Journal
STRUCTURE
Volume 22, Issue 6, Pages 866-877Publisher
CELL PRESS
DOI: 10.1016/j.str.2014.04.012
Keywords
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Funding
- Methusalem grant (Ghent University, Ghent, Belgium)
- Fonds Wetenschappelijk Onderzoek (Brussels, Belgium)
- ERC [340941]
- European Research Council (ERC) [340941] Funding Source: European Research Council (ERC)
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Leptin activates its cognate receptor (LR) to regulate body weight and metabolically costly processes, such as reproduction and immune responses. Despite such benevolent pleiotropy, leptin-mediated signaling has been implicated in autoimmune diseases and breast cancer, thereby rejuvenating interest in leptin antagonism. We present comparative biochemical and structural studies of the LR ectodomain (LRecto) in complex with wild-type and antagonist leptin variants. We show that high-affinity binding of leptin to the cytokine receptor homology 2 domain of LRecto primes interactions with the Ig-domain (LRIg) of another leptin-bound LRecto to establish a quaternary assembly. In contrast, antagonist leptin variants carrying mutations at the LRIg binding site only enable binary complexes with LRecto. Acetylation of free cysteines in LRecto also abrogates quaternary complexes, suggesting a functional role for intrareceptor disulfides. We propose a revised conceptual framework for LR activation whereby leptin activates predimerized LR at the cell surface to seed higher order complexes with 4:4 stoichiometry.
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