A new Kunitz-type plasmin inhibitor from scorpion venom. (November 2015)
- Record Type:
- Journal Article
- Title:
- A new Kunitz-type plasmin inhibitor from scorpion venom. (November 2015)
- Main Title:
- A new Kunitz-type plasmin inhibitor from scorpion venom
- Authors:
- Ding, Li
Wang, Xiaobo
Liu, Hongyan
San, Mingkui
Xu, Yue
Li, Jian
Li, Shan
Cao, Zhijian
Li, Wenxin
Wu, Yingliang
Chen, Zongyun - Abstract:
- Abstract: Kunitz-type peptides from venomous animals are an important source of lead drug candidates towards human plasmin, a target of protease-associated diseases. However, no Kunitz-type plasmin inhibitor from venomous scorpion has been characterized. Here, we first investigated plasmin inhibiting activities of eight known Kunitz-type scorpion toxins Hg1, BmKTT-1, BmKTT-2, BmKTT-3, LmKTT-1a, LmKTT-1b, LmKTT-1c and BmKPI, and found a new plasmin inhibitor BmKTT-2, a Kunitz-type toxin peptide from the scorpion Buthus martensi karch . Protease inhibitory activity assay showed that BmKTT-2 potently inhibited plasmin with a Ki value of 8.75 ± 2.05 nM. Structure–function relationship studies between BmKTT-2 and plasmin showed that BmKTT-2 is a classical Kunitz-type plasmin inhibitor: Lys13 in BmKTT-2 is the P1 site, and Ala14 in BmKTT-2 is the P1′ site. Interestingly, BmKTT-2 has potent inhibiting activities towards three important digestive serine proteases trypsin, chymotrypsin and elastase, suggesting a good stability for administering oral medications. To the best of our knowledge, BmKTT-2 is the first Kunitz-type human plasmin inhibitor from scorpion venom, providing novel insights into drug developments targeting human plasmin protease. Highlights: No Kunitz-type plasmin inhibitor from venomous scorpion has been characterized. We found a Kunitz-type plasmin inhibitor BmKTT-2 from the scorpion Buthus martensi karch with a Ki value of 8.75 ± 2.05 nM. BmKTT-2 has potentAbstract: Kunitz-type peptides from venomous animals are an important source of lead drug candidates towards human plasmin, a target of protease-associated diseases. However, no Kunitz-type plasmin inhibitor from venomous scorpion has been characterized. Here, we first investigated plasmin inhibiting activities of eight known Kunitz-type scorpion toxins Hg1, BmKTT-1, BmKTT-2, BmKTT-3, LmKTT-1a, LmKTT-1b, LmKTT-1c and BmKPI, and found a new plasmin inhibitor BmKTT-2, a Kunitz-type toxin peptide from the scorpion Buthus martensi karch . Protease inhibitory activity assay showed that BmKTT-2 potently inhibited plasmin with a Ki value of 8.75 ± 2.05 nM. Structure–function relationship studies between BmKTT-2 and plasmin showed that BmKTT-2 is a classical Kunitz-type plasmin inhibitor: Lys13 in BmKTT-2 is the P1 site, and Ala14 in BmKTT-2 is the P1′ site. Interestingly, BmKTT-2 has potent inhibiting activities towards three important digestive serine proteases trypsin, chymotrypsin and elastase, suggesting a good stability for administering oral medications. To the best of our knowledge, BmKTT-2 is the first Kunitz-type human plasmin inhibitor from scorpion venom, providing novel insights into drug developments targeting human plasmin protease. Highlights: No Kunitz-type plasmin inhibitor from venomous scorpion has been characterized. We found a Kunitz-type plasmin inhibitor BmKTT-2 from the scorpion Buthus martensi karch with a Ki value of 8.75 ± 2.05 nM. BmKTT-2 has potent inhibiting activities towards three digestive serine proteases trypsin, chymotrypsin and elastase. BmKTT-2 is the first Kunitz-type plasmin inhibitor from scorpion venom. … (more)
- Is Part Of:
- Toxicon. Volume 106(2015)
- Journal:
- Toxicon
- Issue:
- Volume 106(2015)
- Issue Display:
- Volume 106, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 106
- Issue:
- 1
- Issue Sort Value:
- 2015-0106-0001-0000
- Page Start:
- 7
- Page End:
- 13
- Publication Date:
- 2015-11
- Subjects:
- Plasmin -- BmKTT-2 -- Peptide inhibitor -- Kunitz-type -- Scorpion venom
Toxins -- Periodicals
Venom -- Periodicals
615.9 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00410101 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.toxicon.2015.09.004 ↗
- Languages:
- English
- ISSNs:
- 0041-0101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8873.050000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9208.xml