Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Sci. Signal., 28 January 2014
Vol. 7, Issue 310, p. pe3
[DOI: 10.1126/scisignal.2005021]


Biasing GPCR Signaling from Inside

Arun K. Shukla1,2*

1 Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.
2 Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India.

Abstract: The discovery of "functional selectivity" or "biased signaling" through G protein–coupled receptors (GPCRs) has redefined the classical GPCR signaling paradigm. Moreover, the therapeutic potential of biased signaling by and biased ligands for GPCRs is changing the landscape of GPCR drug discovery. The concept of biased signaling has primarily been developed and discussed in the context of ligands that bind to the extracellular regions of GPCRs. However, two recent reports demonstrate that it is also possible to bias GPCR signaling from inside the cell by targeting intracellular regions of these receptors. These findings present a novel handle for delineating the functional outcomes of biased signaling by GPCRs. Moreover, these approaches also uncover a previously unexplored framework for biasing GPCR signaling for drug discovery.

* Corresponding author. E-mail: arun.shukla{at}

Citation: A. K. Shukla, Biasing GPCR Signaling from Inside. Sci. Signal. 7, pe3 (2014).

Read the Full Text

To Advertise     Find Products

Science Signaling. ISSN 1937-9145 (online), 1945-0877 (print). Pre-2008: Science's STKE. ISSN 1525-8882