LONG-ACTING PROTEIN CONJUGATES FOR BRAIN TARGETING, A PREPARATION METHOD THEREOF, AND A COMPOSITION COMPRISING THE SAME

TECHNICAL FIELD

The present invention relates to a long-acting protein conjugate capable of targeting the brain and a method of preparing the same. Additionally, the present invention relates to a novel peptide for brain targeting and use thereof.

BACKGROUND ART

Despite the growing need for effective delivery of therapeutic agents to the brain, the development of new agents for the brain is progressing at a much slower rate than those for the rest of the body. This slow progress is largely due to the situation where most drugs cannot penetrate into the brain through the brain capillary wall that forms the blood-brain barrier (hereinafter, BBB). The BBB is a structure established by tight junctions between the endothelial cells of the cerebral blood vessels and astrocytes that further strengthen these tight junctions, and it has the role of preventing substances in the blood from diffusing freely into the brain parenchyma through the blood vessel walls. For this reason, many drugs developed for the treatment of brain diseases have a problem in that they cannot pass through the BBB well. Almost 100% of macro-molecular drugs and over 98% of small-molecule drugs cannot pass through the BBB. Only a very small number of drugs, for example, small-molecule drugs which have high lipid solubility and molecular weights of 400 to 500 daltons or less, can actually pass through the BBB. Additionally, among these small molecules capable of passing through the BBB, only a small fraction can pass through the BBB in a pharmaceutically significant amount.

Only some brain diseases, such as depression, affective disorder, chronic pain, and epilepsy, can respond to small-molecule drugs that pass through the BBB. A greater majority of brain diseases, such as Alzheimer's disease, stroke/neuroprotection, brain and spinal cord injury, brain cancer, HIV infection in the brain, ataxia-producing disorders, amyotrophic lateral sclerosis (ALS), Huntington disease, childhood inborn genetic errors affecting the brain, Parkinson's disease, and multiple sclerosis do not respond to conventional lipid-soluble small-molecular weight drugs.

Currently, development of carriers capable of delivering drugs through the BBB is actively underway. Meanwhile, although peptides with specific amino acid sequences are known to pass through the BBB and are able to deliver drugs, siRNAs, etc., however, the research on the possibility of delivering a large-sized physiologically active material with a particular structure is still far below expectation (Kumar et al., Nature. 2007, 448: 39 to 43). Additionally, there is an increased need for the development and study of new and improved drugs with respect to the treatment of brain diseases, for which only a very few effective small-molecule drugs are available.

DISCLOSURE
Technical Problem

An object of the present invention is to provide a long-acting conjugate for brain targeting, which can pass through the blood-brain barrier (BBB), maintain effectiveness of physiological activity, and contain a bio-compatible material capable of extending the half-life of a physiologically active material.

Specifically, an object of the present invention is to provide a long-acting conjugate for brain targeting, in which a physiologically active material and a peptide for brain targeting are each independently linked to an immunoglobulin Fc region by a peptide linker or a non-peptide linker.

More specifically, an object of the present invention is to provide a long-acting conjugate for brain targeting, in which a physiologically active material is linked, by a mutual binding, to an immunoglobulin Fc region of a peptide for brain targeting to which the immunoglobulin Fc region is fused.

Another object of the present invention is to provide a polynucleotide encoding the long-acting conjugate for brain targeting; an expression vector comprising the same; a host cell comprising the polynucleotide or the expression vector; and a kit comprising at least one of the above.

Still another object of the present invention is to provide a composition, e.g., a pharmaceutical composition, which comprises the long-acting conjugate for brain targeting.

Still another object of the present invention is to provide a use of the long-acting conjugate for brain targeting in the preparation of pharmaceutical agents.

Still another object of the present invention is to provide a method for preparing the long-acting conjugate for brain targeting.

Still another object of the present invention is to provide a peptide for brain targeting; a polynucleotide encoding the same; an expression vector comprising the polynucleotide; a host cell comprising the polynucleotide or the expression vector comprising the polynucleotide; and a kit comprising at least one of the above.

Technical Solution

To achieve the above objects, an aspect of the present invention provides a long-acting conjugate for brain targeting, which can pass though the blood-brain barrier, maintain effectiveness of physiological activity, and contain a bio-compatible material capable of extending the half-life of a physiologically active material.

In a specific embodiment, the present invention relates to a long-acting conjugate for brain targeting, in which a physiologically active material and a peptide for brain targeting are each independently linked to an immunoglobulin Fc region by a peptide linker or a non-peptide linker.

In the conjugate according to the previous embodiment, the conjugate is one in which a physiologically active material is linked, by a mutual binding, to an immunoglobulin Fc region of a peptide for brain targeting to which the immunoglobulin Fc region is fused.

In the conjugate according to any one of the previous embodiments, the conjugate is represented by the following Formula 1:

X-L₁-F-L₂-Y [Formula 1]

wherein:

X is a physiologically active material;

Y is a brain targeting peptide (BTP)

L₁and L₂are peptide linkers or non-peptide linkers, in which when L₁and L₂are peptide linkers, the peptide linkers comprise 0 to 1,000 amino acids; and

F is an immunoglobulin constant region comprising an FcRn-binding region.

In the conjugate according to any one of the previous embodiments, F and the immunoglobulin Fc region may be in a dimeric form.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the long-acting conjugate is characterized in that it passes through the blood-brain barrier and delivers a physiologically active material into the brain tissue.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the peptide for brain targeting includes a peptide, protein, or antibody, and in which each of the peptide, protein, or antibody contains an amino acid sequence allowing passage through the blood-brain barrier.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the peptide for brain targeting may pass through the blood-brain barrier through a pathway by passive transport or a pathway by receptor-mediated transport, but the transport pathway is not limited thereto. For example, the peptide for brain targeting may be a peptide, protein, or antibody that can pass through the blood-brain barrier, but their types and sizes are not particularly limited.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the peptide for brain targeting passes through the blood-brain barrier through a pathway by receptor-mediated transport.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the pathway by receptor-mediated transport is characterized in that the passage through the blood-brain barrier is performed by a receptor-mediated transport pathway through any one selected from the group consisting of an insulin receptor, transferrin receptor, low-density lipoprotein receptor, low-density lipoprotein receptor-related protein, leptin receptor, nicotinic acetylcholine receptor, glutathione transporter, calcium-activated potassium channel, and receptor for advanced glycation endproducts (RAGE), and ligands of the receptors and antibody binding to the receptors or ligands, but is not limited thereto. The peptide for brain targeting may be selected from the group consisting of a peptide, protein, or antibody that can pass through the blood-brain barrier, or it may be a partial peptide sequence isolated from the peptide, protein, or antibody, but is not limited thereto.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the physiologically active material may be selected from the group consisting of toxins; or glucagon like peptide-1 (GLP-1) receptor agonists; glucagon receptor agonists; gastric inhibitory polypeptide (GIP) receptor agonists; fibroblast growth factor (FGF) receptor agonists; cholecystokinin receptor agonists; gastrin receptor agonists; melanocortin receptor agonists; human growth hormone; growth hormone-releasing hormone; growth hormone-releasing peptide; interferons; interferon receptors; colony-stimulating factors (granulocyte colony-stimulating factors); interleukins; interleukin receptors; enzymes; interleukin-binding proteins; cytokine-binding proteins; macrophage-activating factors; macrophage peptides; B cell factors; T cell factors; protein A; allergy-inhibiting factors; necrosis glycoproteins; immunotoxins; lymphotoxins; tumor necrosis factors; tumor suppressors; transforming growth factors; α-1 antitrypsin; albumin; α-lactalbumin; apolipoprotein-E; erythropoietin; high-glycosylated erythropoietin; angiopoietins; hemoglobins; thrombin; thrombin receptor-activating peptide; thrombomodulin; blood coagulation factor VII; blood coagulation factor VIIa; blood coagulation factor VIII; blood coagulation factor IX; blood coagulation factor XIII; plasminogen activators; fibrin-binding peptides; urokinase; streptokinase; hirudin; protein C; C-reactive protein; renin inhibitor; collagenase inhibitors; superoxide dismutase; leptin; platelet-derived growth factor; epithelial growth factor; epidermal growth factor; angiostatin; angiotensin; bone morphogenetic growth factor; bone morphogenetic protein; calcitonin; insulin; atriopeptin; cartilage-inducing factor; elcatonin; connective tissue-activating factor; tissue factor pathway inhibitor; follicle-stimulating hormone; luteinizing hormone; luteinizing hormone-releasing hormone; nerve growth factors; axogenesis factor-1; brain-natriuretic peptide; glial-derived neurotrophic factor; netrin; neutrophil inhibitory factor; neurotrophic factor; neurturin; parathyroid hormone; relaxin; secretin; somatomedin; insulin-like growth factor; adrenocortical hormone; glucagon; cholecystokinin; pancreatic polypeptides; gastrin-releasing peptides; corticotropin-releasing factor; thyroid-stimulating hormone; autotaxin; lactoferrin; myostatin; activity-dependent neuroprotective protein (ADNP), β-secretase1 (BACE1), amyloid precursor protein (APP), neural cell adhesion molecule (NCAM), amyloid (3, Tau, receptor for advanced glycation endproducts (RAGE), α-synuclein, or agonists or antagonists thereof; receptors, receptor agonists; cell surface antigens; monoclonal antibody; polyclonal antibody; antibody fragments; virus-derived vaccine antigens; hybrid polypeptides or chimeric polypeptides that activate at least one receptor agonist; and analogues thereof.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the toxin is selected from the group consisting of maytansine or a derivative thereof, auristatin or a derivative thereof, duocarmycin or a derivative thereof, and pyrrolobenzodiazepine (PBD) or a derivative thereof;

the glucagon like peptide-1 (GLP-1) receptor agonist is selected from the group consisting of native exendin-3 or native exendin-4, and analogues thereof;

the FGF receptor agonist is selected from the group consisting of FGF1 or an analogue thereof, FGF19 or an analogue thereof, FGF21 or an analogue thereof, and FGF23 or an analogue thereof;

the interferon is selected from the group consisting of interferon-α, interferon-β, and interferon-γ;

the interferon receptor is selected from the group consisting of interferon-α receptor, interferon-β receptor, interferon-γ receptor, and soluble type I interferon receptors;

the interleukin is selected from the group consisting of interleukin-1, interleukin-2, interleukin-3, interleukin-4, interleukin-5, interleukin-6, interleukin-7, interleukin-8, interleukin-9, interleukin-10, interleukin-11, interleukin-12, interleukin-13, interleukin-14, interleukin-15, interleukin-16, interleukin-17, interleukin-18, interleukin-19, interleukin-20, interleukin-21, interleukin-22, interleukin-23, interleukin-24, interleukin-25, interleukin-26, interleukin-27, interleukin-28, interleukin-29, and interleukin-30;

the interleukin receptor is interleukin-1 receptor or interleukin-4 receptor;

the enzyme is selected from the group consisting of β-glucosidase, α-galactosidase, β-galactosidase, iduronidase, iduronate-2-sulfatase, galactose-6-sulfatase, acid α-glucosidase, acid ceramidase, acid sphingomyelinsase, galactocerebrosidsase, arylsulfatase A, arylsulfatase B, β-hexosaminidase A, β-hexosaminidase B, heparin N-sulfatase, α-D-mannosidase, β-glucuronidase, N-acetylgalactosamine-6 sulfatase, lysosomal acid lipase, α-N-acetyl-glucosaminidase, glucocerebrosidase, butyrylcholinesterase, chitinase, glutamate decarboxylase, imiglucerase, lipase, uricase, platelet-activating factor acetylhydrolase, neutral endopeptidase, myeloperoxidase, α-galactosidase-A, agalsidase α, agalsidase β, α-L-iduronidase, butyrylcholinesterase, chitinase, glutamate decarboxylase, and imiglucerase;

the interleukin-binding protein is IL-18 bp;

the cytokine-binding protein is tumor necrosis factor (TNF)-binding protein;

the nerve growth factors are selected from the group consisting of nerve growth factor, ciliary neurotrophic factor, axogenesis factor-1, brain-natriuretic peptide, glial-derived neurotrophic factor, netrin, neutrophil inhibitory factor, neurotrophic factor, and neurturin;

the myostatin receptor is selected from the group consisting of TNFR (P75), TNFR (P55), IL-1 receptor, VEGF receptor, and B cell activating factor receptor;

the myostatin receptor antagonist is IL1-Ra;

the cell surface antigen is selected from the group consisting of CD2, CD3, CD4, CD5, CD7, CD11a, CD11b, CD18, CD19, CD20, CD23, CD25, CD33, CD38, CD40, CD45, and CD69; and

the antibody fragments are selected from the group consisting of scFv, Fab, Fab′, F(ab)₂, and Fd.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the GLP-1 receptor agonist is selected from the group consisting of a native exendin-4; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is deleted; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is substituted with a hydroxyl group; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is modified with a dimethyl group; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is substituted with a carboxyl group; an exendin-4 derivative in which the α-carbon of the 1^stamino acid of exendin-4, histidine, is deleted; an exendin-4 derivative in which the 12^thamino acid of exendin-4, lysine, is substituted with serine, and an exendin-4 derivative in which the 12^thamino acid of exendin-4, lysine, is substituted with arginine.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, L₁is linked to the N-terminal region of F, and L₂is linked to the C-terminal region of F.

In the conjugate according to any one of the previous embodiments, L₁is linked to the N-terminus or C-terminus of X, and L₂is linked to the N-terminal region or C-terminal region of Y.

In the conjugate according to any one of the previous embodiments, L₁is linked to the N-terminus or C-terminus of X, and L₂is linked to the N-terminal region of Y.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the F-L₂-Y of Formula 1 is represented by the following Formula 2:

embedded image

wherein:

F_aand F_bare each a single-stranded polypeptide chain, which comprises a hinge region, CH2 domain, and CH3 domain, in which F_aand F_bare linked by a disulfide bond in the hinge region, whereby the conjugate comprises an Fc fragment, and F_aand L₁are covalently bonded;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2an, being the same as or different from one another, is a peptide linker; and

each of L_2b1, . . . , L_2bn′, being the same as or different from one another, is a peptide linker;

wherein n and n′ are each independently an integer.

In the conjugate according to any one of the previous embodiments, each of L_2a1, . . . , L_2an, being the same as or different from one another, is a peptide linker, and each of L_2b1, . . . , L_2bn′, being the same as or different from one another, is a peptide linker, wherein n and n′ are each independently an integer.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, L₁is linked to the N-terminus of F_a, and L_2a1and L_2b1are each linked to the C-terminus of F_aand F_b.

In the conjugate according to any one of the previous embodiments, the X-L₁-F-L₂-Y of Formula 1 has a structure represented by the following Formula 3:

embedded image

wherein,

X is a physiologically active material;

L_1aand L_1bare each independently a peptide linker or a non-peptide linker;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2anis independently a peptide linker or a non-peptide linker; and

each of L_2b1, . . . , L_2bn′ is independently a peptide linker or a non-peptide linker;

wherein n and n′ are each independently an integer.

In the conjugate according to any one of the previous embodiments, L_1aand L_1bare each linked to the N-terminus of F_aand F_b, and L_2a1and L_2b1are each linked to the C-terminus of F_aand F_b.

In the conjugate according to any one of the previous embodiments, the X-L₁-F-L₂-Y of Formula 1 has a structure represented by the following Formula 4:

embedded image

wherein:

X is a physiologically active material;

L₁is a peptide linker or a non-peptide linker;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2anis independently a peptide linker or a non-peptide linker; and

each of L_2b1, . . . , L_2bn′ is independently a peptide linker or a non-peptide linker;

wherein n and n′ are each independently an integer.

In the conjugate according to any one of the previous embodiments,

each of L_2a1, . . . , L_2an, being the same as or different from one another, is a peptide linker; and each of L_2b1, . . . , L_2bn′, being the same as or different from one another, is a peptide linker, wherein n and n′ are each independently an integer.

In the conjugate according to any one of the previous embodiments, L₁is linked to the N-terminus of F_a, and L_2a1and L_2b1are each linked to the C-terminus of F_aand F_b.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, n=n′, and each fulfills the conditions of L_2a1=L_2b1, . . . . , L_2an=L_2bn′ and BTP_a1=BTP_b1, . . . , BTP_an=BTP_bn′.

In the conjugate according to any one of the previous embodiments, in the Formula 1, F is F_aF_b, and L₂-Y is (L_2a-Ya)n and (L_2b-Yb)n′, in which the conjugate is represented by the following Formula 5:

embedded image

wherein,

X is a physiologically active material;

L₁is a peptide linker or a non-peptide linker;

F_aand F_bare each an immunoglobulin Fc region, which comprises a hinge region, CH2 domain, and CH3 domain, specifically F_aand F_bare each a single-stranded polypeptide chain, which comprises a hinge region, CH2 domain, and CH3 domain, in which F_aand F_bare linked by a disulfide bond in the hinge region, whereby the conjugate comprises an Fc fragment, and F_ais covalently bonded with L₁;

each of Y_aand Y_b, being the same as or different from one another, is a peptide for brain targeting; and

each of L_2aand L_2b, being the same as or different from one another, is a peptide linker;

wherein n and n′ are each independently an integer of 1 or more.

In the conjugate according to any one of the previous embodiments, in Formula 1, X is X_aand X_b; L₁is L_1aand L_1b; F is F_aand F_b; and L₂-Y is (L_2a-Y_a)_nand (L_2b-Y_b)_n′, in which the conjugate is represented by the following Formula 6:

embedded image

wherein,

X is a physiologically active material;

L_1aand L_1bare each independently a peptide linker or a non-peptide linker, specifically a peptide linker;

the peptide linker may comprise 0 to 1,000 amino acids;

each of Y_aand Y_b, being the same as or different from one another, is a peptide for brain targeting; and

each of L_2aand L_2b, being the same as or different from one another, is a peptide linker;

wherein n and n′ are each independently an integer of 1 or more.

In the conjugate according to any one of the previous embodiments, each of BTP_a1, . . . , BTP_an, being the same as one another, is a peptide for brain targeting; each of BTP_b1, . . . , BTP_bn′, being the same as one another, is a peptide for brain targeting; each of L_2a1, . . . , L_2anis a peptide linker; and each of L_2b1, . . . , L_2bn′ is a peptide linker.

In the conjugate according to any one of the previous embodiments, each of BTP_a1, . . . , BTP_an, being different from one another, is a peptide for brain targeting; each of BTP_b1, . . . , BTP_bn′, being different from one another, is peptide for brain targeting; each of L_2a1, . . . , L_2anis a peptide linker; and each of L_2b1, . . . , L_2bn′ is a peptide linker.

In the conjugate according to any one of the previous embodiments, n=n′, and fulfills any one of the conditions of BTP_a1≠BTP_b1, . . . and BTP_an≠BTP_bn′.

In the conjugate according to any one of the previous embodiments, n=n′, and each fulfills the conditions of L_2a1≠L_2b1, . . . , L_2an≠L_2bn′, and/or BTP_a1≠BTP_b1, . . . , BTP_an≠BTP_bn′.

In the conjugate according to any one of the previous embodiments, each of BTP_a1, . . . , BTP_an, being different from one another, is a peptide for brain targeting; each of BTP_b1, . . . , BTP_bn′, being different from one another, is a peptide for brain targeting; each of L_2a1, . . . , L_2anis a peptide linker; and each of L_2b1, . . . , L_2bn′ is a peptide linker.

In the conjugate according to any one of the previous embodiments, n and n′ are each independently an integer of 1 to 5, that is, 1, 2, 3, 4, or 5.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, L₁is linked to an amine group or thiol group of X.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, L₁L_1a, or L_1bis linked to the N-terminal amine group of X, the amine group located at a side chain of a lysine residue, or the —SH group (thiol group) located at a side chain of a cysteine residue.

In the conjugate according to any one of the previous embodiments, the peptide for brain targeting (BTP) comprises an amino acid selected from amino acid sequences of SEQ ID NOS: 2, 4, 6, 8, 10, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, and 85.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, X, which is a physiologically active material, is a polypeptide consisting of 2 to 1,000 amino acids.

In the conjugate according to any one of the previous embodiments, L₁, L_1a, or L_1bis a non-peptide linker having a size of 0.5 kDa to 100 kDa.

In the conjugate according to any one of the previous embodiments, the non-peptide linker is polyethylene glycol.

In the conjugate according to any one of the previous embodiments, L₁, L_1a, or L_1bis a peptide linker comprising 0 to 1,000 amino acids.

In the conjugate according to any one of the previous embodiments, L₂is a peptide linker.

In the conjugate according to any one of the previous embodiments, the peptide linker is (GS)_m, (GGS)_m, (GGGS)_m, or (GGGGS)_m, in which m is 1 to 10.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, L₂is a peptide linker ((GS)_m, (GGS)_m, (GGGS)_m, or (GGGGS)_m, in which m is 1 to 10).

The long-acting conjugate for brain targeting according to any one of the previous embodiments is a fusion protein which is fused at the gene level, in which L_1aand L_1bare each linked to the C-terminal region of X and the N-terminal region of F_aand F_b; and L_2aand L_2bare each linked to the C-terminal region of F_aand F_b.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, L₁and L₂are peptide linkers ((GS)_m, (GGS)_m, (GGGS)_m, or (GGGGS)_m, in which m is 1 to 10), and the long-acting conjugate for brain targeting is in the form of a fusion protein.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the physiologically active material is a therapeutic enzyme, the conjugate is in the form of a fusion protein, and the fusion protein is one in which the stability is increased and the binding affinity to a lysosome receptor is decreased compared to a therapeutic enzyme in which the Fc region is not fused.

In the conjugate according to any one of the previous embodiments, one of L₁and L₂is a peptide linker and the other is a non-peptide linker.

In the conjugate according to any one of the previous embodiments, L₁and L₂are both peptide linkers.

In the conjugate according to any one of the previous embodiments, when L₁is a non-peptide linker or a peptide linker and L₂is a peptide linker, the peptide linker comprises 0 to 1,000 amino acids.

In the conjugate according to any one of the previous embodiments, the long-acting conjugate for brain targeting of Formula 1 is one in which the N-terminus of X and the N-terminus of F are linked by L₁and the N-terminus of Y and the C-terminus of F are linked by L₂.

In the long-acting conjugate according to any one of the previous embodiments, the long-acting conjugate for brain targeting of Formula 1 is one in which an end of L₁is linked to a lysine residue or cysteine residue, etc of X and the other end of L₁is linked to the N-terminus of F; and the N-terminus of Y and the C-terminus of F are linked by L₂.

