Patent Application
20220119792
The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety as a part of the present specification and application. Such ASCII format Sequence Listing, entitled 596_SeqListing_ST25.txt, was created on Dec. 19, 2021, and is 8,032 bytes in size.
The present invention relates to a gene expression cassette for expressing an N-terminal-methionine-truncated target protein and a method of producing an N-terminal-methionine-truncated target protein using the same, and more particularly to a gene expression cassette for expressing an N-terminal-methionine-truncated target protein comprising a nucleic acid encoding a target protein and a nucleic acid encoding a cysteine protease, in which a cysteine protease recognition sequence is inserted between methionine (Met), which is the first amino acid at the N-terminus of the target protein, and the second amino acid, so N-terminal methionine is cleaved with the cysteine protease, and a method of producing an N-terminal-methionine-truncated target protein using the same.
The production of polypeptides and proteins having biological activity is capable of being utilized for the manufacture of pharmaceutical formulations, enzymes, and other specific chemicals for humans and animals. Recombinant DNA techniques using bacterial cells, fungal cells, and mammalian cells as expression hosts have been employed as particularly useful means for the production of large amounts of polypeptides.
In general, recombinant production of a target protein includes a process of subjecting an expression vector including a signal regulating the expression of a gene to transfection into a host cell when it is operably linked to a gene encoding a protein. The transfected cell grows under conditions suitable for expression of the recombinant protein, and the expressed target protein is recovered, thereby producing the target protein.
The protein thus produced has fewer side effects than typical chemical synthetic drugs and has excellent efficacy against diseases in the human body, resulting in a high clinical trial success rate. However, cutting-edge technologies such as DNA manipulation technology, mass fermentation technology, advanced protein purification technology and the like are required for industrial application thereof. Since the launching of five major protein drugs (insulin, human growth hormone, interferon, EPO, and G-CSF) between 1982 and 1991, thorough research into recombinant protein medicines has been ongoing.
Meanwhile, removal of N-formyl-methionine or methionine (Met), which is a translation initiator, from a recombinant protein such as human hemoglobin, interleukin-2, growth hormone, or the like plays an important role in the function and stability of the recombinant protein. Therefore, many attempts have been made to manufacture a protein in which Met is removed from the N-terminus of a native protein. First, there is a method of using cyanogen bromide to cleave Met under highly acidic conditions, but this may only be applied to proteins having no Met residue therein (Boix et al., 1996). Second, there is a method in which a protease-specific oligopeptide is introduced before a target protein and is then removed by proteases, for example, factor Xa, enterokinase, and cathepsin C (Belagaje et al. 1997). Third, there is a method in which N-terminal Met of the protein may be removed in vitro using aminopeptidase of Aeromonas proteolytica (Shapiro et al., 1988; Notomista et al., 1999). Fourth, there is a method in which a signal peptide is introduced before a target protein and processed in vivo during secretion, but the method has a problem in that the yield is very low (1-5 mg per liter of a culture, Huang et al. 1998).
Against this technical background, the present inventors have made great efforts to develop a novel method for producing an N-terminal-methionine-truncated target protein at high yield, and thus ascertained that, when a cysteine protease recognition sequence is inserted between methionine (Met), which is the first amino acid at the N-terminus of a target protein, and the second amino acid and is expressed along with a cysteine protease, an N-terminal-methionine-truncated target protein may be produced with high efficiency, thereby culminating in the present invention.
It is an object of the present invention to provide a gene expression cassette capable of producing an N-terminal-methionine-truncated target protein and a method of producing a target protein at high yield using the same.
In order to achieve the above and other objects, the present invention provides a gene expression cassette comprising a nucleic acid encoding a target protein and a nucleic acid encoding a cysteine protease, in which a cysteine protease recognition sequence is inserted between methionine (Met), which is the first amino acid at the N-terminus of the target protein, and the second amino acid.
In addition, the present invention provides a recombinant vector into which the gene expression cassette is introduced.
In addition, the present invention provides a recombinant microorganism into which the gene expression cassette is introduced.
