CN1167799C - Method for secreting and expressing acid fibroblast growth factor - Google Patents
Method for secreting and expressing acid fibroblast growth factor Download PDFInfo
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- CN1167799C CN1167799C CNB001140108A CN00114010A CN1167799C CN 1167799 C CN1167799 C CN 1167799C CN B001140108 A CNB001140108 A CN B001140108A CN 00114010 A CN00114010 A CN 00114010A CN 1167799 C CN1167799 C CN 1167799C
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Abstract
The present invention relates to a method for producing an acid fibroblast growth factor., particularly a method for using the co-expression of a molecular partner and the human acid fibroblast growth factor in a procaryote body to produce soluble acid fibroblast growth factor protein.
Description
The present invention relates to the method for production acid fibroblast growth factor, particularly relate to and utilize molecular chaperones and human acid fibroblast growth factor, to produce the proteic method of soluble acid fibroblast growth factor at the intravital coexpression of prokaryotic organism.
The growth factor family that fibroblast growth factor (FGF) is made up of protein (FGF 1-9) relevant at least 9 kinds of structures, wherein understanding is clear that acid fibroblast growth factor (aFGF or title FGF-1) and Prostatropin (bFGF or title FGF-2) most.The member of known FGF family is the various types of cytoid mitogen in mesoderm and neuroderm source, and these factors also have the vasculogenesis of promotion, neural axon extension, neuron regeneration and various biological functions such as survival, bone or cartilaginous tissue reparation and sarcoplast differentiation.In general, the core sequence between each member of FGF family has the amino acid sequence homology of about 25-55%, so FGF family may have common first ancestor gene.
AFGF and bFGF can with same receptors bind, but can not get rid of the possibility that both respectively have its special acceptor.Recently, the someone finds that each aFGF molecule can combine with two acceptor molecules.Also find to have in the different tissues aFGF and the bFGF of different molecular weight, infer that this situation may be because these molecules stand the different post-treatment processes of transcribing and cause in different cells.
In general, the total chemical feature of aFGF and bFGF is that these factors can be combined closely with heparin, but wherein aFGF is littler than bFGF to the affinity of heparin, and the iso-electric point of while aFGF is slant acidity (pH 5-7) more.Known heparin can be regulated the function (Loss of FGF molecule by several modes, Eur.J.Clin.Invest., 18:321-326,1988), for example heparin or heparin-like molecule can directly act on FGF, activate or strengthen activity (Uhlrich et al., the Biochem.Biophys.Res.Comm. of aFGF and bFGF, 137:1205-1213,1986).In addition, find that as if the synergism of solubility heparin selective to aFGF, and it strengthens the active degree of aFGF and bigger 10 times than bFGF.Heparin sample material also is the particularly preferred stabilizer of aFGF of FGF.
The angiogenic activity of the uniqueness of FGF and cell-proliferation activity make it to be specially adapted to promote the particularly healing of deep wound of tissue wounds.For example United States Patent (USP) 4,378,347 and European patent 0505811 address natural bFGF respectively and can be used for treating neurodegenerative disorders (Wallicke et al., PNAS, USA 83:3012-3016,1986) such as presenile dementia and Parkinson's disease.International monopoly WO 93/08828 and European patent 0741143 disclose the method for using aFGF active fragments protection axoneuron and improving brain function respectively.It is the pharmaceutical composition that is used to promote bone tissue restoration and/or growth of primary activity composition with aFGF that international patent application 96/38167 has been described.
With regard to biologic activity, though aFGF is more much lower than bFGF, but have found that, aFGF is at damage location to be treated, particularly at the most damage location (as superficial tissues damage and stomach ulcer) that is in sour environment, aFGF is easier to bring into play its temperature than bFGF and closes and persistent biologic activity, thereby more helps the clinical application under these conditions.
Many prior art documents have been reported with recombinant DNA technology and have been produced the method for aFGF (for example referring to Biotechnology 5:960,1987; J.Biol.Chem.263:1 6471,1988; EP 0219052 etc.).In recent years, for biologic activity, expression efficiency that improves product that further improves aFGF and the stability that increases expression product, some laboratories have made up the recombinant expression system (as referring to WO 96/08572, WO 98/32869, EP406738 etc.) of many improvement.On the other hand, some patent applications also disclose biologic activity and/or stable aFGF analogue or the mutant (as suggestion WO 96/22369, WO 92/11366, WO 91/11459) with raising.But also the someone proves, the activity of the overall length aFGF of integration form is than other forms aFGF that has removed the auspicious part amino in N end active approximately high 3 times (referring to EP O505811).
