Patent Application
20050272035
The present invention relates to novel high-throughput functional genomic methods for determining gene and protein function in a cellular context. The method also has utility in identifying novel chemical modulators of gene and protein/enzyme activity.
The large amounts of gene sequence, gene expression and protein expression data arising from the Human Genome Project, and from further downstream investigative efforts, have the potential to allow identification of many new drug targets. Realisation of this potential will require significant efforts in determining the function of new gene products and validating these proteins as drug targets.
Obtaining valid functional information on gene and protein function requires function to be determined (or confirmed) in-context; i.e. the function of the gene/protein should be determined in the presence of other genes/proteins which are likely to interact with it. Consequently there is a need for cell-based approaches for functional screening that enable functional information to be derived in-situ in a cellular environment where dynamic interactions between components may require other cellular components not available in a solution assay.
Moving high-throughput biology into cellular assays can build on and parallel previous work correlating and clustering transcription and interaction data derived from micro-array and protein-protein interaction studies (Ge et al. (2001) Nature Genetics 29, 482-486). Aided by high throughput analysis technologies, cellular screening based approaches can begin to address the complexity necessary to unravel intracellular pathways and control in mammalian cells (Giese et al. (2002) Drug Discovery Today 7, 179-185), with the ultimate aim of producing sufficiently detailed description to allow a representation of cellular processes at a system level (Endy & Brent (2001) Nature 409,391-395; Kitano (2002) Science 295, 1662-1664).
To achieve functional screening in a cellular context two elements are required;
In current procedures a test system is interrogated for the effects of genetic or chemical variance (i.e. up- or down-regulating expression of one gene, or the presence or absence of a candidate drug respectively), either alone or in combination. Consequently the effects (and by inference the function) of a gene (effector) or a drug (modulator) on a read-out from a test cell can be measured in isolation or in combination by observation of the behaviour of the test system. By using combinations of effectors and modulators of known and unknown function it is possible to begin to derive functional linkage between known and unknown entities and hence to assign function.
Use of cell-based assays for such screens (Croston (2002) Trends in Biotechnology 20,110-5; Zheng & Chan 2002 Current Issues in Molecular Biology 4, 33-43) is becoming more widely adopted for reasons of acquiring contextual information as described above. Such assays employ a wide variety of assay methodologies, including reporter gene assays, cell growth, pre-cursor incorporation, cell transformation, cell morphology, and fluorescent enzyme assays. These approaches to functional screening have typically used pre-existing assays and instrumentation (e.g. measurement of a luciferase reporter gene in a luminometer) which require assay development prior to the screening process and which yield data averaged for a cell population under test.
U.S. Pat. No. 6,322,973 (Iconix Pharmaceuticals) describes surrogate means for discovering chemical modulators of genes of unknown function. A heterologous gene of unknown function is expressed in a host cell (e.g. expression of a human gene in a yeast cell) and the host cell is evaluated for a resulting change in phenotype which can then be used as the basis of a cellular assay. Consequent exposure of the host cell exhibiting an altered phenotype to a test substance and assaying for an effect of the test substance on the cellular assay identifies test substances which are modulators of the function of the heterologous gene.
U.S. Pat. No. 6,340,595 (Galapagos Genomics) describes means for identifying the function of the products of a library of sample nucleic acids by expression of the library of nucleic acids in adenoviral vectors. The sample nucleic acids are synthetic oligonucleotides, DNA, or cDNA and encode polypeptides, antisense nucleic acids, or genetic suppressor elements. The sample nucleic acids are expressed in a host and the resultant altered phenotype used to assign a biological function to the product encoded by the sample nucleic acid. WO0202740 (Rosetta Inpharmatics) describes methods and systems (e.g., computer systems and computer program products) for characterising cellular constituents, particularly genes and gene products. The invention provides methods for assigning or determining the biological function of uncharacterised genes and gene products by using response profiles derived from measurements of pluralities of cellular constituents in cells having a modified gene or gene product, as phenotypic markers for the gene product. Methods are provided for clustering such response profiles so that similar or correlated response profiles are organised into the same cluster. The invention also provides databases of response profiles to which the response profile of an uncharacterised gene or gene product are compared.