In the conjugate according to any one of the previous embodiments, the non-peptide linker is selected from the group consisting of polyethylene glycol, polypropylene glycol, an ethylene glycol-propylene glycol copolymer, polyoxyethylated polyol, polyvinyl alcohol, a polysaccharide, dextran, polyvinyl ethyl ether, a biodegradable polymer, a lipid polymer, chitins, hyaluronic acid, a fatty acid, a high molecular weight polymer, a low molecular weight compound, a nucleotide, and a combination thereof.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, when any one or both of L₁and L₂of Formula 1 are a peptide linker, X and F, or F and Y are linked to each other by L₁and L₂via a covalent chemical bond, non-covalent chemical bond, or a combination thereof and L₁and L₂each comprise 0 to 1,000 amino acids. When the peptide linker contains zero amino acid, they are linked by a peptide bond, which is a covalent bond.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, when any one or both of L₁and L₂of Formula 1 are a peptide linker, L₁and L₂consist of 0 amino acid, in which (i) X and F, or F and Y are linked by a peptide bond; or (ii) X and F, and F and Y are linked by a peptide bond.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, when any one of L₁and L₂is a peptide linker and the other of the two is a non-peptide linker, the peptide linker is a linker containing 0 to 1,000 amino acid(s) and the non-peptide linker is polyethylene glycol.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, F of Formula 1 includes an immunoglobulin Fc region.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the immunoglobulin Fc region includes one to four domains selected from the group consisting of CH1, CH2, CH3, and CH4 domains.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the immunoglobulin Fc region further includes a hinge region.

In the conjugate according to any one of the previous embodiments, the immunoglobulin Fc region is derived from IgG, IgA, IgD, IgE, or IgM.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the immunoglobulin Fc region is an Fc region of IgG.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, with respect to the immunoglobulin Fc region, the constant region is derived from IgG1 or IgG4.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the immunoglobulin Fc region is an IgG4 Fc region.

In the long-acting conjugate for brain targeting according to any one of the previous embodiments, the immunoglobulin Fc region is an aglycosylated IgG4 Fc region of a human sequence.

In the conjugate according to any one of the previous embodiments, each domain of the immunoglobulin Fc region is a hybrid of a domain having different origins derived from an immunoglobulin selected from the group consisting of IgG, IgA, IgD, IgE, and IgM.

In the conjugate according to any one of the previous embodiments, the immunoglobulin Fc region is a dimer or a multimer consisting of a short chain immunoglobulin composed of domains of the same origin.

In the conjugate according to any one of the previous embodiments, the immunoglobulin Fc region comprises an amino acid sequence of a native immunoglobulin Fc region or a modified amino acid sequence thereof.

In the conjugate according to any one of the previous embodiments, the immunoglobulin Fc region comprises a variation selected from the group consisting of substitution, addition, deletion, modification, and a combination thereof of at least one amino acid in a native immunoglobulin Fc region.

In the conjugate according to any one of the previous embodiments, the immunoglobulin Fc region is one in which the chain exchange function may not be occur.

In the conjugate according to any one of the previous embodiments, the hinge region constituting the immunoglobulin Fc region may comprise or essentially consist of an amino acid sequence of SEQ ID NO: 14, or may be one in which serine (Ser, S), the 2^ndamino acid, is modified to proline (Pro, P) in the amino acid sequence of SEQ ID NO: 14.

In the conjugate according to any one of the previous embodiments, the CH2 domain constituting the immunoglobulin Fc region may comprise or essentially consist of an amino acid sequence of SEQ ID NO: 15, or may be one in which asparagine (Asn, N), the 67^thamino acid, is modified to glutamine (Gln, Q) in the amino acid sequence of SEQ ID NO: 15.

In the conjugate according to any one of the previous embodiments, F is in the form of a dimer in which two single-stranded polypeptide chains comprising a hinge region, CH2 domain, and CH3 domain derived from IgG are linked by a disulfide bond, wherein the hinge region comprises an amino acid sequence of SEQ ID NO: 14 or an amino acid sequence in which serine (Ser, S), the 2^ndamino acid, is modified to proline (Pro, P) in the amino acid sequence of SEQ ID NO: 14; and/or the CH2 domain comprises an amino acid sequence of SEQ ID NO: 15 or an amino acid sequence in which asparagine (Asn, N), the 67^thamino acid, is modified to glutamine (Gln, Q) in the amino acid sequence of SEQ ID NO: 15; and/or the CH3 domain comprises an amino acid sequence of SEQ ID NO: 16.

In the conjugate according to any one of the previous embodiments, in a single-stranded polypeptide chain comprising an immunoglobulin constant region constituting F, the 2^ndamino acid is substituted with proline; the 71^stamino acid is substituted with glutamine; or the 2nd amino acid is substituted with proline and the 71^stamino acid is substituted with glutamine in an amino acid sequence of SEQ ID NO: 105.

In the conjugate according to any one of the previous embodiments, the single-stranded polypeptide chain comprising an immunoglobulin constant region constituting F comprises an amino acid sequence of SEQ ID NO: 106.

In the conjugate according to any one of the previous embodiments, the conjugate includes two immunoglobulin Fc regions (a dimeric form of an Fc region in which monomeric Fc regions are linked), and the physiologically active material which respectively binds to each of the two immunoglobulin Fc regions may be linked to a single site of the immunoglobulin Fc region (a monomer Fc region) or both sites of the two immunoglobulin Fc regions (each dimeric form of Fc region).

In the conjugate according to any one of the previous embodiments, the chemical binding between the two immunoglobulin constant region chains may be a covalent bond, more specifically a disulfide bond, and even more specifically a disulfide bond formed in a hinge region of two immunoglobulin Fc regions.

In the conjugate according to any one of the previous embodiments, the conjugate may be in a form in which a dimer is formed by a chemical bond between (i) a first immunoglobulin Fc region, in which a peptide for brain targeting is linked to the C-terminal region of one molecule of an immunoglobulin Fc region through the above-described peptide linker (e.g., a peptide bond), and (ii) a second immunoglobulin Fc region, in which a peptide for brain targeting is linked to the C-terminal region of one molecule of an immunoglobulin Fc region through the above-described peptide linker (e.g., a peptide bond), and one molecule of a physiologically active material may be linked to the N-terminal region of one of the two immunoglobulin Fc region molecules; or may be in a form in which a physiologically active material is linked to each of the N-terminal regions of both of the immunoglobulin Fc region molecules.

In the conjugate according to any one of the previous embodiments, the first immunoglobulin Fc region and the second immunoglobulin Fc region are in the form of a fusion protein, wherein the immunoglobulin Fc regions are in-frame fused with a peptide for brain targeting by a peptide bond and wherein the immunoglobulin Fc regions are in the form comprising a hinge region, CH2 domain, and CH3 domain.

In the conjugate according to any one of the previous embodiments, the chemical bond between the first and second immunoglobulin Fc regions may specifically be a covalent bond, more specifically a disulfide bond, and more specifically, a disulfide bond formed in the hinge region of the two immunoglobulin Fc regions.

Another aspect of the present invention provides a polynucleotide encoding the long-acting conjugate for brain targeting; an expression vector comprising the same; and a host cell comprising the polynucleotide or the expression vector.

In a specific embodiment, the polynucleotide is a polynucleotide encoding the long-acting conjugate for brain targeting, which is in the form of a fusion protein consisting of an amino acid sequence.

Still another aspect of the present invention provides a composition comprising the conjugate for brain targeting.

In a specific embodiment, the composition is a pharmaceutical composition.

Still another aspect of the present invention provides a use of the long-acting conjugate for brain targeting in the preparation of pharmaceutical agents.

Still another aspect of the present invention provides a method for preparing the long-acting conjugate for brain targeting.

In a specific embodiment, the preparation method comprises:

(a) culturing the host cell; and (b) recovering a long-acting conjugate for brain targeting from the cultured host cell or a culture thereof.

In another specific embodiment, the preparation method comprises:

(i) preparing:

- (a) X-L₁-F, wherein X, which is a physiologically active material, L₁, which is a peptide or non-peptide linker, and F comprising an immunoglobulin Fc region, are linked; and
- (b) L₂-Y, wherein Y, which is a peptide for brain targeting, and L₂, which is a peptide or non-peptide linker, are linked; and

(ii) linking (a) X-L₁-F and (b) L₂-Y.

In still another embodiment, the preparation method comprises:

(i) preparing:

- (a) X-L₁, wherein X, which is a physiologically active material, and L₁, which is a peptide or non-peptide linker, are linked; and
- (b) F-L₂-Y, wherein Y, which is a peptide for brain targeting, L₂, which is a peptide or non-peptide linker, and F are linked; and

(ii) linking (a) X-L₁and (b) F-L₂-Y.

In still another embodiment, the preparation method comprises:

(a) reacting any one of a reactive functional group of L₁, which is a non-peptide polymer having the same or different reactive functional groups at both termini, with X, which is a freed physiologically active material, to obtain X-L₁, which is a linked material in which the non-peptide polymer is covalently bonded with the physiologically active material via the termini; and

(b) linking F-L₂-Y to the reactive functional group at the unreacted terminus of the linked material to obtain X-L₁-F-L₂-Y.

In the preparation method according to the previous embodiments, in step (b), the reactive functional group at the unreacted terminus of the linked material is linked to F_aof the following Formula 2:

embedded image

wherein:

F_aand F_bare each a single-stranded polypeptide chain, which comprises a hinge region, CH2 domain, and CH3 domain, in which F_aand F_bare linked by a disulfide bond in the hinge region and thereby the conjugate comprises an Fc fragment, and F_ais covalently bonded with L₁;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2anis independently a peptide linker or a non-peptide linker; and

each of L_2b1, . . . , L_2bn′ is independently a peptide linker or a non-peptide linker;

wherein n and n′ are each independently an integer.

In the preparation method according to the previous embodiments, the reactive functional group is selected from the group consisting of an aldehyde group, a maleimide group, and a succinimide derivative.

In the preparation method according to the previous embodiments, the aldehyde group is a propionaldehyde group or a butyraldehyde group.

In the preparation method according to the previous embodiments, the succinimide derivative is succinimidyl carboxymethyl, succinimidyl valerate, succinimidyl methylbutanoate, succinimidyl methylpropionate, succinimidyl butanoate, succinimidyl propionate, N-hydroxysuccinimide, or succinimidyl carbonate.

In the preparation method according to the previous embodiments, the reactive functional groups at both termini are aldehyde groups.

In the preparation method according to the previous embodiments, the non-peptide polymer has, as reactive functional groups, each of an aldehyde group and a maleimide group at its termini.

In the preparation method according to the previous embodiments, the non-peptide polymer has, as reactive functional groups, each of an aldehyde group and a succinimide group at its termini.

In still another embodiment, the preparation method comprises: culturing a host cell comprising an expression cassette encoding X-L_1a-F_a-(L_2a1-BTP_a1)- . . . -(L_2an-BTP_an) of the following Formula 3 and an expression cassette encoding X-L_1b-F_b-(L_2b1-BTP_b1)- . . . -(L_2bn′-BTP_bn) of Formula 3; and obtaining a conjugate of Formula 3 from the cultured host cell or a culture thereof:

embedded image

wherein:

X is a physiologically active material;

L_1aand L_1bare peptide linkers;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2anis a peptide linker; and

each of L_2b1, . . . , L_2bn′ is a peptide linker;

wherein n and n′ are each independently an integer.

In the preparation method according to the previous embodiments, the X-L_1a-F_a-(L_2a1-BTP_a1)- . . . -(L_2an-BTP_an) and X-L_1b-F_b-(L_2b1-BTP_b1)- . . . -(L_2bn′-BTP_bn′) are expressed in the form of a fusion protein, and in the refolding process, the binding between F_aand F_bis formed to form the conjugate.

To achieve the above objects, still another aspect of the present invention provides a novel peptide for brain targeting.

In a specific embodiment, the peptide for brain targeting (BTP) comprises or essentially consists of an amino acid sequence selected from the group consisting of amino acid sequences of SEQ ID NOS: 2, 4, 6, 8, 10, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, and 85.

To achieve the above objects, still another aspect of the present invention provides an separated polynucleotide encoding the peptide for brain targeting; a recombinant expression vector comprising the same; a host cell comprising the polynucleotide or the recombinant expression vector; and a kit comprising at least one of the above.

Advantageous Effects

The long-acting conjugate for brain targeting of the present invention, which contains a peptide for brain targeting and a physiologically active material, has the effects that it can pass through the blood-brain barrier (BBB) in vivo, maintain physiological activity, and significantly increase blood half-life. The long-acting conjugate for brain targeting also has improved stability and thus can be used as a therapeutic agent for treating brain-related diseases. Additionally, the present invention provides a novel peptide for brain targeting, and thus a novel long-acting conjugate for brain targeting can be prepared for use as a therapeutic agent for treating brain-related diseases.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows the experimental results of transcytosis confirming the level of passage of peptides for brain targeting through the blood-brain barrier.

FIG. 2 shows the results of a brain distribution experiment performed in mice confirming the level of passage of peptides for brain targeting through the blood-brain barrier.

FIG. 3 shows the results confirming the level of passage of peptides for brain targeting, to which an immunoglobulin Fc region is linked, through the blood-brain barrier and the level of passage of an immunoglobulin Fc region alone through the blood-brain barrier.

FIG. 4 shows the experimental results of transcytosis confirming the level of passage of a long-acting conjugate for brain targeting, which contains a GIP derivative (i.e., a physiologically active material), through the blood-brain barrier.

FIG. 5 shows the results confirming the ability of a long-acting conjugate for brain targeting containing idursulfase (i.e., a physiologically active material) with regard to the maintenance of physiological activity.

FIG. 6 shows the results confirming the brain distribution of a fusion protein in which an immunoglobulin Fc region and a peptide for brain targeting are linked.

FIG. 7 shows the results confirming iduronate 2-sulfatase-Fc-BTP22, which is a recombinant protein, using SDS-PAGE.

FIG. 8 shows the result confirming the iduronate 2-sulfatase-10 kDa PEG-Fc-BTP28 conjugate using SDS-PAGE.

FIG. 9 shows the results confirming the in vitro enzyme activity of the iduronate 2-sulfatase-Fc-BTP22 fusion protein and iduronate 2-sulfatase-Fc-BTP28 conjugate.

FIG. 10 shows the results confirming the distribution of brain tissues of the iduronate 2-sulfatase-Fc-BTP22 fusion protein.

FIG. 11 shows the experimental results confirming the in vivo efficacy of the iduronate 2-sulfatase-Fc-BTP22 fusion protein and iduronate 2-sulfatase-Fc-BTP28 conjugate.

DETAILED DESCRIPTION OF THE INVENTION

Hereinafter, the present invention will be described in detail.

Meanwhile, each of the explanations and exemplary embodiments disclosed herein can be applied to their respective other explanations and exemplary embodiments. That is, all of the combinations of various factors disclosed herein belong to the scope of the present invention. Additionally, the scope of the present invention should not be limited by the specific disclosure provided hereinbelow.

Additionally, an ordinary person skilled in the art will recognize or be able to confirm using no more than routine experimentation with respect to a number of equivalents to the specific embodiments of the invention described in the present invention. Additionally, such equivalents are intended to be included in the present invention.

Over the entire specification of the present invention, the conventional one-letter and three-letter codes for amino acids are used. Additionally, three-letter codes which are generally allowed for other amino acids, such as diaminopropionic acid (DAP), are used. Additionally, the amino acids mentioned herein are abbreviated according to the nomenclature rules of IUPAC-IUB.

An aspect of the present invention provides a long-acting conjugate for brain targeting which comprises a peptide for brain targeting and a physiologically active material.

More specifically, the long-acting conjugate for brain targeting may be one in which a peptide for brain targeting, which is linked based on an immunoglobulin Fc region by a peptide linker and/or non-peptide linker, and a physiologically active material are linked, but is not limited thereto.

The long-acting conjugate for brain targeting of the present invention is characterized in that a peptide for brain targeting is linked to an immunoglobulin Fc region by a peptide linker (includes direct fusion via peptide bond) or non-peptide linker, but is not linked to a physiologically active material.

In a more specific embodiment, the present invention provides a long-acting conjugate for brain targeting of Formula 1 below:

X-L₁-F-L₂-Y [Formula 1]

in Formula 1,

X is a physiologically active material;

Y is a peptide for brain targeting;

L₁and L₂are peptide linkers or non-peptide linkers;

when L₁and L₂are peptide linkers, the peptide linkers contain 0 to 1,000 amino acids; and

F is an immunoglobulin constant region comprising an FcRn-binding region.

The long-acting conjugate form of the present invention is characterized in that a physiologically active material is linked to a peptide for brain targeting based on an Fc region.

Specifically, the long-acting conjugate of the present invention is characterized in that the peptide for brain targeting is linked to an immunoglobulin Fc region by a peptide linker and the physiologically active material is linked thereto by a non-peptide linker; or the long-acting conjugate of the present invention is characterized in that both the peptide for brain targeting and the physiologically active material are linked to an immunoglobulin Fc region by a peptide linker, but the present invention is not particularly limited thereto.

Both types of the peptide for brain targeting and physiologically active material may be linked by a peptide linker and/or non-peptide linker, but the linkage is not limited thereto.

The peptide linker may be a linker containing 0 to 1,000 amino acid(s), but any peptide linker which can form the conjugate of the present invention can be included without limitation. When the peptide linker contains no amino acids, the conjugate may be in a form linked by a peptide bond.

The “F-L₂-Y” of Formula 1 of the long-acting conjugate for brain targeting may be a long-acting conjugate for brain targeting having the structure of Formula 2 below.

embedded image

In Formula 2 above,

F_aand F_bare each a single-stranded polypeptide chain, which comprises a hinge region, CH2 domain, and CH3 domain, in which F_aand F_bare linked by a disulfide bond in the hinge region and thereby the conjugate comprises an Fc fragment, and F_aand L₁are covalently bonded with each other;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2an, is independently a peptide linker or a non-peptide linker; and

each of L_2b1, . . . , L_2bn′ is independently a peptide linker or a non-peptide linker;

wherein n and n′ are each independently an integer.

More specifically, in Formula 2, each of L_2a1, . . . , L_2an, being the same as or different from one another, may be a peptide linker, and each of L_2b1, . . . , L_2bn′, being the same as or different from one another, may be a peptide linker, wherein n and n′ may be each independently an integer, but the present invention is not particularly limited thereto.

In the long-acting conjugate for brain targeting, L₁may be linked to the N-terminus of F_aand L_2a1and L_2b1may be each linked to the C-terminus of F_aand F_b, respectively.

In the long-acting conjugate for brain targeting of Formula 2, n=n′, and each may fulfill the conditions of L_2a1=, L_2b1, . . . , L_2an=L_2bn′ and BTP_a1=BTP_b1, . . . , BTP_an=BTP_bn′, but the conditions are not limited thereto.

More specifically, the “X-L₁-F-L₂-Y” of Formula 1 may have the structure of Formula 3 below. That is, the conjugate may be represented by the following Formula 3:

embedded image

wherein:

X is a physiologically active material;

L_1aand L_1bare each independently a peptide linker or a non-peptide linker;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2anis independently a peptide linker or a non-peptide linker; and

each of L_2b1, . . . , L_2bn′ is independently a peptide linker or a non-peptide linker;

wherein n and n′ are each independently an integer.

More specifically, in Formula 3, each of L_2a1, . . . , L_2an, being the same as or different from one another, may be a peptide linker, and each of L_2b1, . . . , L_2bn′, being the same as or different from one another, may be a peptide linker, wherein n and n′ may be each independently an integer.

Further more specifically, in Formula 3, each L may be a peptide linker, and the conjugate represented by Formula 3 may be in the form of a fusion protein, but the present invention is not particularly limited thereto.

In Formula 3, L_1aand L_1bare/may be each linked to the N-terminus of F_aand F_b; L_2a1and L_2b1are/may be each linked to the C-terminus of F_aand F_b; L_1aand L_1bare/may be each linked to the C-terminus of X-; and L_2a1and L_2b1are each linked to the N-terminus of the peptide for brain targeting (BTP) linked thereto, but these are not particularly limited thereto.

More specifically, the “X-L₁-F-L₂-Y” of Formula 1 may have the structure of the following Formula 4:

embedded image

wherein:

X is a physiologically active material;

L₁is a peptide linker or a non-peptide linker;

F_aand F_bare each a single-stranded polypeptide chain, which comprises a hinge region, CH2 domain, and CH3 domain, in which F_aand F_bare linked by a disulfide bond in the hinge region and thereby the conjugate comprises an Fc fragment, and F_aand covalently bonded with L₁;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2anis independently a peptide linker or a non-peptide linker; and

each of L_2b1, . . . , L_2bn′ is independently a peptide linker or a non-peptide linker;

wherein n and n′ are each independently an integer.

More specifically, in Formula 4, each of L_2a1, . . . , L_2an, being the same as or different from one another, may be a peptide linker, and each of L_2b1, . . . , L_2bn′, being the same as or different from one another, may be a peptide linker, wherein n and n′ may be each independently an integer, but the present invention is not particularly limited thereto.

In Formula 4, L₁is/may be linked to the N-terminus of F_a; L_2a1and L_2b1are/may be each linked to the C-terminus of F_aand F_b; L₁is/may be linked to the N-terminus of X; and L_2a1and L_2b1may be each linked to the N-terminus of the peptide for brain targeting (BTP) linked thereto, but the present invention is not particularly limited thereto.

In the above Formula(s), n=n′, and each may fulfill the conditions of L_2a1=L_2b1, . . . , L_2an=L_2bn′ and BTP_a1=BTP_b1, . . . , BTP_an=BTP_bn′, but the present invention is not particularly limited thereto.

When n and n′ are each independently an integer of 2 or more, the long-acting conjugate for brain targeting may be one in which at least two of the same or different peptides for brain targeting are linked, and the at least two same or different peptides for brain targeting may be in a form linked in tandem, but the linkage form is not limited thereto.

n and n′ may be an integer of 1 or 2 or more, and n and n′ may be the same or different integers, but n and n′ are not limited thereto. n and n′ may be 1 to 10, and 1 to 5, for example, n and n′ may be each 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, but the number of n is included without limitation, if the Fc region and a physiologically active material, being linked as parts constituting a moiety of the long-acting conjugate for brain targeting of the present invention to be delivered by passing through the BBB.

In Formula 1, F is F_aand F_band L₂-Y is (L_2a-Ya)n and (L_2b-Yb)n′, and the conjugate may be represented by the following Formula 5:

embedded image

wherein,

X is a physiologically active material;

L₁is a peptide linker or a non-peptide linker, specifically a non-peptide linker;

each of Y_aand Y_b, being the same as or different from one another, is a peptide for brain targeting; and

each of L_2aand L₂b, being the same as or different from one another, is a peptide linker;

wherein n and n′ are each independently an integer of 1 or more.

The long-acting conjugate for brain targeting may be one in which the N-terminal region of X and the N-terminal region of F are linked by L₁, and the N-terminal region of Y and the C-terminal region of F are linked by L₂. Additionally, the long-acting conjugate for brain targeting may be in a form in which an end of L₁is linked to a lysine residue or cysteine residue, etc. of X and the other end of L₁is linked to the N-terminal region of F; and the N-terminal region of Y and the C-terminal region of F are linked by L₂.

The long-acting conjugate for brain targeting may be in a form in which L₁is linked to the N-terminal region of F, and L₂is linked to the C-terminal region of F; or L₁is linked to the N-terminal region of F_a, and L_2aand L₂b are each linked to the C-terminal region of F_aand F_b, respectively.

