2014
DOI: 10.1021/cb500651d
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Allele-Specific Chemical Genetics: Concept, Strategies, and Applications

Abstract: The relationship between DNA and protein sequences is well understood, yet because the members of a protein family/subfamily often carry out the same biochemical reaction, elucidating their individual role in cellular processes presents a challenge. Forward and reverse genetics have traditionally been employed to understand protein functions with considerable success. A fundamentally different approach that has gained widespread application is the use of small organic molecules, known as chemical genetics. How… Show more

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Cited by 29 publications
(29 citation statements)
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References 162 publications
(362 reference statements)
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“…brain fog, neurodegeneration, and other CNS pathologies (Yamauchi et al, 2012;Kombo and Bencherif, 2013;Rankovic, 2015). Regrettably, relatively little consideration has concentrated on the development of a7 nAChR antagonists as potential pharmaceutical candidates, even though a7 nAChR selective antagonists have been believed to be useful in the medication of neuropathology and complaint (Garcia-Delgado et al, 2010;Crestey et al, 2013;Islam, 2015). Thus, the development of selective a7 nAChR antagonists is certainly a new research area in medicinal chemistry.…”
Section: Introductionmentioning
confidence: 99%
“…brain fog, neurodegeneration, and other CNS pathologies (Yamauchi et al, 2012;Kombo and Bencherif, 2013;Rankovic, 2015). Regrettably, relatively little consideration has concentrated on the development of a7 nAChR antagonists as potential pharmaceutical candidates, even though a7 nAChR selective antagonists have been believed to be useful in the medication of neuropathology and complaint (Garcia-Delgado et al, 2010;Crestey et al, 2013;Islam, 2015). Thus, the development of selective a7 nAChR antagonists is certainly a new research area in medicinal chemistry.…”
Section: Introductionmentioning
confidence: 99%
“…In this report, we present a novel chemical genetics strategy to acutely modulate kinase activity and visualize kinase target engagement, combining precise gene editing with the design and application of complementary covalent inhibitors. The field of chemical genetics has previously generated tools to aid in kinase target validation 54,55 , such as the powerful "analog-sensitive" (AS) technology, where the gatekeeper residue is changed into a less bulky residue, enabling the kinase of interest to accommodate bulky ATP analogs in its active site. 56 However, these analogs do not form covalent adducts with the kinase and therefore do not readily allow visualization of target engagement.…”
Section: Discussionmentioning
confidence: 99%
“…Chemical-genetic approaches have been successfully used to study the function of proteins for which the identification of specific inhibitors has remained elusive 36,37 . For ATPases such as kinases or motor proteins (including myosins and kinesins), such approaches have involved enlargement of the ATP binding pocket to accommodate a nucleotide or inhibitor analogue that contains a bulky substituent complementing the enlarged pocket.…”
Section: Discussionmentioning
confidence: 99%