Targetable vector particles

This invention relates to “targetable” vector particles. More particularly, this invention relates to vector particles which include a receptor binding region that binds to a receptor of a target cell of a human or non-human animal.

Vector particles are useful agents for introducing gene(s) or DNA (RNA) into a cell, such as a eukaryotic cell. The gene(s) is controlled by an appropriate promoter. Examples of vectors which may be employed to generate vector particles include prokaryotic vectors, such as bacterial vectors; eukaryotic vectors, including fungal vectors such as yeast vectors; and viral vectors such as DNA virus vectors, RNA virus vectors, and retroviral vectors. Retroviral vectors which have been employed for generating vector particles for introducing genes or DNA (RNA) into a cell include Moloney Murine Leukemia Virus, spleen necrosis virus, and vectors derived from retroviruses such as Rous Sarcoma Virus and Harvey Sarcoma Virus. The term “introducing” as used herein encompasses a variety of methods of transferring genes or DNA (RNA) into a cell, such methods including transformation, transduction, transfection, and infection.

Vector particles have been used for introducing DNA (RNA) into cells for gene therapy purposes. In general, such a procedure involves obtaining cells from a patient and using a vector particle to introduce desired DNA (RNA) into the cells and then providing the patient with the engineered cells for a therapeutic purpose. It would be desirable to provide alternative procedures for gene therapy. Such an alternative procedure would involve genetically engineering cells in vivo. In such a procedure, a vector particle which includes the desired DNA (RNA) would be administered directly to the target cells of a patient in vivo.

It is therefore an object of the present invention to provide gene therapy by introduction of a vector particle, such as, for example, a retroviral vector particle, directly into a desired target cell of a patient.

In accordance with an aspect of the present invention, there is provided a retroviral vector particle which includes a receptor binding region or ligand that binds to a receptor of a target cell. The receptor of the target cell is a receptor other than the amphotropic cell receptor.

Retroviruses have an envelope protein which contains a receptor binding region. Applicants have found that retroviruses can be made “targetable” to a specific type of cell if the receptor binding region of the retrovirus, which may be amphotropic, ecotropic, or xenotropic, among other types, is modified such that the receptor binding region of the envelope protein includes a receptor binding region which binds to a receptor of a target cell. For example, at least a portion of the receptor binding region of the envelope protein of the retrovirus is deleted and replaced with a receptor binding region or a ligand which binds to a receptor of a target cell. Thus, there is provided a retroviral vector wherein at least a portion of the DNA (RNA) which encodes the receptor binding region of the envelope protein of the retrovirus has been deleted and replaced with DNA (RNA) encoding a receptor binding region or a ligand which binds to a receptor of a target cell.

In one embodiment, the retrovirus is a murine leukemia virus.

The envelope of murine leukemia viruses includes a protein known as gp70. Such viruses can be made “targetable” to a specific type of cell if a portion of the gp70 protein is deleted and replaced with a receptor binding region or a ligand which binds to a receptor of a target cell. Thus, in a preferred embodiment, there is provided a retroviral vector wherein a portion, but not all, of the DNA (RNA) encoding gp70 protein has been deleted and replaced with DNA (RNA) encoding a receptor binding region or a ligand which binds to a receptor of a target cell.

In general, gp70 protein includes the following regions: (i) the secretory signal or “leader” sequence; (ii) the receptor binding domain; (iii) the hinge region; and (iv) the body portion. Preferably, at least a portion of the DNA (RNA) encoding the receptor binding domain of gp70 protein is deleted and replaced with DNA (RNA) encoding a receptor binding region or a ligand which binds to a receptor of a target cell. More preferably, DNA (RNA) encoding the entire receptor binding domain of gp70 protein is deleted and replaced with DNA (RNA) encoding a receptor binding region or a ligand which binds to a receptor of a target cell. In another embodiment, DNA. (RNA) encoding the entire receptor binding domain of gp70 protein, plus all or a portion of the DNA (RNA) encoding the hinge region of gp70 protein is deleted and replaced with DNA (RNA) encoding a receptor binding region or a ligand of a target cell.

The gp70 protein may be derived from an ecotropic murine leukemia virus, a xenotropic murine leukemia virus, or an amphotropic murine leukemia virus. Ecotropic gp70 (or eco gp70) (SEQ ID NO:1) is a protein having 469 amino acids, and is encoded by (SEQ ID:2). Amino acid residues 1-33 constitute the leader sequence; amino acid residues 34-263 constitute the receptor binding domain; amino acid residues 264-312 constitute the hinge region; and amino acid residues 313-469 constitute the body portion. Preferably, DNA (RNA) encoding at least a portion of the receptor binding region is removed and replaced with DNA (RNA) encoding a receptor binding region or a ligand which binds to a receptor of a target cell. More preferably, DNA (RNA) encoding some or all of amino acid residues 34 to 263 (i.e., the receptor binding domain) is removed and replaced with DNA (RNA) encoding a receptor binding region or a ligand which binds to a receptor of a target cell.

Xenotropic gp70 (or xeno gp70) (SEQ ID NO:3) has 443 amino acid residues and is encoded by (SEQ ID NO:4). Amino acid residues 1-30 constitute the leader sequence; amino acid residues 31-232 constitute the receptor binding domain; amino acid residues 233-286 constitute the hinge region; and amino acid residues 287-443 constitute the body portion. Preferably, DNA (RNA) encoding at least a portion of the receptor binding region is removed and replaced with DNA (RNA) encoding a receptor binding region or a ligand which binds to a receptor of a target cell. More preferably, DNA (RNA) encoding some or all of amino acid residues 31 to 232 is removed and replaced with DNA (RNA) encoding a receptor binding region or a ligand which binds to a receptor of a target cell.

Target cells to which the retroviral vector particle may bind include, but are not limited to, liver cells, T-cells, lymphocytes, endothelial cells, T4 helper cells, and macrophages. In one embodiment, the retroviral vector particle binds to a liver cell, and in particular to hepatocytes. To enable such binding, the retroviral vector particle contains a chimeric protein encoded by DNA (RNA) in which at least a portion of the DNA (RNA) encoding the receptor binding domain of gp70 protein is removed and is replaced with DNA (RNA) which encodes a protein which binds to an asialoglycoprotein receptor (or ASG-R) of hepatocytes.

Proteins which bind to the asialoglycoprotein receptor of liver cells include, but are not limited to, asialoglycoproteins such as, for example, alpha-1-acid glycoprotein (AGP), also known as orosomucoid, and asialofetuin. AGP is a natural high-affinity ligand for ASG-R. The asialoglycoprotein receptor, or ASG-R, is expressed only by hepatocytes. The receptor is present at about 3×10

5

copies per cell, and such receptors have a high affinity for asialoglycoproteins such as AGP. Thus, the engineering of retroviral vector particles to contain asialoglycoprotein in place of the natural receptor binding domain of gp70 generates retroviral vector particles which bind to the asialoglycoprotein receptor of hepatocytes, which provides for an efficient means of transferring genes of interest to liver cells.

