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NMR identification of a conserved Drp1 cardiolipin-binding motif essential for stress-induced mitochondrial fission
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NMR identification of a conserved Drp1 cardiolipin-binding motif essential for stress-induced mitochondrial fission
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NMR identification of a conserved Drp1 cardiolipin-binding motif essential for stress-induced mitochondrial fission
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Journal Article
NMR identification of a conserved Drp1 cardiolipin-binding motif essential for stress-induced mitochondrial fission
2021
Overview
Mitochondria form tubular networks that undergo coordinated cycles of fission and fusion. Emerging evidence suggests that a direct yet unresolved interaction of the mechanoenzymatic GTPase dynamin-related protein 1 (Drp1) with mitochondrial outer membrane–localized cardiolipin (CL), externalized under stress conditions including mitophagy, catalyzes essential mitochondrial hyperfragmentation. Here, using a comprehensive set of structural, biophysical, and cell biological tools, we have uncovered a CL-binding motif (CBM) conserved between the Drp1 variable domain (VD) and the unrelated ADP/ATP carrier (AAC/ANT) that intercalates into the membrane core to effect specific CL interactions. CBM mutations that weaken VD–CL interactions manifestly impair Drp1-dependent fission under stress conditions and induce “donut” mitochondria formation. Importantly, VD membrane insertion and GTP-dependent conformational rearrangements mediate only transient CL nonbilayer topological forays and high local membrane constriction, indicating that Drp1–CL interactions alone are insufficient for fission. Our studies establish the structural and mechanistic bases of Drp1–CL interactions in stressinduced mitochondrial fission.
Publisher
National Academy of Sciences
Subject
/ Binding
/ Biophysics and Computational Biology
/ Dynamin
/ Fission
/ Humans
/ Intrinsically Disordered Proteins - chemistry
/ Intrinsically Disordered Proteins - genetics
/ Intrinsically Disordered Proteins - metabolism
/ Magnetic Resonance Spectroscopy
/ Mitochondrial Dynamics - physiology
/ Mitochondrial Membranes - metabolism
/ Mitochondrial Membranes - pathology
/ Mutation
/ NMR
