SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni.
Blood flukes of the genus Schistosoma are platyhelminth parasites that infect 200 million people worldwide. Digestion of nutrients from the host bloodstream is essential for parasite development and reproduction. A network of proteolytic enzymes (proteases) facilitates hydrolysis of host hemoglobin...
Main Authors: | , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2009-06-01
|
Series: | PLoS Neglected Tropical Diseases |
Online Access: | http://europepmc.org/articles/PMC2685030?pdf=render |
id |
doaj-d630d31d733041269814da1a6ab5b58b |
---|---|
record_format |
Article |
spelling |
doaj-d630d31d733041269814da1a6ab5b58b2020-11-25T02:47:00ZengPublic Library of Science (PLoS)PLoS Neglected Tropical Diseases1935-27271935-27352009-06-0136e44910.1371/journal.pntd.0000449SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni.Jan DvorákSusan T MashiyamaMohammed SajidSimon BraschiMelaine DelcroixEric L SchneiderWilson H McKerrowMahmoud BahgatElizabeth HansellPatricia C BabbittCharles S CraikJames H McKerrowConor R CaffreyBlood flukes of the genus Schistosoma are platyhelminth parasites that infect 200 million people worldwide. Digestion of nutrients from the host bloodstream is essential for parasite development and reproduction. A network of proteolytic enzymes (proteases) facilitates hydrolysis of host hemoglobin and serum proteins.We identified a new cathepsin L termed SmCL3 using PCR strategies based on S. mansoni EST sequence data. An ortholog is present in Schistosoma japonicum. SmCL3 was heterologously expressed as an active enzyme in the yeast, Pichia pastoris. Recombinant SmCL3 has a broad pH activity range against peptidyl substrates and is inhibited by Clan CA protease inhibitors. Consistent with a function in degrading host proteins, SmCL3 hydrolyzes serum albumin and hemoglobin, is localized to the adult gastrodermis, and is expressed mainly in those life stages infecting the mammalian host. The predominant form of SmCL3 in the parasite exists as a zymogen, which is unusual for proteases. This zymogen includes an unusually long prodomain with alpha helical secondary structure motifs. The striking specificity of SmCL3 for amino acids with large aromatic side chains (Trp and Tyr) at the P2 substrate position, as determined with positional scanning-synthetic combinatorial library, is consistent with a molecular model that shows a large and deep S2 pocket. A sequence similarity network (SSN) view clusters SmCL3 and other cathepsins L in accordance with previous large-scale phylogenetic analyses that identify six super kingdoms.SmCL3 is a gut-associated cathepsin L that may contribute to the network of proteases involved in degrading host blood proteins as nutrients. Furthermore, this enzyme exhibits some unusual sequence and biophysical features that may result in additional functions. The visualization of network inter-relationships among cathepsins L suggests that these enzymes are suitable 'marker sequences' for inclusion in future phylogenetic analyses.http://europepmc.org/articles/PMC2685030?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jan Dvorák Susan T Mashiyama Mohammed Sajid Simon Braschi Melaine Delcroix Eric L Schneider Wilson H McKerrow Mahmoud Bahgat Elizabeth Hansell Patricia C Babbitt Charles S Craik James H McKerrow Conor R Caffrey |
spellingShingle |
Jan Dvorák Susan T Mashiyama Mohammed Sajid Simon Braschi Melaine Delcroix Eric L Schneider Wilson H McKerrow Mahmoud Bahgat Elizabeth Hansell Patricia C Babbitt Charles S Craik James H McKerrow Conor R Caffrey SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni. PLoS Neglected Tropical Diseases |
author_facet |
Jan Dvorák Susan T Mashiyama Mohammed Sajid Simon Braschi Melaine Delcroix Eric L Schneider Wilson H McKerrow Mahmoud Bahgat Elizabeth Hansell Patricia C Babbitt Charles S Craik James H McKerrow Conor R Caffrey |
author_sort |
Jan Dvorák |
title |
SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni. |
title_short |
SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni. |
title_full |
SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni. |
title_fullStr |
SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni. |
title_full_unstemmed |
SmCL3, a gastrodermal cysteine protease of the human blood fluke Schistosoma mansoni. |
title_sort |
smcl3, a gastrodermal cysteine protease of the human blood fluke schistosoma mansoni. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Neglected Tropical Diseases |
issn |
1935-2727 1935-2735 |
publishDate |
2009-06-01 |
description |
Blood flukes of the genus Schistosoma are platyhelminth parasites that infect 200 million people worldwide. Digestion of nutrients from the host bloodstream is essential for parasite development and reproduction. A network of proteolytic enzymes (proteases) facilitates hydrolysis of host hemoglobin and serum proteins.We identified a new cathepsin L termed SmCL3 using PCR strategies based on S. mansoni EST sequence data. An ortholog is present in Schistosoma japonicum. SmCL3 was heterologously expressed as an active enzyme in the yeast, Pichia pastoris. Recombinant SmCL3 has a broad pH activity range against peptidyl substrates and is inhibited by Clan CA protease inhibitors. Consistent with a function in degrading host proteins, SmCL3 hydrolyzes serum albumin and hemoglobin, is localized to the adult gastrodermis, and is expressed mainly in those life stages infecting the mammalian host. The predominant form of SmCL3 in the parasite exists as a zymogen, which is unusual for proteases. This zymogen includes an unusually long prodomain with alpha helical secondary structure motifs. The striking specificity of SmCL3 for amino acids with large aromatic side chains (Trp and Tyr) at the P2 substrate position, as determined with positional scanning-synthetic combinatorial library, is consistent with a molecular model that shows a large and deep S2 pocket. A sequence similarity network (SSN) view clusters SmCL3 and other cathepsins L in accordance with previous large-scale phylogenetic analyses that identify six super kingdoms.SmCL3 is a gut-associated cathepsin L that may contribute to the network of proteases involved in degrading host blood proteins as nutrients. Furthermore, this enzyme exhibits some unusual sequence and biophysical features that may result in additional functions. The visualization of network inter-relationships among cathepsins L suggests that these enzymes are suitable 'marker sequences' for inclusion in future phylogenetic analyses. |
url |
http://europepmc.org/articles/PMC2685030?pdf=render |
work_keys_str_mv |
AT jandvorak smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT susantmashiyama smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT mohammedsajid smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT simonbraschi smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT melainedelcroix smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT ericlschneider smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT wilsonhmckerrow smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT mahmoudbahgat smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT elizabethhansell smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT patriciacbabbitt smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT charlesscraik smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT jameshmckerrow smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni AT conorrcaffrey smcl3agastrodermalcysteineproteaseofthehumanbloodflukeschistosomamansoni |
_version_ |
1724755329746468864 |