Cell lines which generate retroviral vector particles that are capable of targeting the hepatocyte's asialoglycoprotein receptor without the removal of the particle's terminal sialic acid groups by neuraminidase treatment, can be developed by selection with the cytotoxic lectin, wheat germ agglutinin (WGA). Cell lines which express the retroviral proteins gag and pol become retroviral vector packaging cell lines after they are transfected with the plasmids encoding chimeric envelope genes. These cell lines express the corresponding chimeric gp 70 glycoproteins. Upon exposure to successively higher concentrations of WGA, the outgrowth of cells which synthesize glycoproteins that lack terminal sialic acid groups, is favored. (Stanley, et al.,

Somatic Cell Genetics,

Vol. 3, pgs. 391-405 (1977)). This selection permits the isolation of cells which synthesize oligosaccharides terminating in galactosyl sugar groups. Such cells will allow the construction of packaging cell lines that are capable of generating retroviral vector particles which target the asialoglycoprotein receptor. It is also possible to select subpopulations of packaging cells which have other distinct glycotypes, such cells yielding viral vectors that potentially are capable of targeting cells other than hepatocytes. Macrophages, for example, express unique, high-mannose receptors. The PHA-resistant subpopulation will have N-linked oligosaccharides which terminate in high-mannose groups (Stanley, et al.,

In Vitro,

Vol. 12, pgs. 208-215 (1976)). Therefore, such a cell population will be capable of producing viral vector particles capable of targeting macrophoges via this receptor. Cells with mutant glycotypes which synthesize other novel oligosaccharides after selection with other cytotoxic lectins may also prove to be useful in targeting vector particles to other cell types such as lymphocytes or endothelial cells.

In another embodiment, the receptor binding region is a receptor binding region of a human virus. In one embodiment, the receptor binding region of a human virus is a hepatitis B virus surface protein binding region, and the target cell is a liver cell.

In another embodiment, the receptor binding region of a human virus is the gp46 protein of HTLV-I virus, and the target cell is a T-cell.

In yet another embodiment, the receptor binding region of a human virus is the HIV gp120 CD4 binding region, and the target cell is a T4 helper cell.

In one embodiment, the retroviral vector may be of the LN series of vectors, as described in Bender, et al.,

J. Virol.,

Vol. 61, pgs. 1639-1649 (1987), and Miller, et al.,

Biotechniques,

Vol. 7, pgs. 98-990 (1989).

In another embodiment, the retroviral vector includes a multiple restriction enzyme site, or multiple cloning site. The multiple cloning site includes at least four cloning, or restriction enzyme sites, wherein at least two of the sites have an average frequency of appearance in eukaryotic genes of less than once in 10,000 base pairs; i.e., the restriction product has an average size of at least 10,000 base pairs.

In general, such restriction sites, also sometimes hereinafter referred to as “rare” sites, which have an average frequency of appearance in eukaryotic genes of less than once in 10,000 base pairs, contain a CG doublet within their recognition sequence, such doublet appearing particularly infrequently in the mammalian genome. Another measure of rarity or scarcity of a restriction enzyme site in mammals is its representation in mammalian viruses, such as SV40. In general, an enzyme whose recognition sequence is absent in SV40 may be a candidate for being a “rare” mammalian cutter.

Examples of restriction enzyme sites having an average frequency of appearance in eukaryotic genes of less than once in 10,000 base pairs include, but are not limited to the NotI, SnaBI, SalI, XhoI, ClaI, SacI, EagI, and SmaI sites. Preferred cloning sites are selected from the group consisting of NotI, SnaBI, SalI, and XhoI.

Preferably, the multiple cloning site has a length no greater than about 70 base pairs, and preferably no greater than about 60 base pairs. In general, the multiple restriction enzyme site, or multiple cloning site is located between the 5′ LTR and 3′ LTR of the retroviral vector. The 5′ end of the multiple cloning site is no greater than about 895 base pairs from the 3′ end of the 5′ LTR, preferably at least about 375 base pairs from the 3′ end of the 5′ LTR. The 3′ end of the multiple cloning site is no greater than about 40 base pairs from the 5′ end of the 3′ LTR, and preferably at least 11 base pairs from the 5′ end of the 3′ LTR.

Such vectors may be engineered from existing retroviral vectors through genetic engineering techniques known in the art such that the retroviral vector includes at least four cloning sites wherein at least two of the cloning sites are selected from the group consisting of the NotI, SnaBI, SalI, and XhoI cloning sites. In a preferred embodiment, the retroviral vector includes each of the NotI, SnaBI, SalI, and XhoI cloning sites.

Such a retroviral vector may serve as part of a cloning system for the transfer of genes to such retroviral vector. Thus, there may be provided a cloning system for the manipulation of genes in a retroviral vector which includes a retroviral vector including a multiple cloning site of the type hereinabove described, and a shuttle cloning vector which includes at least two cloning sites which are compatible with at least two cloning sites selected from the group consisting of NotI, SnaBI, SalI, and XhoI located on the retroviral vector. The shuttle cloning vector also includes at least one desired gene which is capable of being transferred from said shuttle cloning vector to said retroviral vector.

The shuttle cloning vector may be constructed from a basic “backbone” vector or fragment to which are ligated one or more linkers which include cloning or restriction enzyme recognition sites. Included in the cloning sites are the compatible, or complementary cloning sites hereinabove described. Genes and/or promoters having ends corresponding to the restriction sites of the shuttle vector may be ligated into the shuttle vector through techniques known in the art.

The shuttle cloning vector may be employed to amplify DNA sequences in prokaryotic systems. The shuttle cloning vector may be prepared from plasmids generally used in prokaryotic systems and in particular in bacteria. Thus, for example, the shuttle cloning vector may be derived from plasmids such as pBR322; pUC18; etc.

Such retroviral vectors are transfected or transduced into a packaging cell line, whereby there are generated infectious vector particles which include the retroviral vector. In general, the vector is transfected into the packaging cell line along with a packaging defective helper virus which includes genes encoding the gag and pol, and the env proteins of the virus. Representative examples of packaging cell lines include, but are not limited to, the PE501 and PA317 cell lines disclosed in Miller, et al.,

Biotechniques,

Vol. 7 pgs. 980-990 (1989).

The vector particles generated from the packaging cell line, which are also engineered with a protein containing a receptor binding region that binds to a receptor of a target cell, said receptor being other than the amphotropic cell receptor, are targetable, whereby the receptor binding region enables the vector particles to bind to a target cell. The retroviral vector particles thus may be directly administered to a desired target cell ex vivo, and such cells may then be administered to a patient as part of a gene therapy procedure.

Although the vector particles may be. administered directly to a target cell, the vector particles may be engineered such that the vector particles are “injectable” as well as targetable; i.e., the vector particles are resistant to inactivation by human serum, and thus the targetable vector particles may be administered to a patient by intravenous injection, and travel directly to a desired target cell or tissue without being inactivated by human serum.

The envelope of retroviruses also includes a protein known as p15E, and Applicants have found that retroviruses are susceptible to inactivation by human serum a a result of the action of complement protein(s) present in serum on the p15E protein portion of the retrovirus. Applicants have further found that such retroviruses can be made resistant to inactivation by human serum by mutating such p15E protein.

In one embodiment, therefore, the retroviral vector is engineered such that a portion of the DNA (RNA) encoding p15E protein (shown in the accompanying sequence listing as SEQ ID NO:7), has been mutated to render the vector particle resistant to inactivation by human serum; i.e., at least one amino acid but not all of the amino acids of the p15E protein has been changed, or mutated.

p15E protein is a viral protein having 196 amino acid residues. In viruses, sometimes all 196 amino acid residues are present, and in other viruses, amino acid residues 181 to 196 (known as the “r” peptide), are not present, and the resulting protein is the “mature” form of p15E known as p12E. Thus, viruses can contain both the p15E and p12E proteins. p15E protein is anchored in the viral membrane such that amino acid residues residues 1 to 134 are present on the outside of the virus. Although this embodiment of the present invention is not to be limited to any of the following reasoning, Applicants believe complement proteins may bind to this region whereby such binding leads to inactivation and/or lysis of the retrovirus. In particular, the p15E protein includes two regions, amino acid residues 39 to 61 (sometimes hereinafter referred to as region 1), and amino acid residues 101 to 123 (sometimes hereinafter referred to as region 2), which Applicants believe have an external location in the three-dimensional structure of the p15E protein; i.e., such regions are directly exposed to human serum. Region 2 is a highly conserved region in many retroviruses, even though the amino acid sequences of this region are not identical in all retroviruses. Such regions are complement binding regions. Examples of complement proteins which may bind to the complement binding regions are ClS and ClQ, which bind to regions 1 and 2.

In order to inactivate the retrovirus, complement proteins bind to both region 1 and region 2. Thus, in a preferred embodiment, at least one portion of DNA encoding a complement binding region of p15E protein has been mutated. Such a mutation results in a change of at least one amino acid residue of a complement binding region of p15E protein. The change in at least one amino acid residue of a complement binding region of p15E protein prevents binding of a complement protein to the complement binding region, thereby preventing complement inactivation of the retrovirus. In one embodiment, at least one amino acid residue in both complement binding regions of p15E protein is changed, whereas in another embodiment, at least one amino acid residue in one of the complement binding regions is changed.

It is to be understood, however, that the entire DNA sequence encoding p15E protein cannot be mutated because such a change renders the vectors unsuitable for in vivo use.

In one embodiment, the mutation of DNA (RNA) encoding p15E protein may be effected by deleting a portion of the p15E gene, and replacing the deleted portion of the p15E gene, with fragment(s) or portion(s) of a gene encoding another viral protein. In one embodiment, one portion of DNA encoding the p15E protein is replaced with a fragment of the gene encoding the p21 protein, which is an HTLV-I transmembrane protein. HTLV-I virus has been found to be resistant to binding by complement proteins and thus HTLV-I is resistant to inactivation by human serum (Hoshino, et al.,

Nature,

Vol. 310, pgs. 324-325 (1984)). Thus, in one embodiment, there is also provided a retroviral vector particle wherein a portion of the p15E protein has been deleted and replaced with a portion of another viral protein, such as a portion of the p21 protein.

p21 protein (as shown in the accompanying sequence listing as SEQ ID NO:8) is a protein having 176 amino acid residues, and which, in relation to p15E, has significant amino acid sequence homology. In one embodiment, at least amino acid residues 39 to 61, and 101 to 123 are deleted from p15E protein, and replaced with amino acid residues 34 to 56 and 96 to 118 of p21 protein. In one alternative, at least amino acid residues 39 to 123 of p15E protein are deleted and replaced with amino acid residues 34 to 118 of p21 protein.

In another embodiment, amino acid residues 39 to 69 of p15E protein are deleted and replaced with amino acid residues 34 to 64 of p21 protein, and amino acid residues 96 to 123 of p15E protein are deleted and replaced with amino acid residues 91 to 118 of p21 protein.

Vector particles generated from such packaging lines, therefore, are “targetable” and “injectable,” whereby such vector particles, upon administration to a patient, travel directly to a desired target cell or tissue.

The targetable vector particles are useful for the introduction of desired heterologous genes into target cells ex vivo. Such cells may then be administered to a patient as a gene therapy procedure, whereas vector particles which are targetable and injectable may be administered in vivo to the patient, whereby the vector particles travel directly to a desired target cell.

Thus, preferably, the vectors or vector particles of the present invention further include at least one heterologous gene. Heterologous or foreign genes which may be placed into the vector or vector particles include, but are not limited to, genes which encode cytokines or cellular growth factors, such as lymphokines, which are growth factors for lymphocytes. Other examples of foreign genes include, but are not limited to, genes encoding Factor VIII, Factor IX, tumor necrosis factors (TNF's), ADA, ApoE, ApoC, and Protein C.

The vectors of the present invention include one or more promoters. Suitable promoters which may be employed include, but are not limited to, the retroviral LTR; the SV40 promoter; and the human cytomegalovirus (CMV) promoter described in Miller, et al.,

Biotechniques,

Vol. 7, No. 9, pgs 980-990 (1989), or any other promoter (e.g., cellular promoters such as eukaryotic cellular promoters including, but not limited to, the histone, pol III, and B-actin promoters). Other viral promoters which may be employed include, but are not limited to, adenovirus promoters, TK promoters, and B19 parvovirus promoters. The selection of a suitable promoter will be apparent to those skilled in the art from the teachings contained herein.

The vectors of the present invention may contain regulatory elements, where necessary to ensure tissue specific expression of the desired heterologous gene(s), and/or to regulate expression of the heterologous gene(s) in response to cellular or metabolic signals.

Although the invention has been described with respect to retroviral vector particles, other viral vector particles (such as, for example, adenovirus, adeno-associated virus, and Herpes Simplex virus particles), or synthetic particles may be constructed such that the vector particles include a receptor binding region that binds to a receptor of a target cell, wherein the receptor of a human target cell is other than the amphotropic cell receptor. Such vector particles are suitable for in vivo administration to a desired target cell.

