分子病毒学 8病毒载体_PPT课件
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• Elements needed to generate amplicon
– Transfer Vector: plasmid (promoter, gene of interest, ori, packaging signal)
– Packaging vector (cosmid or cell lines): provide the viral structural proteins for packaging of transfer vector
host cells
• Specific target cells: depending on the viral
attachment proteins (capsid or glycoproteins)
• Gene replacement: non-essential genes of
virus are deleted and exogenous genes are inserted
Methods of gene delivery
• Viral Vectors:
– Adenovirus – Retrovirus – Lentivirus – Adeno-associated virus (AAV) – Herpes simplex virus (HSV)
• Non-viral vector based
Generation of viral vector for gene therapy
• Replication-competent virus • Replication-defective virus
– Amplicon: doesn’t encode structural proteins
– Can’t replicate beyond the first cycle of infection
• Disadvantages
– Transient expression ( not good for genetic diseases) – Highly immunogenic – High titers of virus can be toxic – More suitable for cancer immunotherapy
Early generations of adenoviral vector (replication defective)
Gutless Adenoviral vector (Amplicon)
Modification of the tropism of adenovirus vector
• Adenovirus fiber binds to CAR (coxsakie and
Adenoviral vectors
• Non-enveloped ds DNA, 36 kilobases • Early proteins (E1A, E1B, E2,E3 and E4), late proteins
(L1-L5)
• Causes a benign respiratory infections in human • Serotypes 2 and 5 are commonly used as vectors
adenovirus receptor, CAR), receptor which is ubiquitous
• Modify the fiber protein
Characteristics of adenoviral vector
• Advantages
– High titers – Both dividing and non-dividing cells – Wide tissue tropism – Easily modify tissue tropism
Retroviral vector
• Moloney murine leukemia virus (MuLV) • Generation of replication defective retroviral vector
– Transfer plasmid vector:
• Gene of interest • Long terminal repeats(LTR): promoter, polyA, integration,
replication and reverse transcription
• Primer binding site (PBS) (origin of replication) • RNA packaging signal • Poly purine tract (important for replication)
– Naked DNA (plasmid DNA): injection or genegun – Liposomes (cationic lipids): mix with genes
• Ex-vivo • In vivo
Why use viral vectors
• Virus are obligate intracellular parasites • Very efficient at transferring viral DNA into
– Helper virus (packaging of transfer vector): deleted Packaging signal sequence
Generation of adeno-associated virus vector
Characteristics of AAV vector
• Advantages
– Integration and persistent expression – No insertional mutagenesis – Infecting dividing and nondividinwenku.baidu.com cells – Safe
• Disadvantages
– Size limitation, 4.9 kb – Low titer of virus, low level of gene expression
– Transfer Vector: plasmid (promoter, gene of interest, ori, packaging signal)
– Packaging vector (cosmid or cell lines): provide the viral structural proteins for packaging of transfer vector
host cells
• Specific target cells: depending on the viral
attachment proteins (capsid or glycoproteins)
• Gene replacement: non-essential genes of
virus are deleted and exogenous genes are inserted
Methods of gene delivery
• Viral Vectors:
– Adenovirus – Retrovirus – Lentivirus – Adeno-associated virus (AAV) – Herpes simplex virus (HSV)
• Non-viral vector based
Generation of viral vector for gene therapy
• Replication-competent virus • Replication-defective virus
– Amplicon: doesn’t encode structural proteins
– Can’t replicate beyond the first cycle of infection
• Disadvantages
– Transient expression ( not good for genetic diseases) – Highly immunogenic – High titers of virus can be toxic – More suitable for cancer immunotherapy
Early generations of adenoviral vector (replication defective)
Gutless Adenoviral vector (Amplicon)
Modification of the tropism of adenovirus vector
• Adenovirus fiber binds to CAR (coxsakie and
Adenoviral vectors
• Non-enveloped ds DNA, 36 kilobases • Early proteins (E1A, E1B, E2,E3 and E4), late proteins
(L1-L5)
• Causes a benign respiratory infections in human • Serotypes 2 and 5 are commonly used as vectors
adenovirus receptor, CAR), receptor which is ubiquitous
• Modify the fiber protein
Characteristics of adenoviral vector
• Advantages
– High titers – Both dividing and non-dividing cells – Wide tissue tropism – Easily modify tissue tropism
Retroviral vector
• Moloney murine leukemia virus (MuLV) • Generation of replication defective retroviral vector
– Transfer plasmid vector:
• Gene of interest • Long terminal repeats(LTR): promoter, polyA, integration,
replication and reverse transcription
• Primer binding site (PBS) (origin of replication) • RNA packaging signal • Poly purine tract (important for replication)
– Naked DNA (plasmid DNA): injection or genegun – Liposomes (cationic lipids): mix with genes
• Ex-vivo • In vivo
Why use viral vectors
• Virus are obligate intracellular parasites • Very efficient at transferring viral DNA into
– Helper virus (packaging of transfer vector): deleted Packaging signal sequence
Generation of adeno-associated virus vector
Characteristics of AAV vector
• Advantages
– Integration and persistent expression – No insertional mutagenesis – Infecting dividing and nondividinwenku.baidu.com cells – Safe
• Disadvantages
– Size limitation, 4.9 kb – Low titer of virus, low level of gene expression