Phos-tag-based analysis of myosin regulatory light chain phosphorylation in human uterine myocytes

• Published in: PloS one 2011-06, Vol.6 (6), p.e20903
• Main Authors: Aguilar, Hector N, Tracey, Curtis N, Tsang, Siu Cheung F, McGinnis, Justin M, Mitchell, Bryan F
• Format: Article
• Language: English
• Subjects: Antagonists; Binding Sites; Biology; Cell Extracts; Chains; Comparative analysis; Data processing; Dentistry; Dipeptides - pharmacology; Electrophoretic mobility; Female; Gel electrophoresis; Humans; Kinases; Light; Medicine; Migration; Motility; Muscle Cells - cytology; Muscle Cells - drug effects; Muscle Cells - enzymology; Muscle Cells - metabolism; Muscle proteins; Myocytes; Myosin; Myosin Light Chains - chemistry; Myosin Light Chains - metabolism; Myosin-light-chain kinase; Myosin-Light-Chain Kinase - metabolism; Oxytocin; Oxytocin - pharmacology; Phorbol esters; Phorbol Esters - pharmacology; Phosphates; Phosphoproteins - chemistry; Phosphoproteins - metabolism; Phosphorylation; Phosphorylation - drug effects; Physiology; Pregnancy; Proteins; Proteomics; Reproducibility of Results; Rho-associated kinase; rho-Associated Kinases - metabolism; Serine - metabolism; Signal Transduction - drug effects; Smooth muscle; Sodium lauryl sulfate; Stoichiometry; Uterus; Uterus - cytology; Western blotting
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0020903

The 'phosphate-binding tag' (phos-tag) reagent enables separation of phospho-proteins during SDS-PAGE by impeding migration proportional to their phosphorylation stoichiometry. Western blotting can then be used to detect and quantify the bands corresponding to the phospho-states of a target protein. We present a method for quantification of data regarding phospho-states derived from phos-tag SDS-PAGE. The method incorporates corrections for lane-to-lane loading variability and for the effects of drug vehicles thus enabling the comparison of multiple treatments by using the untreated cellular set-point as a reference. This method is exemplified by quantifying the phosphorylation of myosin regulatory light chain (RLC) in cultured human uterine myocytes. We have evaluated and validated the concept that, when using an antibody (Ab) against the total-protein, the sum of all phosphorylation states in a single lane represents a 'closed system' since all possible phospho-states and phosphoisotypes are detected. Using this approach, we demonstrate that oxytocin (OT) and calpeptin (Calp) induce RLC kinase (MLCK)- and rho-kinase (ROK)-dependent enhancements in phosphorylation of RLC at T18 and S19. Treatment of myocytes with a phorbol ester (PMA) induced phosphorylation of S1-RLC, which caused a mobility shift in the phos-tag matrices distinct from phosphorylation at S19. We have presented a method for analysis of phospho-state data that facilitates quantitative comparison to a reference control without the use of a traditional 'loading' or 'reference' standard. This analysis is useful for assessing effects of putative agonists and antagonists where all phospho-states are represented in control and experimental samples. We also demonstrated that phosphorylation of RLC at S1 is inducible in intact uterine myocytes, though the signal in the resting samples was not sufficiently abundant to allow quantification by the approach used here.