In addition, the present invention provides a method of producing a target protein comprising:
Unless otherwise defined, all technical and scientific terms used herein have the same meanings as those typically understood by those skilled in the art to which the present invention belongs. Generally, the nomenclature used herein and the test method described below are well known in the art and are typical.
In the present invention, in order to produce an N-terminal-methionine-truncated target protein in a recombinant microorganism, a gene expression cassette capable of co-expression in a microorganism by introducing a cysteine protease recognition sequence downstream of N-terminal methionine of a target protein and additionally selecting a cysteine protease is developed, and the effect of the gene expression cassette is verified using a human growth hormone as a representative target protein showing protein activity through cleavage of N-terminal methionine, from which it is found that a mature human growth hormone from which N-terminal methionine is effectively cleaved, even without a separate methionine cleavage process, is expressed at high yield.
In the present invention, the expression of the nucleic acid encoding the target protein and the nucleic acid encoding the cysteine protease may be regulated using a separate promoter, and the promoter may be selected from the group consisting of a T3 promoter, a T5 promoter, a T7 promoter, a tac promoter, a trc promoter, a trp promoter, an arabinose promoter, a Lacuv5 promoter, and a Lad promoter, but is not limited thereto.
In the present invention, the cysteine protease may be reverse caspase-3, reverse caspase-6 (NCBI Accession No. P55212.2), or reverse caspase-9 (NCBI Accession No. BAA82697.1), and is preferably reverse caspase-3, but is not limited thereto.
In the present invention, the cysteine protease recognition sequence may be DEVD, VEID, VEHD or LEHD, but is not limited thereto.
Specifically, in the present invention, when the cysteine protease is reverse caspase-3, the cysteine protease recognition sequence may be DEVD, when the cysteine protease is reverse caspase-6, the cysteine protease recognition sequence may be VEID or VEHD, or when the cysteine protease is reverse caspase-9, the cysteine protease recognition sequence may be LEHD, but the present invention is not limited thereto.
In order to improve the efficiency of expression of the target protein in the present invention, an enhancer may be inserted upstream of a translation initiation codon of the nucleic acid encoding the target protein, and the enhancer may be an A/U-rich sequence, but is not limited thereto.
In the present invention, the target protein may be human hemoglobin, interleukin-2, interferon-beta, or human growth hormone protein, but is not limited thereto, and may be applied to all recombinant proteins that are utilized by cleaving N-terminal methionine or cleaving a specific N-terminal sequence.
In the present invention, a tag may be additionally attached to the N-terminus of the cysteine protease recognition sequence, and the tag may be selected from the group consisting of a His tag, DH6 tag, AH6 tag, NH6 tag, KH6 tag, HAK tag, T7 tag, S-tag, Flag-tag, HA-tag, V5 epitope, PelB, and Xpress epitope, but is not limited thereto. In the present invention, the tag may affect the expression level of the target protein or the cleavage efficiency using cysteine protease depending on the type thereof, and when a human growth hormone is expressed as the target protein, it is confirmed that an N-methionine-truncated human growth hormone is produced at the highest yield when using DH6 or KH6. This is deemed to be due to the different contribution to protein translation stability depending on the type of tag, and the different contribution to the caspase accessibility and the structural stability of the target protein-caspase. Based on the results of analysis in silico, it is expected that there will be a difference in the lifespan of mRNA due to a difference in the 5′-site hairpin structure of mRNA, leading to a difference in expression level.
Nucleic acid sequences comprising the tag and the cysteine protease recognition sequence that may be used in the present invention are shown in Table 1 below, but only some examples according to the present invention are listed, and the scope of the present invention is not limited only to these nucleic acid sequences. Meanwhile, in the following sequences, the three nucleic acids (A, T, and G) at the 5′ end are the nucleic acid sequence encoding methionine, which is the first amino acid of the target protein.
In an embodiment of the present invention, the gene expression cassette may be manufactured in a form comprising a first gene structure in which the first N-terminal amino acid sequence methionine of a human growth hormone, the tag sequence H6, the cysteine protease recognition sequence DEVD, and the second amino acid phenylalanine sequence of the human growth hormone to the last amino acid sequence are operably linked downstream of the T7 promoter, which is the first promoter, and a second gene structure in which reverse caspase-3, which is the cysteine protease, is operably linked downstream of the T7 promoter, which is the second promoter.
