A disulfide-bond cascade mechanism for arsenic(III) S-adenosylmethionine methyltransferase

Kavitha Marapakala, Charles Packianathan, A. Abdul Ajees, Dharmendra S. Dheeman, Banumathi Sankaran, Palani Kandavelu, Barry P. Rosen

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Abstract

Methylation of the toxic metalloid arsenic is widespread in nature. Members of every kingdom have arsenic(III) S-adenosylmethionine (SAM) methyltransferase enzymes, which are termed ArsM in microbes and AS3MT in animals, including humans. Trivalent arsenic(III) is methylated up to three times to form methylarsenite [MAs(III)], dimethylarsenite [DMAs(III)] and the volatile trimethylarsine [TMAs(III)]. In microbes, arsenic methylation is a detoxification process. In humans, MAs(III) and DMAs(III) are more toxic and carcinogenic than either inorganic arsenate or arsenite. Here, new crystal structures are reported of ArsM from the thermophilic eukaryotic alga Cyanidioschyzon sp. 5508 (CmArsM) with the bound aromatic arsenicals phenylarsenite [PhAs(III)] at 1.80Å resolution and reduced roxarsone [Rox(III)] at 2.25Å resolution. These organoarsenicals are bound to two of four conserved cysteine residues: Cys174 and Cys224. The electron density extends the structure to include a newly identified conserved cysteine residue, Cys44, which is disulfide-bonded to the fourth conserved cysteine residue, Cys72. A second disulfide bond between Cys72 and Cys174 had been observed previously in a structure with bound SAM. The loop containing Cys44 and Cys72 shifts by nearly 6.5Å in the arsenic(III)-bound structures compared with the SAM-bound structure, which suggests that this movement leads to formation of the Cys72-Cys174 disulfide bond. A model is proposed for the catalytic mechanism of arsenic(III) SAM methyltransferases in which a disulfide-bond cascade maintains the products in the trivalent state.

Original languageEnglish
Pages (from-to)505-515
Number of pages11
JournalActa Crystallographica Section D: Biological Crystallography
Volume71
DOIs
Publication statusPublished - 01-01-2015

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S-Adenosylmethionine
Methyltransferases
Arsenic
Disulfides
Cysteine
Poisons
Methylation
Roxarsone
Metalloids
Arsenicals
Electrons
Enzymes

All Science Journal Classification (ASJC) codes

  • Structural Biology
  • Medicine(all)

Cite this

Marapakala, Kavitha ; Packianathan, Charles ; Ajees, A. Abdul ; Dheeman, Dharmendra S. ; Sankaran, Banumathi ; Kandavelu, Palani ; Rosen, Barry P. / A disulfide-bond cascade mechanism for arsenic(III) S-adenosylmethionine methyltransferase. In: Acta Crystallographica Section D: Biological Crystallography. 2015 ; Vol. 71. pp. 505-515.
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abstract = "Methylation of the toxic metalloid arsenic is widespread in nature. Members of every kingdom have arsenic(III) S-adenosylmethionine (SAM) methyltransferase enzymes, which are termed ArsM in microbes and AS3MT in animals, including humans. Trivalent arsenic(III) is methylated up to three times to form methylarsenite [MAs(III)], dimethylarsenite [DMAs(III)] and the volatile trimethylarsine [TMAs(III)]. In microbes, arsenic methylation is a detoxification process. In humans, MAs(III) and DMAs(III) are more toxic and carcinogenic than either inorganic arsenate or arsenite. Here, new crystal structures are reported of ArsM from the thermophilic eukaryotic alga Cyanidioschyzon sp. 5508 (CmArsM) with the bound aromatic arsenicals phenylarsenite [PhAs(III)] at 1.80{\AA} resolution and reduced roxarsone [Rox(III)] at 2.25{\AA} resolution. These organoarsenicals are bound to two of four conserved cysteine residues: Cys174 and Cys224. The electron density extends the structure to include a newly identified conserved cysteine residue, Cys44, which is disulfide-bonded to the fourth conserved cysteine residue, Cys72. A second disulfide bond between Cys72 and Cys174 had been observed previously in a structure with bound SAM. The loop containing Cys44 and Cys72 shifts by nearly 6.5{\AA} in the arsenic(III)-bound structures compared with the SAM-bound structure, which suggests that this movement leads to formation of the Cys72-Cys174 disulfide bond. A model is proposed for the catalytic mechanism of arsenic(III) SAM methyltransferases in which a disulfide-bond cascade maintains the products in the trivalent state.",
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A disulfide-bond cascade mechanism for arsenic(III) S-adenosylmethionine methyltransferase. / Marapakala, Kavitha; Packianathan, Charles; Ajees, A. Abdul; Dheeman, Dharmendra S.; Sankaran, Banumathi; Kandavelu, Palani; Rosen, Barry P.

In: Acta Crystallographica Section D: Biological Crystallography, Vol. 71, 01.01.2015, p. 505-515.

Research output: Contribution to journalArticle

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