WO0171023 (Genetrace) describes methods for deciphering genetic function. The method provides a matrix of cell lines in which target-specific modified cell lines differ from parental cells in the activity or concentration of a selected protein or nucleic acid. The matrix of cells is exposed to one or more stimuli or test compounds and the cell matrix profiled for response(s) to the stimuli or test compounds. Analysis of the resulting profiles yields information on the genetic function of elements that differ in activity or concentration across the matrix of cells.
All of the above prior-art methods are characterised by one or more of the following;
A significant problem encountered in the prior art assays described above is that they rely on pre-existing assays and are thus, a priori, limited in scope, coverage of biological events being limited by the availability of known assays. This leads to the further problem that assignment of function is limited to those entities which interact with a biological process linked to an available assay read-out. Furthermore, since in general these assays report on cause and effect relationships averaged across a cell population, they do not yield information on the distribution of response across a cell population (e.g. due to cell cycle status, or due to a mixed population of responding and non-responding cells). An additional problem with the prior art methods is that the assays can only be used on stable populations of cells and are not generally suitable for use with non-homogeneous populations of cells such as transiently transfected cells.
Consequently what is required to increase the efficiency of functional screening are methods which do not require pre-existing assays, have the broadest possible coverage of cellular processes and provide data at the individual cell level. The present invention provides methods for functional screening in which assays are generated in concert with screening in an iterative process which expands the scope of biological coverage with each iteration and which uses image-based analysis to yield data at sub-cellular resolution.
The method of the present invention circumvents at least some of the limitations of prior-art methods discussed above by providing means to generate-functionally diagnostic assays which are integrated into a functional screening process. The method takes advantage of the fact that many cellular proteins exhibit a characteristic cellular localisation and in many cases change their cellular localisation in response to certain stimuli. Consequently, given collections of coding nucleic acid sequences and of chemical compounds, where both collections contain members of known and unknown function, it is possible to generate pairings of one nucleic acid sequence with one chemical compound to produce a specific cellular localisation of a marker coupled to the product of the nucleic acid sequence. Such pairings may then be used as diagnostic assays for testing against other collection members and thus build up clusters and linkages therebetween. In this way, using some members of each collection which are of known function, it is possible to assign function to previously uncharacterised elements by linkage to known elements.
Thus the method of the present Invention allows function to be assigned at a molecular and temporal level for any cellular component, chemical, drug or other active moiety which induces a change in behaviour of an endogenous or exogenous cellular component by reference to changes induced by other moieties of known function. Non-destructive single cell analytical methods are used to analyse the cellular behaviour of indicators influenced by genetic effectors and chemical modulators, where the indicators and effectors may be either endogenous or exogenous to the cell.
According to a first aspect of the present invention, there is provided a method for determining the function or effect of a genetic element or a chemical modulator from a library of genetic elements and chemical modulators of known and unknown function on a population of cells, the method comprising
In the context of the present invention, the following terms are to be interpreted as defined below:
In a second aspect of the present invention, there is provided a method for determining the function or effect of a genetic element or a chemical modulator from a library of said genetic elements and chemical modulators of known and unknown function on a population of cells, the method comprising
Suitably, the effector nucleic acid sequence encodes a protein or peptide and is selected from the group consisting of DNA, cDNA, RNA and Protein Nucleic Acid.
Preferably, the effector nucleic acid sequence is an antisense oligonucleotide (cf. Dean (2001) Current Opinion in Biotechnology, 12, 622-625). More preferably, the effector nucleic acid is a small interfering RNA (siRNA) which causes gene silencing (cf. Elbashir et al., (2002) Methods, 26, 199-213). RNA interference (RNAi) is a highly conserved gene silencing mechanism that uses double-stranded RNA as a signal to trigger the degradation of homologous mRNA. The mediators of sequence-specific mRNA degradation are 21- to 23-nt small siRNAs generated by ribonuclease III cleavage from longer double-stranded RNA.
Preferably, there is provided an expression vector comprising suitable expression control sequences operably linked to an indicator or an effector nucleic acid sequence according to the present invention. The DNA construct of the invention may be inserted into a recombinant vector, which may be any vector that may conveniently be subjected to recombinant DNA procedures. The choice of vector will often depend on the host cell into which it is to be introduced. Thus, the vector may be an autonomously replicating vector, ie. a vector which exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g. a plasmid. Alternatively, the vector may be one which, when introduced into a host cell, is integrated into the host cell genome and replicated together with the chromosome(s) into which it has been integrated.