Up to now, particularly the intestinal bacteria conduct is with the proteinic host cell of recombinant technology industrial-scale production mainly to be to use bacterium, and colibacillary major advantage is: be easy to the stability that genetic manipulation also can keep transformant; Cultivate the expression product that can obtain high yield through large volume; And cell is easy to cultivate, thereby can reduce production costs.Yet the use intestinal bacteria production biologically active proteins matter particularly proteic significant drawbacks of eukaryotic cell is that expression product forms so-called " inclusion body ", the i.e. active insoluble polymer of abiology in host's endochylema.The advantage that forms inclusion body is to protect the degraded that is avoided suffering proteolytic enzyme in the host cell by expressed protein, and can at an easy rate inclusion body be separated by enough centrifugal methods.But, must carry out sex change one dissolving one denaturing treatment to inclusion body in order to obtain the protein of biologic activity.This process generally will be finished on the basis of repetition test, and usually can not obtain the gratifying product rate of recovery.In order to solve this difficult problem, people attempt to adopt the molecular chaperones technology, make goal gene assist protein to stride the film transportation, participate in the molecular chaperone coexpression of functions such as the growth keeping the protein higher structure and regulate cell and differentiation with having, under helping at cell institute inherent secreting signal peptide, realize the correct conformation of striding the film secretion and correctly cutting, and keep sophisticated secretory protein of precursor molecule.
Now know, have the closely-related excreted factor of secretion of some and bacterium protein in the intestinal bacteria, as Sec family.These factors and signal peptidase and some other known and unknown factor interactions are participated in the transmembrane transport and the processing of intracellular protein.As an important member of Sec family, SecB is present in the intracytoplasmic shla molecule chaperone of being made up of 155 amino acid (Kumatomo.C.A.et al., Mol.Microbiol.5:19-22,1991) with tetramer form.SecB can combine with most of secreted proteins of synthetic on the rrna or polypeptide, to keep the activity conformation that it is suitable for striding the film transportation.When the peptide chain generation folding of secretor type precursor protein or polypeptide, SecB is by the β laminated structure of molecular skeleton interact with it (Breukink E.et al., Eur.J.Biochem.208:414-425,1992).After precursor protein or polypeptide were transported in the inner membrance, SecB promptly combined with another Sec family member SecA with ATP enzymatic structure feature, and under the help of SecA and other correlation factors, finish molecule stride the film secretion.
An object of the present invention is to provide the recombinant expression vector of secreting, expressing aFGF in intestinal bacteria, wherein said expression vector comprises the coding molecule companion's who is operably connected with first promotor nucleotide sequence, and said sequence downstream is connected with the nucleotide sequence of a coding overall length acid fibroblast growth factor that is operably connected with second promotor.
According to expression vector of the present invention, wherein said molecular chaperones is intestinal bacteria SecB.
According to expression vector of the present invention, wherein said first and second promotors are selected from IacZ promotor, intestinal bacteria alkaline phosphatase promotor and phage T
7Promotor, and first and second promotors are identical or different.
According to expression vector of the present invention, the mutant nucleotide sequence that the nucleotide sequence of wherein said coding aFGF is the wild sequence of screening from natural origin, obtain through induced mutations or modification or the sequence of chemosynthesis.
Another object of the present invention provide a kind of in prokaryotic hosts the method with the soluble form secreting and expressing acid fibroblast growth factor, this method may further comprise the steps:
(1) provide the coding human acid fibroblast growth factor nucleotide sequence;
(2) nucleotides sequence that the nucleotide sequence of step (1) is connected to coding intestinal bacteria molecular chaperones lists, and institute's calling sequence is connected in the suitable expression;
(3) recombinant expression vector with step (2) transforms suitable prokaryotic host cell;
(4) e. coli host cell that the quilt of culturing step (3) transforms under being suitable for the condition of soluble secreted form expressing human acid fibroblast growth factor;
(5) remove insoluble part in the culture, and from soluble fractions, reclaim the required active polypeptide of human acid fibroblast growth factor that has.
