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Unidad de Transferencia GenUnidad de Transferencia GenééticaticaInstituto de OncologInstituto de Oncologíía a “Á“Ángel H. ngel H. RoffoRoffo””
Universidad de Buenos AiresUniversidad de Buenos Aires
Transferencia de Genes aTransferencia de Genes a
CCéélulas Animales en Cultivolulas Animales en Cultivo
Conceptos y TConceptos y Téécnicas de Biotecnologcnicas de Biotecnologíía I a I 2012 2012 –– 2do cuatrimestre2do cuatrimestre
FBMCFBMC--FCENFCEN--UBAUBA
•BACTERIAS (i.e.: Escherichia coli)•HONGOS (i.e.: Saccharomyces cereviseae)•CULTIVOS CELULARES (animales o vegetales)•PLANTASALGASVASCULARES•ANIMALES:PECESAVESMAMÍFEROSBovinosCaprinosOvinosPorcinosHUMANOS: Transgénesis parcial � Terapia Génica
ORGANISMOS TRANSGÉNICOS- INVOLUCRADOS EN BIOTECNOLOGÍA -
Transferencia de Genes a CTransferencia de Genes a Céélulas Animales en Cultivolulas Animales en Cultivo
PROPÓSITOS
•Confirmar identidad de genes
•Caracterizar oncogenes
•Expresar proteínas que necesitan modificaciones post-
traduccionales
•Producir grandes cantidades de proteínas que naturalmente
se encuentran en cantidades limitadas
•Estudiar síntesis y transporte intracelular
•Expresar secuencias genómicas que contienen intrones
•Estudiar mecanismos de edición de genes
•Analizar señales de control de transcripción y su
modulación por drogas, hormonas, estado de diferenciación
Heterologous Protein Production
In Eukaryotic Cells
• Prokaryotic systems are generally cheaper, but…
• Eukaryotic proteins produced in bacteria may be
� Unstable or lack biological activity due to lack of posttranslational modifications or correct assembly
� Possess unacceptable contaminants after purification
Posttranslational Modifications
• Conformation
• Cleavage
• Correct disulfide bond formation
• Protein disulfide isomerase
• Amino acid removal from initial
polypeptide
• O-linked or N-linked glycosylation
� About 30% of eukaryotic proteins are
glycosylated
Examples of O-Glycosylations
Examples of N-Glycosylations
Examples of N-Glycosylations
• Initial groups can be
trimmed and then
expanded to create
different final
modifications
Examples of N-Glycosylations
• Another Variation
Cultivate mammalian cells!!!!
Carrel (surgeon, 1923)
Aseptic techniques
Carrel Flask
Chemically defined media (Eagle, Earle)ConsistencySterilizationReduced chance of contamination
50-s
Growth of Animal Cells in
Culture• In vitro cell culture systems enable scientists to:
– study cell growth and differentiation
– perform genetic manipulations to understand gene
structure and function.
• Culture media contains:
– Serum
– Salts
– Glucose
– Various amino acids and vitamins that the cells do
not make for themselves.
+ compuestos no-definidos: suero sanguíneo (5-15%), cocktail de factores de crecimiento, etc.