The vector is preferably an expression vector in which the effector or indicator nucleic acid sequence is operably linked to additional segments required for transcription of the nucleic acid. In general, the expression vector is derived from plasmid or viral DNA, or may contain elements of both. Preferably, the expression vector is selected from the group consisting of plasmid, retrovirus and adenovirus. The term, “operably linked” indicates that the segments are arranged so that they function in concert for their intended purposes, e.g. transcription initiates in a promoter and proceeds through to protein synthesis.
The promoter may be any DNA sequence which shows transcriptional activity in a suitable host cell of choice, (eg. a mammalian cell, a yeast cell, or an insect cell) for transcription of the indicator or effector nucleic acid sequence. The promoter may be derived from genes encoding proteins either homologous or heterologous to the host cell.
Examples of suitable promoters for directing the transcription of the nucleic acid sequences of the invention in mammalian cells are the CMV promoter (U.S. Pat. No. 5,168,062, U.S. Pat. No. 5,385,839), Ubiquitin C promoter (Wulff et al. (1990) FEBS Lett. 261, 101-105), SV40 promoter (Subramani et al. (1981) Mol. Cell Biol. 1, 854-864) and MT-1 (metallothionein gene) promoter (Palmiter et al. (1983) Science 222, 809-814). An example of a suitable promoter for use in insect cells is the polyhedrin promoter (U.S. Pat. No. 4,745,051; Vasuvedan et al. (1992) FEBS Lett. 311, 7-11). Examples of suitable promoters for use in yeast host cells include promoters from yeast glycolytic genes (Hitzeman et al. (1980) J. Biol. Chem. 255, 12073-12080; Alber & Kawasaki (1982) J. Mol. Appl. Gen. 1, 419-434) or alcohol dehydrogenase genes (Young et al., in Genetic Engineering of Microorganisms for Chemicals (Hollaender et al., eds.), Plenum Press, New York, 1982), or the TPI1 (U.S. Pat. No. 4,599,311) or ADH2-4c (Russell et al., (1983) Nature 304, 652-654) promoters.
The effector and indicator nucleic acid sequences of the present invention may also, if necessary, be operably connected to a suitable terminator, such as the human growth hormone terminator, TPI1 or ADH3 terminators. The vector may further comprise elements such as polyadenylation signals (e.g. from SV40 or the adenovirus 5 Elb region), transcriptional enhancer sequences (e.g. the SV40 enhancer) and translational enhancer sequences (e.g. the ones encoding adenovirus VA RNAs).
The vector may further comprise a DNA sequence enabling internal ribosomal entry and expression of two proteins from one bicistronic transcript mRNA molecule. For example, the internal ribosomal entry sequence from the encephalomyocarditis virus (Rees S, et al. (1996) BioTechniques, 20, 102-110 and U.S. Pat. No. 4,937,190).
The recombinant vector may further comprise a DNA sequence enabling the vector to replicate in the host cell in question. An example of such a sequence (when the host cell is a mammalian cell) is the SV40 origin of replication.
When the host cell is a yeast cell, examples of suitable sequences enabling the vector to replicate are the yeast plasmid 2 μl replication genes REP 1-3 and origin of replication.
The vector may also comprise selectable markers, such as a gene that confers resistance to a drug, e.g. ampicillin, kanamycin, tetracyclin, chloramphenicol, puromycin, neomycin or hygromycin.
The procedures used to ligate the effector and indicator nucleic acid sequences of the invention, the promoter and optionally the terminator and/or targeting sequence, respectively, and to insert them into suitable vectors containing the information necessary for replication, are well known to persons skilled in the art (e.g. Molecular Cloning, Sambrook & Russell, Cold Spring Harbour Press 2001).
Suitably, the indicator nucleic acid sequence comprises a detectable label or encodes a detectable label. Preferably, indicator nucleic acid sequence is created by fusing the effector sequence to a nucleic acid sequence encoding a detectable label.
Suitably, the detectable label is selected from the group consisting of fluorescent protein, enzyme, antigen and antibody.
Fluorescent proteins and fluorescent protein derivatives of chromoproteins have been isolated from a wide variety of organisms, including Aequoria victoria, Anemonia species such as A. majano and A. sulcata, Renilla species, Ptilosarcus species, Discosoma species, Claulada species, Dendronephthyla species, Ricordia species, Scolymia species, Zoanthus species, Montastraea species, Heteractis species, Conylactis species and Goniopara species.