In another embodiment of the present invention, the gene expression cassette may be manufactured in a form comprising a first gene structure in which the first N-terminal amino acid sequence methionine of a human growth hormone, the tag H6, the cysteine protease recognition sequence DEVD, and the second amino acid sequence of the human growth hormone to the last amino acid sequence are operably linked downstream of the tac promoter, which is the first promoter, and a second gene structure in which reverse caspase-3, which is the cysteine protease, is operably linked downstream of the Lacuv5 promoter, which is the second promoter.
In still another embodiment of the present invention, the gene expression cassette may be manufactured in a form comprising a first gene structure in which the first N-terminal amino acid sequence methionine of a human growth hormone, the tag DH6, the cysteine protease recognition sequence DEVD, and the second amino acid sequence of the human growth hormone to the last amino acid sequence are operably linked downstream of the tac promoter, which is the first promoter, and a second gene structure in which reverse caspase-3, which is the cysteine protease, is operably linked downstream of the Lacuv5 promoter, which is the second promoter.
In yet another embodiment of the present invention, the gene expression cassette may be manufactured in a form comprising a first gene structure in which the first N-terminal amino acid sequence methionine of a human growth hormone, the tag AH6, the cysteine protease recognition sequence DEVD, and the second amino acid sequence of the human growth hormone to the last amino acid sequence are operably linked downstream of the tac promoter, which is the first promoter, and a second gene structure in which reverse caspase-3, which is the cysteine protease, is operably linked downstream of the Lacuv5 promoter, which is the second promoter.
In a further embodiment of the present invention, the gene expression cassette may be manufactured in a form comprising a first gene structure in which the first N-terminal amino acid sequence methionine of a human growth hormone, the tag NH6, the cysteine protease recognition sequence DEVD, and the second amino acid sequence of the human growth hormone to the last amino acid sequence are operably linked downstream of the tac promoter, which is the first promoter, and a second gene structure in which reverse caspase-3, which is the cysteine protease, is operably linked downstream of the Lacuv5 promoter, which is the second promoter.
In still a further embodiment of the present invention, the gene expression cassette may be manufactured in a form comprising a first gene structure in which the first N-terminal amino acid sequence methionine of a human growth hormone, the tag KH6, the cysteine protease recognition sequence DEVD, and the second amino acid sequence of the human growth hormone to the last amino acid sequence are operably linked downstream of the tac promoter, which is the first promoter, and a second gene structure in which reverse caspase-3, which is the cysteine protease, is operably linked downstream of the Lacuv5 promoter, which is the second promoter.
In yet a further embodiment of the present invention, the gene expression cassette may be manufactured in a form comprising a first gene structure in which the first N-terminal amino acid sequence methionine of a human growth hormone, the tag HAK, the cysteine protease recognition sequence DEVD, and the second amino acid sequence of the human growth hormone to the last amino acid sequence are operably linked downstream of the tac promoter, which is the first promoter, and a second gene structure in which reverse caspase-3, which the cysteine protease, is operably linked downstream of the Lacuv5 promoter, which is the second promoter.
Another aspect of the present invention pertains to a recombinant vector into which the gene expression cassette is introduced.
In the present invention, the gene expression cassette is introduced into a vector that is selected from the group consisting of a pAPT vector, a pETDuet (pETDuet-1) vector, a pET24a(+) vector, a pQE30 vector, a pMAL-c2x vector, a pTrc99a vector, a pBAD vector, a pUC18 vector, and a pUC1 vector, but the present invention is not limited thereto.
Still another aspect of the present invention pertains to a recombinant microorganism into which the gene expression cassette is introduced.