Advantages of the present invention include the ability to provide vector particles which may be administered directly to a desired target cell or tissues, whereby desired genes are delivered to the target cell or tissue, whereby the target cell or tissue may produce the proteins expressed by such genes.

This invention will now be described with respect to the following examples; however, the scope of the present invention is not intended to be limited thereby.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1

is a map of plasmid pCee;

FIG. 2

is a map of plasmid pAGP-1;

FIG. 3

is a map of plasmid pAGP-3;

FIG. 4

is a map of plasmid pUC18RSVXeno;

FIG. 5

is a map of plasmid pAX2; and

FIG. 6

is a map of plasmid pAX6.

EXAMPLE 1

Plasmid pCee (FIG.

1

), which contains the ecotropic murine leukemia virus gp70 and p15E genes under the control of a CMV promoter, was cut with AccI, and an AccI fragment encoding amino acid residues 1-312 of the eco gp70 protein was removed. Cloned into the AccI site was a PCR fragment containing the eco gp70 secretion signal (or leader, which includes amino acid residues 1-33 of eco gp70), followed by mature rabbit alpha-1 acid glycoprotein (amino acid residues 19-201) (Ray, et al.,

Biochemical and Biophysical Research Communications,

Vol. 178, No. 2, pgs. 507-513 (1991)). The amino acid sequence of rabbit alpha-1 acid glycoprotein is shown in (SEQ ID NO:5), and the DNA sequence encoding therefor is shown in (SEQ ID NO:6). The resulting plasmid pAGP-1 (

FIG. 2

) contains the eco gp70 leader sequence (amino acid residues 1-33 of eco gp70), a sequence encoding the mature rabbit alpha-1 acid glycoprotein (amino acid residues 19-201), and a sequence encoding amino acid residues 313 to 469 of eco gp70.

EXAMPLE 2

Plasmid pCee was cut with SalI and Pf1MI, and a SalI-Pf1MI fragment encoding amino acid residues 1-262 of eco gp70 was removed. Cloned into this site was a PCR generated SalI-Pf1MI fragment containing the eco gp70 leader sequence and the sequence encoding mature rabbit alpha-1 acid glycoprotein. The resulting plasmid, pAGP-3 (

FIG. 3

) thus includes a sequence encoding the leader sequence of eco gp70, a sequence encoding mature rabbit alpha-1 acid glycoprotein; and a sequence encoding amino acid residues 263 to 469 of eco gp70.

EXAMPLE 3

Plasmid pUC18RSVXeno (FIG.

4

), which contains the xenotrophic murine leukemia virus gp70 and p15E genes under the control of an RSV promoter, was cut with AccI and StuI, and an AccI-StuI fragment encoding amino acid residues 1-258 of xeno gp70 was removed. Cloned into this site was a PCR generated AccI-StuI fragment encoding the xeno gp70 leader (amino acid residues 1-30), and the mature rabbit alpha-1 acid glycoprotein. The resulting plasmid, pAX2 (FIG.

5

), thus contains a sequence encoding the xeno gp70 leader, a sequence encoding the mature rabbit alpha-1 acid glycoprotein, and amino acid residues 259-443 of xeno gp70.

EXAMPLE 4

Plasmid pUC18RSVXeno was cut with AccI and ClaI, and a fragment encoding amino acid residues 1-210 of xeno gp70 was removed. Cloned into this site was a PCR generated AccI-Clal fragment encoding the xeno gp70 leader, followed by mature rabbit alpha-1 acid glycoprotein. The resulting plasmid, pAX6 (FIG.

6

), thus includes a sequence encoding the xeno gp70 leader, a sequence encoding mature rabbit alpha-1 acid glycoprotein, and amino acid residues 211-443 of xeno gp70.

EXAMPLE 5

5×10

5

GPL cells on 10 cm tissue culture plates were transfected (using CaPO

4

) with 30 μg/plate of one of plasmids pAGP-1, pAGP-3, pAX2, or pAX6. The CaPO

4

is removed 24 hours later and 10 ml of fresh D10 medium is added for another 24 hours. The D10 medium is then removed and replaced with serum free DX medium for another 24 hours. The DX medium is then collected, filtered, and stored on ice. This supernatant contains the vector particles.

The supernatants were then filtered and collected by standard procedures and then centrifuged. After centrifugation, the virus pellets were reconstituted in a buffer containing 0.1M sodium acetate, 0.15M sodium chloride, and 2 mM calcium chloride; the buffer was sterilized using a Falcon 0.2 millimicron tissue culture filter.

2.2 ml of concentrated supernatant containing viral particles generated from pAGP-1 or pAGP-3, said viral particles sometimes hereinafter referred to as Chimeric-1 or Chimeric-3, were loaded onto two disposable plastic columns which were alcohol sterilized and dried. To each column (1 cm×6 cm), one unit of neuraminidase from

Clostridium perfringens

which was bound to beaded agarose was added as a 2 ml suspension. This represents 1 ml of packed gel or unit of enzyme per column (15.7 mg of agarose/ml and 28 units per gram of agarose). A unit is defined as the amount of neuraminidase which will liberate 1.0 micromole of N-acetylneuraminic acid per minute from NAN-lactose at pH 5.0 and 37° C.

The columns were then washed with a large excess (50 ml) of the buffer hereinabove described to free the resin of all traces of free neuraminidase and to sterilize the resin prior to incubation with virus. The columns were then dried, and the bottoms were sealed with caps and secured with parafilm. The concentrated virus which was reconstituted in the buffer (2.0 ml per sample) was then added to the resin. The tops were placed on the columns and secured with parafilm. The resin was gently re-suspended by hand. The virus was then incubated with the resin for 1 hour at room temperature with gentle rotation on a wheel. The columns were checked periodically to ensure good mixing of resin and virus.

At the end of the incubation period, the Chimera-1 and Chimera-3 viruses were recovered by gentle vacuum filtration and collected into separate sterile 12×75 mm plastic polypropylene Falcon 2063 tubes. Recovery was greater than 90%, giving about 1.8 ml of desialated virus.

