Drug targets: single-cell transcriptomics hastens unbiased discovery
Supporting Files
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October 25 2011
File Language:
English
Details
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Alternative Title:Trends Pharmacol Sci
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Personal Author:
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Description:Drug discovery in neuro- and psychopharmacology is lagging, and the most commonly mentioned cause is the scarcity of drug targets. Using NextGen 'sequencing based single-cell transcriptomics' (SBSCT), several hundred different receptors and channels can be identified in individual neurons, and the functional gene product can subsequently be validated. The use of single-cell transcriptome data to reveal the entire receptor repertoire is crucial, as the copy numbers of mRNAs encoding receptors are low, and when cells are pooled dilution of rare mRNAs leads to loss of signal. These overlooked receptors on key neurons often mediate robust effects that may be therapeutically useful. SBSCT also enables the identification of orphan receptors and can provide strong evidence for receptor heterodimers. Here, we compare SBSCT to other single-cell profiling methods. We argue that the unbiased nature of SBSCT makes it a powerful tool for the identification of new drug targets.
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Subjects:
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Source:Trends Pharmacol Sci. 2011; 33(1):9-16
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Pubmed ID:22032985
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Pubmed Central ID:PMC3259260
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Document Type:
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Funding:U01 NS063560/NS/NINDS NIH HHS/United States ; R37 AG009900/AG/NIA NIH HHS/United States ; R01 AG009900/AG/NIA NIH HHS/United States ; MH88849,/MH/NIMH NIH HHS/United States ; U01 NS063560-03/NS/NINDS NIH HHS/United States ; DP10D004117/DP/NCCDPHP CDC HHS/United States ; R01 MH088849/MH/NIMH NIH HHS/United States ; AG9900/AG/NIA NIH HHS/United States
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Volume:33
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Issue:1
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Collection(s):
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Main Document Checksum:urn:sha256:23d1c994a73046f4087c2a6d1e9432a4aacf183f31465e4154b0498596708b54
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Download URL:
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File Type:
Supporting Files
File Language:
English
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