In the present invention, the recombinant vector may be introduced into E. coli, Corynebacterium glutamicum, Bacillus subtilis, or yeast, but the present invention is not limited thereto. The E. coli that may be used in the present invention may be selected from among all types of E. coli such as a K-12 series and a B series capable of inducing overexpression of target proteins, comprising K-12 W3110, B strain C41 (DE3), and B strain Rosetta2 (DE3), and the yeast may be Pichia pastoris or Saccharomyces cerevisiae, but the range of the recombinant microorganism into which the gene expression cassette according to the present invention may be introduced comprises the entire range of microorganisms available in the art for the production of recombinant proteins, and is not limited to the above exemplary description.
Yet another aspect of the present invention pertains to a method of producing a target protein comprising:
In the present invention, the produced target protein is preferably a mature human growth hormone. In addition thereto, the target protein to be produced may be N-terminal-methionine-truncated human hemoglobin or interleukin-2. Also, any protein requiring cleavage of N-terminal methionine or N-terminal polypeptide may be utilized as the target protein.
As used herein, the term “gene expression cassette” or simply “expression cassette” refers to a recombinantly or synthetically made nucleic acid construct having a nucleic acid element capable of influencing the expression of a structural gene in a host compatible with the sequence. The expression cassette comprises at least a promoter and optionally a transcription termination signal. Typically, a gene expression cassette comprises a nucleic acid to be transcribed (e.g. a heterologous nucleic acid encoding a target protein (polypeptide)) and a promoter. Additional factors required for or assisting in realizing expression may also be used therewith.
As used herein, the term “promoter (or promoter region)” refers to a portion of DNA of a gene that controls the transcription of DNA to which it is operably linked. The promoter region comprises a specific sequence of DNA sufficient for RNA polymerase to initiate recognition, binding and transcription. Also, such a promoter region comprises a sequence that regulates the recognition, binding and transcription initiation activity of RNA polymerase. The promoter may be constitutive or regulated by a cis-acting or trans-acting factor, depending on the nature of the regulation.
As used herein, the term “operably linked” refers to a functional linkage between a nucleic acid expression control sequence (e.g. a promoter, a signal sequence, or a series of transcription-factor-binding sites) and a heterologous nucleic acid sequence. Here, the expression control sequence affects the transcription and/or translation of a nucleic acid corresponding to the heterologous nucleic acid sequence.
As used herein, the term “recombinant” refers to any material (e.g. a vector or microorganism) that may be formed as a result of genetic manipulation.
As used herein, the term “vector” refers to a DNA product comprising a DNA sequence that is operably linked to a suitable control sequence capable of expressing DNA in a suitable host. The vector may be a plasmid, a phage particle, or a simple potential genomic insert. When transformed into an appropriate host, the vector may replicate and function independently of the host genome, or in some cases may be integrated into the genome itself. Since a plasmid is currently the most commonly used form of the vector, the terms “plasmid” and “vector” are sometimes used interchangeably in the specification of the present invention. For the purposes of the present invention, it is preferred to use a plasmid vector. A typical plasmid vector that may be used for this purpose is configured to comprise (a) a replication origin that allows efficient replication to comprise ones to hundreds of plasmid vectors in each host cell, (b) an antibiotic resistance gene that enables selection of a host cell transformed with a plasmid vector, and (c) a restriction enzyme cleavage site into which a foreign DNA fragment may be inserted. Even when an appropriate restriction enzyme cleavage site does not exist, the vector and foreign DNA may be easily ligated using a synthetic oligonucleotide adapter or linker according to a typical method. After ligation, the vector has to be transformed into an appropriate host cell. Transformation may be easily accomplished using a calcium chloride (CaCl2) process or an electroporation process (Neumann, et al., EMBO J., 1:841, 1982).
As the vector that is used for overexpression of the gene according to the present invention, an expression vector known in the art may be used. A base sequence is said to be “operably linked” when placed in a functional relationship with another nucleic acid sequence. This may be a gene and control sequence(s) linked in such a way as to enable gene expression when an appropriate molecule (e.g. a transcriptional activation protein) is bound to the control sequence(s). For example, DNA for a pre-sequence or secretory leader is operably linked to DNA for a polypeptide when expressed as a preprotein that participates in the secretion of the polypeptide, a promoter or enhancer is operably linked to a coding sequence when it affects the transcription of the sequence, a ribosome-binding site is operably linked to a coding sequence when it affects transcription of the sequence, or a ribosome-binding site is operably linked to a coding sequence when placed to facilitate translation. In general, “operably linked” means that the linked DNA sequence is in contact therewith, or that a secretory leader is in contact therewith and is present in the reading frame. However, the enhancer need not be in contact therewith. The linking of these sequences is accomplished by ligation (linkage) at a convenient restriction enzyme site. When no such site exists, a synthetic oligonucleotide adapter or linker according to a typical method is used.
