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Decoding three distinct states of the Syntaxin17 SNARE motif in mediating autophagosome–lysosome fusion
by
Pan, Lifeng
, Xu, Xiaolong
, Li, Ying
, Cheng, Xiaofang
, Fu, Tao
, Gong, Xinyu
, Liu, Jianping
, Wang, Yaru
, Zhou, Zixuan
, Wang, Yingli
, Li, Miao
in
Amino Acid Motifs
/ Apoptosis Regulatory Proteins - metabolism
/ Autophagosomes - physiology
/ Autophagy-Related Protein 8 Family - metabolism
/ Binding
/ Biological Sciences
/ Biophysics and Computational Biology
/ Crystal structure
/ Escherichia coli
/ GABARAP protein
/ Humans
/ Lysosomes - physiology
/ Membrane fusion
/ Microtubule-Associated Proteins - metabolism
/ N-Ethylmaleimide
/ NMR
/ Nuclear magnetic resonance
/ Protein structure
/ Proteins
/ Qa-SNARE Proteins - metabolism
/ Qb-SNARE Proteins - metabolism
/ Qc-SNARE Proteins - metabolism
/ R-SNARE Proteins - metabolism
/ SNAP receptors
2020
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Decoding three distinct states of the Syntaxin17 SNARE motif in mediating autophagosome–lysosome fusion
by
Pan, Lifeng
, Xu, Xiaolong
, Li, Ying
, Cheng, Xiaofang
, Fu, Tao
, Gong, Xinyu
, Liu, Jianping
, Wang, Yaru
, Zhou, Zixuan
, Wang, Yingli
, Li, Miao
in
Amino Acid Motifs
/ Apoptosis Regulatory Proteins - metabolism
/ Autophagosomes - physiology
/ Autophagy-Related Protein 8 Family - metabolism
/ Binding
/ Biological Sciences
/ Biophysics and Computational Biology
/ Crystal structure
/ Escherichia coli
/ GABARAP protein
/ Humans
/ Lysosomes - physiology
/ Membrane fusion
/ Microtubule-Associated Proteins - metabolism
/ N-Ethylmaleimide
/ NMR
/ Nuclear magnetic resonance
/ Protein structure
/ Proteins
/ Qa-SNARE Proteins - metabolism
/ Qb-SNARE Proteins - metabolism
/ Qc-SNARE Proteins - metabolism
/ R-SNARE Proteins - metabolism
/ SNAP receptors
2020
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Decoding three distinct states of the Syntaxin17 SNARE motif in mediating autophagosome–lysosome fusion
by
Pan, Lifeng
, Xu, Xiaolong
, Li, Ying
, Cheng, Xiaofang
, Fu, Tao
, Gong, Xinyu
, Liu, Jianping
, Wang, Yaru
, Zhou, Zixuan
, Wang, Yingli
, Li, Miao
in
Amino Acid Motifs
/ Apoptosis Regulatory Proteins - metabolism
/ Autophagosomes - physiology
/ Autophagy-Related Protein 8 Family - metabolism
/ Binding
/ Biological Sciences
/ Biophysics and Computational Biology
/ Crystal structure
/ Escherichia coli
/ GABARAP protein
/ Humans
/ Lysosomes - physiology
/ Membrane fusion
/ Microtubule-Associated Proteins - metabolism
/ N-Ethylmaleimide
/ NMR
/ Nuclear magnetic resonance
/ Protein structure
/ Proteins
/ Qa-SNARE Proteins - metabolism
/ Qb-SNARE Proteins - metabolism
/ Qc-SNARE Proteins - metabolism
/ R-SNARE Proteins - metabolism
/ SNAP receptors
2020
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Decoding three distinct states of the Syntaxin17 SNARE motif in mediating autophagosome–lysosome fusion
Journal Article
Decoding three distinct states of the Syntaxin17 SNARE motif in mediating autophagosome–lysosome fusion
2020
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Overview
Syntaxin17, a key autophagosomal N-ethylmaleimide–sensitive factor attachment protein receptor (SNARE) protein, can associate with ATG8 family proteins SNAP29 and VAMP8 to facilitate the membrane fusion process between the double-membraned autophagosome and single-membraned lysosome in mammalian macroautophagy. However, the inherent properties of Syntaxin17 and the mechanistic basis underlying the interactions of Syntaxin17 with its binding proteins remain largely unknown. Here, using biochemical, NMR, and structural approaches, we systemically characterized Syntaxin17 as well as its interactions with ATG8 family proteins, SNAP29 and VAMP8. We discovered that Syntaxin17 alone adopts an autoinhibited conformation mediated by a direct interaction between its Habc domain and the Qa- SNARE motif. In addition, we revealed that the Qa-SNARE region of Syntaxin17 contains one LC3-interacting region (LIR) motif, which preferentially binds to GABARAP subfamily members. Importantly, the GABARAP binding of Syntaxin17 can release its autoinhibited state. The determined crystal structure of the Syntaxin17 LIR–GABARAP complex not only provides mechanistic insights into the interaction between Syntaxin17 and GABARAP but also reveals an unconventional LIR motif with a C-terminally extended 310 helix for selectively binding to ATG8 family proteins. Finally, we also elucidated structural arrangements of the autophagic Syntaxin17–SNAP29–VAMP8 SNARE core complex, and uncovered its conserved biochemical and structural characteristics common to all other SNAREs. In all, our findings reveal three distinct states of Syntaxin17, and provide mechanistic insights into the Syntaxin17-mediated autophagosome–lysosome fusion process.
Publisher
National Academy of Sciences
Subject
/ Apoptosis Regulatory Proteins - metabolism
/ Autophagy-Related Protein 8 Family - metabolism
/ Binding
/ Biophysics and Computational Biology
/ Humans
/ Microtubule-Associated Proteins - metabolism
/ NMR
/ Proteins
/ Qa-SNARE Proteins - metabolism
/ Qb-SNARE Proteins - metabolism
/ Qc-SNARE Proteins - metabolism
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