A Chemical Strategy for Protease Substrate Profiling-Reference-Cited by-同舟云学术

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A Chemical Strategy for Protease Substrate Profiling

Published:2019-06 Issue:6 Volume:26 Page:901-907.e6
ISSN:2451-9456
Container-title:Cell Chemical Biology
language:en
Short-container-title:Cell Chemical Biology

Author:

Griswold Andrew R.,Cifani Paolo,Rao Sahana D.,Axelrod Abram J.,Miele Matthew M.,Hendrickson Ronald C.,Kentsis Alex,Bachovchin Daniel A.

Funder

Josie Robertson Foundation

Cancer-Innovative Research

Entertainment Industry Foundation

American Association for Cancer Research

Pew Charitable Trusts

Pershing Square Sohn Cancer Research Alliance

NIH

Burroughs Wellcome Fund

Alex’s Lemonade Stand Foundation

Gabrielle's Angel Foundation

Damon Runyon Cancer Research Foundation

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,Biochemistry

Reference46 articles.

1. PT-100, a small molecule dipeptidyl peptidase inhibitor, has potent antitumor effects and augments antibody-mediated cytotoxicity via a novel immune mechanism;Adams;Cancer Res.,2004

2. Stromal cell-derived factors 1alpha and 1beta, inflammatory protein-10 and interferon-inducible T cell chemo-attractant are novel substrates of dipeptidyl peptidase 8;Ajami;FEBS Lett.,2008

3. In vivo half-life of a protein is a function of its amino-terminal residue;Bachmair;Science,1986

4. Inhibition of food intake in obese subjects by peptide YY3-36;Batterham;N. Engl. J. Med.,2003

5. Dipeptidyl peptidases 8 and 9: specificity and molecular characterization compared with dipeptidyl peptidase IV;Bjelke;Biochem. J.,2006

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