The method according to this invention, the recombinant expression vector of saying wherein comprises second promoter sequence that first promoter sequence that lists of nucleotides sequence that is operably connected to the coding human acid fibroblast growth factor and the nucleotides sequence that is operably connected to the coding molecule companion that is positioned at its upstream list.
The method according to this invention, wherein said first and second promotors are lacZ promotor, intestinal bacteria alkaline phosphatase promotor or phage T
7Promotor.
The method according to this invention, wherein said molecular chaperone protein is intestinal bacteria SecB.
Fig. 1 shows aminoacid sequence (top) and its nucleotide coding sequence (below) of SecB.
Fig. 2 shows the structure that is used at the recombinant expression vector of intestinal bacteria coexpression secretion signal SecB and people aFGF.
The present invention relates to produce with recombinant DNA technology the method for aFGF, particularly relate to As the host, produce people aFGF (haFGF) with the solubility secreted form with the prokaryotes body Method. More specifically he says, the present invention relates to for secreting egg Escherichia coli with solubility White formal representation people aFGF's is recombinant expressed, is transformed by said recombinant expression carrier Recombinant cell, and press the haFGF polypeptide that the inventive method is produced. The present invention is further The haFGF that relates to by method preparation of the present invention is treating owing to vascular lesion, miocardial infarction Or the ischemic disease that causes of cerebral hemorrhage, promote in tissue repair and the wound healing should With.
The recombinant expression carrier that the present invention is used for secreting, expressing aFGF comprises that is expressed a molecule First transcript unit of chaperone and be used for to express second transcript unit of aFGF, wherein Said first transcript unit and second transcript unit can be one another in series be connected in same heavy In the group carrier, but also can be present in respectively two of the same prokaryotic host cell of cotransformation not In the recombinant vector together.
With regard to the two transcript units mode that is connected in series to each other, of the present invention recombinant expressed Carrier comprises that at first one is operably connected to coding molecule companion's on first promoter Nucleotide sequence and the insertion site that can grasp into second transcript unit. Insert by this The angle of striking can be inserted in said expression vector at an easy rate basically by coding aFGF Nucleotide sequence and its upstream second start molecular second transcript unit. In addition, Power between the dna sequence dna of second promoter of second transcript unit and the aFGF polypeptide of encoding An extra signal peptide sequence is arranged, and add one in the downstream of the fusion that so obtains Individual tanscription termination subsequence.
The method for optimizing that obtains encoding human aFGF gene is artificial synthesis, because like this Can make the protein optimization of translation, and be easy to gene order is carried out induced mutations. Can Come synthetic gene with the amino acid sequence based on the aFGF that derives from human body or other animal tissues. Such as can be based on the people such as Gimenes-Gallego (Science 230:1385-1388,1985) Described ox amino acid sequence or based on the people such as Gimenes-Gallego (Biochem, Biophys, Res. Comm.138:611-617,1986) described human amino acid sequence is synthetic Ox or people aFGF gene. Can be according to the people such as Itatura (Science 198:1056-1063,1977) The nucleotide sequence of described technology composite coding aFGF. Perhaps, also can be according to Aviv And the described side of Leder (Proc.Natl Acad.Sci.USA 69:1408-1412,1972) Method, from expressing the cell of aFGF, for example people's pituitary, breast cancer, brain, brain stem or lower Extract the RNA contain poly (A) in the thalamus cell, with the cDNA of the haFGF that obtains encoding. Also can use people (the DNA Cloning Techniques:A Practical such as Huynh V.T. Approach, IRL Press, Oxford, 1984) λ gt 10 carriers, from these tissues MRNA obtain cDNA library, and utilize resulting hybridization clone to reclaim coding aFGF Complete sequence.
In general, for the expression efficiency that improves gene and the productive rate of product, should be suitably Selection is more suitable in the best of breed of the promoter of specific coding sequence, host and carrier. Use escherichia coli host to express in the situation of aFGF, preferably use strong T7Start sublist Reach aFGF cDNA. In addition, consider the finiteness of host cell self-energy, we are preferred The lacZ promoters driven Escherichia coli molecular chaperones base of (institute's energy requirement is less) relatively The expression of cause.