As is well known in the art, in order to increase the expression level of a transformed gene in a host cell, the gene has to be operably linked to a transcriptional and translational expression control sequence that functions in the selected expression host. Preferably, the expression control sequence and the corresponding gene are comprised in a single recombinant vector that comprises both a bacterial selection marker and a replication origin.
The recombinant microorganism that is transformed by the recombinant vector described above constitutes another aspect of the present invention. As used herein, the term “transformation” refers to introduction of DNA into a host such that DNA becomes replicable as an extrachromosomal factor or through chromosomal integration.
Here, it is to be understood that not all vectors function equally in expressing the DNA sequence of the present invention. Likewise, not all hosts function equally for the same expression system. However, those skilled in the art will be able to make an appropriate selection from among various vectors, expression control sequences and hosts without undue experimentation and without departing from the scope of the present invention. For example, a vector may be selected in consideration of the host. This is because the vector has to be replicated in the host. The number of copies of a vector, ability to control the number of copies, and expression of another protein encoded by the vector, for example, an antibiotic marker, also have to be taken into consideration.
Moreover, the gene expression cassette according to the present invention may be introduced into the genome of a host cell and may be present as a chromosomal factor. It will be apparent to those skilled in the art to which the present invention belongs that, even when the gene expression cassette is inserted into the genome chromosome of a host cell, it has the same effect as when the recombinant vector is introduced into the host cell as described above.
A better understanding of the present invention may be obtained through the following examples. These examples are merely set forth to illustrate the present invention, and are not to be construed as limiting the scope of the present invention.
1-1. Selection of Gene Promoter for Inducing Overexpression of Target Protein
For system construction, an isopropyl beta-D-1-thiogalactopyranoside (Isopropyl-βIPTG) responsive gene promoter, commonly used in molecular biology research, was selected. Three types of promoters (tac, T7, Lacuv5) known to be capable of strongly inducing and regulating gene expression were selected.
1-2. Selection of Synthetic Tag for Induction of Overexpression of Target Protein and Cleavage of N-Terminal Methionine
A tag in which five histidines (5x-histidine, H5), a specific amino acid, and a cysteine protease recognition sequence (DEVD) were attached to downstream of N-terminal methionine of a target protein was selected as a basic synthetic tag structure (MHHHHHXaa). Xaa may include lysine, arginine, or histidine, and may also be deleted. In addition, a tag in the form of MXaaXaaXaaXaaHHHHHXaa was used by adding a specific amino acid to the N-terminus of the basic synthetic tag. Specifically, 4 types of tags (aspartate-6x-histidine, DH6; alanine-6x-histidine, AH6; asparagine-6x-histidine, NH5; and lysine-6x-histidine, KH6) were manufactured, and a complex histidine synthetic tag (histidine-alanine-lysine-(4x-alanine-histidine)-glycine-histidine-alanine-histidine (HAK)) in which histidine, alanine, and lysine were used in combination was also manufactured.
1-3. Selection of Cysteine Protease for Cleavage of N-Terminal Methionine
Referring to a paper (Srinivasa M. Srinivasula et al., J Biol Chem., 1998 Apr. 24; 273(17):10107-11) in which subunits of cysteine protease were rebuilt so as to exhibit protein activity even in E. coli, a reverse caspase-3 (rev-CASP3) gene was selected. The amino acid sequence and the nucleic acid sequence of reverse caspase-3 that was used in the present invention were as follows.