6-well plates containing about 105 receptor-positive (Hep G2) or receptor-negative (SK HepI) human hepatocytes in 2 ml D10 media were employed as target cells. 24 hours after the cells were plated, 1 ml of D10 was removed from the first well and 2 ml of neuraminidase-treated (or untreated as a control) viral supernatant containing Chimeric-1 or Chimeric-3 was added and mixed well. 200 ul from the first well was diluted into the 2 ml present in the second well, was then mixed; and then 200 ul from the second well was diluted into the 1.8 ml present in the third well, thereby giving approximate dilutions of 2/3, 1/15, and 1/150. 8 ug/ml of Polybrene was included in each well during the transduction. The viral particles were left in contact with the cells overnight, followed by removal of media containing viral particles, and replaced with D10 containing 1,000 mg/ml of G418. The medium was changed with fresh D10 and G418 every 4 to 5 days as necessary. G418-resistant colonies were scored after 2 to 3 weeks.

EXAMPLE 6

The pre-packaging cell line GP8, which expresses the retroviral proteins gag and pol, and the packaging cell lines derived from them which also express the chimeric gp70 glycoproteins encoded by the plasmids pAGP-1, pAGP-3, pAX2, or pAX6 were maintained in cell culture and exposed to successively higher concentrations of wheat germ agglutinin; starting with 15 ug/ml. The cell lines were maintained under WGA selection in cell culture for 6 to 8 weeks until populations resistant to 40-50 ug/ml WGA were obtained. The latter were then subjected to fluoresence-activated cell sorting using FITC-conjugated lectins to enrich for the cells expressing the desired mutant glycotype (e.g., FITC-

Erythrina Cristagalli

agglutinin for beta-D-galactosyl groups, and FITC-concanavalin A for alpha-D-mannosyl groups). Retroviral vector packaging and producer cell lines were then generated from the resulting populations by standard techniques.

It is to be understood, however, that the scope of the present invention is not to be limited to the specific embodiments described above. The invention may be practiced other than as particularly described and still be within the scope of the accompanying claims.

SEQUENCE LISTING

(1) GENERAL INFORMATION:

(iii) NUMBER OF SEQUENCES: 8

(2) INFORMATION FOR SEQ ID NO: 1:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 469 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: <Unknown>

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(ix) FEATURE:

(A) NAME/KEY: Ecotropic gp70 Protein

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 1:

Met Ala Arg Ser Thr Leu Ser Lys Pro Leu

5 10

Lys Asn Lys Val Asn Pro Arg Gly Pro Leu

15 20

Ile Pro Leu Ile Leu Leu Met Leu Arg Gly

25 30

Val Ser Thr Ala Ser Pro Gly Ser Ser Pro

35 40

His Gly Val Tyr Asn Ile Thr Trp Glu Val

45 50

Thr Asn Gly Asp Arg Glu Thr Val Trp Ala

55 60

Thr Ser Gly Asn His Pro Leu Trp Thr Trp

65 70

Trp Pro Asp Leu Thr Pro Asp Leu Cys Met

75 80

Leu Ala His His Gly Pro Ser Tyr Trp Gly

85 90

Leu Glu Tyr Gln Ser Pro Phe Ser Ser Pro

95 100

Pro Gly Pro Pro Cys Cys Ser Gly Gly Ser

105 110

Ser Pro Gly Cys Ser Arg Asp Cys Glu Glu

115 120

Pro Leu Thr Ser Leu Thr Pro Arg Cys Asn

125 130

Thr Ala Trp Asn Arg Leu Lys Leu Asp Gln

135 140

Thr Thr His Lys Ser Asn Glu Gly Phe Tyr

145 150

Val Cys Pro Gly Pro His Arg Pro Arg Glu

155 160

Ser Lys Ser Cys Gly Gly Pro Asp Ser Phe

165 170

Tyr Cys Ala Tyr Trp Gly Cys Glu Thr Thr

175 180

Gly Arg Ala Tyr Trp Lys Pro Ser Ser Ser

185 190

Trp Asp Phe Ile Thr Val Asn Asn Asn Leu

195 200

Thr Ser Asp Gln Ala Val Gln Val Cys Lys

205 210

Asp Asn Lys Trp Cys Asn Pro Leu Val Ile

215 220

Arg Phe Thr Asp Ala Gly Arg Arg Val Thr

225 230

Ser Trp Thr Thr Gly His Tyr Trp Gly Leu

235 240

Arg Leu Tyr Val Ser Gly Gln Asp Pro Gly

245 250

Leu Thr Phe Gly Ile Arg Leu Arg Tyr Gln

255 260

Asn Leu Gly Pro Arg Val Pro Ile Gly Pro

265 270

Asn Pro Val Leu Ala Asp Gln Gln Pro Leu

275 280

Ser Lys Pro Lys Pro Val Lys Ser Pro Ser

285 290

Val Thr Lys Pro Pro Ser Gly Thr Pro Leu

295 300

Ser Pro Thr Gln Leu Pro Pro Ala Gly Thr

305 310

Glu Asn Arg Leu Leu Asn Leu Val Asp Gly

315 320

Ala Tyr Gln Ala Leu Asn Leu Thr Ser Pro

325 330

Asp Lys Thr Gln Glu Cys Trp Leu Cys Leu

335 340

Val Ala Gly Pro Pro Tyr Tyr Glu Gly Val

345 350

Ala Val Leu Gly Thr Tyr Ser Asn His Thr

355 360

Ser Ala Pro Ala Asn Cys Ser Val Ala Ser

365 370

Gln His Lys Leu Thr Leu Ser Glu Val Thr

375 380

Gly Gln Gly Leu Cys Ile Gly Ala Val Pro

385 390

Lys Thr His Gln Ala Leu Cys Asn Thr Thr

395 400

Gln Thr Ser Ser Arg Gly Ser Tyr Tyr Leu

405 410

Val Ala Pro Thr Gly Thr Met Trp Ala Cys

415 420

Ser Thr Gly Leu Thr Pro Cys Ile Ser Thr

425 430

Thr Ile Leu Asn Leu Thr Thr Asp Tyr Cys

435 440

Val Leu Val Glu Leu Trp Pro Arg Val Thr

445 450

Tyr His Ser Pro Ser Tyr Val Tyr Gly Leu

455 460

Phe Glu Arg Ser Asn Arg His Lys Arg

465

(2) INFORMATION FOR SEQ ID NO: 2:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 1446 bases

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: viral DNA

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 2:

