Proteomics

Dataset Information

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Proteomic QSAR analysis of calpain substrate specificity


ABSTRACT: Calpains are intracellular Ca2+-regulated cysteine proteases that are essential for various cellular functions. Mammalian conventional calpains (calpain-1 and calpain-2) modulate the structure and function of their substrates by limited proteolysis; however, their substrate specificity remains unclear because the amino acid (aa) sequences around their cleavage sites are very diverse. To clarify calpains’ substrate specificities, 84 20-mer oligopeptides, corresponding to P10-P10’ of reported cleavage site sequences, were proteolyzed by calpains, and the catalytic efficiencies (kcat/Km) were globally determined by LC/MS. This analysis revealed 483 cleavage site sequences, including 360 novel ones. The kcat/Kms for 119 sites ranged from 12.5~1,710 M-1s-1. Most sites were cleaved by both calpain-1 and -2 with a similar kcat/Km. The aa compositions of the novel sites were not significantly different from the 420 previously reported sites, suggesting calpains have a strict implicit rule for sequence specificity, and that the limited proteolysis of intact substrates is due to the substrates’ higher-order structures. Cleavage position frequencies indicated that longer sequences N-terminal to the cleavage site (P-sites) than C-terminal (P’-sites) were preferred for proteolysis. Quantitative structure-activity relationship (QSAR) analyses using partial least-squares regression and >1,300 aa descriptors achieved kcat/Km prediction with r=0.834, and binary-QSAR modeling attained 64.8% prediction accuracy for 132 reported calpain cleavage sites independent of our model construction. These results outperformed previous calpain cleavage predictors, and revealed the importance of the P2, P3’, P4’, and P1-P2 contexts. This study increases our understanding of calpain substrate specificities, and opens calpains to “next-generation,” i.e., activity-related quantitative and context-dependent analyses.

INSTRUMENT(S): 4800 Proteomics Analyzer, QSTAR

ORGANISM(S): Rattus Norvegicus (rat) Homo Sapiens (human) Bos Taurus (bovine) Gallus Gallus (chicken) Oryctolagus Cuniculus Algirus Ovis Aries Sus Scrofa Domesticus (domestic Pig) Mus Musculus (mouse)

SUBMITTER: Hiroyuki Sorimachi  

LAB HEAD: Hiroyuki Sorimachi

PROVIDER: PXD002532 | Pride | 2016-07-19

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
C1_48_1_20090828_12.mzXML Mzxml
C1_48_1_20090828_20_49124.mzXML Mzxml
C1_48_1_20090828_7.mzXML Mzxml
C1_48_2_20090928_49183-4.mzXML Mzxml
C1_48_2_20090928_49185-7.mzXML Mzxml
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Publications

Predictions of Cleavability of Calpain Proteolysis by Quantitative Structure-Activity Relationship Analysis Using Newly Determined Cleavage Sites and Catalytic Efficiencies of an Oligopeptide Array.

Shinkai-Ouchi Fumiko F   Koyama Suguru S   Ono Yasuko Y   Hata Shoji S   Ojima Koichi K   Shindo Mayumi M   duVerle David D   Ueno Mika M   Kitamura Fujiko F   Doi Naoko N   Takigawa Ichigaku I   Mamitsuka Hiroshi H   Sorimachi Hiroyuki H  

Molecular & cellular proteomics : MCP 20160121 4


Calpains are intracellular Ca(2+)-regulated cysteine proteases that are essential for various cellular functions. Mammalian conventional calpains (calpain-1 and calpain-2) modulate the structure and function of their substrates by limited proteolysis. Thus, it is critically important to determine the site(s) in proteins at which calpains cleave. However, the calpains' substrate specificity remains unclear, because the amino acid (aa) sequences around their cleavage sites are very diverse. To cla  ...[more]

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