The use of Green Fluorescent Protein (GFP) derived from Aequorea victoria has revolutionised research into many cellular and molecular-biological processes. However, as the fluorescence characteristics of wild type (native) GFP (wtGFP) are not ideally suited for use as a cellular reporter, significant effort has been expended to produce variant mutated forms of GFP with properties more suitable for use as an intracellular reporter (Heim et al., (1994), Procedings of the National Acadamy of Sciences (USA), 91, 12501; Ehrig et al., 1995, FEBS Letters, 367,163-6; WO96/27675; Crameri, A. et al., (1996), Nature Biotechnology 14, 315-9; U.S. Pat. No. 6,172,188; Cormack, B. P. et al., (1996) Gene 173, 33-38; U.S. Pat. No. 6,194,548; U.S. Pat. No. 6,077,707 and GB Patent Number 2374868 (‘Amersham Biosciences UK Ltd.’). Preferred embodiments disclosed in GB Patent No 2374868 comprise GFP derivatives selected from the group consisting of: F64L-V163A-E222G-GFP, F64L-S175G-E222G-GFP, F64L-S65T-S175G-GFP and F64L-S65T-V163A-GFP.
In a preferred embodiment, the fluorescent protein is a modified Green Fluorescent Protein (GFP) having one or more mutations selected from the group consisting of Y66H, Y66W, Y66F, S65T, S65A, V68L, Q69K, Q69M, S72A, T203I, E222G, V163A, I167T, S175G, F99S, M153T, V163A, F64L, Y145F, N149K, T203Y, T203Y, T203H, S202F and L236R.
Preferably, the modified GFP has three mutations selected from the group consisting of F64L-V163A-E222G, F64L-S175G-E222G, F64L-S65T-S175G and F64L-S65T-V163 as disclosed in GB Patent Number 2374868.
Preferably, the enzyme is selected from the group consisting of β-galactosidase, nitroreductase, alkaline phosphatase and β-lactamase. The indicator nucleic acid sequence can thus be detected by the action of the enzyme on a suitable substrate added to the cell. Examples of such substrates include nitro-quenched CyDyes™ (Amersham Biosciences, nitroreductase substrate), ELF 97 (Molecular Probes, alkaline phosphate substrate) and CCF2 (Aurora Biosciences, β-lactamase substrate).
Suitably, the modulator is selected from the group consisting of organic compound, inorganic compound, peptide, polypeptide, protein, carbohydrate, lipid, nucleic acid, polynucleotide and protein nucleic acid. Preferably, the modulator is selected from a combinatorial library comprising similar organic compounds such as analogues or derivatives.
Suitably, the cell is a eukaryotic cell. Preferably, the eukaryotic cell is selected from the group consisting of mammal, plant, bird, fungus, fish, insect and nematode, which cell may or may not be genetically modified. More preferably, the mammalian cell is a human cell, which cell may or may not be genetically modified.
Preferably, the localisation of the detectable label is determined using an imaging system. A suitable Imaging System is the In Cell Analyzer, as described in WO 99/47963 and PCT/GB03/01816.
In a third aspect of the present invention, there is provided an automated system for determining the function or effect of a chemical and/or a genetic element on a population of cells comprising use of the method as hereinbefore described together with an imaging system and a computerised data processing device.
To achieve the method of the current invention one or more of a collection of nucleic acid sequences [10] (
Expression of the detectable fusion protein in a population of host cells [30] yields a distribution of the detectable protein characteristic of the distribution of the protein encoded by the nucleic acid sequence [10]. Expression of the fusion protein in a second population of host cells [50] in the presence of a test compound [40] will in certain circumstances yield a distribution of the fusion protein [70] which differs from that in the absence of the test compound [60]. In such cases of combinations of [20] and [40] which yield distribution patterns where [60] differs from [70] the particular combination of test compound and detectable fusion protein provide a basis for further investigations. It is an important aspect of this process that it does not require knowledge of the identity or biological function of either component [10] or [40] to be known, beyond that required to follow the process as described; e.g. sufficient sequence information for [10] to enable assembly of the fusion construct [20]. This process establishes combinations of fusion proteins [20] and test compounds [40] which together engineer a defined and responsive cellular phenotype, i.e. a cell-based assay which can be used in further functional screening.
