Cryo-EM structure of the native butyrylcholinesterase tetramer reveals a dimer of dimers stabilized by a superhelical assembly

Miguel Ricardo Leung, Laura S. van Bezouwen, Lawrence M Schopfer, Joel L. Sussman, Israel Silman, Oksana Lockridge, Tzviya Zeev-Ben-Mordehai

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

The quaternary structures of the cholinesterases, acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), are essential for their localization and function. Of practical importance, BChE is a promising therapeutic candidate for intoxication by organophosphate nerve agents and insecticides, and for detoxification of addictive substances. Efficacy of the recombinant enzyme hinges on its having a long circulatory half-life; this, in turn, depends strongly on its ability to tetramerize. Here, we used cryoelectron microscopy (cryo-EM) to determine the structure of the highly glycosylated native BChE tetramer purified from human plasma at 5.7 Å. Our structure reveals that the BChE tetramer is organized as a staggered dimer of dimers. Tetramerization is mediated by assembly of the C-terminal tryptophan amphiphilic tetramerization (WAT) helices from each subunit as a superhelical assembly around a central lamellipodin-derived oligopeptide with a proline-rich attachment domain (PRAD) sequence that adopts a polyproline II helical conformation and runs antiparallel. The catalytic domains within a dimer are asymmetrically linked to the WAT/PRAD. In the resulting arrangement, the tetramerization domain is largely shielded by the catalytic domains, which may contribute to the stability of the human BChE (HuBChE) tetramer. Our cryo-EM structure reveals the basis for assembly of the native tetramers and has implications for the therapeutic applications of HuBChE. This mode of tetramerization is seen only in the cholinesterases but may provide a promising template for designing other proteins with improved circulatory residence times.

Original languageEnglish (US)
Pages (from-to)13270-13275
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume115
Issue number52
DOIs
StatePublished - Dec 26 2018

Fingerprint

Butyrylcholinesterase
Cryoelectron Microscopy
Cholinesterases
Proline
Catalytic Domain
Oligopeptides
Organophosphates
Acetylcholinesterase
Insecticides
Tryptophan
Half-Life
Enzymes
Therapeutics
Proteins

Keywords

  • Acetylcholinesterase
  • Bioscavenger
  • Butyrylcholinesterase
  • Cryoelectron microscopy
  • Superhelical assembly

ASJC Scopus subject areas

  • General

Cite this

Cryo-EM structure of the native butyrylcholinesterase tetramer reveals a dimer of dimers stabilized by a superhelical assembly. / Leung, Miguel Ricardo; van Bezouwen, Laura S.; Schopfer, Lawrence M; Sussman, Joel L.; Silman, Israel; Lockridge, Oksana; Zeev-Ben-Mordehai, Tzviya.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 115, No. 52, 26.12.2018, p. 13270-13275.

Research output: Contribution to journalArticle

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abstract = "The quaternary structures of the cholinesterases, acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), are essential for their localization and function. Of practical importance, BChE is a promising therapeutic candidate for intoxication by organophosphate nerve agents and insecticides, and for detoxification of addictive substances. Efficacy of the recombinant enzyme hinges on its having a long circulatory half-life; this, in turn, depends strongly on its ability to tetramerize. Here, we used cryoelectron microscopy (cryo-EM) to determine the structure of the highly glycosylated native BChE tetramer purified from human plasma at 5.7 {\AA}. Our structure reveals that the BChE tetramer is organized as a staggered dimer of dimers. Tetramerization is mediated by assembly of the C-terminal tryptophan amphiphilic tetramerization (WAT) helices from each subunit as a superhelical assembly around a central lamellipodin-derived oligopeptide with a proline-rich attachment domain (PRAD) sequence that adopts a polyproline II helical conformation and runs antiparallel. The catalytic domains within a dimer are asymmetrically linked to the WAT/PRAD. In the resulting arrangement, the tetramerization domain is largely shielded by the catalytic domains, which may contribute to the stability of the human BChE (HuBChE) tetramer. Our cryo-EM structure reveals the basis for assembly of the native tetramers and has implications for the therapeutic applications of HuBChE. This mode of tetramerization is seen only in the cholinesterases but may provide a promising template for designing other proteins with improved circulatory residence times.",
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AU - Leung, Miguel Ricardo

AU - van Bezouwen, Laura S.

AU - Schopfer, Lawrence M

AU - Sussman, Joel L.

AU - Silman, Israel

AU - Lockridge, Oksana

AU - Zeev-Ben-Mordehai, Tzviya

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