As with the molecular chaperone of nucleotide sequence coexpression of coding aFGF, this Bright optimized encoding has the nucleotide sequence of the molecular chaperones SecB albumen of secreting function. SecB Uniquely in the Escherichia coli EF Sec family to be present in intracytoplasmic soluble protein Matter, other EFs such as SecA, SecD, SecE, SecF and SecY are then all located On cell membrane. SecB can be combined with most of albumen or polypeptide, makes it to keep that it is special Loose folding, be in the space conformation that is of value to the molecule transhipment. SecB is the egg of combination with it After white matter is transported on the cell membrane, further be combined with SecA, and at other EFs The collaborative lower transportation of finishing destination protein or polypeptide. Because the SecB binding site is without the need for the spy Fixed amino acid sequence, and as long as with single positive charge and have β-pleated sheet zone, institute Can be combined with most protein or polypeptide with it. Yet, owing to be subjected to bacterial cell intrinsic The restriction of the factors such as SecB protein content, a large amount of synthetic exogenous proteins are normal on ribose Often accumulate in the cell, the random folding and molecular aggregates of precursor molecule take place, make these before The body molecule can not with various correlation molecule companions (particularly SecB) protein combination, thereby the funeral Lose it and stride the film transport capacity. In order to overcome this defective, we attempt the SecB gene is connected Arrive upstream or the catchment of the nucleotides of coding aFGF, in the hope of realizing the secreting, expressing of aFGF. Perhaps, both are carried on respectively on two different carriers, and with resulting two Individual recombinant vector transforms same escherichia coli host, reaches both and expresses synchronously the justacrine expression The purpose of aFGF.
What should particularly point out is, for the secreting, expressing of realizing aFGF and improve its expression, and must be at upstream and the promoter (T of haFGF coded sequence7Promoter) inserts between the downstream Enter a secretory signal sequence. This sequence comprises translation initiation codon in 5 ' → 3 ' direction (ATG), be the Shina-Dalgarno sequence then, be terminator codon (TAA) at last. Preferably Burst is ATG TAGT CGA TTA AAT AAG GAG GAA (ginseng See Schoner et al., Proc.Natl.Acad.Sci.USA 93:8506-8510,1986). For For the purpose of convenient, can be when the aFGF that synthesizes with the preparation of pcr amplification method, at amplimer The such sequence of middle adding.
Can use any carrying of being suitable in escherichia coli host, stably keeping and copying Body makes up recombinant expression carrier of the present invention through genetic manipulation. Available initial plasmid bag Draw together pBR322, pUC18, pUC119, pSP64, pGEM-3, pTE-3 and pT7-7. The present invention is preferably with T7The multicopy plasmid pT of promoter7-7。
Can use any being suitable for therein with high efficiency coexpression desired protein (aFGF And secB) e. coli strains is as the host, such bacterial strain comprise Escherichia coli MM294, DH-1, C600, DE-3 and BL21 etc. The preferred host of the present invention is coli strain BL21.
Can carry out separation and synthetic, the clone of gene and express according to technology known in the art Vector construction, dna sequence analysis and evaluation, host cell transform and cultivate, and table Reach the operations such as the separation of product and purifying (referring to Sambrook et al., Molecular Cloning: A Laboratory Mannual, Cold Spring Harbor Laboratory Press, Cola Spring Harbor, NY, 1989).
Be purpose of the present invention, can be at first with the chromosomal DNA with Escherichia coli YU537 Be template, the SecB that obtains through the PCK amplification imports with (first startup of lacE promoter Son) in the plasmid pUC18. Perhaps, also can with previously prepared, comprise that lacZ starts Son and SecB gene first transcript unit are directly connected to the expression vector pT that the present invention selects7T in-77The upstream of (second promoter) of promoter obtains recombinant plasmid pT7-SecB. In order effectively to express the base of the coding SecB that does not basically have host's endogenous dna sequence Cause can connect a termination signal in the downstream of molecular chaperone in case of necessity, or in design And add such terminator sequence during the cloning molecular chaperone. Can suitably adjust Distance between one promoter sequence and the molecular chaperone is transcribed efficient to obtain the best.