1-4. Construction of System for Overexpression of Target Protein
A system for overexpression of a target protein was constructed using the factors selected in Examples 1-1, 1-2, and 1-3. In order to test the system, a gene expression cassette was designed and manufactured for a growth hormone protein (human growth hormone (hGH)). The amino acid sequence and the nucleic acid sequence of the human growth hormone that was used in the present invention were as follows.
Meanwhile, a pETDuet-1 plasmid (EMD Millipore Corp.) and a pAPT plasmid (AP Tech.) were used as vectors for cloning.
A DNA fragment (H6-DEVD-hGH) was amplified by performing PCR such that the basic synthetic tag (H6-DEVD) to which six histidines and a reverse caspase-3 recognition sequence were linked was attached to DNA encoding the growth hormone protein. The amplified DNA fragment and the pETDuet-1 plasmid cleaved with restriction enzymes NcoI/HindIII were purified through gel extraction, and were then cloned through homologous recombination. In order to insert the DNA fragment encoding reverse caspase-3, the plasmid subjected to primary cloning was cleaved with restriction enzymes NdeI/XhoI, and was then secondarily cloned in a homologous recombination manner. The manufacture d plasmid is pETDuet-H6-DEVD-hGH-T7-rev-CASP3, the manufacture thereof is schematically shown in
For the pAPT plasmid, an A/U-rich sequence (GCTCTTTAACAATTTATCAGATCCAATAGGAGGAACAAT) as an enhancer for increasing protein translation efficiency was inserted upstream of the translation initiation codon, and the corresponding plasmid was called pAPT-Y. The pAPT-Y cloning is schematically shown in
As shown in
Thereby, pETDuet-H6-DEVD-hGH-T7-rev-CASP3, pAPT-Y-H6-DEVD-hGH-Lacuv5-rev-CASP3, pAPT-Y-DH6-DEVD-hGH-Lacuv5-rev-CASP3, pAPT-Y-AH6-DEVD-hGH-Lacuv5-rev-CASP3, pAPT-Y-NH6-DEVD-hGH-Lacuv5-rev-CASP3, pAPT-Y-KH6-DEVD-hGH-Lacuv5-rev-CASP3, and pAPT-Y-HAK-DEVD-hGH-Lacuv5-rev-CASP3 plasmids were obtained, and are schematically shown in
2-1. Evaluation of Expression Level of N-Terminal-Methionine-Truncated Mature Growth Hormone Protein
20 μL of E. coli (Escherichia coli K-12 W3110 or Escherichia coli C41 (DE3) or Escherichia coli Rosetta2 (DE3)) manufactured to enable transformation was dispensed in an amount of 1.0×106 cells or more into each tube, mixed with 10 ng of the plasmid manufactured above, and then allowed to stand on ice for 5 minutes. The E. coli-DNA mixture was transferred into a 0.2 cm cuvette for electroporation, current at 2.5 kV was applied thereto, 500 μL of a SOC medium (super optimal broth with catabolite repression) was mixed therewith, and the mixture was cultured at 37° C. for 30 minutes. 100 μL of the culture solution was spread on an LB (Luria-Bertani) solid medium (agar plate) containing a 100 μg/mL kanamycin antibiotic, followed by stationary culture at 37° C. for 16 hours to thus complete transformation. The strains showing resistance to kanamycin were randomly selected, inoculated in 5 mL of an LB liquid medium (100 μg/mL), and then cultured at 37° C. When the optical density (OD) of the culture solution was measured to be 0.8-1.3 at a wavelength of 600 nm, 1 mM IPTG (Isopropyl β) was added to the culture solution to induce expression of the growth hormone protein and reverse caspase-3 for 3 hours. The expression levels of growth hormone protein and reverse caspase-3 were calculated using SDS-PAGE (sodium dodecyl sulfate-polyacrylamide gel electrophoresis) and Bio-Rad Image Lab software version 5.2.1.
Compared with the strain in which N-terminal methionine was maintained due to the absence of reverse caspase-3, it was confirmed that expression of the growth hormone protein from which N-terminal methionine was removed was induced when expressed along with reverse caspase-3 (
2-2. Evaluation of Cleavage of N-Terminal Methionine and Synthetic Tag 1
Western blot was performed on the growth hormone protein and the synthetic tag in order to confirm whether N-terminal methionine was cleaved.
