 O). 1 .mu.l aliquots of each fraction (in 5.mu.l 4M ammonium acetate pH 7.0) were spotted onto a dry nitrocellulose filter and screened by dot hybridization under stringent conditions. A .sup.32 P-labeled probe was prepared from the pm.beta.N-9Gl insert by a published procedure utilizing calf thymus DNA fragments as primers in a Klenow Pol 1 reaction. The filter was hybridized with .about.10.sup.7 cpm in 50 mM NaPO.sub.4 pH 7.0, 5X Denhardt's solution, 5XSSC, 50 .mu.g/ml sonicated herring sperm DNA, 100.mu.M rATP, 1 mM NaH.sub.2PO.sub.4 -sodium pyrophosphate, and 50 percent formamide at 42.degree. C. for 18 hrs. The filter was washed 20 minutes (3 times) in 0.2X SSC-0.1 percent SDS at 42.degree. C. and exposed to film. Hybridization results localized the NGF message to fractions 11 and 12. Oligo dT-primed cDNA wasprepared by standard methods using 10 .mu.l each of fractions 11 and 12. The cDNA longer than 600 bp was eluted from gel slices after electrophoresis on a 5 percent polyacrylamide gel. Approximately 40 ngm cDNA from fraction 11 and 20 ngm from fraction 12 were d(C)-tailed and annealed with d(G)-tailed pBR322. About 3300 clones from fraction 11 and 1500 clones from fraction 12 were screened as colonies by filter hybridization under stringent conditions using a .sup.32 P-labeled internal HpaII fragment (216 bp) from pm.beta.N-9Gl. Filters were hybridized with 50.times.10.sup.6 cpm at 42.degree. C. for 18 hrs, washed,and exposed to X-ray film as before. Five clones from fraction 12 were "positive" with this probe. Restriction analyses showed they were siblings. pm.beta.N-12E4 was completely sequenced by the Maxam-Gilbert method. Two clones from fraction 11 were "positive". The largest, pm.beta.N-8B3, was completely sequenced by Maxam-Gilbert method.

Pharmaceutical Compositions

The human .beta.-NGF of the present invention can be formulated according to known methods to prepare pharmaceutically useful compositions whereby the .beta.-NGF is combined in admixture with a pharmaceutically acceptablecarrier vehicle. Suitable vehicles and their formulation, inclusive of other human proteins, e.g. human serum albumin, are described for example in Remington's Pharmaceutical Sciences by E. W. Martin, which is hereby incorporated by reference. Such compositions will contain an effective amount of the protein hereof together with a suitable amount of vehicle inorder to prepare pharmaceutically acceptable compositions suitable for effective parenteral administration to the host.

The human .beta.-NGF hereof may be parenterally administered to subjects suffering from nerve damage or other conditions for which it is therapeutically effective. Dosage and dose rate may parallel that currently in use in clinical investigations of such agents derived, for example, from mouse salivary glands.

Notwithstanding that reference has been made to particular preferred embodiments, it will be further understood that the present invention is not to be construed as limited to such, rather to the lawful scope of the appended claims.

Claims

1. A process which comprises transforming an E. Coli host cell with a replicable expression vector capable, in the host cell transformed with the vector, of expressing an isolated first DNA sequence which encodes a polypeptide comprising the human mature .beta.NGF amino acid sequence ##STR1## operably linked with a second DNA sequence capable of effecting expression of the first DNA sequence in the host cell transformed with the operably linked DNA sequences.

2. An isolated DNA sequence which encodes a polypeptide comprising the human mature .beta.NGF amino acid sequence ##STR2##

3. A replicable expression vector capable, in a host cell transformed with the vector, of expressing the DNA sequence of claim 2.

4. The vector of claim 3 comprising a signal sequence for the human .beta.NGF.

5. A host cell transformed with a replicable expression vector capable of expressing in the host cell the DNA sequence of claim 2.

6. The host cell of claim 5 that is eukaryotic.

7. A host cell according to claim 6 that is a Chinese hamster ovary cell line.

8. A host cell according to claim 5 which is an E. coli strain.

9. The DNA sequence of claim 2 that further comprises a signal sequence for the human .beta.NGF.

10. A host cell according to claim 5 which is prokaryotic.

11. A host cell according to claim 5 which is a mammalian cell.

12. A host cell according to claim 5 which is a yeast cell.

13. Plasmid ph.beta.NGFtrpl.

14. A host cell transformed with the plasmid of claim 13.

15. A host cell according to claim 14 which is a strain of E. coli.

16. A replicable vector comprising an isolated nucleic acid encoding the human pro .beta.NGF pro sequence ##STR3##

17. An isolated first DNA sequence which encodes a polypeptide comprising the human mature .beta.NGF amino acid sequence ##STR4## operably linked with a second DNA sequence capable of effecting expression of the first DNA sequence in a host cell transformed with the operably linked DNA sequences.