GGCTGCCGAC CCCGGGGGTG GACCATCCTC TAGACTGACA TGGCGCGTTA AACGCTCTCA 60

AAACCCCTTA AAAATAAGGT TAACCCGCGA GGCCCCCTAA TCCCCTTAAT TCTTCTGATG 120

CTCAGAGGGG TCAGTACTGC TTCGCCCGGC TCCAGTCCTC ATCAAGTCTA TAATATCACC 180

TGGGAGGTAA CCAATGGAGA TCGGGAGACG GTATGGGCAA CTTCTGGCAA CCACCCTCTG 240

TGGACCTGGT GGCCTGACCT TACCCCAGAT TTATGTATGT TAGCCCACCA TGGACCATCT 300

TATTGGGGGC TAGAATATCA ATCCCCTTTT TCTTCTCCCC CGGGGCCCCC TTGTTGCTCA 360

GGGGGCAGCA GCCCAGGCTG TTCCAGAGAC TGCGAAGAAC CTTTAACCTC CCTCACCCCT 420

CGGTGCAACA CTGCCTGGAA CAGACTCAAG CTAGACCAGA CAACTCATAA ATCAAATGAG 480

GGATTTTATG TTTGCCCCGG GCCCCACCGC CCCCGAGAAT CCAAGTCATG TGGGGGTCCA 540

GACTCCTTCT ACTGTGCCTA TTGGGGCTGT GAGACAACCG GTAGAGCTTA CTGGAAGCCC 600

TCCTCATCAT GGGATTTCAT CACAGTAAAC AACAATCTCA CCTCTGACCA GGCTGTCCAG 660

GTATGCAAAG ATAATAAGTG GTGCAACCCC TTAGTTATTC GGTTTACAGA CGCCGGGAGA 720

CGGGTTACTT CCTGGACCAC AGGACATTAC TGGGGCTTAC GTTTGTATGT CTCCGGACAA 780

GATCCAGGGC TTACATTTGG GATCCGACTC AGATACCAAA ATCTAGGACC CCGCGTCCCA 840

ATAGGGCCAA ACCCCGTTCT GGCAGACCAA CAGCCACTCT CCAAGCCCAA ACCTGTTAAG 900

TCGCCTTCAG TCACCAAACC ACCCAGTGGG ACTCCTCTCT CCCCTACCCA ACTTCCACCG 960

GCGGGAACGG AAAATAGGCT GCTAAACTTA GTAGACGGAG CCTACCAAGC CCTCAACCTC 1020

ACCAGTCCTG ACAAAACCCA AGAGTGCTGG TTGTGTCTAG TAGCGGGACC CCCCTACTAC 1080

GAAGGGGTTG CCGTCCTGGG TACCTACTCC AACCATACCT CTGCTCCAGC CAACTGCTCC 1140

GTGGCCTCCC AACACAAGTT GACCCTGTCC GAAGTGACCG GACAGGGACT CTGCATAGGA 1200

GCAGTTCCCA AAACACATCA GGCCCTATGT AATACCACCC AGACAAGCAG TCGAGGGTCC 1260

TATTATCTAG TTGCCCCTAC AGGTACCATG TGGGCTTGTA GTACCGGGCT TACTCCATGC 1320

ATCTCCACCA CCATACTGAA CCTTACCACT GATTATTGTG TTCTTGTCGA ACTCTGGCCA 1380

AGAGTCACCT ATCATTCCCC CAGCTATGTT TACGGCCTGT TTGAGAGATC CAACCGACAC 1440

AAAAGA 1446

(2) INFORMATION FOR SEQ ID NO: 3:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 453 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: <Unknown>

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(ix) FEATURE:

(A) NAME/KEY:xenotropic gp70 protein

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 3:

Met Glu Gly Ser Ala Phe Ser Lys Pro Leu

5 10

Lys Asp Lys Ile Asn Pro Trp Gly Pro Leu

15 20

Ile Val Met Gly Ile Leu Val Arg Ala Gly

25 30

Ala Ser Val Gln Arg Asp Ser Pro His Gln

35 40

Ile Phe Asn Val Thr Trp Arg Val Thr Asn

45 50

Leu Met Thr Gly Gln Thr Ala Asn Ala Thr

55 60

Ser Leu Leu Gly Thr Met Thr Asp Thr Phe

65 70

Pro Lys Leu Tyr Phe Asp Leu Cys Asp Leu

75 80

Pro Lys Leu Tyr Phe Asp Leu Cys Asp Leu

85 90

Val Gly Asp Tyr Trp Asp Asp Pro Glu Pro

95 100

Asp Ile Gly Asp Gly Cys Arg Thr Pro Gly

105 110

Gly Arg Arg Arg Thr Arg Leu Tyr Asp Phe

115 120

Tyr Val Cys Pro Gly His Thr Val Pro Ile

125 130

Gly Cys Gly Gly Pro Gly Glu Gly Tyr Cys

135 140

Gly Lys Trp Gly Cys Glu Thr Thr Gly Gln

145 150

Ala Tyr Trp Lys Pro Ser Ser Ser Trp Asp

155 160

Leu Ile Ser Leu Lys Arg Gly Asn Thr Pro

165 170

Lys Asp Gln Gly Pro Cys Tyr Asp Ser Ser

175 180

Val Ser Ser Gly Val Gln Gly Ala Thr Pro

185 190

Gly Gly Arg Cys Asn Pro Leu Val Leu Glu

195 200

Phe Thr Asp Ala Gly Arg Lys Ala Ser Trp

205 210

Asp Ala Pro Lys Val Trp Gly Leu Arg Leu

215 220

Tyr Arg Ser Thr Gly Ala Asp Pro Val Thr

225 230

Arg Phe Ser Leu Thr Arg Gln Val Leu Asn

235 240

Val Gly Pro Arg Val Pro Ile Gly Pro Asn

245 250

Pro Val Ile Thr Asp Gln Leu Pro Pro Ser

255 260

Gln Pro Val Gln Ile Met Leu Pro Arg Pro

265 270

Pro His Pro Pro Pro Ser Gly Thr Val Ser

275 280

Met Val Pro Gly Ala Pro Pro Pro Ser Gln

285 290

Gln Pro Gly Thr Gly Asp Arg Leu Leu Asn

295 300

Leu Val Glu Gly Ala Tyr Gln Ala Leu Asn

305 310

Leu Thr Ser Pro Asp Lys Thr Gln Glu Cys

315 320

Trp Leu Cys Leu Val Ser Gly Pro Pro Tyr

325 330

Tyr Glu Gly Val Ala Val Leu Gly Thr Tyr

335 340

Ser Asn His Thr Ser Ala Pro Ala Asn Cys

345 350

Ser Val Ala Ser Gln His Lys Leu Thr Leu

355 360

Ser Glu Val Thr Gly Gln Gly Leu Cys Val

365 370

Gly Ala Val Pro Lys Thr His Gln Ala Leu

375 380

Cys Asn Thr Thr Gln Lys Thr Ser Asp Gly

385 390

Ser Tyr Tyr Leu Ala Ala Pro Ala Gly Thr

395 400

Ile Trp Ala Cys Asn Thr Gly Leu Thr Pro

405 410

Cys Leu Ser Thr Thr Val Leu Asn Leu Thr

415 420

Thr Asp Tyr Cys Val Leu Val Glu Leu Trp

425 430

Pro Lys Val Thr Tyr His Ser Pro Asp Tyr

435 440

Val Tyr Gly Gln Phe Glu Lys Lys Thr Lys

445 450

Tyr Lys Arg

(2) INFORMATION FOR SEQ ID NO: 4:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 1356 bases