L₁may be linked to an amine group or thiol group of X; and L₁may be linked to the N-terminal amine group of X, the amine group located at a side chain of a lysine residue, or the —SH group (thiol group) located at a side chain of a cysteine residue, but is not limited thereto.

As used herein, the term “N-terminal region” refers to the amino terminal of a peptide or protein, and for the purposes of the present invention, refers to a site capable of binding to a linker including a non-peptide linker, etc. For example, the amino acid residues around the N-terminal region as well as the most terminal amino acid residues of the N-terminal region may all be included, and specifically, may include the first to twentieth amino acid residues from the most terminal region, but the sites of the amino acid residues are not particularly limited thereto.

As used herein, the term “C-terminal region” refers to the carboxyl terminal of a peptide or protein, and for the purposes of the present invention, refers to a site capable of binding to a linker including a non-peptide linker, etc. For example, the amino acid residues around the C-terminal as well as the most terminal amino acid residues of the C-terminal region may all be included, and specifically, may include the first to twentieth amino acid residues from the most terminal, but the sites of the amino acid residues are not particularly limited thereto.

In Formula 1, X is X_aand X_b; L₁is L_1aand L_1b; F is F_aand F_b; and L₂-Y is (L_2a-Y_a)_nand (L₂b-Y_b)_n′. The conjugate may be represented by the following Formula 6:

embedded image

wherein:

X is a physiologically active material;

L_1aand L_1bare each independently a peptide linker or a non-peptide linker, specifically a peptide linker;

the peptide linker may comprise 0 to 1,000 amino acids;

F_aand F_bare each a single-stranded polypeptide chain, which comprises a hinge region, CH2 domain, and CH3 domain, in which F_aand F_bare linked by a disulfide bond in the hinge region and thereby the conjugate comprises an Fc fragment, and F_aand F_bare each covalently bonded with L_1aand L_1b, respectively;

each of Y_aand Y_b, being the same as or different from one another, is a peptide for brain targeting; and

each of L_2aand L₂b, being the same as or different from one another, is a peptide linker;

wherein n and n′ are each independently an integer.

In the above Formula(s), n and n′ may be 1 to 5, for example, n and n′ may be 1, 2, 3, 4, or 5, but these are not particularly limited thereto. Herein, n=n′, but is not limited thereto.

Meanwhile, L₁, L_1a, or L_1bis linked to the N-terminal amine group of X, the amine group located at a side chain of a lysine residue, or the —SH group (thiol group) located at a side chain of a cysteine residue, but is not particularly limited thereto.

In the above Formula(s), n=n′, and each may fulfill the conditions of L_2a1=L_2b1, . . . , L_2an=L_2bn′ and BTP_a1=BTP_b1, . . . , BTP_an=BTP_bn′. In particular, each of BTP_a1, . . . , BTP_an, being the same as one another, may be a peptide for brain targeting, each of BTP_b1, . . . , BTP_bn′, being the same as one another, may be a peptide for brain targeting, each of L_2a1, . . . , L_2anmay be a peptide linker, and each of L_2b1, . . . , L_2bn′ may be a peptide linker; or each of BTP_a1, . . . , BTP_an, being different from one another, may be a peptide for brain targeting, each of BTP_b1, . . . , BTP_bn′, being different from one another, may be a peptide for brain targeting, each of L_2a1, . . . , L_2anmay be a peptide linker, and each of L_2b1, . . . , L_2bn′ may be a peptide linker, but these are not limited thereto.

In the above Formula(s), n=n′, and each may fulfill any one of the conditions of BTP_a1≠BTP_b1, . . . and BTP_an≠BTP_bn′. For example, each may fulfill the conditions of L_2a1≠L_2b1, . . . , L_2an≠L_2bn′, BTP_a1≠BTP_b1, . . . , BTP_an≠ BTP_bn′, and a≠b. In particular, each of BTP_a1, . . . , BTP_an, being the same as one another, may be a peptide for brain targeting, each of BTP_b1, . . . , BTP_bn′, being the same as one another, may be a peptide for brain targeting, each of L_2a1, L_2anmay be a peptide linker, and each of L_2b1, . . . , L_2bn′ may be a peptide linker; or each of BTP_a1, . . . , BTP_an, being different from one another, may be a peptide for brain targeting, each of BTP_b1, . . . , BTP_bn′, being different from one another, may be a peptide for brain targeting, each of L_2a1, . . . , L_2anmay be a peptide linker, and each of L_2b1, . . . , L_2bn′ may be a peptide linker, but these are not limited thereto.

The long-acting conjugate for brain targeting is a fusion protein fused at the genetic level, wherein L₁may be linked to the C-terminal region of X, specifically L_1aand L_1bmay be each linked to the C-terminal region of X, and L₂a and L₂b may be each linked to the C-terminal region of F_aand F_b, respectively, but the present invention is not particularly limited thereto.

In such long-acting fusion protein for brain targeting, L₁(L_1aand L_1b) and L₂(L₂a and L₂b) are peptide linkers. For examples, the peptide linkers may be (GS)_m, (GGS)_m, (GGGS)_m, or (GGGGS)_m, in which m is 1 to 10, but these are not particularly limited thereto.

As used herein, the term “long-acting conjugate for brain targeting” refers to a conjugate, which includes a peptide for brain targeting and a physiologically active material, and an immunoglobulin constant region, and has a structure in which the peptide for brain targeting and physiologically active material are each linked directly or indirectly to an FcRn-binding region, respectively. In the present invention, the term “long-acting enzyme conjugate for brain targeting” may be used interchangeably with “long-acting conjugate for brain targeting” or “long-acting conjugate”.

The term “long-acting conjugate for brain targeting” may be used interchangeably with “long-acting conjugate”, and it refers to a material, where a physiologically active material that is included in the long-acting conjugate is linked to a biocompatible material which includes an immunoglobulin constant region capable of extending the duration of activity of the physiologically active material and has an FcRn-binding region, and the peptide linker and/or non-peptide linker containing 0 to 1,000 amino acid(s).

The long-acting conjugate for brain targeting can deliver a physiologically active material into the brain tissue by passing through the blood-brain barrier, but is not particularly limited thereto.

Hereinafter, the elements constituting the long-acting conjugate for brain targeting will be described in more detail.

As used herein, the term “peptide for brain targeting” includes a peptide, or protein, or antibody that contains an amino acid sequence that can pass through the BBB. The peptide for brain targeting corresponds to one moiety that constitutes a long-acting conjugate for brain targeting of the present invention.

Additionally, the peptide for brain targeting may be a sequence which is separated from known peptides, proteins, or antibodies and has an activity that can pass through the BBB.

As used herein, the term “amino acid” refers to an amino acid moiety which includes any naturally occurring or non-naturally occurring or synthetic amino acid residue, that is, any moiety which includes at least one carboxyl residue and at least one amino residue, which are directly linked by one, two, three, or more carbon atom(s), typically by a single (a) carbon atom.

The peptide for brain targeting of the present invention may be characterized in that it can pass through the blood-brain barrier through a pathway by passive transport or a pathway by receptor-mediated transport, but the transport pathway is not limited thereto. For example, the peptide for brain targeting may be a peptide, protein, or antibody that can pass through the blood-brain barrier, but their types and sizes are not particularly limited.

Meanwhile, the peptide for brain targeting may be one that passes through the blood-brain barrier through a pathway by receptor-mediated transport.

Specifically, the peptide for brain targeting may pass through the blood-brain barrier by the receptor-mediated transport pathway through any one selected from the group consisting of an insulin receptor, transferrin receptor, low-density lipoprotein receptor, low-density lipoprotein receptor-related protein, leptin receptor, nicotinic acetylcholine receptor, glutathione transporter, calcium-activated potassium channel, and receptor for advanced glycation endproducts (RAGE), and ligands of the receptors and an antibody binding to the receptors or ligands, but the pathway is not particularly limited thereto; and in addition, may be selected from the group consisting of peptides, proteins, and antibodies that can pass through the blood-brain barrier, or may be partial peptide sequences isolated from the peptides, proteins, and antibodies, but the pathway is not particularly limited thereto. For example, HAITYPRH peptide (BTP1 peptide) of SEQ ID NO: 2, THR peptide (BTP2 peptide) of SEQ ID NO: 4, Angiopep-2 peptide (BTP3 peptide) of SEQ ID NO: 6, ApoB peptide (BTP4 peptide) of SEQ ID NO: 8, ApoE peptide (BTP5 peptide) of SEQ ID NO: 10, etc. may be used, but any peptide which can deliver the linked F-L₂-Y structure to the brain by passing through the blood-brain barrier can be included without limitation.

In another specific embodiment, BTP6 peptide of SEQ ID NO: 20, BTP7 peptide of SEQ ID NO: 22, BTP8 peptide of SEQ ID NO: 24, BTP5 peptide of SEQ ID NO: 26, BTP10 peptide of SEQ ID NO: 28, BTP11 peptide of SEQ ID NO: 30, BTP12 peptide of SEQ ID NO: 32, BTP13 peptide of SEQ ID NO: 34, BTP14 peptide of SEQ ID NO: 36, BTP15 peptide of SEQ ID NO: 38, BTP16 peptide of SEQ ID NO: 40, or BTP17 peptide of SEQ ID NO: 85, but the peptide is not limited thereto.

In another specific embodiment, the peptide for brain targeting may be:

(1) Angiopep-2: TFFYGGSRGKRNNFKTEEY-OH (SEQ ID NO: 41),

(2) ApoB (3371-3409): SVIDALQYKLEGTTRLTRKRGLKLATALSLSNKFVEGS (SEQ ID NO: 42),

(3) ApoE (159-167)₂: (LRKLRKRLL)₂(SEQ ID NO: 10),

(4) Peptide-22: Ac-C(&)MPRLRGC(&)-NH₂(SEQ ID NO: 43),

(5) THR: THRPPMWSPVWP-NH₂(SEQ ID NO: 44),

(6) THR retro-enantio: pwvpswmpprht-NH₂(SEQ ID NO: 45),

(7) CRT: C(&)RTIGPSVC(&) (SEQ ID NO: 46),

(8) Leptin 30: YQQILTSMPSRNVIQISNDLENLRDLLHVL (SEQ ID NO: 47),

(9) RVG29: YTIWMPENPRPGTPCDIFTNSRGKRASNG-OH (SEQ ID NO: 48)

(10) ^DCDX: GreirtGraerwsekf-OH (SEQ ID NO: 49)

(11) Apamin: C(&₁)NC(&₂)KAPETALC(&₁)-ARRC(&₂)QQH-NH₂(SEQ ID NO: 50),

(12) MiniAp-4: [Dap](&)KAPETALD(&) (SEQ ID NO: 51),

(13) GSH: γ-L-glutamyl-CG-OH

(14) G23: HLNILSTLWKYRC (SEQ ID NO: 52),

(15) g7: GFtGFLS(O-β-Glc)-NH₂(SEQ ID NO: 53),

(16) TGN: TGNYKALHPHNG (SEQ ID NO: 54),

(17) TAT (47-57): YGRKKRRQRRR-NH₂(SEQ ID NO: 55),

(18) SynB1: RGGRLSYSRRRFSTSTGR (SEQ ID NO: 56),

(19) Diketopiperazines: &(N-MePhe)-(N-MePhe)diketopiperazines, or

(20) PhPro: (Phenylproline)₄-NH₂(SEQ ID NO: 57),

but the peptide is not limited thereto.

In the sequences above, & is a symbol according to the nomenclature for cyclic peptides described in (J. Pept. Res., 2005, 65, 550 to 555; J. Spengler et al.), and “&” indicates the connecting point. For example, the first “&” in a single chain indicates the position of an end of a chemical bond and the second “&” indicates the position to which the chemical bond is attached. For example, “&Ala-Ala-Phe-Leu-Pro&” means that a chemical bond is formed between alanine and proline and thereby forms a cyclic peptide. In the case where two or more chemical bonds are present, codes such as &1 and &2 may be used so as to indicate the position where the corresponding chemical bond is formed. For example, in the case where it is indicated as “&1Asp(&2)-Trp-Phe-Dpr(&2)-Leu-Met&1”, it means that a chemical bond is formed between Asp and Met, and a chemical bond is formed between Asp and Dpr. Meanwhile, [Dap] stands for diaminopropionic acid.

As used herein, the term “physiologically active material”, which may be a constitution that forms a moiety of the long-acting conjugate for brain targeting, collectively refers to materials which have certain physiological activity in vivo, and these materials have a variety of physiological activities. The physiologically active material, X, may be a polypeptide consisting of 2 amino acids to 1,000 amino acids, 2 amino acids to 950 amino acids, 2 amino acids to 900 amino acids, 2 amino acids to 850 amino acids, 2 amino acids to 800 amino acids, 2 amino acids to 750 amino acids, 2 amino acids to 700 amino acids, 5 amino acids to 700 amino acids, 5 amino acids to 650 amino acids, 5 amino acids to 600 amino acids, 5 amino acids to 550 amino acids, 5 amino acids to 500 amino acids, 5 amino acids to 450 amino acids, 5 amino acids to 400 amino acids, 5 amino acids to 350 amino acids, 5 amino acids to 300 amino acids, 5 amino acids to 250 amino acids, 5 amino acids to 200 amino acids, 5 amino acids to 150 amino acids, 5 amino acids to 100 amino acids, 5 amino acids to 90 amino acids, about 5 amino acids to about 80 amino acids, 5 amino acids to 70 amino acids, 5 amino acids to 60 amino acids, 5 amino acids to 50 amino acids, 5 amino acids to 40 amino acids, 5 amino acids to 30 amino acids, 5 amino acids to 25 amino acids, or 5 amino acids to 20 amino acids, but is not limited thereto. The polypeptides that constitute the physiologically active material include all of peptides, oligopeptides, polypeptides, or proteins.

The physiologically active material may be a toxin or physiologically active polypeptide, and may include various physiologically active polypeptides, such as cytokines, interleukin, interleukin-binding proteins, enzymes, antibodies, growth factor, transcription factors, blood coagulation factors, vaccines, structural proteins, ligand proteins or receptors, cell surface antigens, and receptor antagonists which are used for the purpose of preventing or treating human diseases, physiologically active peptides secreted in the small intestine and the pancreas which exhibit a therapeutic effect for diabetes and obesity, and G protein-coupled receptors (GPCR) agonists or antagonists, or analogues thereof but the physiologically active materials are not limited thereto.

As used herein, the term “analogue of X” refers to a material which can exhibit the same type of activity as that of X, and it includes all of agonists of X, derivatives of X, fragments of X, variants of X, etc.

Specifically, the toxin may be selected from maytansine and/or a derivative thereof, auristatin and/or a derivative thereof, duocarmycin and/or a derivative thereof, pyrrolobenzodiazepine (PBD) and/or a derivative thereof, which are effective for the apoptosis of cancer cells, but any toxin which exhibits an effect for the apoptosis of cancer cells can be included without limitation.

Specifically, examples of the physiologically active polypeptide may include GLP-1 receptor agonists, glucagon receptor agonists, gastric inhibitory polypeptide (GIP) receptor agonists, fibroblast growth factor (FGF) receptor agonists (FGF1, FGF19, FGF21, FGF23, etc.), cholecystokinin receptor agonists, gastrin receptor agonists, melanocortin receptor agonists, human growth hormone, growth hormone-releasing hormone, growth hormone-releasing peptide, interferons and interferon receptors (e.g., interferon-α, 43 and -γ, soluble type I interferon receptors, etc.), colony-stimulating factors, interleukins (e.g., interleukin-1, -2, -3, -4, -5, -6, -7, -8, -9, -10, -11, -12, -13, -14, -15, -16, -17, -18, -19, -20, -21, -22, -23, -24, -25, -26, -27, -28, -29, -30, etc.) and interleukin receptors (e.g., IL-1 receptor, IL-4 receptor, etc.), enzymes (e.g., β-glucosidase), α-galactosidase, β-galactosidase, iduronidase, iduronate-2-sulfatase, galactose-6-sulfatase, acid α-glucosidase, acid ceramidase, acid sphingomyelinsase, galactocerebrosidsase, arylsulfatase A, B, β-hexosaminidase A, B, heparin N-sulfatase, α-D-mannosidase, β-glucuronidase, N-acetylgalactosamine-6 sulfatase, lysosomal acid lipase, α-N-acetyl-glucosaminidase, glucocerebrosidase, butyrylcholinesterase, chitinase, glutamate decarboxylase, imiglucerase, lipase, uricase, platelet-activating factor acetylhydrolase, neutral endopeptidase, myeloperoxidase, α-galactosidase-A, agalsidase α, (3, α-L-iduronidase, butyrylcholinesterase, chitinase, glutamate decarboxylase, imiglucerase, lipase, uricase, platelet-activating factor acetylhydrolase, neutral endopeptidase, and myeloperoxidase, etc.), interleukins and cytokine-binding proteins (e.g., IL-18 bp, TNF-binding protein, etc.), macrophage-activating factors, macrophage peptides, B cell factors, T cell factors, protein A, allergy-inhibiting factors, necrosis glycoproteins, immunotoxins, lymphotoxins, tumor necrosis factors, tumor suppressors, transforming growth factors, α-1 antitrypsin, albumin, α-lactalbumin, apolipoprotein-E, erythropoietin, high-glycosylated erythropoietin, angiopoietin, hemoglobins, thrombin, thrombin receptor-activating peptide, thrombomodulin, blood coagulation factor VII, blood coagulation factor VIIa, blood coagulation factor VIII, blood coagulation factor IX, blood coagulation factor XIII, plasminogen activators, fibrin-binding peptide, urokinase, streptokinase, hirudin, protein C, C-reactive protein, renin inhibitor, collagenase inhibitors, superoxide dismutase, leptin, platelet-derived growth factor, epithelial growth factor, epidermal growth factor, angiostatin, angiotensin, bone morphogenetic growth factor; bone morphogenetic protein, calcitonin, insulin, atriopeptin, cartilage-inducing factor, elcatonin, connective tissue-activating factor, tissue factor pathway inhibitor, follicle-stimulating hormone, luteinizing hormone, luteinizing hormone-releasing hormone, nerve growth factors (e.g., nerve growth factor, ciliary neurotrophic factor, axogenesis factor-1, brain-natriuretic peptide, glial-derived neurotrophic factor, netrin, neutrophil inhibitory factor, neurotrophic factor, neurturin), parathyroid hormone, relaxin, secretin, somatomedin, insulin-like growth factor, adrenocortical hormone, glucagon, cholecystokinin, pancreatic polypeptide, gastrin-releasing peptides, corticotropin-releasing factor, thyroid-stimulating hormone, autotaxin, lactoferrin, myostatin, activity-dependent neuroprotective protein (ADNP), β-secretase1 (BACE1), amyloid precursor protein (APP), neural cell adhesion molecule (NCAM), amyloid β, Tau, receptor for advanced glycation endproducts (RAGE), α-synuclein, or agonists or antagonists thereof, receptors thereof (e.g., TNFR(P75), TNFR(P55), IL-1 receptor, VEGF receptor, B cell activating factor receptor, etc.), receptor antagonist (e.g., IL1-Ra, etc.), cell surface antigens (e.g., CD 2, 3, 4, 5, 7, 11a, 11b, 18, 19, 20, 23, 25, 33, 38, 40, 45, 69, etc.), monoclonal antibody, polyclonal antibody, antibody fragments (e.g., scFv, Fab, Fab′, F(ab′)₂and Fd), virus-derived vaccine antigens, hybrid polypeptides or chimeric polypeptides that activate at least one receptor agonist, etc., but the physiologically active polypeptide is not limited thereto.

As used herein, the term “iduronate-2-sulfatase”, which is a sulfatase enzyme related to Hunter syndrome (MPS-II), is an enzyme necessary for lysosomal degradation of heparin sulfate and dermatan sulfate. In a specific embodiment of the present invention, “idursulfase”, which is a purified type of iduronate-2-sulfatase, may be used as iduronate-2-sulfatase, and it is obvious that idursulfase is included in the iduronate-2-sulfatase. The idursulfase may be, for example, idursulfase α or idursulfase β, but is not limited thereto.

Iduronate-2-sulfatase can be prepared or manufactured by a method known in the art, and specifically, it can be purified from animal cells into which an animal cell expression vector was inserted and cultured and after cultivation thereof, or enzymes commercially available may be purchased for use, but the preparation methods of iduronate-2-sulfatase are not limited thereto.

The physiologically active polypeptide to be applicable in the present invention may be in a native form, or those prepared by genetic recombination in a prokaryotic cell such as Escherichia coli or a eukaryotic cell such as a yeast cell, insect cell, or animal cell. Additionally, the physiologically active polypeptide may be an analogue having activity equivalent to that of the native form or of the same species (e.g., a mutant derivative at one or more amino acid positions), but the applicable physiologically active polypeptide is not limited thereto.

Meanwhile, the GLP-1 receptor agonist may be selected from the group consisting of a native exendin-4; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is deleted; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is substituted with a hydroxyl group; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is modified with a dimethyl group; an exendin-4 derivative in which the N-terminal amine group of exendin-4 is substituted with a carboxyl group; an exendin-4 derivative in which the α-carbon of the 1^stamino acid of exendin-4, histidine, is deleted; an exendin-4 derivative in which the 12^thamino acid of exendin-4, lysine, is substituted with serine, and an exendin-4 derivative in which the 12^thamino acid of exendin-4, lysine, is substituted with arginine, but the GLP-1 receptor agonist is not particularly limited thereto.

In a specific embodiment, the present invention provides a long-acting conjugate for brain targeting which is characterized in that a physiologically active material is linked by a mutual binding to an immunoglobulin Fc region of a peptide for brain targeting, which is fused with the immunoglobulin Fc region.

As used herein, the term “F” refers to a material which includes an immunoglobulin constant region and an FcRn-binding region, and specifically, it corresponds to one moiety that constitutes the long-acting conjugate for brain targeting of the present invention. For example, F may be an immunoglobulin Fc region including an FcRn-binding region.

Since an immunoglobulin Fc region is a biodegradable polypeptide that can be metabolized in vivo, it is safe for use as a drug carrier. Additionally, the immunoglobulin Fc region has a relatively low molecular weight compared to the whole molecule of immunoglobulin, it is advantageous in terms of preparation, purification, and yield of a conjugate. In addition, as the Fab region, which exhibits high heterogeneity due to the difference in amino acid sequences from antibody to antibody, is removed, it is expected that the homogeneity of materials can be greatly increased and the risk of inducing blood antigenicity can also be lowered.

The peptide conjugate for brain targeting, which is fused with an immunoglobulin Fc region, is linked to the immunoglobulin Fc region by a peptide bond and is produced as a long-acting conjugate in host cells expressing the same. The expression host may be a microorganism such as Escherichia coli or a yeast cell, insect cell, animal cell, etc., without limitation.

As used herein, the term “immunoglobulin constant region” may be a constitution that forms a moiety of a long-acting conjugate for brain targeting, and includes the heavy chain constant region 2 (CH2) and the heavy chain constant region 3 (CH3), excluding the heavy chain and the light chain variable regions and the light chain constant region (CL1) of the immunoglobulin. A hinge region may be included in the heavy chain constant regions.