0.0940.094L-Valine
0.63510.10379L-Tyrosine • 2Na •2H2O
0.0160.016L-Tryptophan
0.0950.095L-Threonine
0.0420.042L-Serine
0.0660.066L-Phenylalanine
0.03—L-Methionine
0.1461.46L-Lysine • HCl
0.1050.105L-Leucine
0.1050.105L-Isoleucine
0.0420.042L-Histidine • HCl • H2O
0.030.03Glycine
0.0626—L-Cystine • 2HCl
0.0840.084L-Arginine • HCl
Amino Acids
0.1090.109Sodium Phosphate Monobasic (anhydrous)
6.46.4Sodium Chloride
3.73.7Sodium Bicarbonate
0.40.4Potassium Chloride
0.097670.09767Magnesium Sulfate (anhydrous)
0.00010.0001Ferric Nitrate • 9H2O
0.20.2Calcium Chloride
Inorganic Salts
Ejemplo de medio de cultivo de células de mamífero:
Dulbecco Modified Eagle medium (DMEM)
0.5840.584L-Glutamine
Add
—0.11Pyruvic Acid • Na
—0.0159Phenol Red • Na
4.54.5D-Glucose
Other
0.0040.004Thiamine • HCl
0.00040.0004Riboflavin
0.0040.004Pyridoxine • HCl
——Pyridoxal • HCl
0.0040.004D-Pantothenic Acid(hemicalcium)
0.0040.004Niacinamide
0.00720.0072myo-Inositol
0.0040.004Folic Acid
0.0040.004Choline Chloride
Vitamins
Serum
• 0-20% Serum
– Growth factors
– Transferrin (Fe)
– Lipids
– Insulin
– Shear protection
– Detoxification
Problems
– Infectious agents (viruses, mycoplasm, prions)
– serum composition is
poorly defined and the
batches vary.
– Expensive
�Completely mammalian origin free (MOF)
�chemically defined medias
Growth of Animal Cells in Culture
• Primary cultures are the
original cultures
established from a tissue.
• Permanent (or immortal)
cell lines are embryonic
stem cells or tumor cells
that proliferate indefinitely
in culture.
0.0
0.0
0.0
0.0
0.1
1.0
10.0
0 50 100Time (h)
Cx
(g/l
)
YeastHybridoma
Growth curves in yeasts and
mammalian cells are different
Minimumdensity Lag phase
exponential
Stationary
decline
Ejemplo: historia del desarrollo de la línea
HEK-293
Graham, et al., J. Gen. Virol., 36:59-72, 1977
Dificultades suplementarias
• El tiempo de división aumenta con la talla:
– Las células animales necesitan condiciones de asepsia muy estrictas
• Adhesión obligatoria:
– Ciertas líneas de células de mamíferos necesitan un soporte para ser
viables. Esto:
– presenta un problema de escalado
– las vuelve particularmente susceptibles a la disrupción
Ej: tapiz celular de mioblastos Cultivo sobre microcarriers
MODALIDAD
•Transitoria: s/ Integración: Expresión 12-72 horas
•Permanente: c/ Integración: Expresión 1-3 semanas
PARÁMETROS A CONSIDERAR
•Tipos celulares disponibles
•Expresión transitoria o permanente (estable)
•Elementos de control de expresión adecuados
Canine KidneyEpithelial
Common cell lines
CHO
HeLa
MDCK
BHK
Vero
WI-38
3T3
Chinese Hamster OvaryEpithelial
Mouse fibroblastFibroblast
Monkey KidneyFibroblast
Epithelial Human cervical carcinoma
Human fetal lungFibroblast
Baby Hamster KidneyFibroblast
MARCADORES FENOTMARCADORES FENOTÍÍPICOSPICOS
••Crecimiento en agarCrecimiento en agar••Crecimiento con bajo sueroCrecimiento con bajo suero••Cambios morfolCambios morfolóógicosgicos••Rescate de la muerte de cultivos celulares primariosRescate de la muerte de cultivos celulares primarios