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: viral DNA

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 4:

GCGACAACTC CTCCAGCCGG GAACAGCATG GAAGGTTCAG CGTTCTCAAA ACCCCTTAAA 60

GATAAGATTA ACCCGTGGGG CCCCCTAATA GTTATGGGGA TCTTGGTGAG GGCAGGAGCT 120

TCGGTACAAC GTGACAGCCC TCACCAGATC TTCAATGTTA CTTGGAGAGT TACCAACCTA 180

ATGACAGGAC AAACAGCTAA CGCCACCTCC CTCCTGGGGA CGATGACAGA CACCTTCCCT 240

AAACTATATT TTGACCTGTG TGATTTAGTA GGAGACTACT GGGATGACCC AGAACCCGAT 300

ATTGGGGATG GTTGCCGCAC TCCCGGGGGA AGAAGAAGGA CAAGACTGTA TGACTTCTAT 360

GTTTGCCCCG GTCATACTGT ACCAATAGGG TGTGGAGGGC CGGGAGAGGG CTACTGTGGC 420

AAATGGGGAT GTGAGACCAC TGGACAGGCA TACTGGAAGC CATCATCATC ATGGGACCTA 480

ATTTCCCTTA AGCGAGGAAA CACTCCTAAG GATCAGGGCC CCTGTTATGA TTCCTCGGTC 540

TCCAGTGGCG TCCAGGGTGC CACACCGGGG GGTCGATGCA ACCCCCTGGT CTTAGAATTC 600

ACTGACGCGG GTAGAAAGGC CAGCTGGGAT GCCCCCAAAG TTTGGGGACT AAGACTCTAT 660

CGATCCACAG GGGCCGACCC GGTGACCCGG TTCTCTTTGA CCCGCCAGGT CCTCAATGTA 720

GGACCCCGCG TCCCCATTGG GCCTAATCCC GTGATCACTG ACCAGCTACC CCCATCCCAA 780

CCCGTGCAGA TCATGCTCCC CAGGCCTCCT CATCCTCCTC CTTCAGGCAC GGTCTCTATG 840

GTACCTGGGG CTCCCCCGCC TTCTCAACAA CCTGGGACGG GAGACAGGCT GCTAAATCTG 900

GTAGAAGGAG CCTACCAAGC ACTCAACCTC ACCAGTCCTG ACAAAACCCA AGAGTGCTGG 960

TTGTGTCTGG TATCGGGACC CCCCTACTAC GAAGGGCTTG CCGTCCTAGG TACCTACTCC 1020

AACCATACCT CTGCCCCAGC TAACTGCTCC GTGGCCTCCC AACACAAGCT GACCCTGTCC 1080

GAAGTAACCG GACAGGGACT CTGCGTAGGA GCAGTTCCCA AAACCCATCA GGCCCTGTGT 1140

AATACCACCC AGAAGACGAG CGACGGGTCC TACTATCTGG CTGCTCCCGC CGGGACCATC 1200

TGGGCTTGCA ACACCGGGCT CACTCCCTGC CTATCTACTA CTGTACTCAA CCTCACCACC 1260

GATTACTGTG TCCTGGTTGA GCTCTGGCCA AAGGTAACCT ACCACTCCCC TGATTATGTT 1320

TATGGCCAGT TTGAAAAGAA AACTAAATAT AAAAGA 1356

(2) INFORMATION FOR SEQ ID NO: 5:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 201 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: <Unknown>

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(ix) FEATURE:

(A) NAME/KEY:rabbit alpha-1-acid glycoprotein

(x) PUBLICATION INFORMATION

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 5:

Met Ala Leu Pro Trp Ala Leu Ala Val Leu

5 10

Ser Leu Leu Pro Leu Leu His Ala Gln Asp

15 20

Pro Ala Cys Ala Asn Phe Ser Thr Ser Pro

25 30

Ile Thr Asn Ala Thr Leu Asp Gln Leu Ser

35 40

His Lys Trp Phe Phe Thr Ala Ser Ala Phe

45 50

Arg Asn Pro Lys Tyr Lys Gln Leu Val Gln

55 60

His Thr Gln Ala Ala Phe Phe Tyr Phe Thr

65 70

Ala Ile Lys Glu Glu Asp Thr Leu Leu Leu

75 80

Arg Glu Tyr Ile Thr Thr Asn Asn Thr Cys

85 90

Phe Tyr Asn Ser Ser Ile Val Arg Val Gln

95 100

Arg Glu Asn Gly Thr Leu Ser Lys His Asp

105 110

Gly Ile Arg Asn Ser Val Ala Asp Leu Leu

115 120

Leu Leu Arg Asp Pro Gly Ser Phe Leu Leu

125 130

Val Phe Phe Ala Gly Lys Glu Gln Asp Lys

135 140

Gly Met Ser Leu Tyr Thr Asp Lys Pro Lys

145 150

Ala Ser Thr Glu Gln Leu Glu Glu Phe Tyr

155 160

Glu Ala Leu Thr Cys Leu Gly Met Asn Lys

165 170

Thr Glu Val Val Tyr Thr Asp Trp Thr Lys

175 180

Asp Leu Cys Glu Pro Leu Glu Lys Gln His

185 190

Glu Glu Glu Arg Lys Lys Glu Lys Ala Glu

195 200

Ser

(2) INFORMATION FOR SEQ ID NO: 6

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 759 bases

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: genomic DNA

(x) PUBLICATION INFORMATION:

(A) AUTHORS: Ray, et al.

(B) TITLE:

(C) JOURNAL: Biochem. and Biophys. Res. Comm.

