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Multiplexed single-molecule enzyme activity analysis for counting disease-related proteins in biological samples.


ABSTRACT: We established an ultrasensitive method for identifying multiple enzymes in biological samples by using a multiplexed microdevice-based single-molecule enzymatic assay. We used a paradigm in which we "count" the number of enzyme molecules by profiling their single enzyme activity characteristics toward multiple substrates. In this proof-of-concept study of the single enzyme activity-based protein profiling (SEAP), we were able to detect the activities of various phosphoric ester-hydrolyzing enzymes such as alkaline phosphatases, tyrosine phosphatases, and ectonucleotide pyrophosphatases in blood samples at the single-molecule level and in a subtype-discriminating manner, demonstrating its potential usefulness for the diagnosis of diseases based on ultrasensitive detection of enzymes.

SUBMITTER: Sakamoto S 

PROVIDER: S-EPMC7065886 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

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Multiplexed single-molecule enzyme activity analysis for counting disease-related proteins in biological samples.

Sakamoto Shingo S   Komatsu Toru T   Watanabe Rikiya R   Zhang Yi Y   Inoue Taiki T   Kawaguchi Mitsuyasu M   Nakagawa Hidehiko H   Ueno Takaaki T   Okusaka Takuji T   Honda Kazufumi K   Noji Hiroyuki H   Urano Yasuteru Y  

Science advances 20200311 11


We established an ultrasensitive method for identifying multiple enzymes in biological samples by using a multiplexed microdevice-based single-molecule enzymatic assay. We used a paradigm in which we "count" the number of enzyme molecules by profiling their single enzyme activity characteristics toward multiple substrates. In this proof-of-concept study of the single enzyme activity-based protein profiling (SEAP), we were able to detect the activities of various phosphoric ester-hydrolyzing enzy  ...[more]

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