Then, use based on the synthetic antisense oligonucleotide primer of the nucleotide sequence of aFGF cDNA Thing, and with the aFGF cDNA that makes as stated above as template, get through pcr amplification To the synthetic bifilar aFGF gene order of normal chain end with the NdeI site. With The plasmid pT that SmaI+Nde I double digestion makes by preceding method7Behind-the SecB, resulting aFGF coded sequence is connected on the SmaI-NdeI large fragment, and then obtains connecting with series system, contain the SecB gene that is under the lacZ promoters driven and be in T7Recombinant vector (the pUCSec-T of the aFGF gene under the promoters driven7-aFGF)。
Can be according to a conventional method (such as CaCl2Facture) turns to carrying above-mentioned first and second The suitable coli strain of recombinant plasmid transformed of record unit is (as referring to Proc.Natl.Acad. Sci.USA 69:2110,1972), and by method well known to those skilled in the art, for example The transformant that uses LB culture medium fermented and cultured to obtain through screening.
After fermentation is finished, can be with simple centrifuging separation and Culture thing supernatant, and with known three step chromatography (high performance liquid chromatography (HPLC) of cation-exchange chromatography-heparin-Sepharose affinity column-oppositely is (referring to United States Patent (USP) 5,312,911) aFGF is purified to the pure basically homogeneous state that silver-colored painted SDS-polyacrylamide gel electrophoresis is single band.Available amino end acid compositional analysis method and N-terminal sequential detection method are identified the proteic structure verity of haFGF, and inoblast (Babl/c 3T3 A31 clone) the mitotic division method of further using people (J.Biol.Chem.225:5517-5520,1980) such as Thomas is estimated the biologic activity of the rhaFGF of purifying.
Can with by the rhaFGF of the inventive method preparation be selected from human serum albumin, polyglycine, metallic cation (as Zn
++, Mn and Mg
2+) and the active protein protective material of low molecular weight peptide; the stablizer that is selected from polyoxyethylene glycol, carboxymethyl cellulose alkali metal salt, heparin, heparin sulfate or its analogue, sulfated polysaccharide, gsh mixes; and add pharmaceutical carrier well known to those skilled in the art or vehicle; make and be suitable for, particularly the compositions of administration outside gi tract through the gi tract approach.Can be according to the ordinary method of pharmacy field, such pharmaceutical composition made be suitable in the intravascular, intramuscular or the solution of intraperitoneal administration, the tablet or the powder agent of footpath oral administration, or make formulations such as the suppository that is suitable for external application, ointment, creme, emulsifying agent.
Pharmaceutical composition of the present invention can be used for promoting the reparation or the healing of the soft tissue, tendon, ligament, cartilage or the osseous tissue wound that cause because of burn or other mechanical traumas.Said soft tissue comprises the institute except that bone and cartilaginous tissue such as skin, muscle, blood vessel, internal organs and cornea tissue in a organized way.In general, the local or subcutaneous dosage of aFGF is about 1-100 μ g/cm
2/ day.When being used to promote that skeletal muscle and cartilage injury are repaired, preferably at the damage location of surgical operation or the wound pharmaceutical composition of the present invention that comes into operation.Be used to promote that the dosage of skeletal muscle healing is about 10-100 μ g/cm
3/ day.Pharmaceutical composition of the present invention also can be used for treating vascular tissue injury, as promoting angiogenic growth (vasculogenesis) and blood vessel reparation (promoting the vascular endothelial cell proliferation of damaged part).Can be at the damage location innerlich anwenden, to bring into play angiogenic activity in its body, dosage is about 10-100 μ g/cm
2/ day.Pharmaceutical composition of the present invention also can be used for promotion maincenter and peripheral nerve tissue repair, comprises the growth that stimulates hippocampal neuron impaired in Alzheimer's disease (presenile dementia) pathologic process.As active ingredient in pharmaceutical of the present invention, aFGF can stimulate the nervous tissue that sustains damage because of a variety of causes, makes it the new neurone of mitotic division regeneration by neuroblast, recovers the neuronal cell population of damaged part, and promotes the extension of aixs cylinder.