MARCADORES BIOQUMARCADORES BIOQUÍÍMICOSMICOS
IndicadoresIndicadores••Anticuerpos especAnticuerpos especííficosficos••ChloramphenicolChloramphenicol acetyltransferaseacetyltransferase ((catcat))••ββ--galactosidasegalactosidase ((ββ--galgal))••LuciferaseLuciferase
SelectoresSelectores••ThymidineThymidine kinasekinase ((tktk))••XantineXantine guanineguanine phosphoribosylphosphoribosyl transferasetransferase ((xgprtxgprt))••AminoglicosideAminoglicoside phosphotransferasephosphotransferase ((aphtapht//neoneorr))••DihydrofolateDihydrofolate reductasereductase ((dhfrdhfr))••HygromycinHygromycin B B phosphotransferasephosphotransferase ((hyghygrr)
Indicadores/SelectoresIndicadores/Selectores••GreenGreen/Blue/Red /Blue/Red fluorescencefluorescence proteinsproteins ((gfpgfp//bfpbfp//rfprfp) )
MARCADORES BIOQUMARCADORES BIOQUÍÍMICOSMICOS
IndicadoresIndicadores
•Anticuerpos específicosAg + AbI � Ag.AbIAg.AbI + AbII.� � Ag.Ab.AbII.� ����: enzima, grupo fluorescente, grupo radioactivo
•Chloramphenicol acetyltransferase (cat)[14C] Chloramphenicol � Ac- [14C] Chloramphenicol � (Ac)2-[
14C] Chloramphenicol
•β-galactosidase (β-gal, lac Z)lactosa � galactosa + glucosaONPG � o-nitrofenol (amarillo) + galactosaXgal � X (azul) + galactosa
•LuciferaseLuciferina + ATP � Luciferina + ADP + hν (luz)
Indicadores/SelectoresIndicadores/Selectores•Green/Blue/Red fluorescence proteins (gfp/bfp/rfp)
XFP + hν1 (luz) � XFP + hν2 (luz) νννν1 >νννν2 Selector: FACS
Fluorescence-activated cell sorter
Reporter gene systems
1. chloramphenicol acetyl transferase (CAT)
CAT is a bacterial enzyme that catalyzes the transfer of acetyl groups from acetyl-coenzyme A to the antibiotic chloramphenicol.(chloramphenicol deactivation)
For mammalian cells
it is laborous and expensive.
Extract protein and measure activity…
thin-layer chromatographic sheetChloramphenicol
is radiolabelled
β-galactosidase (βgal) systems
luciferase (luc) systemsfirefly species Photinus pyralis
oxidation of compounds called luciferans( ATP-dependent process)
luciferans emit fluorescense
Expressed luciferase catalyses
mouse with a strain of salmonella
Mice are injected
with LUC+ salmonellas.
Sensitive digital cameras
allow non-invasive detection.
For GT vectors pictures
look the same
luminometer measurement
Green fluorescent protein (GFP)autofluorescent protein from Pacific Northwest jellyfish Aequorea victoriaGFP is an extremely stable proteinof 238 amino acids with unique post-translationallycreated and covalently-attached chromophore from oxidised residues 65-67, Ser-Tyr-Gly
ultraviolet light causes GFP to autofluoresce
In a bright green color
Jellyfish do nothing with UV,
The activate GFP by aequorin
(Ca++ activated,
biolumuniscent helper)
Green fluorescent protein (GFP)
GFP expression is harmless
for cells and animals
GFP transgenic mice from Osaka University (Masaru Okabe)
GFP construct could be used for construct tracking in living organism
GFP labelled image of a human tumor.
