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% File src/library/datasets/man/Puromycin.Rd% Part of the R package, https://www.R-project.org% Copyright 1995-2014 R Core Team% Distributed under GPL 2 or later\name{Puromycin}\docType{data}\alias{Puromycin}\title{Reaction Velocity of an Enzymatic Reaction}\description{The \code{Puromycin} data frame has 23 rows and 3 columns of thereaction velocity versus substrate concentration in an enzymaticreaction involving untreated cells or cells treated with Puromycin.}\usage{Puromycin}\format{This data frame contains the following columns:\describe{\item{\code{conc}}{a numeric vector of substrate concentrations (ppm)}\item{\code{rate}}{a numeric vector of instantaneous reaction rates (counts/min/min)}\item{\code{state}}{a factor with levels\code{treated}\code{untreated}}}}\details{Data on the velocity of an enzymatic reaction were obtainedby Treloar (1974). The number of counts per minute of radioactiveproduct from the reaction was measured as a function of substrateconcentration in parts per million (ppm) and from these counts theinitial rate (or velocity) of the reaction was calculated(counts/min/min). The experiment was conducted once with the enzymetreated with Puromycin, and once with the enzyme untreated.}\source{Bates, D.M. and Watts, D.G. (1988),\emph{Nonlinear Regression Analysis and Its Applications},Wiley, Appendix A1.3.Treloar, M. A. (1974), \emph{Effects of Puromycin onGalactosyltransferase in Golgi Membranes}, M.Sc. Thesis, U. ofToronto.}\seealso{\code{\link{SSmicmen}} for other models fitted to this dataset.}\examples{require(stats); require(graphics)\dontshow{options(show.nls.convergence=FALSE)}plot(rate ~ conc, data = Puromycin, las = 1,xlab = "Substrate concentration (ppm)",ylab = "Reaction velocity (counts/min/min)",pch = as.integer(Puromycin$state),col = as.integer(Puromycin$state),main = "Puromycin data and fitted Michaelis-Menten curves")## simplest form of fitting the Michaelis-Menten model to these datafm1 <- nls(rate ~ Vm * conc/(K + conc), data = Puromycin,subset = state == "treated",start = c(Vm = 200, K = 0.05))fm2 <- nls(rate ~ Vm * conc/(K + conc), data = Puromycin,subset = state == "untreated",start = c(Vm = 160, K = 0.05))summary(fm1)summary(fm2)## add fitted lines to the plotconc <- seq(0, 1.2, length.out = 101)lines(conc, predict(fm1, list(conc = conc)), lty = 1, col = 1)lines(conc, predict(fm2, list(conc = conc)), lty = 2, col = 2)legend(0.8, 120, levels(Puromycin$state),col = 1:2, lty = 1:2, pch = 1:2)## using partial linearityfm3 <- nls(rate ~ conc/(K + conc), data = Puromycin,subset = state == "treated", start = c(K = 0.05),algorithm = "plinear")}\keyword{datasets}