Cells in which protein expression was induced through IPTG were collected and then lysed ten times each for 10 seconds at 20% intensity (amplitude) using a cell lysis buffer (50 mM Tris-HCl (pH 8.5), 10 mM EDTA) and a sonicator. The lysed cells were centrifuged at 12,000×g at 4° C. for 30 minutes to afford a soluble protein and an insoluble protein (inclusion body). Protein electrophoresis was performed by loading total protein and soluble and insoluble proteins on a 4-12% Bis-Tris gel under the same conditions as in SDS-PAGE, after which protein transfer was carried out using a PVDF membrane (polyvinylidene fluoride membrane). Blocking was performed in order to reduce nonspecific binding to the membrane, and binding of primary antibodies anti-His, anti-hGH, and anti-CASP3 was induced. A secondary antibody to which a fluorescent factor was attached was allowed to react therewith, after which the presence or absence of the growth hormone protein, synthetic tag, and reverse caspase-3 was observed using an Odyssey Infrared Imaging System. The results of Western blot were analyzed using Li-COR Image studio analysis software version 3.1.
Compared with the strain in which N-terminal methionine was maintained due to the absence of reverse caspase-3, it was confirmed that 96.12% of the N-terminal methionine of the growth hormone protein and the synthetic tag was cleaved when expressed along with reverse caspase-3 (
2-3. Evaluation of Cleavage of N-Terminal Methionine and Synthetic Tag 2
N-terminal sequencing was performed on the growth hormone protein and the synthetic tag in order to confirm whether N-terminal methionine was cleaved. The insoluble protein of Example 2-2 was loaded on a 4-12% Bis-Tris gel and SDS-PAGE was performed, after which the growth hormone protein was identified and acquired through staining with Coomassie blue. The protein thus obtained was subjected to trypsinization (trypsin-based enzymatic digestion), followed by N-terminal sequencing through liquid chromatography-mass spectrometry (LC-MS). Here, the liquid chromatography column that was used was an Acclaim RSLC 120, C18, 2.2 μm Analytical (2.1 mm×25 cm; 2.2 μm packing C18), the mobile phase A was 0.1% formic acid in water, the mobile phase B was 0.1% formic acid in acetonitrile, and analysis was performed under UV radiation at 214 nm. Mass spectrometry was performed in the range of 300-1,900 m/z using a Thermo Q-Exactive Plus-Quad-Orbitrap MS system.
For the strain in which N-terminal methionine was maintained due to the absence of reverse caspase-3, the ‘GSHHHHHHDEVDFPTIPLSR’ sequence to which the synthetic tag was attached was identified. For the strain expressed along with reverse caspase-3, the ‘FPTIPLSR’ sequence, in which the N-terminal methionine of the growth hormone protein and the synthetic tag were cleaved, was identified (
From the above description, those skilled in the art to which the present invention belongs will appreciate that the present invention may be embodied in other specific forms without changing the technical spirit or essential features thereof. In this regard, the embodiments described above should be understood to be non-limiting and illustrative in every way. The scope of the present invention is defined by the claims below rather than the aforementioned detailed description, and all changes or modified forms that are capable of being derived from the meaning, range, and equivalent concepts of the appended claims should be construed as being comprised in the scope of the present invention.
When a gene expression cassette according to the present invention is used, N-terminal methionine of a target protein is cleaved by a cysteine protease that is introduced along with the target protein, so methionine is removed without a separate methionine removal process, thus making it possible to simplify the process of producing a target protein and to produce a target protein having activity at high yield.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2018-0170531 | Dec 2018 | KR | national |
This is a United States national phase under 35 USC § 371 of International Patent Application PCT/KR20219/018464 filed Dec. 26, 2019, which in turn claims priority under 35 USC § 119 of Korean Patent Application 10-2018-0170531 filed Dec. 27, 2018. The disclosures of all such applications are hereby incorporated herein by reference, in their entireties, for all purposes.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2019/018464 | 12/26/2019 | WO | 00 |