Vessel on the tumor surface
are visible in black
MARCADORES BIOQUMARCADORES BIOQUÍÍMICOSMICOS
SelectoresSelectores
•Thymidine kinase (tk):)dT +ATP ����dTMP +ADP ½ select. céls. tk-: HAT (hipoxantina, aminopterina, timidina)dUMP ���� dTTP inhib: aminopterina
•Xantine-guanine phosphorybosil transferase (xgprt)Xantina →→→→XMP →→→→ GMP ←←←← ←←←← guanina ½ selectivo p/toda cél.: AAMX
↑↑↑↑ inhib: ac. aminofenólico (adenosina, aminopterina,precursores →→→→ →→→→ IMP inhib: aminpoterina ac. Aminofenólico, xantina)
↓↓↓↓ASMP →→→→ AMP ASMP: ac. adenilosuccínico
•Aminoglicoside phosphotransferase (apht/neor)neomicina/kanamicina/geneticina (G418) →→→→ antibiótico fosforilado (inactivo)
•Dihydrofolate reductase (dhfr)DHF→→→→THF½ selectivo en céls. dhfr-: ausencia de nucleósidos½ selectivo p/toda cél.: methotrexate (MTX)
•Hygromycin B phosphotransferase (hygr)Hygromicina B →→→→ antibiótico fosforilado (inactivo)
Gene amplification
• Vectores virales
• Vectores no virales
TRANSFERENCIA GENTRANSFERENCIA GENÉÉTICA:TICA:METODOLOGIAMETODOLOGIA
Direccionamiento de vectores
• Via de administración
• Receptores celulares
• Promotores específicos de tejido
•• Vectores ViralesVectores Virales
Virus naturales (silvestres):•Crecen en todas las células•Infectan todas las células•Son patogénicos
Virus terapeúticos (recombinantes):•Sólo crecen en células empaquetadoras•Infectan todas las células•No son patogénicos
Figure 1. Construction of recombinant adenoviral vectors. cDNA of interest is cloned into a shuttle vector which provides cDNAexpression cassette (adenovirusITR, E1 enhancer, adenovirus encapsidation signal, CMV promoter, and SV40 a polyadenylation signal). Homologous recombination sequences arealso cloned in this vector. Adenovirus genome (e.g., pJM17 shown in the figure) and the shuttle vector containing the cDNA are cotransfected in 293 cells.Intracellular homologous recombination between the two DNAs results in a E1- recombinant genome; the numbers 0, 20, 100 represent the approximatemap units. This recombinant genome is replication defective. However, in the presence of E1 proteins (provided in trans by 293 cells), the recombinantgenome will replicate and form adenoviral particles.
Cytopathic Effect
• Cytopathic Effect can
be seen in cell
monolayer
• CPE is assessed at day 2,
4 and 7
Plaque Forming Units
• In serial viral dilutions,
areas of lysis are
observed where cells
are destroyed
• Crystal Violet
staining
VECTORES VIRALES
Retrovirus Adenovirus Herpes virus Virus Adenoasociados
Tamaño máximo del gen terapeútico
8 kb 35 kb 30 kb 4,8 kb
Células objetivo Sólo en división activa
En división activa o sin
división
En división activa o sin
división
En división o quizás sin división
Administración Ex vivo o in
situ
Ex vivo o in
situ
Ex vivo o in
situ
Ex vivo o in
situ
Expresión del gen terapeútico
Estable Transitoria Transitoria Posiblemente estable
Indice de expresión del gen terapeútico
Moderado Elevado Moderado Moderado
Riesgos Posible integración mutagénica
Reacciones inflamatorias/inmunitarias
Posible integración mutagénica
Posible integración mutagénica
Inmunidad preexistente en el hospedador
No Sí Sí Sí
Recombinación con el hospedador
Improbable Posible Posible Improbable
Recombinación con el virus parental
Imposible Posible Posible Posible
•• VectoresVectores no no ViralesVirales
•Microinyección / Perforación (DNA desnudo)•Precipitación con fosfato de calcio•Liposomas aniónicos•Complejos DNA/lípido catiónico: lipoplex•Complejos DNA/polycatión: polyplex•Conjugados moleculares•Dendrímeros: PEI•Hydrogel•Nanoesferas Biopolímero-DNA •Complejos LPD•Inyección a presión•Electroporación•Cañón génico•Ultrasonido•Campo magnético
TransfectionMicroinjection
Lipofection Electroporation
Liposomes
Why naked DNA?
Lets’ wrap it in something safe
to increase transfection rate
Therapeutic drugs
Lipids – is an obvious idea !
Liposomes are formed by the self-assembly of phospholipid
molecules in an aqueous environment.
www.emc.maricopa.edu/faculty/ farabee/BIOBK/
Anionic liposome
Cationic liposomes
positively charged lipid dropletscan interact with negatively charged DNA
to wrap it up and deliver to cells
Positively charged lipid heads
Lipofectin, lipofectamine, lipofectase….
Inside liposomes DNA is resistant to degradation
Lab procedure for liposome
preparation
Lípidos catiónicos: Citofectinas
Complejo DNA/lípido catiónico: Lipoplex
Electron photomicrographs of lipid-DNA complexes.
