Unknown

Dataset Information

0

Proteolytic activation of human cathepsin A.


ABSTRACT: Galactosialidosis is a human lysosomal storage disease caused by deficiency in the multifunctional lysosomal protease cathepsin A (also known as protective protein/cathepsin A, PPCA, catA, HPP, and CTSA; EC 3.4.16.5). Previous structural work on the inactive precursor human cathepsin A (zymogen) led to a two-stage model for activation, where proteolysis of a 1.6-kDa excision peptide is followed by a conformational change in a blocking peptide occluding the active site. Here we present evidence for an alternate model of activation of human cathepsin A, needing only cleavage of a 3.3-kDa excision peptide to yield full enzymatic activity, with no conformational change required. We present x-ray crystallographic, mass spectrometric, amino acid sequencing, enzymatic, and cellular data to support the cleavage-only activation model. The results clarify a longstanding question about the mechanism of cathepsin A activation and point to new avenues for the design of mechanism-based inhibitors of the enzyme.

SUBMITTER: Kolli N 

PROVIDER: S-EPMC4002070 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

Proteolytic activation of human cathepsin A.

Kolli Nilima N   Garman Scott C SC  

The Journal of biological chemistry 20140305 17


Galactosialidosis is a human lysosomal storage disease caused by deficiency in the multifunctional lysosomal protease cathepsin A (also known as protective protein/cathepsin A, PPCA, catA, HPP, and CTSA; EC 3.4.16.5). Previous structural work on the inactive precursor human cathepsin A (zymogen) led to a two-stage model for activation, where proteolysis of a 1.6-kDa excision peptide is followed by a conformational change in a blocking peptide occluding the active site. Here we present evidence f  ...[more]

Similar Datasets

| S-EPMC7343387 | biostudies-literature
| S-EPMC4338073 | biostudies-literature
| S-EPMC10038901 | biostudies-literature
| S-EPMC4795699 | biostudies-literature
| S-EPMC5666837 | biostudies-literature
| S-EPMC7360561 | biostudies-literature
| S-EPMC8630017 | biostudies-literature
| S-EPMC1934589 | biostudies-literature
| S-EPMC3688724 | biostudies-literature
| S-EPMC6207624 | biostudies-literature