Although the biologic activity of known aFGF is starkly lower than Prostatropin (bFGF), a large amount of experimental studies prove that aFGF is relatively more gentleer than the bFGF effect, and particularly aFGF is more suitable for the low pH environment in most of wounds.Therefore, pharmaceutical composition of the present invention can be made the preparation that is suitable for oral administration, be used for the treatment of stomach or duodenal ulcer, perhaps make suitable external preparation, be used for the wound treatment of (comprising operation wound, the particularly local deep wound that is the acid pH environment).Our result of study (data not shown goes out) shows as if when uniting use with other somatomedins, particularly Urogastron that are used for wound (as skin incision or stomach ulcer) reparation, aFGF has better result of treatment than bFGF.AFGF can make the inoblast of wound site and epidermic cell keep better reproduction ratio, obtains better physiology repairing effect.
The following example is intended to further illustrate the present invention, rather than limits the await the reply scope of claim of the present invention by any way.
The preparation of embodiment 1:SecB gene
Be used for intestinal bacteria excreted factor SecB gene of the present invention in order to prepare, at first (every liter contains peptone 10g at the LB substratum that contains penbritin (100ug/ml) with coli strain YK537 (being provided by the MAKART YAMASAK1 of Tokyo Univ Japan) cultivation, female extract 5g of acid and sodium-chlor 10g) in, chromosomal DNA separated after the cell proliferation according to a conventional method.
With the total DNA of the karyomit(e) of YK537 cell is template, and uses synthetic Oligonucleolide primers (1): 5 '-G
GAATTCGATGTCAGAACAAAACAACAC-3 ' (SEQID NO:1) and primer (2): 3 '-AA
CTGCAGTTATCAGGCATCCTGATGTTC-5 ' (SEQ ID NO:2) carries out PCR reaction (90 ° of sex change 30 seconds, 50 ℃ of annealing 60 seconds in the presence of the Taq polysaccharase, 72 ℃ of polymerizations 60 seconds), after the circulation, 72 ℃ were extended 10 minutes for coreaction 30, with amplification obtain two ends have respectively EcoRI (
GAATTC) and the fragment of the about 480bp of length of Pst1 (CTGCAG) restriction enzyme site.Electrophoresis (1% low melting point glue) separates the PCR reaction mixture, and the dyeing back is downcut from gel and is equivalent to the electrophoretic band of 480bp and reclaims it.
The plasmid pUC18 that has lacZ promotor (as first promotor) then with the EcoRI+Pst1 enzymic digestion, reclaim after the big fragment in the presence of the T4 dna ligase, above-mentioned 480bp fragment is connected on this big fragment, obtains carrying the recombinant plasmid pUC-SecB of SecB gene after the cyclisation.With gained plasmid transformed competence colibacillus bacillus coli DH 5 cell (BethesdaResearch Labs).Cultivate the propagation back and from the transformant clone, separate strand EcoRI-PstT fragment.By currently known methods and use universal primer to measure the forward and the reverse dna sequence dna of junction fragment, the result shows that resulting fragment is 155 proteic nucleotide sequences of amino acid whose SecB of coding, thereby obtains required SecB gene fragment.
Embodiment 2: the recombinant plasmid pT that carries the SecB gene
7The structure of-SecB
In order to utilize T
7Promotor is as expressing proteic second promotor of aFGF, and we at first are connected to the SecB gene of preparation among the embodiment 1 in the expression vector.For this reason, at first use Bgl II digested plasmid pT
7-7 (Dept.Of Biol.Chem., Harvard MedicalSchool, Boston, Mass.02115), big section of separation quality grain is also used S
1Nuclease is accomplished flush end with its end.In the presence of the T4 dna ligase, with its with used S
1The above-mentioned SecB gene (PvuII-PstI) that nuclease is handled links together, and obtains carrying the middle interstitial granules pT of SecB gene after the cyclisation
7--SecB.