Zabner J et al. J. Biol. Chem. 1995;270:18997-19007
Electron photomicrographs of lipid-DNA complexes. Lipid-DNA complexes were prepared at a ratio of 5:1 (w/w). PanelA shows appearance of plasmid DNA without lipid. Panels B-Fshow examples of the various types of complexes that were observed. In panelB the open arrow shows uncomplexed plasmid and the solid arrow shows plasmid complexed with lipid. Bar indicates 100 nm. DMRIE:DOPE 1:1
Electron photomicrographs of COS cells transfected with gold-labeled DNA complexed with lipid (DMRIE:DOPE 1:1).
Zabner J et al. J. Biol. Chem. 1995;270:18997-19007
Electron photomicrographs of COS cells transfected with gold-labeled DNA complexed with lipid. Cells were exposed to DMRIE/DOPE•DNA complexes and then removed for electron microscopy at the following times: panel A, 5 min;panel B, 30 min; panel C, 1 h;panel D, 6 h; panel E, 24 h;panel F, 24 h. Cells transfectedwith plasmid that had not been labeled with gold are shown inpanelF. Bar indicates 100 nm.
Protein-mediated plasmid nuclear import. Transcription factors and other nuclear proteins normally enter the nucleus through interactions between their NLSs and importin family members. However, if plasmids containing certain sequences that act as scaffolds for transcription factors and other DNA binding proteins (termed ‘DTS’, or DNA nuclear targeting sequences) are deposited into the cytoplasm during transfection, they can form complexes with these proteins, thereby attaching NLSs to the DNA. Some, but not all, of these NLSs may be in a conformation able to interact with importins for transport of the DNA–protein complex into the nucleus through the nuclear pore complex.
Methods to enhance plasmid nuclear import. A number of different approaches have been developed to promote recognition of plasmids by importin family members to increase nuclear import. These include peptide-nucleic acid clamp-conjugated NLS peptides bound to DNA, sequence-specific DNA binding proteins bound to DNA, NLS peptides covalently attached to DNA and NLS peptides electrostatically bound to DNA.
••Lipids / Lipids / PolycationsPolycations / DNA (LPD) Complexes/ DNA (LPD) Complexes
LPD-I: Cationic Liposome Entraped,Polycation – Condensed DNA →→→→
←←←← LPD-II: Anionic Liposome Entraped,Polycation – Condensed DNA
How to make the gene expressed in the target
cell?
Four basic types of expression vectors :
1.Minimal promoters used to study gene regulatory elements such
as enhancer elements (in the lab studies).
2. Constitutive promoters used to direct expression of gene products
to produce enough target protein.
3. Cell-specific promoters used to specify expression to target cells
(tissue-specific promoters in case of GT)
4. Regulated promoters used to control the on/off expression
of cloned genes.