The immunoglobulin constant region may be an immunoglobulin Fc region.

The immunoglobulin constant region of F may include one to four domains selected from the group consisting of CH1, CH2, CH3, and CH4 domains.

The immunoglobulin constant region of the present invention may be 1) a CH1 domain, a CH2 domain, a CH3 domain, and a CH4 domain, 2) a CH1 domain and a CH2 domain, 3) a CH1 domain and a CH3 domain, 4) a CH2 domain and a CH3 domain, and 5) a combination between one or two or more domains selected from a CH1 domain, a CH2 domain, a CH3 domain, and a CH4 domain and a hinge region (or part of a hinge region) of an immunoglobulin (e.g., a combination between a CH2 domain and a CH3 domain and a hinge region (or part of the hinge region)), and 6) a dimer between each domain of the heavy chain constant region and the light chain constant region. The hinge region of the present invention includes not only a native hinge region but also a part of all of the hinge regions known in the art.

Specifically, the immunoglobulin constant region of F may include a hinge region, a CH2 domain, and a CH3 domain, but is not particularly limited thereto.

Additionally, the immunoglobulin Fc region of the present invention includes not only the native amino acid sequence but also a sequence derivative (mutant) thereof. An amino acid sequence derivative refers to an amino acid sequence which has a difference in at least one amino acid residue due to deletion, insertion, non-conservative or conservative substitution, or a combination thereof. For example, the amino acid residues at positions 214 to 238, 297 to 299, 318 to 322, or 327 to 331, which are known to be important in the conjugation of an immunoglobulin Fc, may be used as suitable sites for modification. Additionally, various other kinds of derivatives are possible, including one that has a deletion of a region capable of forming a disulfide bond, or a deletion of some amino acid residues at the N-terminus of native Fc or an addition of a methionine residue at the N-terminus of native Fc. Further, to remove effector functions, a deletion may occur in a complement-binding site, such as a C1q-binding site and an antibody dependent cell mediated cytotoxicity (ADCC) site. Techniques of preparing such sequence derivatives of the immunoglobulin Fc region are disclosed in International Patent Publication Nos. WO 97/34631, WO 96/32478, etc.

Amino acid exchanges in proteins and peptides, which do not generally alter the activity of the proteins or peptides, are known in the art (H. Neurath, R. L. Hill, The Proteins, Academic Press, New York, 1979). The most commonly occurring exchanges are Ala/Ser, Val/Ile, Asp/Glu, Thr/Ser, Ala/Gly, Ala/Thr, Ser/Asn, Ala/Val, Ser/Gly, Thy/Phe, Ala/Pro, Lys/Arg, Asp/Asn, Leu/Ile, Leu/Val, Ala/Glu, and Asp/Gly. In some cases, the Fc region may be modified by phosphorylation, sulfation, acrylation, glycosylation, methylation, farnesylation, acetylation, amidation, etc.

The above-described immunoglobulin constant region derivatives may be those which show biological activity identical to that of the immunoglobulin constant region of the present invention and have improved structural stability against heat, pH, etc.

For example, the immunoglobulin Fc region may be one in which the chain exchange function may not occur.

Additionally, F, specifically the immunoglobulin Fc region, may be in a dimeric form in which two single-stranded polypeptide chains comprising a hinge region, CH2 domain, and CH3 domain are linked by a disulfide bond.

The hinge region constituting the immunoglobulin Fc region may comprise or essentially consist of an amino acid sequence of SEQ ID NO: 14, or may be one in which serine (Ser, S), the 2^ndamino acid, is modified to proline (Pro, P) in the amino acid sequence of SEQ ID NO: 14, but is not particularly limited thereto.

The CH2 domain constituting the immunoglobulin Fc region may comprise or essentially consist of an amino acid sequence of SEQ ID NO: 15, or may be one in which asparagine (Asn, N), the 67^thamino acid, is modified to glutamine (Gln, Q) in the amino acid sequence of SEQ ID NO: 15, but is not particularly limited thereto.

More specifically, F is in a dimeric form in which two single-stranded polypeptide chains comprising a hinge region, CH2 domain, and CH3 domain derived from IgG are linked by a disulfide bond, wherein the hinge region comprises an amino acid sequence of SEQ ID NO: 14 or an amino acid sequence in which serine (Ser, S), the 2^ndamino acid, is modified to proline (Pro, P) in the amino acid sequence of SEQ ID NO: 14, and/or the CH2 domain comprises an amino acid sequence of SEQ ID NO: 15 or an amino acid sequence in which asparagine (Asn, N), the 67^thamino acid, is modified to glutamine (Gln, Q) in the amino acid sequence of SEQ ID NO: 15, and/or the CH3 domain comprises an amino acid sequence of SEQ ID NO: 16, but it is not limited thereto.

Specifically, the single-stranded polypeptide chain comprising the immunoglobulin constant region constituting F may be one in which the 2^ndamino acid in the amino acid sequence of SEQ ID NO: 105 is substituted with proline; the 71^stamino acid is substituted with glutamine; or the 2^ndamino acid is substituted with proline and the 71^stamino acid is substituted with glutamine. More specifically, the single-stranded polypeptide chain comprising the immunoglobulin constant region constituting F may be one including the amino acid sequence of SEQ ID NO: 106, but is not particularly limited thereto.

Additionally, the immunoglobulin Fc region may be obtained from native forms isolated in vivo from humans or animals such as cows, goats, pigs, mice, rabbits, hamsters, rats, guinea pigs, etc., or may be recombinants or derivatives thereof, obtained from transformed animal cells or microorganisms. Herein, the Fc region may be obtained from a native immunoglobulin by isolating a whole immunoglobulin from a living human or animal body and treating the isolated immunoglobulin with protease. When the whole immunoglobulin is treated with papain, it is cleaved into Fab and Fc regions, whereas when the whole immunoglobulin is treated with pepsin, it is cleaved into pF′c and F(ab)₂fragments. These fragments can be isolated using size exclusion chromatography, etc. In a more specific embodiment, the immunoglobulin Fc region may be a recombinant immunoglobulin Fc region obtained from a microorganism with regard to a human-derived Fc region.

Additionally, the immunoglobulin constant region may be in the form of native glycan, increased or decreased glycans compared to the native type, or in a deglycosylated form. The increase, decrease, or removal of the immunoglobulin Fc glycans may be achieved by conventional methods such as a chemical method, enzymatic method, and genetic engineering method using a microorganism. The immunoglobulin Fc region obtained by removal of glycans from the Fc region shows a significant decrease in binding affinity to the complement (Clq part) and a decrease or loss in antibody-dependent cytotoxicity or complement-dependent cytotoxicity, and thus it does not induce unnecessary immune responses in vivo. In this regard, an immunoglobulin Fc region in a deglycosylated or aglycosylated immunoglobulin Fc region may be a more suitable form to meet the original object of the present invention as a drug carrier.

As used herein, the term “deglycosylation” refers to enzymatically removing sugar moieties from an Fc region, and the term “aglycosylation” refers to an unglycosylated immunoglobulin constant region produced in prokaryotes, more specifically, E. coli.

Meanwhile, the immunoglobulin Fc region may be derived from humans or animals including cows, goats, pigs, mice, rabbits, hamsters, rats, and guinea pigs, and preferably, it is derived from humans.

Additionally, the immunoglobulin (Ig) Fc region may be derived from IgG, IgA, IgD, IgE, IgM, or a combination or hybrid thereof. For example, it may be derived from IgG or IgM, which are among the most abundant proteins in human blood, and it may be derived from IgG, which is known to enhance the half-lives of ligand-binding proteins. Meanwhile, as used herein, the term “combination” means that polypeptides encoding single-chain immunoglobulin Fc regions of the same origin are linked to a single-chain polypeptide of a different origin to form a dimer or multimer. That is, a dimer or multimer may be prepared from two or more fragments selected from the group consisting of IgG Fc, IgA Fc, IgM Fc, IgD Fc, and IgE Fc fragments.

As used herein, the term “hybrid” means that sequences corresponding to two or more immunoglobulin Fc fragments of different origins are present in a single-chain of an immunoglobulin Fc region. In the present invention, various hybrid forms are possible. That is, the hybrid domain may be composed of one to four domains selected from the group consisting of CH1, CH2, CH3, and CH4 of IgG Fc, IgM Fc, IgA Fc, IgE Fc, and IgD Fc, and may further include a hinge region.

Meanwhile, IgG may also be divided into the IgG1, IgG2, IgG3, and IgG4 subclasses, and the present invention may include combinations or hybrids thereof, for example, the IgG2 and IgG4 subclasses, and specifically, the Fc region of IgG4 rarely having effector functions such as complement dependent cytotoxicity (CDC), but is not limited thereto. Additionally, in an embodiment, the immunoglobulin Fc region may be the IgG1 Fc region or IgG4 Fc region, but is not limited thereto.

As used herein, the term “L₁and/or L₂” of Formula 1, which is a constituting element that forms a moiety of the long-acting conjugate for brain targeting, refers to a linker that links a peptide for brain targeting or physiologically active material to an immunoglobulin Fc region. The linker basically refers to a linking body that can link two fusion partners using a covalent bond, etc. In addition to linking fusion partners, a linker can also have a role of providing a gap of a certain size between the fusion partners or providing flexibility or rigidity, but the roles of a linker are not particularly limited thereto.

In a specific embodiment, one of L₁and L₂of Formula 1 may be a peptide linker and the other of L₁and L₂of Formula 1 may be a non-peptide linker. Alternatively, one of L₁and L₂of Formula 1 may be a peptide linker, the other of L₁and L₂of Formula 1 may be a non-peptide linker, and both L₁and L₂may be a peptide linker while both L₁and L₂may be a non-peptide linker, but L₁and L₂of Formula 1 are not particularly limited thereto.

In another specific embodiment, when any one or both of L₁and L₂of Formula 1 are a non-peptide linker, the non-peptide linker may be selected from the group consisting of polyethylene glycol, polypropylene glycol, an ethylene glycol-propylene glycol copolymer, polyoxyethylated polyol, polyvinyl alcohol, a polysaccharide, dextran, polyvinyl ethyl ether, a biodegradable polymer, a lipid polymer, chitins, hyaluronic acid, a fatty acid, a high molecular weight polymer, a low molecular weight compound, a nucleotide, and a combination thereof, but the non-peptide linker is not limited thereto.

In still another specific embodiment, when L₁is a non-peptide linker and L₂is a peptide linker, the peptide linker may contain 0 to 1,000 amino acid(s). In another specific embodiment, when L₁is a non-peptide linker and L₂is a peptide linker, and the peptide linker contains no amino acids, F and Y, which is a peptide for brain targeting, may be directly formed by fusion (e.g., a peptide bond).

In still another specific embodiment, when any one or both of L₁and L₂are a peptide linker, X and F, or F and Y are linked to each other by L₁and L₂via a covalent chemical bond, non-covalent chemical bond, or a combination thereof; and L₁and L₂each contain 0 to 1,000 amino acid(s). When the peptide linker contains no amino acids, X and F, or F and Y may be linked by a peptide bond.

In still another specific embodiment, when any one or both of L₁and L₂are a peptide linker, and L₁and L₂each consists of 0 amino acid, (i) X and F, or F and Y may be linked by a peptide bond; or (ii) X and F, or F and Y may be linked by a peptide bond.

As used herein, the term “peptide linker” includes a peptide conjugate connecting two fusion partners or a polymer of amino acids. Specifically, the peptide linker may contain 0 to 1,000 amino acid sequences, and more specifically, 0 to 900 amino acid sequences, 0 to 800 amino acid sequences, 0 to 700 amino acid sequences, 0 to 600 amino acid sequences, 0 to 500 amino acid sequences, 0 to 400 amino acid sequences, 0 to 300 amino acid sequences, 0 to 250 amino acid sequences, 0 to 200 amino acid sequences, 0 to 150 amino acid sequences, 0 to 100 amino acid sequences, 0 to 90 amino acid sequences, 0 to 80 amino acid sequences, 0 to 70 amino acid sequences, 0 to 60 amino acid sequences, 0 to 50 amino acid sequences, 0 to 40 amino acid sequences, 0 to 30 amino acid sequences, 0 to 25 amino acid sequences, 0 to 20 amino acid sequences, 0 to 15 amino acid sequences, or 0 to 10 amino acid sequences, but the number of amino acid sequences is not particularly limited thereto.

Additionally, examples of the peptide linker may include peptides which consist of an amino acid sequence, which is in a form where a GGGGS (SEQ ID NO: 58) motif, GS motif, GGGS (SEQ ID NO: 59) motif, or GGSG (SEQ ID NO: 60) motif is repeated, and these motifs may be repeated 1 to 10 times, but the motifs are not particularly limited thereto.

Additionally, when L₂is a peptide linker, L₂is (GS), (GGS)_m, (GGGS)_m, or (GGGGS)_m, and m may be 1 to 10, but is not limited thereto.

In still another specific embodiment, when any one of L₁and L₂is a peptide linker and the other of the two is a non-peptide linker, the peptide linker is a linker containing 0 to 1,000 amino acid(s) and the non-peptide linker is polyethylene glycol, but the linkers are not limited thereto.

As used herein, the term “non-peptide linker” refers to a biocompatible linker in which two or more repeating units are linked, and the repeating units are linked to each other through any covalent bond other than a peptide bond.

In still another specific embodiment, when the non-peptide linker and X and Y are each linked by their respective functional groups, the functional group of the non-peptide linker may be selected from the group consisting of an aldehyde group, a maleimide group, and a succinimide derivative. L₁may be a non-peptide polymer having a functional group at both ends, and the functional group at both ends may be an amine-reactive group or thiol-reactive group, and the functional group at both ends may be the same kind as each other or different kinds from each other, but is not limited thereto.

The non-peptide polymer, which is a non-peptide linker to be used in the present invention, may be selected from the group consisting of polyethylene glycol, polypropylene glycol, an ethylene glycol-propylene glycol copolymer, polyoxyethylated polyol, polyvinyl alcohol, a polysaccharide, dextran, polyvinyl ethyl ether, biodegradable polymers such as polylactic acid (PLA) and polylactic-glycolic acid (PLGA), a lipid polymer, chitins, hyaluronic acid, an oligonucleotide, and a combination thereof, and for example polyethylene glycol, but the non-peptide polymer is not limited thereto. Derivatives thereof already known in the art and derivatives which can be easily prepared at the technical level of the art are also included within the scope of the present invention.

With respect to the non-peptide polymer to be used in the present invention, any polymer having resistance to protein degradation in vivo may be used without limitation. The molecular weight of the non-peptide polymer may be in the range of exceeding 0 kDa to about 100 kDa, e.g., about 0.5 kDa to about 100 kDa, about 1 kDa to about 100 kDa, or about 1 kDa to about 20 kDa, but the molecular weight is not limited thereto.

As used herein, the term “about” refers to a range which includes all of ±0.5, ±0.4, ±0.3, ±0.2, ±0.1, etc., and includes all of the values that are equivalent or similar to those following the values, but the range is not limited thereto.

Additionally, with respect to the non-peptide linker, not only a single kind of a polymer but also a combination of different kinds of polymers may be used.

Meanwhile, the non-peptide polymer, which is a non-peptide linker used in the present invention, may have a functional group to be linked to the functional group of F and X or Y, so that an immunoglobulin Fc region and a physiologically active material can form a covalent bond between them.

Specifically, the non-peptide linker may have at least two terminal functional groups, specifically 2 or 3 terminal functional groups, and more specifically two terminal functional groups.

The functional group may be selected from the group consisting of an aldehyde group, a maleimide group, and a succinimide derivative, but the functional group is not limited thereto.

In the above, examples of the aldehyde group may include a propionaldehyde group or butyraldehyde group, but the aldehyde group is not limited thereto.

In the above, examples of the succinimide derivative may include succinimidyl valerate, succinimidyl methylbutanoate, succinimidyl methylpropionate, succinimidyl butanoate, succinimidyl propionate, N-hydroxysuccinimide, hydroxy succinimidyl, succinimidyl carboxymethyl, or succinimidyl carbonate, but the succinimide derivative is not limited thereto.

The functional groups of both ends of the non-peptide linker may be the same as or different from each other.

For example, the functional group at one end of the non-peptide linker may be a maleimide group and the functional group at the other end may be an aldehyde group (e.g., propionaldehyde group or butyraldehyde group). When polyethylene glycol having a hydroxyl functional group at both ends is used as the non-peptide polymer, it is possible to activate the hydroxyl group by a known chemical reaction in the various reactive groups or to prepare the conjugate of the present invention using polyethylene glycol having a commercially available modified reactive group.

Additionally, the non-peptide polymer may be a homo-functional non-peptide polymer in which all of two ends or three ends of the non-peptide linker are aldehyde groups.

For example, the non-peptide linker may be a non-peptide polymer having a propionaldehyde group at both ends, and specifically polyethylene glycol having a propionaldehyde group at both ends, but is not particularly limited thereto.

When the non-peptide linker has a functional group of a reactive aldehyde group at both ends, it is effective in minimizing non-specific reactions and for linking to a physiologically active polypeptide and an immunoglobulin at both ends, respectively. The final product formed by reductive amination by an aldehyde bond is significantly more stable compared to those by an amide bond. The aldehyde functional group reacts selectively at the N-terminus at low pH and can form a covalent bond with a lysine residue at high pH (e.g., pH 9.0).

The conjugate includes an immunoglobulin Fc region (a dimeric form of an Fc region in which monomeric Fc regions are linked), which consists of two chains, and the physiologically active material which binds to each of the two immunoglobulin Fc regions may be linked to a single site of the immunoglobulin Fc region (a monomer Fc region) or both sites of the two immunoglobulin Fc regions (each dimeric form of Fc region).

The chemical binding may be a covalent bond, more specifically a disulfide bond, and even more specifically a disulfide bond formed in a hinge region of two immunoglobulin Fc regions, but the binding is not particularly limited thereto.

More specifically, the long-acting conjugate for brain targeting may be in a form in which a dimer is formed by a chemical bond between (i) a first immunoglobulin Fc region, in which a peptide for brain targeting is linked to the C-terminal region of one molecule of an immunoglobulin Fc region through the above-described peptide linker (e.g., a peptide bond) and (ii) a second immunoglobulin Fc region, in which a peptide for brain targeting is linked to the C-terminal region of one molecule of an immunoglobulin Fc region through the above-described peptide linker (e.g., a peptide bond), and one molecule of a physiologically active material may be linked to the N-terminal region of one of the two immunoglobulin Fc region molecules; or may be in a form in which a physiologically active material is linked to each of the N-terminal regions of both of the immunoglobulin Fc region molecules, but the forms are not particularly limited thereto. The first and second immunoglobulin Fc regions, which are in the form of a fusion protein, may be fused in-frame by a peptide bond between the immunoglobulin Fc region and the peptide for brain targeting, and the immunoglobulin Fc region may include a hinge region, CH2 domain, and CH3 domain, but the immunoglobulin Fc region is not particularly limited thereto.

The chemical bond between the first and second immunoglobulin Fc regions may specifically be a covalent bond, more specifically a disulfide bond, and more specifically, a disulfide bond formed in the hinge region of the two immunoglobulin Fc regions, but the chemical bond is not particularly limited thereto.

Still another aspect of the present invention provides a separated polynucleotide encoding the conjugate; an expression vector comprising the polynucleotide; and a host cell comprising the expression vector.

The separated polynucleotide encoding the conjugate includes a polynucleotide sequence having an identity to the corresponding sequence of at 75% or higher, specifically 85% or higher, more specifically 90% or higher, even more specifically 95%, are included within the scope of the present invention.

The recombinant vector according to the present invention may typically be constructed as a vector or vector for expression for cloning, and may be constructed using prokaryotic or eukaryotic cells as a host cell.

As used herein, the term “vector” refers to a recombinant vector capable of expressing a target protein in an appropriate host cell, which is a gene construct including essential regulatory factors operably linked to enable the expression of a gene insert.

The long-acting conjugate for brain targeting of the present invention can be obtained by performing transformation or transfection of the recombinant vector into a host cell.

In the present invention, the polynucleotide encoding the conjugate can be operably linked to a promoter.

The method for transforming the recombinant vector containing a polynucleotide according to the present invention is not limited to the above embodiments, and the transforming or transfection methods conventionally used in the art can be used without limitation.

The transformant of the present invention can be obtained by introducing a recombinant vector containing the polynucleotide according to the present invention into a host cell.

An appropriate host to be used in the present invention may not be particularly limited as long as it can express the polynucleotide of the present invention. Examples of the appropriate host may include bacteria belonging to the genus Escherichia such as E. coli; bacteria belonging to the genus Bacillus such as Bacillus subtilis; bacteria belonging to the genus Pseudomonas such as Pseudomonas putida; yeasts such as Pichia pastoris, Saccharomyces cerevisiae, or Schizosaccharomyces pombe; insect cells such as Spodoptera frugiperda (Sf9), and animal cells such as CHO, COS, or BSC etc.

Still another aspect of the present invention provides a composition comprising the long-acting conjugate for brain targeting.

In a specific embodiment, the composition may be a pharmaceutical composition.

Still another aspect of the present invention provides a use of the long-acting conjugate for brain targeting in the preparation of pharmaceutical agents.

Still another aspect of the present invention provides a method for preparing the long-acting conjugate for brain targeting.

In a specific embodiment, the preparation method may comprise (a) culturing the host cell; and (b) recovering a long-acting conjugate for brain targeting from the cultured host cell or a culture thereof.

In another specific embodiment, the preparation method may comprise:

(i) preparing:

- (a) X-L₁-F, wherein X, which is a physiologically active material, L₁, which is a peptide or non-peptide linker, and F comprising an immunoglobulin Fc region, are linked; and
- (b) L₂-Y, wherein Y, which is a peptide for brain targeting, and L₂, which is a peptide or non-peptide linker, are linked; and

(ii) linking (a) X-L₁-F and (b) L₂-Y.

In particular, in still another specific embodiment, L₁of (a) may be a peptide linker and L₂of (b) may be a non-peptide linker.

In another specific embodiment, the preparation method may comprise:

(i) preparing:

- (a) X-L₁, wherein X, which is a physiologically active material, and L₁, which is a peptide or non-peptide linker, are linked; and
- (b) F-L₂-Y, wherein Y, which is a peptide for brain targeting, L₂, which is a peptide or non-peptide linker, and F are linked; and

(ii) linking (a) X-L₁and (b)

In particular, in still another specific embodiment, L₁of (a) may be a non-peptide linker and L₂of (b) may be a peptide linker.

In another specific embodiment, the preparation method may comprise:

(b) linking F-L₂-Y to the reactive functional group at the unreacted terminus of the linked material to obtain X-L₁-F-L₂-Y.

In the preparation method according to the previous embodiments, in (b), the reactive functional group at the unreacted terminus of the linked material may be linked to F_aof the following Formula 2:

embedded image

wherein:

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2anis independently a peptide linker or a non-peptide linker; and

each of L_2b1, . . . , L_2bn′ is independently a peptide linker or a non-peptide linker;

wherein n and n′ are each independently an integer.