Embodiment 3: the structure of the proteic recombinant vectors of secreting, expressing aFGF
To comprise being connected with and be in the SecB gene under the lacZ promotor control and be in T in order to make up with series system
7Promotor control down and comprise the recombinant expression vector of the aFGF gene of a secretory signal sequence in the upstream, at first with aFGF cDNA library as template, and use aminoacid sequence chemistry synthetic Oligonucleolide primers (3): 5 '-TGT based on aFGF
ATG TATCGATTAAATAAGGAGGAATTCAAT
CTGCCAC(wherein the part of following stroke thick black line is a secretory signal sequence to-3 ' (SEQ ID NO:3), the part of drawing thin black line down is the NdeI restriction enzyme site), and primer (4): 3 '-TTAGTCAGAGCTCAC-5 ' (SEQ ID NO:4), with conventional PCR reaction (92 ℃ of sex change 30 seconds, annealed 45 seconds for 50 ℃, 70 ℃ of polymerizations 60 seconds, 72 ℃ were extended 10 minutes after 35 circulations) amplification obtains 5 ' end and has secretion signal, and 3 ' end has the nucleotide fragments of the coding aFGF of a NdeI restriction enzyme site.
Cut the plasmid pT that makes among the embodiment 2 with the NdeI enzyme
7-SecB, and with the T4 dna ligase will encode aFGF nucleotide sequence together with its 5 ' end secretory signal sequence be connected to pT
7The downstream of SecB gene order among the-SecB, thus recombinant expression plasmid pUCSec-T of the present invention obtained
7-aFGF.
Proteic secreting, expressing of embodiment 4:aFGF and purifying
According to conventional CaCl
2The facture recombinant vectors transformed competence colibacillus e. coli strain bl21 (Stratagene) of embodiment 3.In the LB substratum that contains 1% peptone, 0.5% yeast extract, 0.5%NaCl, 0.4% glucose and about 50 μ g/ml penicillin, cultivate transformant for 37 ℃.When the 560nm of cell culture optical density(OD) reaches 0.6 approximately, add IPTG to final concentration be 1mM, and continue to cultivate 18 hours.After cultivation is finished, centrifugal collection culture supernatant, and use Zeo-karb, heparin-Sepharose mixture and reverse high performance liquid phase layer Ke method (HPLC) purifying aFGF protein successively.
, at first will be suspended in about 0.1M phosphate buffered saline buffer (pH6.0) for this reason, and add the cationite CM-Sephadex (6ml/ restrains protein) that has crossed with same damping fluid balance through the culture supernatants of dialysis.4 ℃ after static 2 hours, collect resin in the glass column and wash post 3 times with phosphate buffered saline (PBS) (pH6.2).Use the phosphate buffered saline (PBS) elute protein that contains 0.5MNaCl after washing post.In eluate, add the heparin-Sopharose (1ml/ restrains protein) that crosses with 10mM phosphate buffered saline buffer (pH7.0) balance then.4 ℃ vibrate and place about 1 hour gently after, collect resin-protein complex and also fill out post.After washing post with the 20mM phosphate buffered saline buffer that contains 0.6M NaCl, with the required protein of same buffer solution elution that contains 1.0M NaCl. collect eluate (monitoring 280nm light absorption ratio) at last and be added on and use 5mM trifluoroacetic acid (TFA) equilibrated C4 reversed-phase HPLC post (on the 5mm * 25cm), with TFA (0-100%)+CH
3CN (0-60%) gradient elution is collected the aFGF protein that obtains high purity (about 98%) after the single main protein peak value part.
The product albumen matter of purifying is separated with the electric arteries and veins of polyacrylamide gel (15% separation gel) after reducing, and demonstrates the single band of the about 16.1KD of molecular weight after the silver dyeing.By amino acid composition analysis and the further verity that confirms by the aFGF of the inventive method preparation of N-terminal sequencing.
Embodiment 5: the biologic activity of the haFGF of secreting, expressing
With reference to the described method of people such as Thomas (Proc.Natl.Acad.Sci.USA 81:357-361,1984), according to
3The H-thymus pyrimidine mixes the amount in the Babl/c mouse 3T3 cell DNA, the mitogenic activity of the reorganization aFGF of estimation purifying.Briefly, in the substratum that contains 10% foetal calf serum with Babl/c 3T3 cell (5 * 10
4/ hole) be cultured to individual layer and converge after, change substratum and continue and cultivated 24 hours.The cultivation back adds test sample (10 μ l) in each hole, be incubated to add 0.2 μ Ci after 12 hours again
3The thymus pyrimidine (Sigma) of H-thymus pyrimidine (NewEnglamd Nuclear) and 0.3 μ g end mark continues insulation 12 hours.The radioactivity (cpm) that mixes in the cell DNA is detected in the insulation back.Wherein adding sample is 2 times of diluents of successive, and crosses at least 3 orders of magnitude between background peak value DNA is synthetic.A concentration that stimulates unit to be decided to be the required aFGF diluent of the maximum reaction of generation half.The stimulation units of every milligram of pure aFGF is decided to be compares mitogen activation.The synthetic required concentration of hormesis of aFGF generation maximum DNA that makes by method of the present invention is about 3.2ng/ml.