JUST TATA box and reporter
Sites for constitutive transfactors
Sites for cell-specific transfactors
Sites for small ligand responsive transfactors
www.biochem.arizona.edu
Examples of often used promoters
Moderately high level gene expression in
mammalian cells
simian virus 40 early
enhancer/prom. SV40
Regulated by doxycycline (tetracycline)TET-off and TET-on systems
based on tet-resistance
operon of the E. coli Tn10
transposon
steroid-regulated gene expression in mammalian cells
mouse mammary tumor virus long terminal repeat enhancer/promoter MMTV)
Regulated
promoters
targeted expression of genes to mouse thymocytes for immunological studies
lymphocyte-specific tyrosine kinasepromoter (LCK)
targeted expression of genes to mammary
tissue in animals
whey acidic protein promoter (WAP)
Cell-specific
promoters
high level gene expression in mammalian
cells
cytomegalovirus
immediate early promoter
(CMV)
High activity
constitutive
promoters
a ubiquitous low level promoter that is used to construct
reporter genes
deleted Drosophila alcohol
dehydrogenase promoterMinimal promoter
Generalized Eukaryotic Cloning
Vector
• Prokaryotic origin of
replication, selectable
marker
• Eukaryotic origin,
selectable marker
• MCS with eukaryotic
promoter and
transcriptional
terminator/polyadenylatio
n signal
Mammalian Systems
• Sometimes insect cells simply don’t carry
out proper/necessary glycosylations
• Other processing may also not occur
• Mammalian cell systems are more
expensive by may be required for active
product
Mammalian Expression Vector
• “I” is an intron that enhances expression
• Other signals similar to insect and prokaryotic
vectors
Translation Control Elements
• K - Kozak Sequence (equiv. To rbs)
• S - for secretion signal peptide
• T – tag peptide for purification
• P – proteolytic cleavage sequence
• SC – stop codon for translation
• 3’UTR – proper sequences for efficient translation and
mRNA stability (e.g. polyadenylation sequence)
Two Vector Expression System
•Useful for proteins of two different polypeptides
Two Gene Expression Vector
Bicistronic Expression Vector
IRES from mammalian virus
•Gives more uniform level of expression of two genes
Tetracycline-responsible systemsManfred Gossen and Hermann Bujard
www.biochem.arizona.edu
control the expression of genes that have been cloned downstream of a
promoter containing tetracycline receptor (TetR) binding sites.
The "Tet-off" system is repressed
in the presence of the doxycycline
VP is derived from the herpes simplex virus VP16 protein.
TET-VP producing vector
Gene of interest
expressing vector
VP – RNA pol interacting part
TetR - tet binding part
TET-OFF system
"Tet-on" system is activated in the presence of
doxycyclinethe DNA binding domain of the Tet-on regulator (rTetR) contains mutations
repressor that only binds DNA in the absence of ligandis converted to a ligand-dependent DNA binding protein.
RNA-pol
VECTORESNO VIRALES
Conjugadosmoleculares
Transfecc. Liposomascatiónicos
Vector ideal
Capacidad de inserción
Irrestricto Irrestricto Irrestricto 1-1000 kb
Eficiencia detransferencia
Eficiente Eficiente Eficiente Muy eficiente
Integración No No/Rara No Sí/No
Generación virus recombinantes
No No No No
Oncogenicidad ? ? ? No
Expresión deproteínas virales
No No No No
Expresión estable Transitoria Transitoria Transitoria Sí/No
Administraciónin vivo
? Sí Sí Sí
Transmisión acéls. quiescentes
No Sí Sí Sí
Top Fifteen Biopharmaceuticals (1999 Sales)
Epogen Amgen Erythropoeitin αααα $1,770
Neupogen Amgen G-CSF $1,245
Infergen Schering-Plough Interferon $1,010
Humulin Eli Lilly Insulin $ 880
Avonex Biogen Interferon ββββ 1a $ 570
Engerix SmithKline Beecham Hepatitis B vaccine $ 505
KoGENate Bayer Corporation Factor VIII $ 470
Cerezyme Genzyme Tissue Repair Glucocerebrosidase $ 430
Betaseron Berlex Laboratories Interferon ββββ 1b $ 395
GenoTropin Pharmacia & Upjohn Human growth hormone $ 380
Enbrel Immunex TNF αααα receptor $ 340
ReoPro Centocor Monoclonal antibody $ 335
Gonal-F Serono Laboratories Follicle stimulating hormone $ 320
RECOMBIVAX HB Merck Heptatis B vaccine $ 275
Synagis MedImmune Monoclonal antibody $ 275
TOTAL: $9,200
http://www.lonza.com/group/en/news/downloads/speeches.Par.0028.File2.tmp/part2.pdf
The resulting proteins are found to have comparable structures and activity profiles
although strictly speakingnot being necessarily identical
Just a few products could be produced by using both mammalian and microbial systems
Mammalian system demands on the
grow
http://www.lonza.com/group/en/news/downloads/speeches.Par.0028.File2.tmp/part2.pdf