In the preparation method, the reactive functional group may be selected from the group consisting of an aldehyde group, a maleimide group, and a succinimide derivative.

The aldehyde group may be a propionaldehyde group or a butyraldehyde group.

The succinimide derivative may be succinimidyl carboxymethyl, succinimidyl valerate, succinimidyl methylbutanoate, succinimidyl methylpropionate, succinimidyl butanoate, succinimidyl propionate, N-hydroxysuccinimide, or succinimidyl carbonate.

The reactive functional groups at both termini of the non-peptide polymer may be aldehyde groups.

Meanwhile, the non-peptide polymer may have, as reactive functional groups, each of an aldehyde group and a maleimide group at its termini.

Meanwhile, the non-peptide polymer may have, as reactive functional groups, each of an aldehyde group and a succinimide group at its termini.

The preparation method may comprise: culturing a host cell comprising an expression cassette encoding X-L_1a-F_a-(L_2a1-BTP_a1)- . . . -(L_2an-BTP_an) of the following Formula 3 and an expression cassette encoding X-L_1b-F_b-(L_2b1-BTP_b1)- . . . -(L_2bn′-BTP_bn′) of Formula 3; and obtaining a conjugate of Formula 3 from the cultured host cell or a culture thereof:

embedded image

wherein:

X is a physiologically active material;

L_1aand L_1bare peptide linkers;

each of BTP_a1, . . . , BTP_an, being the same as or different from one another, is a peptide for brain targeting;

each of BTP_b1, . . . , BTP_bn′, being the same as or different from one another, is a peptide for brain targeting;

each of L_2a1, . . . , L_2anis a peptide linker; and

each of L_2b1, . . . , L_2bn′ is a peptide linker;

wherein n and n′ are each independently an integer.

In particular, the X-L_1a-F_a-(L_2a1-BTP_a1)- . . . -(L_2an-BTP_an) and X-L_1b-F_b-(L_2b1-BTP_b1)- . . . -(L_2bn′-BTP_bn′) may be expressed in the form of a fusion protein, and in the refolding process, the binding between F_aand F_bmay be formed to form the conjugate.

Still another aspect of the present invention provides the peptide for brain targeting, a separated polynucleotide which encodes the peptide for brain targeting, an expression vector containing the polynucleotide, and a transformant containing the expression vector.

Meanwhile, the peptide for brain targeting may include all of those in the form of the peptide itself, a salt thereof (e.g., a pharmaceutically acceptable salt of the peptide), or a solvate thereof.

Additionally, the peptide for brain targeting may be in any pharmaceutically acceptable form.

The kind of the salt is not particularly limited. However, the salt is preferably one that is safe and effective to a subject, e.g., a mammal, but is not particularly limited thereto.

The term “pharmaceutically acceptable” refers to a material which can be effectively used for the intended use within the scope of pharmaco-medical decisions without inducing excessive toxicity, irritation, allergic responses, etc.

As used herein, the term “pharmaceutically acceptable salt” refers to a salt derived from pharmaceutically acceptable inorganic salts, organic salts, or bases. Examples of the suitable salts may include hydrochloric acid, bromic acid, sulfuric acid, nitric acid, perchloric acid, fumaric acid, maleic acid, phosphoric acid, glycolic acid, lactic acid, salicylic acid, succinic acid, toluene-p-sulfonic acid, tartaric acid, acetic acid, citric acid, methanesulfonic acid, formic acid, benzoic acid, malonic acid, naphthalene-2-sulfonic acid, benzenesulfonic acid, etc. Examples of the salts derived from suitable bases may include alkali metals such as sodium, potassium, etc.; alkali earth metals such as magnesium; ammonium, etc.

As used herein, the term “solvate” refers to a complex formed between the peptide according to the present invention or a salt thereof and a solvent molecule.

The separated polynucleotide encoding the peptide for brain targeting includes polynucleotide sequences which have a sequence identity to the corresponding sequence of 75% or higher, specifically 85% or higher, more specifically 90% or higher, and even more specifically 95%, are included within the scope of the present invention.

Hereinafter, the present invention will be described in more detail with reference to the following Examples. However, these Examples are for illustrative purposes only, and the invention is not intended to be limited by these Examples.

Example 1: Preparation of Fusion Proteins in which Immunoglobulin Fc Region and Peptide for Brain Targeting are Linked

For the preparation of a long-acting conjugate containing a peptide for brain targeting and a physiologically active polypeptide, in which a biocompatible material, which includes an immunoglobulin constant region and has an FcRn-binding region, a peptide for brain targeting, and a physiologically active material are linked by a peptide linker, a fusion protein to which an immunoglobulin Fc region and a peptide for brain targeting are linked was prepared.

In this regard, five kinds of peptides were selected as the peptide for brain targeting (Table 1).

TABLE 1

SEQ

Peptides for

ID

Brain Targeting
Sequence
NO

HAIYPRH
DNA
CATGCAATTTATCCGCGTCATTGA
1

(BTP1)
Protein
HAIYPRH
2

THR
DNA
ACCCATCGTCCGCCGATGTGGAGC
3

(BTP2)

CCGGTTTGGCCGTGA

Protein
THRPPMWSP VWP
4

Angiopep-2
DNA
ACCTTTTTTTATGGTGGCAGCCGT
5

(BTP3)

GGTAAACGCAATAACTTTAAAACC

GAAGAATATTAA

Protein
TFFYGGSRG KRNNFKTEEY
6

ApoB
DNA
AGCGTTATTGATGCACTGCAGTAT
7

(BTP4)

AAACTGGAAGGTACCACACGTCTG

ACCCGCAAACGTGGTCTGAAACTG

GCCACCGCACTGTCACTGAGCAAT

AAATTTGTTGAAGGTAGCTAA

Protein
SVIDALQYK LEGTTRLTRK RGL
8

KLATALSLSNKFVEGS

ApoE
DNA
CTGCGTAAACTGCGCAAACGTCTG
9

(BTP5)

TTACTGCGTAAACTGCGCAAACGT

CTGTTATAA

Protein
LRKLRKRLL LRKLRKRLL
10

As the biocompatible material capable of increasing the half-life of a physiologically active polypeptide linked thereto, IgG4 Fc regions including a hinge region were selected, and the IgG4 Fc regions including a hinge region and the peptides for brain targeting were fused at a gene level, and each of the fusion products was inserted into respective expression vectors.

Fusion proteins were synthesized by linking the IgG4 Fc regions, which include a hinge region, and the peptides for brain targeting by a peptide linker or by a method of direct fusion, and specifically, by linking the IgG4 Fc regions, which include a hinge region, and the peptides for brain targeting by a peptide bond (synthesized by Bioneer Corporation, Korea) (Table 2). As can be seen in the sequences of Table 2 below, the fusion proteins containing the IgG4 Fc region, which includes a hinge region, and a peptide for brain targeting were prepared by linking the N-terminus of a peptide for brain targeting to the C-terminus of an IgG4 Fc region using a linker or by a method of direct fusion.

TABLE 2

SEQ ID

Sequence
NO

Fc-
DNA
IgG4
ATGCCATCATGCCCA
11

BTP1

Hinge

(HAIYPRH)

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCCTGTTCC
12

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

HAIYPRH
CATGCAATTTATCCGCGTCATTGA
1

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTQKSLSLSLGK

HAIYPRH
HAIYPRH
2

Fc-
DNA
IgG4
ATGCCATCATGCCCA
11

BTP2

Hinge

(THR)

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCCTGTTCC
12

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

THR
ACCCATCGTCCGCCGATGTGGAGCCCGGMGGCCGTGA
3

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTQKSLKSLGK

THR
THRPPMWSP VWP
4

Fc-
DNA
IgG4
ATGCCATCATCCA
11

BTP3

Hinge

(Angiopep-

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCCTGTTCC
12

2)

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

Angiopep-
ACCTTTTTTTATGGTGGCAGCCGTGGTAAACGCAATAACTT
5

2
TAAAACCGAAGAATATTAA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTQKSLSLSLGK

Angiopep-
TFFYGGSRG KRNNFKTEEY
6

2

Fc-
DNA
IgG4
ATGCCATCATGCCCA
11

BTP4

Hinge

(ApoB)

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCCTGTTCC
12

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TQGGAGAGCAATQGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

ApoB
AGCGTTATTGATGCACTGCAGTATAAACTGGAAGGTACCAC
7

ACGTCTGACCCGCAAACGTGGTCTGAAACTGGCCACCGCA

CTGTCACTGAGCAATAAATTTGTTGAAGGTAGCTAA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTQKSLSLSLGK

ApoB
SVIDALQYK LEGTTRLTRK RGLKLATALS LSNKFVEGS
8

Fc-
DNA
IgG4
ATGCCATCATGCCCA
11

BTP5

Hinge

(ApoE)

IgG4
GCACCTGAGTTCCTQGGGGGACCATCAGTCTTCCTGTTCC
12

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

ApoE
CTGCGTAAACTGCGCAAACGTCTGTTACTGCGTAAACTGCG
9

CAAACGTCTGTTATAA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTOKSLSLSLGK

ApoE
LRKLRKRLL LRKLRKRLL
10

Fc-
DNA
Ig64
ATGCCATCATGCCCA
11

BTP6

Hinge

(HAIYPRH)

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCCTGTTCC
12

Linker

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

15a.a

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGGAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CQCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCAGGCGGAGGTGGCTCTGGCGGTGGC
17

GGATCG

HAIYPRH
CATGCAATTTATCCGCGTCATTGA
1

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTQKSLSLSLGK

Linker
GGGGSGGGGSGGGGS
18

HAIYPRH
HAIYPRH
2

Fc-
DNA
IgG4
ATGCCATCATGCCCA
11

BTP7

Hinge

(THR)

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCCTGTTCC
12

Linker

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

15a.a

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCAGGCGGAGGTGGCTCTGGCGGTGGC
17

GGATCG

THR
ACCCATCGTCCGCCGATGTGGAGCCCGGTTTGGCCGTGA
3

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDILMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGDPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWCIEGNVF

SCSVMHEALHNHYTOKSISLSIGK

Linker
GGGGSGGGGSGGGGS
18

THR
THRPPMWSP VWP
4

Fc-
DNA
IgG4
ATGCCATCATGCCCA
11

BTP8

Hinge

(Angiopep-

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCCTGTTCC
12

2)

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

Linker

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

15a.a

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCAGGCGGAGGTGCTCTGGCGGTGGC
17

GGATCG

Angiopep-
ACCTTTTTTTATGGTGGCAGCCTGTAAACGCAATAACTT
5

2
TAAAACCGAAGAATATTAA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTQKSLSLSLGK

Linker
GGGGSGGGGSGGGGS
18

Angiopep-
TFFYGGSRG KRNNFKTEEY
6

2

Fc-
DNA
IgG4
ATGCCATCATGCCCA
11

BTP9

Hinge

(ApoB)

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCCTGTTCC
12

Linker

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

15a.a

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCAGGCGGAGGTGGCTCTGGCGGTGGC
17

GGATCG

ApoB
AGCGTTATTGATGACTGCAGTATAAACTGGAAGGTACCAC
7

ACGTCTGACCCGCAAACGTGGTCTGAAACTGGCCACCGCA

CTGTCACTGAGCAATAAATTTGTTGAAGGTAGCTAA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTQKSLSLSLGK

Linker
GGGGSGGGGSGGGGS
18

ApoB
SVDALQYK LEGTTRL TRK RGLKLATALS LSNKFVEGS
8

Fc-
DNA
IqG4
ATGCCATCATCCCA
11

BTP10

Hinge

(ApoE)

IgG4
GCACCTGAGTTCCTGGGGACCATCAGTCTTCTGTTCC
12

Linker

CH2
CCCCAAAACCCAAGGACACCCTCATGATCTCCCGGACCCC

15a.a

TGAGGTCACATGCGTGGTGGTGGACGTGAGCCAGGAAGAC

CCTGAGGTCCAGTTCAACTGGTACGTGGACGGCGTGGAGG

TGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTTCAA

CAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCAC

CAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCT

CCAACAAAGGCCTCCCATCCTCCATCGAGAAAACCATCTCC

AAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTGCCCCCAT
13

CH3
CCCAGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTG

CCIGGICAAAGGCTTCTATCCCAGCGACATCGCCGTGGAG

TGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCA

CGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCAGGAGGG

GAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACA

ACCACTACACGCAGAAGAGCCTCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCAGGCGGAGGTGGCTCTGGCGGTGGC
17

GGATCG

ApoE
CTGCGTAAACTGCGCAAACGTCTGTTACTGCGTAAACTGCG
9

CAAACGTCTGTTATAA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEV
15

CH2
QFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQDWL

NGKEYKCKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWE
16

CH3
SNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVF

SCSVMHEALHNHYTQKSLSLSLGK

Linker
GGGGSGGGGSGGGGS
18

ApoE
LRKLRKRLL LRKLRKRLL
10

Since the gene encoding the peptide for brain targeting, which was fused to the synthesized immunoglobulin Fc region, included NdeI and BamHI at both ends thereof, the gene was inserted into the pET22b expression vector, which is digested by NdeI and BamHI. The expression vector, to which the gene encoding the peptide for brain targeting fused to the synthesized immunoglobulin Fc region was inserted, was inserted into the BL21 (DE3) strain and thereby the long-acting fusion protein, in which the immunoglobulin Fc region and the peptide for brain targeting were linked, was expressed.

Example 2: Preparation of a Peptide for Brain Targeting

For the detection of various peptides for brain targeting which are fused to an immunoglobulin Fc region, additional peptides including BTP1 to BTP5 for brain targeting were designed and synthesized (Table 3).

TABLE 3

SEQ ID

Sequence
NO

BTP1
DNA
CATGCAATTTATCCGCGTCAT
1

Protein
HAIYPRH
2

BTP2
DNA
ACCCATCGTCCGCCGATGTGGAGCCCGGTTTGGCCG
3

Protein
THRPPMWSPVWP
4

BTP3
DNA
ACCTTTTTTTATGGTGGCAGCCGTGGTAAACGCAATAA
5

CTTTAAAACCGAAGAATAT

Protein
TFFYGGSRGKRNNFKTEEY
6

BTP4
DNA
AGCGTTATTGATGCACTGCAGTATAAACTGGAAGGTAC
7

CACACGTCTGACCCGCAAACGTGGTCTGAAACTGGCCA

CCGCACTGTCACTGAGCAATAAATTTGTTGAAGGTAGC

Protein
SVIDALQYKLEGTTRLTRKRGLKLATALSLSNKFVEGS
8

BTP5
DNA
CTGCGTAAACTGCGCAAACGTCTGTTACTGCGTAAACT
9

GCGCAAACGTCTGTTA

Protein
LRKLRKRLLLRKLRKRLL
10

BTP6
DNA
taccaacagatcctcaccagtatgccttccagaaacgtgatccaa
19

atatccaacgacctggagaacctccgggatcttcttcacgtgctg

Protein
YQQILTSMPSRNVIQISNDLENLRDLLHVL
20

BTP7
DNA
tacaccatttggatgcccgagaatccgagacctgggacaccttgt
21

gacatttttaccaatagtagagggaagagagcatccaatggg

Protein
YTIWMPENPRPGTPCDIFTNSRGKRASNG
22

BTP8
DNA
aagtcagtcagaacttggaatgagatcAtAccttcaaaagggtgt
23

ttaagagttggggggaggtgtcatcctcatgtgaacggg

Protein
KSVRTWNEIIPSKGCLRVGGRCHPHVNG
24

BTP9
DNA
CATCTGAATATTCTGAGCACCCTGTGGAAATATCGT
25

Protein
HLNILSTLWKYR
26

BTP10
DNA
CTGCGCAAGCTGCGTAAGCGGCTCCTCCGCGATGCCGA
27

TGACCTGTTACGTAAACTTCGCAAACGTCTGCTTCGTG

ACGCAGACGATCTG

Protein
LRKLRKRLLRDADDLLRKLRKRLLRDADDL
28

BTP11
DNA
ACCGAGGAGCTGCGGGTGCGCCTCGCCTCCCACCTGCG
29

CAAGCTGCGTAAGCGGCTCCTC

Protein
TEELRVRLASHLRKLRKRLL
30

BTP12
DNA
CTGCGGGTGCGCCTCGCCTCCCACCTGCGCAAGCTGCG
31

TAAGCGGCTCCTCTTACGTGTTCGTCTGGCAAGCCATCT

TCGTAAACTTCGCAAACGTCTGCTT

Protein
LRVRLASHLRKLRKRLLLRVRLASHLRKLRKRLL
32

BTP13
DNA
GGTAAAGGCCCGAAATGGATGCGTTGA
33

Protein
GKGPKWMR
34

BTP14
DNA
GGTCATAAAGCAAAAGGCCCGCGTAAATGA
35

Protein
GHKAKGPRK
36

BTP15
DNA
GTTATTGCAAAAATTAAGAAACCGAAATGA
37

Protein
VIAKIKKPK
38

BTP16
DNA
AAGTGGAAAACCCCGAAAGTTCGTGTGTGA
39

Protein
KWKTPKVRV
40

To confirm whether the peptides for brain targeting can actually serve in brain targeting, in vitro and in vivo tests were performed.

Example 3: Transcytosis Assay of Peptides for Brain Targeting

A transcytosis experiment was performed to determine the level of blood-brain barrier (BBB) passage of peptides for brain targeting. The hCMEC/D3 cells, which are human cerebral endothelial cells, were cultured on a microporous membrane at a concentration of 5×10⁴cells/cm²for 10 days. To confirm the BBB formation, a penetration test was performed with FITC-Dextran (70 kDa) and thereby the formation of tight junctions was confirmed. Then, 25 mM FITC-BTP5, FITC-BTP11, FITC-BTP12, FITC-BTP16, and FITC-Exendin4, FITC-P-8 (negative control, P-8) were placed on hCMEC/D3 cells. After 2 hours and 24 hours, the fluorescence intensity of FITC was measured (FIG. 1).

As a result, all of the BTPs showed higher levels of passage compared to those of exendin-4 and the negative control (P-8). It was confirmed that the passage level of the peptides for brain targeting, such as BTP5, BTP11, and BTP16, increased with time.

These results suggest that the peptides for brain targeting confirmed in the present invention could effectively pass through the BBB.

Example 4: Confirmation of Brain Distribution of Peptides for Brain Targeting

A brain distribution test was performed in mice to determine the level of BBB passage of peptides for brain targeting. Mice were administered through the common carotid artery (CCA) of the mice at a concentration of 2 mg/head and the brains of the mice were isolated and cut into fragments, and the level of passage through the BBB of peptides for brain targeting was observed under a microscope using the fluorescence of FITC (FIG. 2).

The peptides for brain targeting injected via CCA must spread to one side of the brain region in light of the injection characteristic, and as a result of the test, it was possible to observe the spreading to one side of the brain with a microscope of 12.5× magnification. Additionally, it was confirmed that the fluorescence of FITC was observed in the region where the cell bodies of the hippocampus, which plays an important role in long-term memory, are present with a microscope at magnification of 200× magnification. From these results, it was confirmed that the peptides for brain targeting passed through the BBB and entered the brain tissue.

These results suggest that the peptides for brain targeting of the present invention can be used for targeting not only in vitro but also into the brain in vivo, suggesting that physiologically active materials, which were linked to the peptides for brain targeting, could also pass through the BBB and be effectively delivered to the brain. Furthermore, these results suggest that with respect to the conjugate of the present invention, which is in the form of a long-acting conjugate, the in vivo duration is increased, and as the duration increases, the targeting to the brain can be more efficiently performed.

Example 5: Preparation of Expression Vector for Fusion Proteins Containing Immunoglobulin Fc Region and Peptide for Brain Targeting

An expression vector was constructed to express additional fusion proteins. IgG4 Fc regions containing a hinge region were selected as a biocompatible material capable of increasing the half-life of the linked physiologically active polypeptide, and the IgG4 Fc regions containing a hinge region and the peptides for brain targeting were fused at the gene level, and the fused products was inserted into respective expression vectors.

Fusion proteins were synthesized by linking the IgG4 Fc regions, which include a hinge region, and the peptides for brain targeting by a peptide linker or by a method of direct fusion, and specifically, by linking the IgG4 Fc regions, which include a hinge region, and the peptides for brain targeting by a peptide bond (synthesized by Bioneer Corporation, Korea) (Table 4). As can be seen in the sequences of Table 4 below, the fusion proteins containing the IgG4 Fc regions, which have the sequences of Table 4 below and include a hinge region, and the peptides for brain targeting were prepared by linking the N-terminus of the peptides for brain targeting to the C-terminus of an IgG4 Fc region using a linker or by a method of direct fusion.

TABLE 4

SEQ ID

Sequence
NO

Fc-BTP11
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP6)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCGT
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP6
TACCAACAGATCCTCACCAGTATGCCTTCCAGAAA
19

CGTGATCCAAATATCCAACGACCTGGAGAACCTC

CGGGATCTTCTTCACGTGCTG

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTIPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP6
YQQILTSMPSRNVIQISNDLENLRDLLHVL
20

Fc-BTP12
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP7)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP7
TACACCATTTGGATGCCCGAGAATCCGAGACCTG
21

GGACACCTTGTGACATTTTTACCAATAGTAGAGGG

AAGAGAGCATCCAATGGG

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP7
YTIWMPENPRPGTPCDIFTNSRGKRASNG
22

Fc-BTP13
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP8)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP8
AAGTCAGTCAGAACTTGGAATGAGATCATACCTTC
23

AAAAGGGTGTTTAAGAGTTGGGGGGAGGTGTCAT

CCTCATGTGAACGGG

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
1S

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP8
KSVRTWNEIIPSKGCLRVGGRCHPHVNG
24

Fc-BTP14
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP9)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTOGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP9
CATCTGAATATTCTGAGCACCCTGTGGAAATATCG
25

T

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPRKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFHWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP9
HLNILSTLWKYR
26

Fc-BTP15
DNA
IgG4
ATGCCATCATGA
11

(BTP10)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP10
CTGCGCAAGCTGCGTAAGCGGCTCCTCCGCGAT
27

GCCGATGACCTGTTACGTAAACTTCGCAAACGTC

TGCTTCGTGACGCAGACGATCTG

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP10
LRKLRKRLLRDADDLLRKLRKRLLRDADDL
28

Fc-BTP16
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP11)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP11
ACCGAGGAGCTGCGGGTGCGCCTCGCCTCCCAC
29

CTGCGCAAGCTGCGTAAGCGGCTCCTC

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP11
TEELRVRLASHLRKLRKRLL
30

Fc-BTP17
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP12)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP12
CTGCGGGTGCGCCTCGCCTCCCACCTGCGCAAG
31

CTGCGTAAGCGGCTCCTCTTACGTGTTCGTCTGG

CAAGCCATCTTCGTAAACTTCGCAAACGTCTGCTT

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP12
LRVRLASHLRKIRKRLLLRVRLASHLRKLRKRLL
32

Fc-BTP18
DNA
IgG4
ATGCCATCATCCCA
11

(BTP13)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP13
GGTAAAGGCCCGAAATGGATGCGTTA
33

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VQKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP13
GKGPKWMR
34

Fc.BTP19
DNA
IgG4
ATGCCATATGCCCA
11

(BTP14)

Hinge

Ig34
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP14
GGTCATAAAGCAAAAGGCCCGCGTAAATGA
35

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP14
GHKAKGPRK
36

Fc-BTP20
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP15)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGOTACGTGGACGGCGTOGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTtCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP15
GTTATTGCAAAAATTAAGAAACGAAATGA
37

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP15
VIAKIKKPK
38

Fc-BTP21
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP16)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGSAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

BTP16
AAGTGGAAAACCCCGAAAGTTCGTGTGTGA
39

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

BTP16
KWKTPKVRV
40

Since the gene encoding the peptide for brain targeting, which was fused to the synthesized immunoglobulin Fc region, included NdeI and BamHI at both ends thereof, the gene was inserted into the pET22b expression vector, which was digested by NdeI and BamHI. The expression vector, to which the gene encoding the peptide for brain targeting fused to the synthesized immunoglobulin Fc region was inserted, was inserted into the BL21 (DE3) strain and thereby the long-acting fusion protein, in which the immunoglobulin Fc region and the peptide for brain targeting were linked, was expressed.

