Bauer R J, Carl A, Kapicka C L, Kenyon J L
Department of Physiology/MS 352, University of Nevada School of Medicine, Reno 89557, USA.
J Neurosci Methods. 1996 Sep;68(1):101-11. doi: 10.1016/0165-0270(96)00013-1.
We developed a method for determining whether channels in a multichannel patch or bilayer have the same or statistically significantly different open probabilities. We use a maximum likelihood method to fit the distribution of (unbinned) current amplitudes and to provide estimates of individual channel open probabilities, single channel currents, and standard deviations of the channel currents. These parameters are used to compare models with increasing constraints on the open probabilities including the model where all channels have different open probabilities and the model where all channels have the same open probability. A chi 2 statistic is used to identify models that are statistically less likely to predict the data. The ability of multichannel data to determine individual open probabilities is limited by two factors: the signal to noise ratio of the record and the fact that changes in amplitude distributions caused by a 0.2 difference in open probabilities are comparable in magnitude to the variations caused by random channel gating. These limitations notwithstanding, we demonstrate the utility of our approach by using it to analyze the open probabilities of 3 large conductance Ca2(+)-activated K+ channels in an artificial lipid bilayer revealing the response of one of those channels to GTP gamma S.
我们开发了一种方法,用于确定多通道膜片或双层膜中的通道是否具有相同的开放概率,或者在统计学上是否存在显著差异。我们使用最大似然法来拟合(未分箱的)电流幅度分布,并提供单个通道开放概率、单通道电流以及通道电流标准差的估计值。这些参数用于比较对开放概率施加越来越多限制的模型,包括所有通道具有不同开放概率的模型和所有通道具有相同开放概率的模型。使用卡方统计量来识别在统计学上不太可能预测数据的模型。多通道数据确定单个开放概率的能力受到两个因素的限制:记录的信噪比,以及开放概率相差0.2所导致的幅度分布变化在大小上与随机通道门控引起的变化相当这一事实。尽管存在这些限制,我们通过使用该方法分析人工脂质双层中3个大电导Ca2(+)-激活K+通道的开放概率,展示了我们方法的实用性,揭示了其中一个通道对GTPγS的反应。