Journal article

AMP-activated protein kinase subunit interactions β1:γ1 Association Requires β1 Thr-263 and Tyr-267

TJ Iseli, JS Oakhill, MF Bailey, S Wee, M Walter, BJ Van Denderen, LA Castelli, F Katsis, LA Witters, D Stapleton, SL Macaulay, BJ Michell, BE Kemp

Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2008

Abstract

AMP-activated protein kinase (AMPK) plays multiple roles in the body's overall metabolic balance and response to exercise, nutritional stress, hormonal stimulation, and the glucose-lowering drugs metformin and rosiglitazone. AMPK consists of a catalytic α subunit and two non-catalytic subunits, β and γ, each with multiple isoforms that form active 1:1:1 heterotrimers. Here we show that recombinant human AMPK α1β1γ1 expressed in insect cells is monomeric and displays specific activity and AMP responsiveness similar to rat liver AMPK. The previously determined crystal structure of the core of mammalian αβγ complex shows that β binds α and γ. Here we show that a β1(186-270)γ1 complex can form i..

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University of Melbourne Researchers