Please use this identifier to cite or link to this item:
|Title:||Molecular aptamer beacon for myotonic dystrophy kinase-related Cdc42-binding kinase α|
Signal transduction proteins
|Citation:||Tok, J., Lai, J., Leung, T., Li, S.F.Y. (2010-04-15). Molecular aptamer beacon for myotonic dystrophy kinase-related Cdc42-binding kinase α. Talanta 81 (1-2) : 732-736. ScholarBank@NUS Repository.|
|Abstract:||A novel strategy for the development of molecular aptamer beacon for a signal transduction protein, myotonic dystrophy kinase-related Cdc42-binding kinase (MRCK) was proposed in this work. MRCK is an important downstream effector protein of Cdc42 that phosphorylates proteins involved in organizing actin structures responsible for forming stress fibres, lamellipodia or filopodia. The simple method for MAB design could potentially be applied to other aptamers for modification into a protein probe. The MRCK aptamer was modified into a MAB by adding nucleotides on the 5′ end, which are complementary to the 3′ end of the aptamer so as to destroy the existing structure and change it into a MB form. In the absence of MRCK, the MAB remained a hairpin structure. However, in the presence of MRCK, the equilibrium was shifted towards the formation of the MRCK-aptamer complex, resulting in the preference for the MRCK-binding conformer, where a fluorescence-quenching pair added to the 5′ and 3′ ends signaled any protein-dependent conformation change. The development of MABs for signal transduction proteins will have the potential to replace antibodies for diagnostic assays as well as protein studies in cellular imaging. © 2010 Elsevier B.V. All rights reserved.|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Mar 5, 2018
WEB OF SCIENCETM
checked on May 1, 2018
checked on Jun 29, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.