Once key combinations of [20] and [40] have been established in which [40] exhibits a reproducible activity in modulating the cellular distribution of [20], a second round of screening may be carried out in which nucleic acid sequences [10] are transfected into cells expressing the detectable fusion protein in the absence [60] and presence [70] of the test compound [40]. Cells are subsequently evaluated for modulation of the engineered phenotype to identify nucleic acid sequences [10] which modulate the cellular distribution of the detectable fusion protein either alone [80], or in combination [90] (antagonism or synergy) with the test compound.
Repetition of the screening process (
Large scale screening using a library of nucleic acid sequences of known and unknown function in combination with a collection of test compounds of characterised or uncharacterised biological activity can therefore be carried out to establish combinations of nucleic acid sequences and chemical entities which operate in concert to modify a detectable cellular phenotype measured by a cellular assay. Since the process inherently generates cellular assays the method has advantages over previously used approaches in that it does not require either prior knowledge of biological activities or pre-existing cell assays; although the process may be used in conjunction with pre-existing cell-based assays, where available.
A number of groups (Bejarano et al. (1999) J Cell Sci 112 (23), 4207-11; Misawa et al. (2000) Proc Natl Acad Sci USA 97, 3062-6; Gonzalez et al. (2000) Trends Cell Biol 10,162-5; Rolls et al., (1999) J. Cell Biol. 146, 29-44; Simpson et al. (2000) EMBO 1, 287-92) have reported using GFP tagging of unknown genes or sequence motifs arising from cDNA libraries or other sources to identify sequences associated with proteins of defined sub-cellular localisation. Developments are already in place to automate cloning (Rolls et al. (1999) J. Cell Biol. 146, 29-44) which allows high-throughput generation of the N- and C-terminal GFP fusions necessary for transfection.
Use of high throughput image based analysis using instruments such as the Amersham Biosciences IN Cell Analyzer (Goodyer et al. (2001), Society for Biomolecular Screening, 7th Annual Conference and Exhibition, Baltimore, USA Screening and signalling events in live cells using novel GFP redistribution assays) permits the use of assays measuring tagged protein localization to be carried out on transiently modulated cells, (e.g. by transient cDNA transfection) with data collected on an individual cell basis. This approach offers a number of benefits, including removal of the need to pre-establish stable indicator cell lines prior to screening yields assay results which are less likely to be distorted by ‘over-expression squelching’ and phenotype distortion arising through cellular selection (Giese et al Drug Discovery Today (2002) 7, 179-186) associated with generation of large numbers of stable cell lines.
The method of the invention may be used to establish functional relationships between genetic elements (effectors), chemical elements (modulators) and cellular assays (indicators). Starting from collections of effectors [210] (
Consequently by collecting data from a large number of triplets where unknown elements are tested in combination with known elements and selecting triplets in which there is an interaction between all three components it is possible to assemble networks of functional linkages which yield information on the biological function of previously uncharacterised elements. For example a triplet [400] (
A collection of cDNAs (Invitrogen & Image Consortium, Table 2) were prepared for expression as cDNA-EGFP fusion proteins by inserting cDNA sequences into the multiple cloning site of pCORON 1000-EGFP-N2 and pCORON1000-EGFP-C1 expression vectors (Amersham Biosciences) using standard molecular cloning techniques (Molecular Cloning, Sambrook & Russell, Cold Spring Harbour Press 2001). These vectors direct the expression of fusion proteins comprising the protein encoded by the inserted cDNA sequence fused at their amino and carboxy termini to EGFP in mammalian cells under the control of a constitutively active CMV promoter.
Expression vectors encoding cDNA-EGFP indicators were transiently transfected into HeLa cells growing in wells of 96 well microtitre plates by chemically mediated transfection (Fugene, Roche) and cells incubated under standard growth conditions for 24 hours to permit synthesis of indicator fusion proteins. Cells were subsequently stained with DRAQ 5, a cell permeable nuclear DNA binding dye (Biostatus), to fluorescently mark cell nuclei, and all wells imaged with dual laser excitation (EGFP 488 nm, DRAQ 5 633 nm) using an IN Cell Analyzer (Amersham Biosciences). Data for green (EGFP) and red (DRAQ 5) fluorescence were collected for all cells (
Data collection and analysis as described above allows cDNA-EGFP fusion proteins to be used as indicators in transiently transfected cell populations by using data thresholding to distinguish transfected from non-transfected cells, so avoiding the need to engineer stable cell lines required for analysis methods which use population average measurements.
