| Literature DB >> 30610604 |
Chandra Sekhar Chirumamilla1, Mobashar Hussain Urf Turabe Fazil2, Claudina Perez-Novo1, Savithri Rangarajan3, Rik de Wijn3, Padma Ramireddy1, Navin Kumar Verma4, Wim Vanden Berghe1.
Abstract
T-Lymphocyte kinases are important checkpoints that control T-cell motility by regulating a diverse range of signal transduction pathways. The distinct configuration of kinase events in T-cell could be used to fingerprint the status of T-cells. However, only small fraction human kinases have been characterized so far and little is known about the dynamics of the kinome in motile T-cells. Although several direct and indirect strategies exist to characterize cellular kinase activities, such as RNA interference, antibody arrays, enzyme kinetics, and mass spectrometry, this chapter focuses on an alternative multiplex phosphopeptide array-based methodology, which allows the kinome-wide identification of hyper-activated kinases involved in the regulation of T-cell migration.Entities:
Keywords: ICAM-1; Kinase; Kinome analysis; LFA-1; Peptide microarray; T-cell
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Year: 2019 PMID: 30610604 DOI: 10.1007/978-1-4939-9036-8_13
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745