(D) VOLUME: 178

(E) ISSUE: NO. 2

(F) PAGES: 507-513

(G) DATE: 1991

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 6:

AGCTCTGCCT GGCTCCAGCG CCTCTGTGTC TCAGCATGGC CCTGCCCTGG GCCCTCGCCG 60

TCCTGAGCCT CCTCCCTCTG CTGCATGCCC AGGACCCAGC GTGTGCCAAC TTCTCGACCA 120

GCCCTATCAC CAATGCCACC CTGGACCAGC TCTCCCACAA GTGGTTTTTT ACCGCCTCGG 180

CCTTCCGGAA CCCCAAGTAC AAGCAGCTGG TGCAGCATAC CCAGGCGGCC TTTTTCTACT 240

TCACCGCCAT CAAAGAGGAG GACACCTTGC TGCTCCGGGA GTACATAACC ACGAACAACA 300

CGTGCTTCTA TAACTGCAGC ATCGTGAGGG TCCAGAGAGA GAATGGGACC CTCTCCAAAC 360

ACGACGGCAT ACGAAATAGC GTGGCCGACC TGCTGCTCCT CAGGGACCCC GGGAGCTTCC 420

TCCTCGTCTT CTTCGCTGGG AAGGAGCAGG ACAAGGGAAT GTCCTTCTAC ACCGACAAGC 480

CCAAGGCCAG CCCGGAACAA CTGGAAGAGT TCTACGAAGC CCTCACGTGC CTGGGCATGA 540

ACAAGACGGA AGTCGTCTAC ACTGACTGGA CAAAGGATCT GTGCGAGCCG CTGGAGAAGC 600

AACACGAGGA GGAGAGGAAG AAGGAAAAGG CAGAGTCATA GGGCACAGCA CCGGCTCCGG 660

GACTCGGGGC CCACCCCCTG CACCTGCCTT TTTGTTTGTT TTGTAAATCT CTGTTCTTTC 720

CCATGGTTGC ATCAATAAAA CTGCTGGACC AGTAAAAAA 759

(2) INFORMATION FOR SEQ ID NO: 7:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 196 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: <Unknown>

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(ix) FEATURE:

(A) NAME/KEY: ecotropic p15E protein.

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 7:

Glu Pro Val Ser Leu Thr Leu Ala Leu Leu

5 10

Leu Gly Gly Leu Thr Met Gly Gly Ile Ala

15 20

Ala Gly Ile Gly Thr Gly Thr Thr Ala Leu

25 30

Met Ala Thr Gln Gln Phe Gln Gln Leu Gln

35 40

Ala Ala Val Gln Asp Asp Leu Arg Glu Val

45 50

Glu Lys Ser Ile Ser Asn Leu Glu Lys Ser

55 60

Leu Thr Ser Leu Ser Glu Val Val Leu Gln

65 70

Asn Arg Arg Gly Leu Asp Leu Leu Phe Leu

75 80

Lys Glu Gly Gly Leu Cys Ala Ala Leu Lys

85 90

Glu Glu Cys Cys Phe Tyr Ala Asp His Thr

95 100

Gly Leu Val Arg Asp Ser Met Ala Lys Leu

105 110

Arg Glu Arg Leu Asn Gln Arg Gln Lys Leu

115 120

Phe Glu Ser Thr Gln Gly Trp Phe Glu Gly

125 130

Leu Phe Asn Arg Ser Pro Trp Phe Thr Thr

135 140

Leu Ile Ser Thr Ile Met Gly Pro Leu Ile

145 150

Val Leu Leu Met Ile Leu Leu Phe Gly Pro

155 160

Cys Ile Leu Asn Arg Leu Val Gln Phe Val

165 170

Lys Asp Arg Ile Ser Val Val Gln Ala Leu

175 180

Val Leu Thr Gln Gln Tyr His Gln Leu Lys

185 190

Pro Ile Glu Tyr Glu Pro

195

(2) INFORMATION FOR SEQ ID NO: 8:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 176 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: <Unknown>

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(ix) FEATURE:

(A) NAME/KEY: HTLV-I p21 protein

(x) PUBLICATION INFORMATION:

(A) AUTHORS: Malik, et al.

(B) TITLE:

(C) JOURNAL: J. Gen. Virol.

(D) VOLUME: 69

(E) ISSUE:

(F) PAGES: 1695-1710

(G) DATE: 1988

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: 8:

Ala Val Pro Val Ala Val Trp Leu Val Ser

5 10

Ala Leu Ala Met Gly Ala Gly Val Ala Gly

15 20

Arg Ile Thr Gly Ser Met Ser Leu Ala Ser

25 30

Gly Lys Ser Leu Leu His Glu Val Asp Lys

35 40

Asp Ile Ser Gln Leu Thr Gln Ala Ile Val

45 50

Lys Asn His Lys Asn Leu Leu Lys Ile Ala

55 60

Gln Tyr Ala Ala Gln Asn Arg Arg Gly Leu

65 70

Asp Leu Leu Phe Trp Glu Gln Gly Gly Leu

75 80

Cys Lys Ala Leu Gln Glu Gln Cys Cys Phe

85 90

Leu Asn Ile Thr Asn Ser His Val Ser Ile

95 100

Leu Gln Glu Arg Pro Pro Leu Glu Asn Arg

105 110

Val Leu Thr Gly Trp Gly Leu Asn Trp Asp

115 120

Leu Gly Leu Ser Gln Trp Ala Arg Glu Ala

125 130

Leu Gln Thr Gly Ile Thr Leu Val Ala Leu

135 140

Leu Leu Leu Val Ile Leu Ala Gly Pro Cys

145 150

Ile Leu Arg Gln Leu Arg His Leu Pro Ser

155 160

Arg Val Arg Tyr Pro His Tyr Ser Leu Ile

165 170

Asn Pro Glu Ser Ser Leu

175

Number	Name	Date	Kind
5328470	Nabel et al.	Jul 1994	A
5354674	Hodgson	Oct 1994	A
5512421	Burns et al.	Apr 1996	A
5591624	Barber et al.	Jan 1997	A
5817491	Yee et al.	Oct 1998	A

Number	Date	Country
334301	Sep 1989	EP
WO 9102805	Mar 1991	WO
WO 9206180	Apr 1992	WO
WO 9214829	Sep 1992	WO
WO 9220316	Nov 1992	WO
WO 9300103	Jan 1993	WO
WO 9314188	Jul 1993	WO
WO 9320221	Oct 1993	WO
WO 9325234	Dec 1993	WO

	Number	Date	Country
Parent	08/326347	Oct 1994	US
Child	08/484126		US
Parent	07/973307	Nov 1992	US
Child	08/326347		US

Targetable vector particles

Information

Patent Number

Date Filed

Date Issued

Inventors

Examiners

CPC

US Classifications

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US

International Classifications

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Abstract

Description

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Parent Case Info

US Referenced Citations (5)

Foreign Referenced Citations (9)

Non-Patent Literature Citations (11)

Continuations (2)

Entry
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Orkin, et al., 1995 Report and Recommendations of the Panel to Assess the NIH Investment in Research on Gene Therapy (Dec. 1995).
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Miller, et al., Biotechniques, vol. 7, No. 9, pp. 980-990 (1989).
Wu, et al., J. Biol. Chem., vol. 262, No. 10, pp. 4429-4432 (Apr. 5, 1981).
Wu, et al., J. Biol. Chem., vol. 232, No. 29, pp. 14621-14624 (Oct. 1988).