Example 6: Preparation of Expression Vector for Fusion Proteins in which an Immunoglobulin Fc Region and at Least Two Peptides for Brain Targeting are Linked

Expression vectors were constructed to express additional fusion proteins to increase receptor binding affinity. IgG4 Fc regions including a hinge region were selected as a biocompatible material capable of increasing the half-life of linked physiologically active polypeptides, and linkers and peptides for brain targeting were inserted into the constructed expression vectors at the gene level by site-directed mutagenesis PCR. Specifically, the linkers and peptides for brain targeting were inserted between the C-terminus of an immunoglobulin Fc region and the N-terminus of the peptides for brain targeting, or the C-terminus of the peptides for brain targeting and the site where the BamHI site of the vector is included, using the primers of SEQ ID NOS disclosed in Table 5. Expression vectors expressing fusion proteins (Table 6) containing two or more replicated peptides for brain targeting were constructed. These fusion proteins had the sequences shown in Table 6. For example, in the Fc-BTP22 conjugate, linkers are intercalated in two units of BTP5 peptides of Table 2 and thereby linked to the C-terminal direction of the CH3 region of an Fc fragment. Specifically, as can be confirmed in Table 6 below, fusion proteins were prepared by linking the C-terminus of an immunoglobulin Fc region and the N-terminus of each of the peptides for brain targeting by a peptide linker, or by a method of direct fusion. In this case, the peptides for brain targeting in a form linked in tandem means that the peptides for brain targeting are in a form where single-unit peptides for brain targeting are linked by a linker.

TABLE 5

SEQ ID

Sequence
NO

Fc-BTP22-F
5′-TCTCCCTGTCTCTGGGTAAAGGTGGAGGCGGTTCACTTC
61

GCAAGTTACGTAAACGCTTACTGTTACGTAAACTTCGGAA

GCGCTTACTGGGCGGAGGTGGCTCTCTGCGTAAACTGCGC

AAACG-3′

Fc-BTP22-R
5′-CGTTTGCGCAGTTTACGCAGAGAGCCACCTCCGCCCAG
62

TAAGCGCTTCCGAAGTTTACGTAACAGTAAGCGTTTACGT

AACTTGCGAAGTGAACCGCCTCCACCTTTACCCAGAGACA

GGGAGA-3′

Fc-BTP23-F
5′-AACTGCGCAAACGTCTGTTAGGCGGTGGCGGATCGCTG
63

CGTAAACTGCGCAAACGTCTGTTACTTCGGAAGCTGAGAA

AACGCTTACTTTAAGGATCCgaattcgagctccG-3′

Fc-BTP23-R
5′-CGGAGCTCGAATTCGGATCCTTAAAGTAAGCGTTTTCTC
64

AGCTTCCGAAGTAACAGACGTTTGCGCAGTTTACGCAGCG

ATCCGCCACCGCCTAACAGACGTTTGCGCAGTT-3′

Fc-BTP24-F
5′-TCTCCCTGTCTCTGGGTAAAGGTGGAGGCGGTTCAACA
65

GAAGAGTTACGTGTTCGTCTGGCAAGCCATTTACGTAAAC

TTCGCAAACGTCTGTTAGGCGGAGGTGGCTCTACCGAGGA

GCTGCGGGTGCG-3′

Fc-BTP24-R
5′-CGCACCCGCAGCTCCTCGGTAGAGCCACCTCCGCCTAA
66

CAGACGTTTGCGAAGTTTACGTAAATGGCTTGCCAGACGA

ACACGTAACTCTTCTGTTGAACCGCCTCCACCTTTACCCA

GAGACAGGGAGA-3′

Fc-BTP25-F
5′-AGCTGCGTAAGCGGCTCCTCGGCGGTGGCGGATCGACG
67

GAAGAACTTCGCGTCCGGTTAGCGTCACATCTTCGGAAAT

TACGGAAGCGCTTGCTGTGAGGATCCgaattcgagctccG-3′

Fc-BTP25-R
5′-CGGAGCTCGAATTCGGATCCTCACAGCAAGCGCTTCCG
68

TAATTTCCGAAGATGTGACGCTAACCGGACGCGAAGTTCT

TCCGTCGATCCGCCACCGCCGAGGAGCCGCTTACGCAGCT-3′

Fc-BTP26-F
5′-TCTCCCTGTCTCTGGGTAAAGGTGGAGGCGGTTCAAAA
69

TGGAAGACACCAAAGGTGCGCGTTGGCGGAGGTGGCTCT

AAGTGGAAAACCCCGAAAGT-3′

Fc-BTP26-R
5′-ACTTTCGGGGTTTTCCACTTAGAGCCACCTCCGCCAACG
70

CGCACCTTTGGTGTCTTCCATTTTGAACCGCCTCCACCTTT

ACCCAGAGACAGGGAGA-3′

Fc-BTP27-F
5′-AAACCCCGAAAGTTCGTGTGGGCGGTGGCGGATCGAAA
71

TGGAAAACTCCTAAAGTACGGGTCTGAGGATCCgaattcgagct

ccG-3′

Fc-BTP27-R
5′-CGGAGCTCGAATTCGGATCCTCAGACCCGTACTTTAGG
72

AGTTTTCCATTTCGATCCGCCACCGCCCACACGAACTTTC

GGGGTTT-3′

TABLE 6

Sequence
SEQ ID NO

Fc-BTP22
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP5 2x)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCA
73

BTP5
CTTCGCAAGTACGTAAACGCTTACTGTTACGTAA
74

Linker
ACTTCGGAAGCGCTTACTG
75

BTP5
CTGCGTAAACTGCGCAAACGTCTACTGTA
9

AACTGCGCAAACGTCTGTTA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

Linker
GGGGS
76

BTP5
LRKLRKRLLLRKLRKRLL
10

Linker
GGGGS
76

BTP5
LRKLRKRLLLRKLRKRLL
10

Fc-BTP23
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP5 3x)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
AGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
GCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCA
73

BTP5
CTTCGCAAGTTACGTAAACGCTTACTGTTACGTAA
74

ACTTCGGAAGCGCTTACTG

Linker
GGCGGAGGTGGCTCT
75

BTP5
CTGCGTAAACTGCGCAAACGTCTGACTGTA
9

AACTGCGCAAACGTCTGTTA

Linker
GGCGGTGGCGGATCG
77

BTP5
CTGCGTAAACTGCGCAAACGTCTGTTACTTCGGA
78

AGCTGAGAAAACGCTTACTTTAA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

Linker
GGGGS
76

BTP5
LRKLRKRLLLRKLRKRLL
10

Linker
GGGGS
76

BTP5
LRKLRKRLLLRKLRKRLL
10

Linker
GGGGS
76

BTP5
LRKLRKRLLLRKLRKRLL
10

Fc-BTP24
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP11 2x)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCA
73

BTP11
ACAGAAGAGTTACGTGTTCGTCTGGCAAGCCATT
79

TACGTAAACTTCGCAAACGTCTGTTA

Linker
GGCGGAGGTGGCTCT
75

BTP11
ACCGAGGAGCTGCGGGTGCGCCTCGCCTCCCAC
29

CTGCGCAAGCTGCGTAAGCGGCTCCTC

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

Linker
GGGGS
76

BTP11
TEELRVRLASHLRKLRKRLL
30

Linker
GGGGS
76

BTP11
TEELRVRLASHLRKLRKRLL
30

Fc-BTP25
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP11 3x)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTGAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGCCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCA
73

BTP11
ACAGAAGAGTTACGTGTTCGTCTGGCAAGCCATT
79

TACGTAAACTTCGCAAACGTCTGTTA

Linker
GGCGGAGGTGGCTCT
75

BTP11
ACCGAGGAGCTGCGGGTGCGCCTCGCCTCCCAC
29

CTGCGCAAGCTGCGTAAGCGGCTCCTC

Linker
GGCGGTGGCGGATCG
77

BTP11
ACGGAAGAACTTCGCGTCCGGTTAGCGTCACATC
80

TTCGGAAATTACGGAAGCGCTTGCTGTGA

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

Hinge
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

Linker
GGGGS
76

BTP11
TEELRVRLASHLRKLRKRLL
30

Linker
GGGGS
76

BTP11
TEELRVRLASHLRKLRKRLL
30

Linker
GGSGS
76

BTP11
TEELRVRLASHLRKLRKRLL
30

Fc-BTP26
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP16 2x)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

Linker
GTGGAGGCGGTTCA
73

BTP16
AAATGGAAGACACCAAAGGTGCGCGTT
81

Linker
GGCGGAGGTGGCTCT
75

BTP16
AAGTGGAAAACCCCGAAAGTTCGTGTGTGA
39

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

Linker
GGGGS
76

BTP16
KWKTPKVRV
40

Linker
GGGGS
76

BTP16
KWKTPKVRV
40

Fc-BTP27
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP16 3x)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGTCTTCC
12

CH2
TGTTCCCCCCAAAACCCAAGGACACCCTCATGAT

CTCCCGGACCCCTGAGGTCACATGCGTGGTGGT

GGACGTGAGCCAGGAAGACCCTGAGGTCCAGTT

CAACTGGTACGTGGACGGCGTGGAGGTGCATAAT

GCCAAGACAAAGCCGCGGGAGGAGCAGTTCAAC

AGCACGTACCGTGTGGTCAGCGTCCTCACCGTCC

TGCACCAGGACTGGCTGAATGGCAAGGAGTACAA

GTGCAAGGTCTCCAACAAAGGCCTCCCATCCTCC

ATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
GGGCAGCCCCGAGAACCACAGGTGTACACCCTG
13

CH3
CCCCCATCCCAGGAGGAGATGACCAAGAACCAG

GTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATC

CCAGCGACATCGCCGTGGAGTGGGAGAGCAATG

GGCAGCCGGAGAACAACTACAAGACCACGCCTC

CCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTA

CAGCAGGCTAACCGTGGACAAGAGCAGGTGGCA

GGAGGGGAACGTCTTCTCATGCTCCGTGATGCAT

GAGGCTCTGCACAACCACTACACGCAGAAGAGCC

TCTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCA
73

BTP16
AAATGGAAGACACCAAAGGTGCGCGTT
81

Linker
GGCGGAGGTGGCTCT
75

BTP16
AAGTGGAAAACCCCGAAAGTTCGTGTG
82

Linker
GGCGGTGGCGGATCG
77

BTP16
AAATGGAAAACTCCTAAAGTACGGGTCTGA
83

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTEVTCVVVDV
15

CH2
SQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTY

RVVSVLTVLHQDWLNGKEYKCKVSNKGLPSSIEKTI

SKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPS
16

CH3
DIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLT

VDKSRWQEGNVFSCSVMHEALHNHYTQKSLSLSLG

K

Linker
GGGGS
76

BTP16
KWKTPKVRV
40

Linker
GGGGS
75

TP
KWKTPKVRV
40

Linker
GGGGS
76

RV
KWKTPKVRV
40

Example 7: Expression of Fusion Proteins in which Immunoglobulin Fc Region and Peptide for Brain Targeting are Fused

The expression of fusion proteins, in which an immunoglobulin Fc region and the peptides for brain targeting were linked, was performed under the control of the T7 promoter of pET22b vector (Novagen). E. coli BL21-DE3 (E. coli B F-dcm ompT hsdS (rB⁻mB⁻) gal λDE3); Novagen) was transformed using each of the constructed expression vectors. The transformation was performed according to the method recommended by Novagen. Single colonies, in which each recombinant expression vector was transformed, were collected and inoculated into 2× Luria broth (LB) media containing ampicillin (50 μg/mL) and cultured at 37° C. for 15 hours. The recombinant strain culture broth and 2×LB media containing 30% glycerol were mixed at a 1:1 ratio (v/v), and each 1 mL of the mixture was aliquoted into cryotubes and stored at −140° C., and the resultant was used as a cell stock for the production of recombinant fusion proteins.

For the expression of conjugates in which an immunoglobulin Fc region and a peptide for brain targeting are fused, each vial of the cell stock was dissolved, inoculated into 500 mL of 2× Luria broth (LB), and cultured in a shaking water bath at 37° C. for 14 to 16 hours. When the OD at 600 nm reached 4.0 or higher, the cultivation was terminated and the resulting culture was used as a seed culture medium. The seed culture medium (1.6 L) was inoculated into a fermentation medium and the initial batch fermentation was begun. The cultivation conditions were 37° C., air supply (2 L/minute; 1 vvm), and stirring speed (650 rpm), and the pH was maintained at 6.70 using a 20% aqueous ammonia solution. With regard to the progress of the fermentation, when the nutrients in the culture media were limited, fed-batch culture was processed by adding a feeding solution. The bacterial growth was monitored based on OD values and when the OD value reached 120 or higher, IPTG was introduced thereto to a final concentration of 0.5 mM. The culture was processed further for about 23 to 25 hours after the introduction. Upon completion of the cultivation, the recombinant strains were collected by a centrifuge and stored at −80° C. until use.

Example 8: Recovery and Refolding of Fusion Proteins in which Immunoglobulin Fc Region and Peptide for Brain Targeting are Fused

Cells were disrupted and refolded to convert the fusion proteins expressed in Example 7, in which each of immunoglobulin Fc regions and each of the peptides for brain targeting were fused, into a soluble form. Cell pellets corresponding to 200 mL of each cell culture broth was resuspended in 200 mL of a lysis buffer (50 mM Tris, pH 9.0, 1 mM EDTA (pH 8.0), 0.2 M NaCl, and 0.5% Triton X-100). The cells were disrupted at a pressure of 15,000 psi using the microfluidizer processor M-110EH (Model M1475C, AC Technology Corp.). The disrupted cell lysate was centrifuged at 12,200×g at 4° C. for 30 minutes and the supernatant was discarded and resuspended in 200 mL of lysis buffer (0.5% Triton X-100 and 20 mM Tris (pH 8.0)). The pellet was resuspended in 200 mL of wash buffer (20 mM Tris (pH 8.0)) after centrifugation at 12,200×g at 4° C. for 30 minutes and then centrifuged in the same manner. The pellet was resuspended in 100 mL of buffer (8 M guanidine-HCl and 50 mM Tris (pH 8.0)) and stirred at room temperature for 2 hours. After 2 hours, the resultant was centrifuged at 12,200×g at 23° C. for 30 minutes and the supernatant was collected. Then, 2.5 mM dithiothreitol was added thereto and the mixture was stirred at 37° C. for 30 minutes. For the refolding of fusion proteins, in which solubilized immunoglobulin Fc regions and the peptides for brain targeting were fused, 3.5 L of buffer (3 M urea, 1 mM cysteine, 0.160 M arginine, 50 mM Tris (pH 9.2), and 20% glycerol) was added thereto at a flow rate of 1 mL/min using a peristaltic pump while stirring at 4° C. for 36 hours. The immunoglobulin Fc regions within the fusion proteins, in which solubilized immunoglobulin Fc regions and the peptides for brain targeting were fused, were expressed as dimers.

Example 9: Purification by Affinity Chromatography

Upon completion of refolding, samples were centrifuged at 12,200×g at 4° C. for 30 minutes and the supernatant was collected and filtered with a Satorius filter (0.22 μm), and the pH of the samples was adjusted to pH 7.5 with 50% HCl. Samples were allowed to bind to a Protein A-sepharose (GE Healthcare) column equilibrated with 10 mM Tris (pH 7.0) buffer, and then conjugate proteins in which the immunoglobulin Fc regions and the peptides for brain targeting were fused were eluted using 10 mM sodium citrate (pH 3.3) and 10% glycerol buffer.

Example 10: Purification by Hydrophobic Chromatography

After introducing 0.6 M ammonium sulfate into the eluted samples, the samples introduced with 0.6 M ammonium sulfate were allowed to bind to a phenyl HP (GE Healthcare) column equilibrated using 10 mM Tris (pH 7.0) buffer and 0.6 M ammonium sulfate as buffer, fusion proteins, in which the immunoglobulin Fc regions and the peptides for brain targeting were fused, were eluted using 10 mM Tris (pH 7.5) buffer in a linear concentration gradient from 0% to 100% with 6 column volumes.

Example 11: Confirmation of Brain Distribution of Fusion Protein in which Immunoglobulin Fc Region and a Peptide for Brain Targeting are Linked

A brain distribution test was performed in mice to determine the level of blood-brain barrier passage of fusion proteins, in which the immunoglobulin Fc regions and the peptides for brain targeting were linked. Mice were administered via intravenous injection at a concentration of 10 mg/kg. After two hours, the brains of the mice were separated and the concentration of the fusion proteins, in which the immunoglobulin Fc regions and the peptides for brain targeting were linked, was measured and thereby the level of blood-brain barrier passage of the fusion proteins was confirmed (FIG. 3).

As a result, the levels of blood-brain barrier passage of the immunoglobulin Fc regions and the peptides for brain targeting measured were shown to be higher compared to those of immunoglobulin Fc regions, and the concentrations of the immunoglobulin Fc regions and the peptides for brain targeting were higher compared to those of immunoglobulin Fc regions in the brain than in the serum. It was confirmed that, in the case a fusion protein where two or more of the same kinds of peptides for brain targeting are linked to an immunoglobulin Fc region, the concentrations was measured higher compared to when only one peptide for brain targeting was linked, and was also shown to have a higher T/S ratio.

These results suggest that the fusion proteins of the present invention, in which the immunoglobulin Fc regions and the peptide for brain targeting can effectively pass through the BBB and delivered into the brain. Furthermore, these results suggest that the fusion proteins of the present invention in the form of a long-acting conjugate increase their in vivo duration, and as the duration increases the targeting into the brain can be more effectively performed.

Hereinafter, further experiments were performed to confirm whether the long-acting fusion proteins of the present invention, even in a case where physiologically active materials are linked to the long-acting fusion proteins in which immunoglobulin Fc regions and peptides for brain targeting are linked, can also be effectively delivered to the brain by passing through the BBB and thereby exhibit physiological activity.

Example 12: Preparation of Conjugate Comprising Idursulfase and PEG

A long-acting conjugate for brain targeting containing idursulfase (approximately 72 kDa) was prepared as an example of a long-acting conjugate for brain targeting that contains a typical size of protein as a physiologically active material. As a precursor of the long-acting conjugate for brain targeting, a mono-pegylated conjugate in which a polyethylene glycol was linked as a linker to idursulfase was prepared first as follows.

After concentrating idursulfase (Shire, Ireland) to an appropriate concentration, for the pegylation of 10 K butyl-ALD(2) PEG (10 kDa polyethylene glycol where the hydrogen at both ends is each modified to butyraldehyde, NOF, Japan), a reaction was performed at 4° C. for about 2 hours, under the conditions where the molar ratio of idursulfase to 10 K butyl-ALD(2) PEG was set at 1:10 and the idursulfase concentration was set at 10 mg/mL. In particular, the reaction was performed by adding sodium cyanoborohydride (NaBH₃CN), i.e., a reducing agent, to 0.1 M potassium phosphate butter (pH 6.0). The idursulfase-10 K PEG, which is a mono-pegylated conjugate, was purified by applying the reactants to the Source 15Q column (GE, USA) using potassium phosphate buffer (pH 6.0) and a concentration gradient of NaCl.

Example 13: Preparation of Idursulfase-10 kDa PEG-Fc-BTP22 Conjugate which is a Long-Acting Conjugate for Brain Targeting

Then, a long-acting conjugate for brain targeting was prepared by linking an idursulfase-10 kDa PEG conjugate to an Fc fragment containing a peptide for brain targeting. A reaction was performed 25° C. for 15 hours by setting the molar ratio of idursulfase-10 K PEG to Fc-BTP22 (i.e., a representative example of a fusion protein for brain targeting) at 1:10 and the idursulfase concentration at 10 mg/mL. In particular, Dulbecco's phosphate buffer (DPBS) and a solution containing 10 mM NaBH₃CN as a reducing agent were added as reactants.

Upon completion of the reaction, the reactants were applied to the Source 15Q column (GE, USA) using sodium phosphate buffer (pH 6.0) and a concentration gradient of NaCl, and then, applied to the Source 15ISO column (GE, USA) using a concentration gradient of ammonium sulfate and sodium phosphate (pH 6.0), and thereby idursulfase-10 K PEG-Fc-BTP22, which is the intended long-acting conjugate for brain targeting, was purified. The idursulfase-10 K PEG-Fc-BTP22 can be used interchangeably with idursulfase-Fc-BTP22.

Example 14: Preparation of Conjugate Comprising GIP Derivative and PEG

A long-acting conjugate for brain targeting of an artificial GIP derivative having glucose-dependent insulinotropic polypeptide (GIP) receptor-stimulating activity, which consists of 40 amino acid residues, was prepared as an example of long-acting conjugates for brain targeting that contains a peptide of a typical size as a physiologically active material. As a precursor of the long-acting conjugate, a mono-pegylated conjugate, to which polyethylene glycol as a linker is linked to the artificial GIP derivative, was prepared as follows.

For the pegylation of 10 K MAL-PEG-ALD (10 kDa polyethylene glycol where the hydrogen atom at one end is modified to 3-[N-β-N-maleimido-1-oxoprolyl)amino]propyl group and the hydrogen atom at the opposite end is modified to 3-oxopropyl group (propylaldehyde group), NOF, Japan) to the C-terminal cysteine of the GIP derivative, a reaction was performed at 4° C. for about 1 hour, under the conditions where the molar ratio of GIP derivative to PEG was set at 1:1.3 and the GIP derivative concentration was set at 3 mg/mL. In particular, the reaction was performed in a solvent (50 mM Tris-HCl (pH 7.5)+45% isopropanol). The GIP derivative-10 K PEG, which is a mono-pegylated conjugate, was purified by applying the SP HP (GE, USA) column, which utilizes sodium citrate buffer (pH 3.0)+45% ethanol and a concentration gradient of KCl.