Indicator proteins derived from a range of cDNAs as described for Example 1 were transfected into HeLa cells and allowed to express for 24 hours. Following expression, cells were transferred into serum-free media for 2 hours to allow effects of stimuli from serum factors such as cortisol to decay. Cells were stained with DRAQ 5, imaged as described in Example 1, returned to complete media and then exposed to 1 μM dexamethasone (a synthetic glucocorticoid agonist) or 1 μM staurosporine (kinase inhibitor and apoptosis inducer) for 5 minutes followed by repeat imaging. Image data were analysed using a nuclear trafficking algorithm (Amersham Biosciences; (cf. Adie et al. (2001) ‘The pharmacological characterisation of a GPCR using pH sensitive cyamine dyes on the LEADseeker Cell Analysis System’ Poster, Society for Biomolecular Screening Conference 10-13th Sep. 2001, Baltimore USA; Goodyer et al. (2001) ‘Screening of signalling events in live cells using novel GFP redistribution assays’ Poster, Society for Biomolecular Screening Conference 10-13th Sep. 2001). The alogorithm returns a numerical description of fluorescence distribution in nucleus and cytoplasm as a ratio (nuclear fluorescence divided by cytoplasmic fluorescence; N/C). This algorithm allows the spatial distribution of cDNA-EGFP fusion proteins to be quantitated in expressing cells: a low N/C ratio indicating a cytoplasmic location for the indicator protein, a high N/C ration indicating a nuclear location. Consequently a change in N/C ratio for an indicator protein induced by a chemical modulator indicates a translocation of the indicator in response to the modulator. This form of analysis permits screening of combinations of indicators/chemical modulators for pairings in which the indicator exhibits translocation in response to the modulator, and may serve as the basis for testing the action of effectors or further modulators on the characterised response.
Results from this analysis are shown in
Data from this example are also shown in
A further group of indicator proteins were transfected into HeLa cells and cells imaged before and after exposure to staurosporine as described in Example 2. Images were analysed with a further two IN Cell Analyzer algorithms, Granularity and Membrane Spot (Amersham Biosciences) (cf. Adie et al. (2001) ‘The pharmacological characterisation of a GPCR using pH sensitive cyamine dyes on the LEADseeker Cell Analysis System’ Poster, Society for Biomolecular Screening Conference 10-13th Sep. 2001, Baltimore USA; Goodyer et al. (2001) ‘Screening of signalling events in live cells using novel GFP redistribution assays’ Poster, Society for Biomolecular Screening Conference 10-13th Sep. 2001). These algorithms return results which quantitate fluorescence in degrees of granularity (i.e. low value indicates uniform distribution, high value indicates punctate distribution) and in terms of membrane localisation. Consequently these algorithms are suitable for examining indicators which no not exhibit cytoplasmic to nuclear differential localisation and hence are unsuitable for analysis by the algorithm used in the previous example.
Results from analysis with these two algorithms on staurosporine treated cells are shown in
A range of cDNA modulators were transiently transfected into CHO cells expressing a NFκB p65-GFP fusion protein. This indicator undergoes a well characterised cytoplasmic to nuclear translocation in response to a number of stimuli, including exposure to Interleukin-1 (IL-1). Cells were incubated for 24 hours post transfection, stained with DRAQ 5, imaged, and then stimulated with IL-1, followed by repeat imaging. N/C ratios were determined for all images using the algorithm described in Example 2, and a scatterplot (
In an experiment of this design where two factors (stimulus and effector) may change the behaviour of the indicator, a number of possibilities may occur;
all of the above may, depending on their combination, result in a modulation of the magnitude of change of the indicator N/C ratio induced by IL-1 stimulus. The scatterplot of
In addition, the diagonal dotted line on
The functional screen of Example 4 was repeated with a second indicator, RAC1 (T)-GFP, in the presence and absence of stimulation with insulin and analysed using the membrane spot algorithm described in Example 3. As in Example 4 it is clear that the effectors used in this experiment are having a range of effects on the distribution of the indicator protein in changing the cellular distribution of the indicator both before and after insulin stimulus and in changing the overall response to insulin stimulation (
| Number | Date | Country | Kind |
|---|---|---|---|
| 0216674.2 | Jul 2002 | GB | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/GB03/02983 | 7/10/2003 | WO | 1/13/2005 |
