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http://dspace.mediu.edu.my:8181/xmlui/handle/1721.1/3948Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.creator | Murugesan, Nivetha | - |
| dc.creator | Du, Tai | - |
| dc.creator | Stephanopoulos, Gregory | - |
| dc.creator | Lee, Jim Yang | - |
| dc.creator | Too, Heng-Phon | - |
| dc.date | 2003-12-16T14:23:30Z | - |
| dc.date | 2003-12-16T14:23:30Z | - |
| dc.date | 2004-01 | - |
| dc.date.accessioned | 2013-10-09T02:33:18Z | - |
| dc.date.available | 2013-10-09T02:33:18Z | - |
| dc.date.issued | 2013-10-09 | - |
| dc.identifier | http://hdl.handle.net/1721.1/3948 | - |
| dc.identifier.uri | http://koha.mediu.edu.my:8181/xmlui/handle/1721 | - |
| dc.description | Intracellular communication controls most cellular functions, which includes cell growth, death, and differentiation. The current challenge in cell biology is to decipher the spatial-temporal interactions of these highly complex intracellular signaling pathways in mediating the various cellular responses. A number of emerging tools are available for the analyses of the proteome or the protein complement of the genome. However, these tools are generally not applicable for the profiling of molecules involved in the signaling pathways. The significant challenges include the lack of sensitivity, specificity and throughput. Conventional protein chip technology with capture moieties immobilized onto solid-surface, promises to be a powerful tool for large scale high-throughput proteome profiling. This approach has a number of drawbacks, among which the stability of the capture moieties in the given format pose a significant problem. Here we report the development and application of a novel multiplexed and high-throughput platform for the quantitative profiling of activated intracellular signalling proteins subsequent to ligand-receptor induced signalling. This spatially addressable biochip platform will allow comprehensive mapping of interconnected signal pathways, through identification of key functional signalling proteins (â nodes’) in each pathway and quantifying their state of activity. | - |
| dc.description | Singapore-MIT Alliance (SMA) | - |
| dc.format | 13793 bytes | - |
| dc.format | application/pdf | - |
| dc.language | en_US | - |
| dc.relation | Molecular Engineering of Biological and Chemical Systems (MEBCS); | - |
| dc.subject | intracellular signaling pathways | - |
| dc.subject | proteome profiling | - |
| dc.subject | ligand-receptor induced signalling | - |
| dc.subject | activated intracellular signalling proteins | - |
| dc.title | Signaling Biochip – Profiling ligand-receptor induced signalling | - |
| dc.type | Article | - |
| Appears in Collections: | MIT Items | |
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