Example 15: Preparation of GIP Derivative-10 K PEG-Fc-BTP22 Conjugate

Then, a long-acting conjugate for brain targeting was prepared by linking a GIP derivative-10 K PEG conjugate to an Fc fragment containing a peptide for brain targeting. A reaction was performed at 4° C. for 16 hours by setting the total reaction concentration at 4.55 mg/mL, while setting the molar ratio of the GIP derivative-10 K PEG (purified in Example 14) to the Fc-BTP22 at 1:2. In particular, DPBS and a solution containing 20 mM NaBH₃CN as a reducing agent were added as reactants.

Upon completion of the reaction, the reactants were applied to the Source 15ISO column (GE, USA) using sodium phosphate buffer (pH 7.5) and a concentration gradient of ammonium sulfate, and then, applied again to the same column, and thereby the GIP derivative-10 K PEG-Fc-BTP22, which is the intended long-acting conjugate for brain targeting, was purified. The GIP derivative-10 K PEG-Fc-BTP22 can be used interchangeably with GIP derivative-Fc BTP22.

Example 16: Analysis of Transcytosis of Long-Acting Conjugates for Brain Targeting

A transcytosis experiment was performed for confirming the passage level of the long-acting conjugates for brain targeting obtained in Examples through the blood-brain barrier. The hCMEC/D3 cells, which are human cerebral endothelial cells, were cultured on a microporous membrane at a concentration of 5×10⁴cells/cm²for 10 days. To confirm the BBB formation, a penetration test was performed with FITC-Dextran (70 kDa) and thereby the formation of tight junctions was confirmed. Then, 25 mM long-acting conjugates were placed on hCMEC/D3 cells. After 2 hours and 4 hours, the protein concentration was measured using the ELISA kit.

As a result, GIP derivative-10 K PEG-Fc-BTP22 of Example 15 showed a higher level of passage through the blood-brain barrier compared to the control group, and it was confirmed that the passage level of the GIP derivative-10 K PEG-Fc-BTP22 increased with time (FIG. 4). A similar passage level was observed for the idursulfase-10 K PEG-Fc-BTP22 of Example 13 (data not shown).

These results suggest that the brain targeting long-acting conjugate confirmed in the present invention could effectively pass through the BBB.

Example 17: Measurement of Activity of Idursulfase-10 kDa PEG-Fc-BTP22 Conjugate

To examine the presence of any change in specific activity of idursulfase according to the preparation of idursulfase-10 K PEG-Fc-BTP22 conjugate, an in vitro experiment for specific activity of enzymes was performed. 4-Methylumbelliferyl-α-L-idopyranosiduronic acid-2-sulfate sodium salt (4MU-α-idopyraA-2), which is known as an enzyme substrate for idursulfase, was reacted with idursulfase β and IDS-Fc-BTP22 at 37° C. for 4 hours, and then, reacted with α-iduronidase, which is a secondary reaction enzyme, at 37° C. for 24 hours. The enzyme activity of 4-methylumbelliferone (4 MU), the final product, was measured by the measurement of the fluorescence of the corresponding substance (FIG. 5).

As a result, the enzyme activity of free idursulfase and idursulfase-10 K PEG-Fc-BTP22 were shown to be 23.4±1.94 nmol/min/μg and 10.8±1.39 nmol/min/μg, respectively. In particular, the values of enzyme activity were calculated in terms of specific activity per converted rate of weight (μg). That is, in the case of free idursulfase, the value was obtained by dividing the number of enzyme reactions by weight, and in the case of idursulfase-10 K PEG-Fc-BTP22, the value was obtained by dividing the number of enzyme reactions by the converted rate of weight possessed by the idursulfase part within the conjugate. Conclusively, the enzyme activity of idursulfase-10 K PEG-Fc-BTP22 was 46.6% and reduced slightly in part, compared to that of idursulfase. However, it was confirmed that even when the enzyme was prepared as the long-acting conjugate for brain targeting of the present invention, a significant enzyme activity was observed in the corresponding conjugate.

Example 18: Preparation of Expression Vector for Fusion Proteins in which Immunoglobulin Fc Region and Peptide for Brain Targeting are Linked

Fusion proteins were synthesized by linking the IgG4 Fc regions, which include a hinge region, and the peptides for brain targeting by a peptide linker or by a method of direct fusion, and specifically, by linking the IgG4 Fc regions, which include a hinge region, and the peptides for brain targeting by a peptide bond (synthesized by Bioneer Corporation, Korea) (Table 7). As can be seen in the sequences of Table 7 below, the fusion proteins containing the IgG4 Fc regions, which have the sequences of Table 7 below and include a hinge region, and the peptides for brain targeting were prepared by linking the N-terminus of the peptides for brain targeting to the C-terminus of an IgG4 Fc region using a linker or by a method of direct fusion.

TABLE 7

Sequence
SEQ ID NO

Fc-BTP28
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP17)

Hinge

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGT
12

CH2
CTTCCTGTTCCCCCCAAAACCCAAGGACA

CCCTCATGATCTCCCGGACCCCTGAGGTC

ACATGCGTGGTGGTGGACGTGAGCCAGGA

AGACCCTGAGGTCCAGTTCAACTGGTACG

TGGACGGCGTGGAGGTGCATAATGCCAAG

ACAAAGCCGCGGGAGGAGCAGTTCAACA

GCACGTACCGTGTGGTCAGCGTCCTCACC

GTCCTGCACCAGGACTGGCTGAATGGCAA

GGAGTACAAGTGCAAGGTCTCCAACAAA

GGCCTCCCATCCTCCATCGAGAAAACCAT

CTCCAAAGCCAAA

IgG4CH3
GGGCAGCCCCGAGAACCACAGGTGTACA
13

CCCTGCCCCCATCCCAGGAGGAGATGACC

AAGAACCAGGTCAGCCTGACCTGCCTGGT

CAAAGGCTTCTATCCCAGCGACATCGCCG

TGGAGTGGGAGAGCAATGGGCAGCCGGA

GAACAACTACAAGACCACGCCTCCCGTGC

TGGACTCCGACGGCTCCTTCTTCCTCTACA

GCAGGCTAACCGTGGACAAGAGCAGGTG

GCAGGAGGGGAACGTCTTCTCATGCTCCG

TGATGCATGAGGCTCTGCACAACCACTAC

ACGCAGAAGAGCCTCTCCCTGTCTCTGGG

TAAA

BTP17
AAGCTGGTGTTCTTTGCAGAAGAT
84

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCV
15

CH2
VVDVSQEDPEVQFNWYVDGVEVHNAKTKP

REEQFNSTYRVVSVLTVLHQDWLNGKEYK

CKVSNKGLPSSIEKTISKAK

IgG4CH3
GQPREPQVYTLPPSQEEMTKNQVSLTCLVK
16

GFYPSDIAVEWESNGQPENNYKTTPPVLDS

DGSFFLYSRLTVDKSRWQEGNVFSCSVMHE

ALHNHYTQKSLSLSLGK

BTP17
KLVFFAED
85

Example 19: Confirmation of Brain Distribution of Fusion Proteins in which Immunoglobulin Fc Region and Peptide for Brain Targeting are Linked

A brain distribution test was performed in mice to determine the level of blood-brain barrier (BBB) passage of fusion proteins in which an immunoglobulin Fc region and a peptide for brain targeting are linked. The mice were intravenously injected at a dose of 10 mg/kg. After 2 hours, the mice's brains were separated and the concentration of the fusion proteins in which the immunoglobulin Fc region and the peptide for brain targeting are linked was measured to determine the level of blood-brain barrier passage (FIG. 6).

Example 20: Preparation of Iduronate-2-sulfatase-Fc-BTP Fusion Protein

(1) Preparation of Expression Vector for Iduronate-2-sulfatase-Fc-BTP Fusion Protein

In order to produce enzyme fusion proteins, an expression vector for fusion proteins was constructed by overlapping PCR using the expression vector (IDS cDNA, Cat No. EX-00003-M02, Gencopoeia) into which native iduronate-2-sulfatase (IDS, SEQ ID NO: 102) is introduced, the synthesized linker (SEQ ID NO: 17), and the IgG4 Fc regions (SEQ ID NOS: 11, 12, and 13). The overlapping PCR technique includes sequences overlapping each other in a primer when PCR-amplifying each enzyme and linker-Fc, and thus the resulting PCR products contain overlapping sequences. In order to amplify the fusion proteins, the primary PCR was performed 25 times at 95° C. for 1 minute, 57° C. for 30 seconds, and 68° C. for 3 minutes; and the secondary PCR was performed 25 times at 95° C. for 1 minute, 57° C. for 30 seconds, and 68° C. for 4 minutes.

Specifically, the IDS was subjected to PCR using the primers of SEQ ID NO NOS: 86 and 87, and the linker-Fc was subjected to PCR using the primers of SEQ ID NOS: 88 and 89, whereby the PCR product of the IDS contained the linker-Fc sequence at 3′ and the PCR product of the linker-Fc contained the IDS sequence at 5′.

The secondary PCR was carried out with the two PCR products, which had been obtained from the primary PCR, as a template using the primers of SEQ ID NOS: 86 and 89, and then a PCR product having the sequence of IDS-Fc was obtained. Thereafter, the overlapping sequence was cleaved with KpnI and XhoI restriction enzymes, and the thus-obtained PCR product was inserted into the XOGC vector to construct a vector expressing the IDS-Fc fusion protein (pX0GC-enzyme-Fc).

TABLE 8

Overlapping PCR Primer

Sequence
SEQ ID NO

IDS-F (KpnI)
5′-CAGGTACCATGCCGCCACCCCGGACC-3′
86

IDS-R (overlap)
5′-TGAACCGCCTCCACCAGGCATCAACAACTGGAA
87

AAGATCTCCAC-3′

L15Fc(IDS)-F
5′-cagttgttgatgcctGGTGGAGGCGGTTCAGGCG-3′
88

L15Fc-R (XhoI)
5′-GACTCGAGTCATTTACCCAGAGACAGGGAGAGG-
89

3′

A site-directed mutagenesis PCR technique was used to remove chain exchange and N-glycosylation sites in the Fc regions of the established fusion protein sequences. Specifically, serine, which is the 2^ndamino acid of the Fc region involved in the chain exchange, was replaced with proline using the primers of SEQ ID NOS: 90 and 91, and asparagine, which is the 71^stamino acid in the Fc regions where N-glycosylation takes place, was replaced with glutamine using the primers of SEQ ID NOS: 92 and 93.

TABLE 9

Mutagenesis primer

Primer
Sequence
SEQ ID NO

Fc(S2P)_F
5′-CTGGCGGTGGCGGATCGCCACCATGCCCAGCACCTGAG
90

TTCCT-3′

Fc(S2P)_R
5′-AGGAACTCAGGTGCTGGGCATGGTGGCGATCCGCCACC
91

GCCAG-3′

Fc(N71Q)_F
5′-AGCCGCGGGAGGAGCAGTTCCAAAGCACGTACCGTGTG
92

GTCAG-3′

Fc(N71Q)_R
5′-CTGACCACACGGTACGTGCTTTGGAACTGCTCCTCCCGC
93

GGCT-3′

A site-directed mutagenesis PCR technique was used in order to insert the BTP sequence into the IDS-Fc fusion protein in which chain exchange and N-glycosylation sites are removed from the Fc region. Specifically, the primary PCR was carried out to insert the BTP5 sequence of Fc-BTP22 by using the primers of SEQ ID NOS: 94 and 95, and as a result, it was confirmed that the BTP5 sequence was inserted into the C-terminus of the Fc region. Thereafter, the secondary PCR was carried out to insert the linker and BTP5 sequence by using the primers of SEQ ID NOS: 96 and 97.

The primary and secondary PCRs were carried out to construct a vector expressing the IDS-Fc-BTP22 fusion protein in the XOGC vector.

TABLE 10

BTP22 insertion primer

Primer
Sequence
SEQ ID NO

BTP5_F
5′-TCTCCCTGTCTCTGGGTAAACTGCGTAAACTGCGCAAAC
94

GTCTGTTACTGCGTAAACTGCGCAAACGTCTGTTATAAGG

ATCCgaattcgagctccG-3′

BTP5_R
5′-CGGAGCTCGAATTCGGATCCTTATAACAGACGTTTGCG
95

CAGTTTACGCAGTAACAGACGTTTGCGCAGTTTACGCAGT

TTACCCAGAGACAGGGAGA-3′

L-BTP5_F
5′-TCTCCCTGTCTCTGGGTAAAGGTGGAGGCGGTTCACTTC
96

GCAAGTTACGTAAACGCTTACTGTTACGTAAACTTCGGAA

GCGCTTACTGGGCGGAGGTGGCTCTCTGCGTAAACTGCGC

AAACG-3′

L-BTP5_R
5′-CGTTTGCGCAGTTTACGCAGAGAGCCACCTCCGCCCAG
97

TAAGCGCTTCCGAAGTTTACGTAACAGTAAGCGTTTACGT

AACTTGCGAAGTGAACCGCCTCCACCTTTACCCAGAGACA

GGGAGA-3′

The vector for expressing the enzyme fusion protein prepared in the above Example was named pX0GC-IDS-Fc-BTP22 vector and has the following sequence (Table 11).

TABLE 1

Sequence
SEQ ID NO

IDS-Fc-
DNA
IDS
ATGCCGCCACCCCGGACCGGCCGAGGCCTTCTCTGGCTGGGT
98

BTP22

CTGGTTCTGAGCTCCGTCTGCGTCGCCCTCGGATCCGAAACGC

(BTP5

AGGCCAACTCGACCACAGATGCTCTGAACGTTCTTCTCATCATC

2x)

GTGGATGACCTGCGCCCCTCCCTGGGCTGTTATGGGGATAAGC

TGGTGAGGTCCCCAAATATTGACCAACTGGCATCCCACAGCCTC

CTCTTCCAGAATGCCTTTGCGCA6CAAGCAGTGTGCGCCCCGA

GCCGCGTTTCTTTCCTCACTGGCAGGAGACCTGACACCACCCG

CCTGTACGACTTCAACTCCTACTGGAGGGTGCACGCTGGAAACT

TCTCCACCATCCCCCAGTACTTCAAGGAGAATGGCTATGTGACC

ATGTCGGTGGGAAAAGTCTTTCACCCTGGGATATCTTCTAACCA

TACCGATGATTCTCCGTATAGCTGGTCTTTTCCACCTTATCATCC

TTCCTCTGAGAAGTATGAAAACACTAAGACATGTCGAGGGCCAG

ATGGAGAACTCCATGCCAACCTGCTTTGCCCTGTGGATGTGCTG

GATGTTCCCGAGGGCACCTTGCCTGACAAACAGAGCACTGAGC

AAGCCATACAGTTGTTGGAAAAGATGAAAACGTCAGCCAGTCCT

TTCTTCCTGGCCGTTGGGTATCATAAGCCACACATCCCCTTCAG

ATACCCCAAGGAATTTCAGAAGTTGTATCCCTTGGAGAACATCA

CCCTGGCCCCCGATCCCGAGGTCCCTGATGGCCTACCCCCTGT

GGCCTACAACCCCTGGATGGACATCAGGCAACGGGAAGACGTC

CAAGCCTTAAACATCAGTGTGCCGTATGGTCCAATTCCTGTGGA

CTTTCAGCGGAAAATCCGCCAGAGCTACTTTGCCTCTGTGTCAT

ATTTGGATACACAGGTCGGCCGCCTCTTGAGTGCTTTGGACGAT

CTTCAGCTGGCCAACAGCACCATCATTGCATTTACCTCGGATCA

TGGGTGGGCTCTAGGTGAACATGGAGAATGGGCCAAATACAGC

AATTTTGATGTTGCTACCCATGTTCCCCTGATATTCTATGTTCCT

GGAAGGACGGCTTCACTTCCGGAGGCAGGCGAGAAGCTTTTCC

CTTACCTCGACCCTTTTGATTCCGCCTCACAGTTGATGGAGCCA

GGCAGGCAATCCATGGACCTTGTGGAACTTGTGTCTCTTTTTCC

CACGCTGGCTGGACTTGCAGGACTGCAGGTTCCACCTCGCTGC

CCCGTTCCTTCATTTCACGTTGAGCTGTGCAGAGAAGGCAAGAA

CCTTCTGAAGCATTTTCGATTCCGTGACTTGGAAGAGGATCCGT

ACCTCCCTGGTAATCCCCGTGAACTGATTGCCTATAGCCAGTAT

CCCCGGCCTTCAGACATCCCTCAGTGGAATTCTGACAAGCCGA

GTTTAAAAGATATAAAGATCATGGGCTATTCCATACGCACCATAG

ACTATAGGTATACTGTGTGGGTTGGCTTCAATCCTGATGAATTTC

TAGCTAACTTTTCTGACATCCATGCAGGGGAACTGTATTTTGTGG

ATTCTGACCCATTGCAGGATCACAATATGTATAATGATTCCCAAG

GTGGAGATCTTTTCCAGTTGTTGATGCCT

Linker
GGTGGAGGCGGUCAGGCGGAGGTGGCTCTGGCGGTGGCGGA
17

TCG

Ig34
CCACCATGCCCA
99

Hinge

IgG4
GCACCTGAGTTCCTGGGCCATCAGTCTTCCTGTTCCCCC
100

CH2
CAAAACCCAAGGACACCCTCATGATCTCCCGGACCCCTGAGGT

CACATGCGTGGTGGTGGACGTGAGCCAGGAAGACCCTGAGGTC

CAGTTCAACTGGTACGTGGACGGCGTGGAGGTGCATAATGCCA

AGACAAAGCCGCGGGAGGAGCAGTTCCAAAGCACGTACCGTGT

GGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGGC

AAGGAGTACAAGTGCAAGGTCTCCAACAAAGGCCTCCCATCCTC

CATCGAGAAAACCATCTCCAAAGCCAAA

IgG4
AGCCCCGAGAACCACAGGTGTACACCCTGCCCCCATCCC
13

CH3
AGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTGCCTGGT

CAAAGGCTTCTATCCCAGCGACATCGCCGTGGAGTGGGAGAGC

AATGGGCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGC

TGGACTCCGACGGCTCCTTCTTCCTCTACAGCAGGCTAACCGTG

GACAAGAGCAGGTGGCAGGAGGGGAACGTCTTCTCATGCTCCG

TGATGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCT

CTCCCTGTCTCTGGGTAAA

Linker
GGTGGAGGCGGTTCA
73

BTP5
CTTCGCAAGTTACGTAAACGCTTACTGTTACGTAAACTTCGGAA
74

GCGCTTACTG

Linker
GGCGGAGGTGGCTCT
75

BTP5
CTGCGTAAACTGCGCAAACGTCTGTTACTGCGTAAACTGCGCAA
101

ACGTCTGTTA

Protein
IDS
MPPPRTGRGLLWLGLVLSSVCVALGSETQANSTTDALNVLLIIVDDL
102

RPSLGCYGDKLVRSPNIDQLASHSLLFQNAFAQQAVCAPSRVSFLT

GRRPDTTRLYDFNSYWRVHAGNFSTIPQYFKENGYVTMSVGKVFH

PGISSNHTDDSPYSWSFPPYHPSSEKYENTKTCRGPDGELHANLL

CPVDVLDVPEGTLPDKQSTEQAIQLLEKMKTSASPFFLAVGYHKPH

IPFRYPKEFQK

LYPLENITLAPDPEVPDGLPPVAYNPWMDIRQREDVQALNISVPYG

PIPVDFQRKIRQSYFASVSYLDTQVGRLLSALDDLQLANSTIIAFTSD

HGWALGEHGEWAKYSNFDVATHPLIFYVPGRTASLPEAGEKLFP

YLDPFDSASQLMEPGRQSMDLVELVSLFPTLAGLAGLQVPPRCPV

PSFHVELCREGKNLLKHFRFRDLEEDPYLPGNPRELIAYSQYPRPS

DIPQWNSKDP

SLKDIKIMGYSIRTIDYRYTVWVGFNPDEFLANFSDIHAGELYFVDSD

PLQDHNMYNDSQGGDLFQLLMP

Linker
GGGGSGGGGSGGGGS
18

IgG4
PPCP
103

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSQEDPEVQFN
104

CH2
WYVDGVEVHNAKTKPREEQFQSTYRVVSVLTVLHQDWLNGKEYK

CKVSNKGLPSSIEKTISKAK

IgG4
GQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSDIAVEWESNG
16

CH3
QPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVFSCSVMHE

ALHNHYTQKSLSLSLGK

Linker
GGGGS
76

BTP5
LRKLRKRLLLRKLRKRLL
10

Linker
GGGGS
76

BTP5
LRKLRKRLLLRKIRKRLL
10

(2) Preparation of Transformed CHO Cell Line for Iduronate 2-sulfatase-Fc-BTP22 Fusion Protein

The recombinant expression vector pX0GC-IDS-Fc-BTP22, which was prepared in the above, was introduced into a DG44/CHO cell line (CHO/dhfr-) (purchased from Dr. Chasin of Columbia University), in which the nucleic acid biosynthetic process is incomplete due to the damage to the DHFR gene, to obtain a transformant. Thereafter, the iduronate 2-sulfatase-Fc-BTP22 fusion protein was expressed from the transformant.

Specifically, the DG44/CHO cell line was cultured enough to cover about 80% to 90% of the bottom of the culture container, and then the cells were washed three times with Opti-MEM (Lifetechnology, Cat. No. 51985034).

Meanwhile, a mixture of Opti-MEM (3 mL) and the expression vector pX0GC-IDS-Fc-BTP22 (5 μg), and a mixture of Opti-MEM (3 mL) and lipofectamine (20 μL; Lifetechnology, Cat. No. 18324-012) were each allowed to stand at room temperature for 30 minutes. Thereafter, each of the mixtures was mixed, added to the cultured DG44/CHO cell line, and then cultured under the conditions of 37° C. and 5% CO₂for about 18 hours, so that the expression vector pXOGC-IDS-Fc-BTP22 was introduced into the DG44/CHO cell line. Further, the cultured cells were washed three times with a DMEM-F12 (Lifetechnology, Cat. No. 11330) medium containing 10% FBS, and then the medium was added thereto and cultured again for 48 hours. The cultured cells were treated with trypsin to separate each of the cultured cells, and these were inoculated into a selective medium (a MEM-α medium (WELGENE, Cat. No. LM008-02) containing no Hypoxanthine-Thymidine (HT) supplement and containing 10% FBS and 1 mg/mL of G418 (Cellgro, Cat. No. 61-234-RG)). The selective medium was cultured while exchanging it every 2 or 3 days until only the transformed cells survived to form colonies, and then the transformed cells were selected from the separated cells. In particular, in order to improve the expression level of the iduronate 2-sulfatase-Fc-BTP22 conjugate in the selected transformed cells, 5 nM MTX (Sigma, Cat. No. M8407) was added to the selective medium to gradually increase the concentration, and then the MTX content was increased to 20 nM after 2 to 3 weeks.