Sequence table
(1) general information
(i) applicant: Biopharmaceutial Research ﹠ Development Center of Jinan University
(ii) denomination of invention: the method for secreting and expressing acid fibroblast growth factor
(iii) sequence number: 4
(iv) address:
(A) contact person: Li Jiaokun
(B) street: Tianhe District Stone steles
(C) city: Guangzhou
(D) country: the People's Republic of China (PRC)
(E) postcode: 510632
(V) computer-reader form:
(A) amboceptor type: 3.5 inches floppy disks
(B) computer: IBM PremiumIII
(C) operating system: WIN.97
(D) software: WORD97
(iv) telecommunication information:
(A) phone: 020-85223275
(B) fax: 86-20-85223275
(2) information of SEQ ID NO:1:
(i) sequence signature:
(A) length: 28 base pairs
(B) type: nucleic acid
(C) chain: strand
(D) topological structure: linearity
(ii) molecule type: CDNA
(iii) sequence description: SEQ ID NO:1
GGAATTCGATGTCAGAACAAAACAACAC
(2) information of SEQ ID NO:2:
(i) sequence signature:
(E) length: 29 base pairs
(F) type: nucleic acid
(G) chain: strand
(H) topological structure: linearity
(ii) molecule type: cDNA
(iii) sequence description: SEQ ID NO:2
AA
CTGCAGTTATCAGGCATCCTGATGTTC
(2) information of SEQ ID NO:3:
(i) sequence signature:
(I) length: 37 base pairs
(J) type: nucleic acid
(K) chain: strand
(L) topological structure: linearity
(ii) molecule type: cDNA
(iii) sequence description: SEQ ID NO:3
TGT
ATG?TATCGATTAAATAAGGAGGAATTCAAT
CTGCCAC
(2) information of SEQ ID NO:4:
(i) sequence signature:
(M) length: 15 base pairs
(N) type: nucleic acid
(O) chain: strand
(P) topological structure: linearity
(ii) molecule type: CDNA
(iii) sequence description: SEQ ID NO:4
TTAGTCAGAGCTCAC
Claims (1)
1. the acid fibroblast growth factor recombinant expression vector of secreting, expressing in intestinal bacteria, wherein said expression vector comprises the SecB gene order that is under the control of 1acZ promotor, and described SecB gene order downstream is connected with a nucleotide sequence that is in the coding total length acid fibroblast growth factor under the control of T7 promotor.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB001140108A CN1167799C (en) | 2000-01-07 | 2000-01-07 | Method for secreting and expressing acid fibroblast growth factor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB001140108A CN1167799C (en) | 2000-01-07 | 2000-01-07 | Method for secreting and expressing acid fibroblast growth factor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1303948A CN1303948A (en) | 2001-07-18 |
| CN1167799C true CN1167799C (en) | 2004-09-22 |
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| Application Number | Title | Priority Date | Filing Date |
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| CNB001140108A Expired - Lifetime CN1167799C (en) | 2000-01-07 | 2000-01-07 | Method for secreting and expressing acid fibroblast growth factor |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2014161405A1 (en) * | 2013-04-03 | 2014-10-09 | Gene-Vinate Limited | Means and method for expression of authentic human epidermal growth factor and/or basic fibrolast growth factor in cytoplasm and/or culture medium of escherichia coli |
| CN110078815B (en) * | 2019-05-24 | 2020-12-11 | 温州医科大学 | Large-scale preparation method of recombinant human acidic fibroblast growth factor |
| CN110526958B (en) * | 2019-07-22 | 2022-04-29 | 广州暨南大学医药生物技术研究开发中心有限公司 | Activity repair peptide Tvigour A and application thereof |
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