TY - JOUR
T1 - OZITX, a pertussis toxin-like protein for occluding inhibitory G protein signalling including Gαz
AU - Keen, Alastair C.
AU - Pedersen, Maria Hauge
AU - Lemel, Laura
AU - Scott, Daniel J.
AU - Canals, Meritxell
AU - Littler, Dene R.
AU - Beddoe, Travis
AU - Ono, Yuki
AU - Shi, Lei
AU - Inoue, Asuka
AU - Javitch, Jonathan A.
AU - Lane, J. Robert
N1 - Publisher Copyright:
© 2022. The Author(s).
PY - 2022
Y1 - 2022
N2 - Heterotrimeric G proteins are the main signalling effectors for G protein-coupled receptors. Understanding the distinct functions of different G proteins is key to understanding how their signalling modulates physiological responses. Pertussis toxin, a bacterial AB5 toxin, inhibits Gαi/o G proteins and has proven useful for interrogating inhibitory G protein signalling. Pertussis toxin, however, does not inhibit one member of the inhibitory G protein family, Gαz. The role of Gαz signalling has been neglected largely due to a lack of inhibitors. Recently, the identification of another Pertussis-like AB5 toxin was described. Here we show that this toxin, that we call OZITX, specifically inhibits Gαi/o and Gαz G proteins and that expression of the catalytic S1 subunit is sufficient for this inhibition. We identify mutations that render Gα subunits insensitive to the toxin that, in combination with the toxin, can be used to interrogate the signalling of each inhibitory Gα G protein.
AB - Heterotrimeric G proteins are the main signalling effectors for G protein-coupled receptors. Understanding the distinct functions of different G proteins is key to understanding how their signalling modulates physiological responses. Pertussis toxin, a bacterial AB5 toxin, inhibits Gαi/o G proteins and has proven useful for interrogating inhibitory G protein signalling. Pertussis toxin, however, does not inhibit one member of the inhibitory G protein family, Gαz. The role of Gαz signalling has been neglected largely due to a lack of inhibitors. Recently, the identification of another Pertussis-like AB5 toxin was described. Here we show that this toxin, that we call OZITX, specifically inhibits Gαi/o and Gαz G proteins and that expression of the catalytic S1 subunit is sufficient for this inhibition. We identify mutations that render Gα subunits insensitive to the toxin that, in combination with the toxin, can be used to interrogate the signalling of each inhibitory Gα G protein.
U2 - 10.1038/s42003-022-03191-5
DO - 10.1038/s42003-022-03191-5
M3 - Journal article
C2 - 35322196
AN - SCOPUS:85126903386
VL - 5
JO - Communications Biology
JF - Communications Biology
SN - 2399-3642
IS - 1
M1 - 256
ER -