In addition, in order to reduce the heterogeneity of the transformed cells, a limiting dilution method was carried out to secure a monoclone. Specifically, the transformed cells diluted to a ratio of 0.7 cells per well were each dispersed in a 96-well plate, and then cultured for 2 to 3 weeks to determine whether a monoclone appeared. When the wells in which a monoclone formed a cluster were detected, the monoclone was transferred to a 24-well plate, and the cell growth rate of each clone and the expression amount of the idursulfase derivative were analyzed by an ELISA method to select the clones having the most excellent expression amount of the idursulfase derivative. Thereafter, the selected cell line was adapted to suspension culture using a serum-free medium (EX-CELL CHO medium; USA, Sigma, Cat. No. 63289C).

(3) Production of Recombinant Protein Using Transformed Iduronate 2-sulfatase-Fc-BTP22/CHO

The expression cell line 1 vial (1×10⁷cells/mL) of the iduronate 2-sulfatase-Fc-BTP22 conjugate, which had been adapted to the suspension culture after being selected from (2) above and stored in a liquid nitrogen tank, was taken out, and was dissolved as quickly as possible in a 37° C. constant-temperature water bath. Thereafter, the resultants were washed once with a seed culture medium (EX-CELL CHO medium (Sigma, Cat. No. 63289C) supplemented with glutamine (0.45 g/L)), centrifuged at 90×g for 5 minutes, and then inoculated into an Erlenmeyer flask (USA, Corning, Cat. No. 431144)) containing 50 mL of the seed culture medium. The resultants were cultured for 1 to 2 days in a CO₂incubator (37° C., 5% CO₂) until the cell concentration reached 10×10⁵cells/mL. Then, the resultants were subcultured in a new Erlenmeyer flask containing a fresh seed culture medium (100 mL) by centrifuging in the same manner as above. Subculture was carried out while increasing the culture volume by 2 times until a sufficient number of cells were obtained using the same method above. When a sufficient number of cells were obtained, the production cells grown in the Erlenmeyer flask were transferred and cultured in a 5 L standard bioreactor (Sartorious, model: biostat). When the concentration of a target cell reached 10×10⁶cells/mL, sodium butyrate (Sigma, Cat No. 58903C) was added to the culture medium, and then incubated at a temperature of 33° C. for 10 days or more. When the culture was completed, the culture medium was centrifuged at 3,000×g for 60 minutes to separate the cells and supernatant. The supernatant was filtered and stored frozen at −20° C.

(4) Purification of Iduronate 2-sulfatase-Fc-BTP Fusion Protein

The culture medium sample cultured in (3) above was conjugated to a column of rProtein A sepharose fast flow (GE Healthcare, USA) equilibrated with 20 mM Tris (pH 7.5) and glycerol buffer, and was eluted using a buffer composed of 0.1 M sodium citrate (pH 3.0 to 4.0), sodium chloride, and glycerol. The eluted sample was applied to Source 15ISO (GE Healthcare, USA) using a concentration gradient of ammonium sulfate and Tris (pH 7.5), and then iduronate 2-sulfatase-Fc-BTP22, which is a recombinant protein, was purified. The purified recombinant protein (i.e., iduronate 2-sulfatase-Fc-BTP22) was confirmed by SDS-PAGE, and the result thereof is shown in FIG. 7.

Example 21: Preparation of Iduronate 2-sulfatase-10 kDa PEG-Fc-BTP28 Conjugate

In order to pegylate 10 K propion-ALD(2) PEG (10 K PEG having one propionaldehyde group at each terminus; NOF, Japan) to the N-terminus of iduronate 2-sulfatase (Shire, Ireland), the reaction was carried out at 2° C. to 8° C. for about 1 to 2 hours at a molar ratio of iduronate 2-sulfatase to PEG (i.e., 1:10 to 20) and at the iduronate 2-sulfatase concentration of 10 mg/mL to 20 mg/mL. In particular, the reaction was carried out by adding a sodium cyanoborohydride (NaCNBH₃) reducing agent at a concentration of 20 mM to a 0.1 M potassium phosphate buffer (pH 6.0). The mono-PEGylated idursulfase-10 K PEG was purified by a Source 15Q column (GE Healthcare, USA) using a concentration gradient of sodium phosphate (pH 6.0) and sodium chloride as the reaction solution.

Next, the reaction was carried out at 2° C. to 8° C. for 16 hours using the molar ratio of the purified mono-PEGylated idursulfase to immunoglobulin Fc-BTP28 (i.e., 1:10 to 15) and the total protein concentration of 10 mg/mL to 20 mg/mL. In particular, 0.1 M potassium phosphate (pH 6.0) and 20 mM sodium cyanoborohydride were added as a reaction solution and a reducing agent, respectively.

After completion of the reaction, the reaction solution was applied to a Source 15Q column (GE Healthcare, USA) using a concentration gradient of a sodium phosphate buffer (pH 5.6) and sodium chloride, and applied to Source 151S0 (GE Healthcare, USA) using a concentration gradient of ammonium sulfate and sodium phosphate (pH 6.0) to prepare the iduronate 2-sulfatase-10 kDa PEG-Fc-BTP28 conjugate (it can be used interchangeably with the term “iduronate 2-sulfatase-Fc-BTP28 conjugate”). The result thereof confirmed by SDS-PAGE is shown in FIG. 8.

Example 22: Confirmation of In Vitro Enzyme Activity of Iduronate 2-sulfatase-Fc-BTP22 Fusion Protein and Iduronate 2-sulfatase-10 kDa PEG-Fc-BTP28 Conjugate

In order to measure the change in enzyme activity according to preparation of the iduronate 2-sulfatase-Fc-BTP22 fusion protein, which was prepared according to Example 20, and the iduronate 2-sulfatase-Fc-BTP28 conjugate, which was prepared according to Example 21, measurement of in vitro test-tube enzyme activity was performed. 4MU-α-IdopyraA-2 (4-methylumbelliferyl α-L-idopyranosiduronic acid-2-sulfate sodium salt), which is known as an enzyme substrate of iduronate 2-sulfatase, was reacted with the iduronate 2-sulfatase-Fc-BTP22 fusion protein and iduronate 2-sulfatase-Fc-BTP28 conjugate at 37° C. for 4 hours, and then reacted again with α-iduronidase (i.e., an enzyme for secondary reaction) at 37° C. for 24 hours. The enzyme activity for the corresponding material was measured by measuring the fluorescence of 4-methylumbelliferone (4MU) finally produced (FIG. 9).

As a result, it was confirmed that the enzyme activity (specific activity) of the iduronate 2-sulfatase-Fc-BTP22 fusion protein and that of the iduronate 2-sulfatase-Fc-BTP28 conjugate were 45.0±11.4 nmol/min/μg and 41.2±1.2 nmol/min/μg, respectively. Consequently, the enzyme activities of the iduronate 2-sulfatase-Fc-BTP22 fusion protein and iduronate 2-sulfatase-Fc-BTP28 conjugate were 95.5% and 87.4%, respectively, compared to that of iduronate 2-sulfatase; and thus it was confirmed that similar levels of the enzyme activities were exhibited even after preparation of the long-acting conjugate for brain targeting and the fusion protein.

Example 23: Confirmation of Brain Tissue Distribution of Iduronate 2-sulfatase-Fc-BTP22 Fusion Protein

In order to determine the level of passage of the iduronate 2-sulfatase-Fc-BTP22 fusion protein, which was prepared according to Example 20, through the blood-brain barrier (BBB), a brain distribution experiment was carried out in normal mice. Normal mice were intravenously injected at a dose of 6.58 nmol/kg. After 1 hour, the mice's brains were separated, and the concentration of each conjugate protein was measured to determine the level of passage of the protein through the BBB (FIG. 10). As a result, the level of passage of the long-acting iduronate 2-sulfatase-Fc-BTP22 fusion protein for brain targeting through the BBB was measured at a higher concentration in the brain compared to that of native iduronate 2-sulfatase; that is the long-acting iduronate 2-sulfatase-Fc-BTP22 fusion protein for brain targeting showed a higher passage level.

Example 24: In Vivo Efficacy Experiment According to Administration of Iduronate 2-sulfatase-Fc-BTP22 Fusion Protein and Iduronate 2-sulfatase-10 kDa PEG-Fc-BTP28 Conjugate in Mice in which Iduronate 2-sulfatase is Knocked-Out

In order to confirm the efficacy according to administration of the iduronate 2-sulfatase-Fc-BTP22 fusion protein, which was prepared according to Example 20, and the iduronate 2-sulfatase-Fc-BTP28 conjugate, which was prepared according to Example 21, mice were prepared in 7 groups.

In the first group of wild-type (WT) mice (n=4), a long-acting iduronate 2-sulfatase excipient for brain targeting was administered. Further, from the second group, mice in which iduronate 2-sulfatase is knocked-out were used as an experimental group. In Group 2, a long-acting iduronate 2-sulfatase excipient for brain targeting was administered; in Group 3, iduronate 2-sulfatase (0.5 mg/kg) was administered intravenously once a week; in Group 4, an iduronate 2-sulfatase-Fc-BTP22 fusion protein (2 mg/kg) was administered intravenously once every two weeks; in Group 5, an iduronate 2-sulfatase-Fc-BTP22 fusion protein (4 mg/kg) was administered subcutaneously once every two weeks; in Group 6, an iduronate 2-sulfatase-Fc-BTP28 conjugate (2 mg/kg) was administered intravenously once every two weeks; and in Group 7, an iduronate 2-sulfatase-Fc-BTP28 conjugate (4 mg/kg) was administered subcutaneously once every two weeks. While the experiment was being conducted, urine was collected before and after the administration at intervals of one week, the content of glycosaminoglycan (GAG) was measured, and the content of creatinine was measured, thereby the GAG content was corrected. For measurement of the GAG content, a urine sample (50 μL) was placed in a 96-well plate, and a dimethylmethylene blue solution (250 μL) was added thereto and then mixed. Thereafter, GAG was quantified at 525 nm by an ELISA reader, and then the resultants were compared to each other. Statistical processing was performed using a one-way ANOVA to compare the excipient groups (control groups) and the experimental group.

As a result of measuring the GAG content, as shown in FIG. 11, it was confirmed that in the groups in which iduronate 2-sulfatase-Fc-BTP22 fusion protein and iduronate 2-sulfatase-Fc-BTP28 conjugate are administered, the amount of GAG reduction in the urine was maintained at the level of the GAG content in normal mice after two weeks of the administration. The above results suggest that the long-acting iduronate 2-sulfatase-Fc-BTP22 fusion protein and iduronate 2-sulfatase-Fc-BTP28 conjugate for brain targeting could have a therapeutic effect on Hunter's syndrome, which is caused by the accumulation of GAG as GAG is not degraded.

Example 25: Preparation of Fusion Protein in which Two or More Peptides for Brain Targeting, which are Different from Each Other, and Immunoglobulin Fc Region are Linked

(1) Preparation of Expression Vector for Fusion Protein in which Two or More Peptides for Brain Targeting, which are Different from Each Other, and Immunoglobulin Fc Region are Linked

In order to express additional fusion proteins, expression vectors were prepared as follows. As the biocompatible material capable of increasing the half-life of a physiologically active polypeptide linked thereto, IgG4 Fc regions including a hinge region were selected, and the IgG4 Fc regions including a hinge region and two or more peptides for brain targeting, which are different from each other, were fused at a gene level, and each of the fusion products was inserted into respective expression vectors.

Fusion proteins were prepared by linking the IgG4 Fc regions, which include a hinge region, to two or more peptides for brain targeting, which are different from each other, or by a method of direct fusion; specifically, fusion proteins having the sequences in Table 13, in which the IgG4 Fc regions, which include a hinge region, is linked to two or more peptides for brain targeting at the direction of the C-terminus of the Fc CH3 regions thereof by a peptide bond, were prepared using the primers shown in Table 12. Specifically, in order to insert the BTP16 sequence and linker into the Fc-BTP28 expression vector, a site-mutagenesis PCR technique was utilized to prepare Fc-BTP29 using the primers of SEQ ID NOS: 107 and 108, and to prepare Fc-BTP30 using the primers of SEQ ID NOS: 109 and 110. As shown in the sequences of Table 13 below, fusion proteins in which the immunoglobulin Fc region and peptides for brain targeting are linked were prepared by linking the N-terminus of two or more peptides for brain targeting to the C-terminus of the IgG4 Fc region by a peptide linker, or by a method of direct fusion.

TABLE 12

BTP29 & 30 insertion primer

Primer
Sequence
SEQ ID NO

BTP29_F
5′-AAACCCCGAAAGTTCGTGTGGGCGGAGGTGGCTCTAA
107

GCTGGTGTTCTTTGCAGAAGATTGAGGATCCgaattcgagct-3′

BTP29_R
5′-AGCTCGAATTCGGATCCTCAATCTTCTGCAAAGAACA
108

CCAGCTTAGAGCCACCTCCGCCCACACGAACTTTCGGGG

TTT-3′

BTP30_F
5′-TGGTGTTCTTTGCAGAAGATGGCGGAGGTGGCTCTAA
109

GTGGAAAACCCCGAAAGTTCGTGTGTAAGGATCCgaattcga

gct-3′

BTP30_R
5′-AGCTCGAATTCGGATCCTTACACACGAACTTTCGGGGT
110

TTTCCACTTAGAGCCACCTCCGCCATCTTCTGCAAAGAA

CACCA-3′

TABLE 13

Sequence
SEQ ID NO

Fc-BTP29
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP16 +

Hinge

BTP17)

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGT
12

CH2
CTTCCTGTTCCCCCCAAAACCCAAGGACA

CCCTCATGATCTCCCGGACCCCTGAGGTC

ACATGCGTGGTGGTGGACGTGAGCCAGGA

AGACCCTGAGGTCCAGTTCAACTGGTACG

TGGACGGCGTGGAGGTGCATAATGCCAAG

ACAAAGCCGCGGGAGGAGCAGTTCAACA

GCACGTACCGTGTGGTCAGCGTCCTCACC

GTCCTGCACCAGGACTGGCTGAATGGCAA

GGAGTACAAGTGCAAGGTCTCCAACAAA

GGCCTCCCATCCTCCATCGAGAAAACCAT

CTCCAAAGCCAAA

IgG4CH3
GGGCAGCCCCGAGAACCACAGGTGTACA
13

CCCTGCCCCCATCCCAGGAGGAGATGACC

AAGAACCAGGTCAGCCTGACCTGCCTGGT

CAAAGGCTTCTATCCCAGCGACATCGCCG

TGGAGTGGGAGAGCAATGGGCAGCCGGA

GAACAACTACAAGACCACGCCTCCCGTGC

TGGACTCCGACGGCTCCTTCTTCCTCTACA

GCAGGCTAACCGTGGACAAGAGCAGGTG

GCAGGAGGGGAACGTCTTCTCATGCTCCG

TGATGCATGAGGCTCTGCACAACCACTAC

ACGCAGAAGAGCCTCTCCCTGTCTCTGGG

TAAA

BTP16
AAGTGGAAAACCCCGAAAGTTCGTGTG
82

Linker
GGCGGAGGTGGCTCT
75

BTP17
AAGCTGGTGTTCTTTGCAGAAGAT
84

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCV
15

CH2
VVDVSQEDPEVQFNWYVDGVEVHNAKTKP

REEQFNSTYRVVSVLTVLHQDWLNGKEYK

CKVSNKGLPSSIEKTISKAK

IgG4CH3
GQPREPQVYTLPPSQEEMTKNQVSLTCLVK
16

GFYPSDIAVEWESNGQPENNYKTTPPVLDS

DGSFFLYSRLTVDKSRWQEGNVFSCSVMHE

ALHNHYTQKSLSLSLGK

BTP16
KWKTPKVRV
40

Linker
GGGGS
76

BTP17
KLVFFAED
85

Fc-BTP30
DNA
IgG4
ATGCCATCATGCCCA
11

(BTP17 +

Hinge

BTP16)

IgG4
GCACCTGAGTTCCTGGGGGGACCATCAGT
12

CH2
CTTCCTGTTCCCCCCAAAACCCAAGGACA

CCCTCATGATCTCCCGGACCCCTGAGGTC

ACATGCGTGGTGGTGGACGTGAGCCAGGA

AGACCCTGAGGTCCAGTTCAACTGGTACG

TGGACGGCGTGGAGGTGCATAATGCCAAG

ACAAAGCCGCGGGAGGAGCAGTTCAACA

GCACGTACCGTGTGGTCAGCGTCCTCACC

GTCCTGCACCAGGACTGGCTGAATGGCAA

GGAGTACAAGTGCAAGGTCTCCAACAAA

GGCCTCCCATCCTCCATCGAGAAAACCAT

CTCCAAAGCCAAA

IgG4CH3
GGGCAGCCCCGAGAACCACAGGTGTACA
13

CCCTGCCCCCATCCCAGGAGGAGATGACC

AAGAACCAGGTCAGCCTGACCTGCCTGGT

CAAAGGCTTCTATCCCAGCGACATCGCCG

TGGAGTGGGAGAGCAATGGGCAGCCGGA

GAACAACTACAAGACCACGCCTCCCGTGC

TGGACTCCGACGGCTCCTTCTTCCTCTACA

GCAGGCTAACCGTGGACAAGAGCAGGTG

GCAGGAGGGGAACGTCTTCTCATGCTCCG

TGATGCATGAGGCTCTGCACAACCACTAC

ACGCAGAAGAGCCTCTCCCTGTCTCTGGG

TAAA

BTP17
AAGCTGGTGTTCTTTGCAGAAGAT
84

Linker
GGCGGAGGTGGCTCT
75

BTP16
AAGTGGAAAACCCCGAAAGTTCGTGTG
82

Protein
IgG4
PSCP
14

Hinge

IgG4
APEFLGGPSVFLFPPKPKDTLMISRTPEVTCV
15

CH2
VVDVSQEDPEVQFNWYVDGVEVHNAKTKP

REEQFNSTYRVVSVLTVLHQDWLNGKEYK

CKVSNKGLPSSIEKTISKAK

IgG4CH3
GQPREPQVYTLPPSQEEMTKNQVSLTCLVK
16

GFYPSDIAVEWESNGQPENNYKTTPPVLDS

DGSFFLYSRLTVDKSRWQEGNVFSCSVMHE

ALHNHYTQKSLSLSLGK

BTP17
KLVFFAED
85

Linker
GGGGS
76

BTP16
KWKTPKVRV
40

The expression vector, to which the gene encoding the peptide for brain targeting fused to the immunoglobulin Fc region was inserted, was inserted into the BL21 (DE3) strain and thereby the long-acting fusion protein, in which the immunoglobulin Fc region and the peptide for brain targeting were linked, was expressed.

(2) Purification of Fusion Protein in which Immunoglobulin Fc Region and Two or More Peptides for Brain Targeting, which are Different from Each Other, are Linked

In order to convert the fusion proteins, which is expressed in (1) above and in which the immunoglobulin Fc region and the peptides for brain targeting are fused, into a soluble form, the cells were disrupted and refolded. Cell pellets corresponding to each culture solution (200 mL) were resuspended in 200 mL of a lysis buffer (50 mM Tris (pH 9.0), 1 mM EDTA (pH 8.0), 0.2 M sodium chloride, and 0.5% Triton X-100). Cells were disrupted using a microfluidizer processor M-110EH (AC Technology Corp. Model M1475C) at a pressure of 15,000 psi. The disrupted cell lysates were centrifuged at 12,200×g at 4° C. for 30 minutes, the supernatants were discarded, and the cell lysates were resuspended in 200 mL of a wash buffer ((0.5% TritonX-100 and 20 mM Tris (pH 7.0)). The pellets were resuspended in 200 mL of a wash buffer (20 mM Tris (pH 7.0)) by centrifugation at 12,200×g at 4° C. for 30 minutes. Thereafter, the resultants were centrifuged using the same method above. The pellets were obtained, resuspended in 400 mL of a buffer (8 M urea, 20 mM Tris (pH 7.0), and 1 mM EDTA), and then stirred at room temperature for 3 hours. After 3 hours, the resultants were centrifuged at 12,200×g at 4° C. for 30 minutes. Then, the supernatants were obtained, and 0.5 mM cysteine was added thereto, followed by stirring at 37° C. for 30 minutes. For refolding of the fusion proteins in which the solubilized immunoglobulin Fc region and the peptides for brain targeting are fused, 600 mL of a buffer (0.11 mM cysteine, 0.5 M arginine, and 50 mM Tris (pH 9.5)) was slowly added thereto using a peristaltic pump, and then stirred at 4° C. for 36 hours. The immunoglobulin Fc region, in the fusion protein in which the immunoglobulin Fc region and peptides for brain targeting are fused, is expressed as a dimer.

The refolded samples were centrifuged at 12,200×g at 4° C. for 30 minutes. The supernatants were obtained, and then filtered using a filter (0.22 μm; Satorius). Thereafter, the pH of the samples was adjusted to pH 7.5 using 50% HCl. After conjugating the samples to a Protein A-sepharose column (GE Healthcare) equilibrated with a buffer (10 mM Tris (pH 7.0)), the conjugate proteins in which the immunoglobulin Fc region and peptides for brain targeting are fused were eluted using 100 mM sodium citrate (pH 3.3) and 10% glycerol buffer.

After inserting 0.6 M ammonium sulfate into the eluted samples, the samples into which 0.6 M ammonium sulfate was inserted were conjugated to a Phenyl FF column (GE Healthcare) equilibrated with a buffer (10 mM Tris (pH 7.5) and 0.6 M ammonium sulfate). Thereafter, the fusion proteins in which the immunoglobulin Fc region and peptide for brain targeting are fused were eluted with a linear concentration gradient of 10 column volumes to a concentration of 0% to 100% using a buffer (10 mM Tris (pH 7.5)).

Due to the peptide for brain targeting linked to an Fc region, the long-acting conjugate prepared above can pass through the blood-brain barrier, maintain the physiological activity of the linked physiologically active material, and thus can provide a long-acting conjugate with improved duration and stability thereby being capable of providing a platform for the development of novel therapeutic agents enabling passage through the BBB.

From the foregoing, a skilled person in the art to which the present invention pertains will be able to understand that the present invention may be embodied in other specific forms without modifying the technical concepts or essential characteristics of the present invention. In this regard, the exemplary embodiments disclosed herein are only for illustrative purposes and should not be construed as limiting the scope of the present invention. On the contrary, the present invention is intended to cover not only the exemplary embodiments but also various alternatives, modifications, equivalents, and other embodiments that may be included within the spirit and scope of the present invention as defined by the appended claims.

Number	Date	Country	Kind
10-2018-0037725	Mar 2018	KR	national
10-2018-0069887	Jun 2018	KR	national

LONG-ACTING PROTEIN CONJUGATES FOR BRAIN TARGETING, A PREPARATION METHOD THEREOF, AND A COMPOSITION COMPRISING THE SAME

Information

Publication Number

Date Filed

Date Published

Inventors

Original Assignees

CPC

International Classifications

Abstract

Description

Claims

Priority Claims (2)

PCT Information