@article{3191558, title = "Elevated In Vitro Kinase Activity in Peripheral Blood Mononuclear Cells ofLeucine-RichRepeat Kinase 2G2019SCarriers: A NovelEnzyme-LinkedImmunosorbent Assay-Based Method", author = "Melachroinou, Katerina and Kang, Min Suk and Liong, Christopher and and Narayan, Sushma and Levers, Najah and Joshi, Neal and Kopil, Katie and and Hutten, Samantha J. and Baptista, Marco A. S. and Padmanabhan, Shalini and and Kang, Un Jung and Stefanis, Leonidas and Alcalay, Roy N. and and Rideout, Hardy J.", journal = "Movement disorders : official journal of the Movement Disorder Society", year = "2020", volume = "35", number = "11", pages = "2095-2100", publisher = "Wiley", doi = "10.1002/mds.28175", keywords = "ELISA; kinase; LRRK2; Parkinson's disease; PBMC", abstract = "Background Leucine-rich repeat kinase 2 kinase inhibitors are being vigorously pursued as potential therapeutic options; however, there is a critical need for sensitive and quantitative assays of leucine-rich repeat kinase 2 function and target engagement. Objectives Our objective was to compare collection and storage protocols for peripheral blood mononuclear cells, and to determine the optimal conditions for downstream analyses of leucine-rich repeat kinase 2 in PD cohorts. Methods Here, we describe enzyme-linked immunosorbent assay-based assays capable of detecting multiple aspects of leucine-rich repeat kinase 2 function at endogenous levels in human tissues. Results In peripheral blood mononuclear cells from both healthy and affected carriers of the G2019S mutation in leucine-rich repeat kinase 2, we report, for the first time, significantly elevated in vitro kinase activity, while detecting a significant increase in pS935/leucine-rich repeat kinase 2 in idiopathic PD patients. Conclusions Quantitative assays such as these described here could potentially uncover specific markers of leucine-rich repeat kinase 2 function that are predictive of disease progression, aid in patient stratification, and be a critical component of upcoming clinical trials. (c) 2020 International Parkinson and Movement Disorder Society" }