Capturing an initial intermediate during the P450nor enzymatic reaction using time-resolved XFEL crystallography and caged-substrate. Issue 1 (December 2017)
- Record Type:
- Journal Article
- Title:
- Capturing an initial intermediate during the P450nor enzymatic reaction using time-resolved XFEL crystallography and caged-substrate. Issue 1 (December 2017)
- Main Title:
- Capturing an initial intermediate during the P450nor enzymatic reaction using time-resolved XFEL crystallography and caged-substrate
- Authors:
- Tosha, Takehiko
Nomura, Takashi
Nishida, Takuma
Saeki, Naoya
Okubayashi, Kouta
Yamagiwa, Raika
Sugahara, Michihiro
Nakane, Takanori
Yamashita, Keitaro
Hirata, Kunio
Ueno, Go
Kimura, Tetsunari
Hisano, Tamao
Muramoto, Kazumasa
Sawai, Hitomi
Takeda, Hanae
Mizohata, Eiichi
Yamashita, Ayumi
Kanematsu, Yusuke
Takano, Yu
Nango, Eriko
Tanaka, Rie
Nureki, Osamu
Shoji, Osami
Ikemoto, Yuka
Murakami, Hironori
Owada, Shigeki
Tono, Kensuke
Yabashi, Makina
Yamamoto, Masaki
Ago, Hideo
Iwata, So
Sugimoto, Hiroshi
Shiro, Yoshitsugu
Kubo, Minoru
… (more) - Abstract:
- Abstract Time-resolved serial femtosecond crystallography using an X-ray free electron laser (XFEL) in conjunction with a photosensitive caged-compound offers a crystallographic method to track enzymatic reactions. Here we demonstrate the application of this method using fungal NO reductase, a heme-containing enzyme, at room temperature. Twenty milliseconds after caged-NO photolysis, we identify a NO-bound form of the enzyme, which is an initial intermediate with a slightly bent Fe-N-O coordination geometry at a resolution of 2.1 Å. The NO geometry is compatible with those analyzed by XFEL-based cryo-crystallography and QM/MM calculations, indicating that we obtain an intact Fe3+ -NO coordination structure that is free of X-ray radiation damage. The slightly bent NO geometry is appropriate to prevent immediate NO dissociation and thus accept H− from NADH. The combination of using XFEL and a caged-compound is a powerful tool for determining functional enzyme structures during catalytic reactions at the atomic level. Using photosensitive caged-compound for femtosecond crystallography at X-ray free electron lasers would allow the structure determination of reaction intermediates. Here the authors demonstrate the feasibility of this approach with a caged NO-compound and present the initial NO-bound intermediate structure of cytochrome P450 nitric oxide reductase.
- Is Part Of:
- Nature communications. Volume 8:Issue 1(2017)
- Journal:
- Nature communications
- Issue:
- Volume 8:Issue 1(2017)
- Issue Display:
- Volume 8, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 8
- Issue:
- 1
- Issue Sort Value:
- 2017-0008-0001-0000
- Page Start:
- 1
- Page End:
- 9
- Publication Date:
- 2017-12
- Subjects:
- Biology -- Periodicals
Physical sciences -- Periodicals
505 - Journal URLs:
- http://www.nature.com/ncomms/index.html ↗
http://www.nature.com/ ↗ - DOI:
- 10.1038/s41467-017-01702-1 ↗
- Languages:
- English
- ISSNs:
- 2041-1723
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6046.280270
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10996.xml