A Human Tyrosine Phosphatase Interactome Mapped by Proteomic Profiling
Author(s) -
Parveen Kumar,
Prathyusha Munnangi,
KVS Rammohan Chowdary,
Varun Jayeshkumar Shah,
Swapnil Rohidas Shinde,
Nanci R. Kolli,
Rachita Ramachandra Halehalli,
Hampapathalu Adimurthy Nagarajaram,
Subbareddy Maddika
Publication year - 2017
Publication title -
journal of proteome research
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.644
H-Index - 161
eISSN - 1535-3907
pISSN - 1535-3893
DOI - 10.1021/acs.jproteome.7b00065
Subject(s) - interactome , protein tyrosine phosphatase , phosphatase , biology , tyrosine , cytokinesis , computational biology , midbody , microbiology and biotechnology , dephosphorylation , phosphorylation , biochemistry , cell division , cell , gene
Tyrosine phosphatases play a critical role in many cellular processes and pathogenesis, yet comprehensive analysis of their functional interacting proteins in the cell is limited. By utilizing a proteomic approach, here we present an interaction network of 81 human tyrosine phosphatases built on 1884 high-confidence interactions of which 85% are unreported. Our analysis has linked several phosphatases with new cellular processes and unveiled protein interactions genetically linked to various human diseases including cancer. We validated the functional importance of an identified interaction network by characterizing a distinct novel interaction between PTPN5 and Mob1a. PTPN5 dephosphorylates Mob1a at Y26 residue. Further, we identify that PTPN5 is required for proper midbody abscission during cytokinesis through regulation of Mob1a dephosphorylation. In conclusion, our study provides a valuable resource of tyrosine phosphatase interactions, which can be further utilized to dissect novel cellular functions of these enzymes.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom