Permeation through the calcium release channel of cardiac muscle

被引:51
作者
Chen, D
Xu, L
Tripathy, A
Meissner, G
Eisenberg, B
机构
[1] RUSH MED COLL, DEPT MOL PHYSIOL & BIOPHYS, CHICAGO, IL 60612 USA
[2] UNIV N CAROLINA, DEPT BIOCHEM & BIOPHYS, CHAPEL HILL, NC 27599 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1016/S0006-3495(97)78167-0
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Current voltage (I-V) relations were measured from the calcium release channel (CRC) of the sarcoplasmic reticulum of cardiac muscle in 12 KCl solutions, symmetrical and asymmetrical, from 25 mM to 2 M. I-V curves are nearly linear, in the voltage range +/- 50 mV approximate to 12kT/e, even in asymmetrical solutions, e.g., 2 M parallel to 100 mM. It is awkward to describe straight lines as sums of exponentials in a wide range of solutions and potentials, and so traditional barrier models have difficulty fitting this data. Diffusion theories with constant fields predict curvilinear I-V relations, and so they are also unsatisfactory. The Poisson and Nernst-Planck equations (PNP) form a diffusion theory with variable fields. They fit the data by using adjustable parameters for the diffusion constant of each ion and for the effective density of fixed (i.e., permanent) charge P(x) along the channel's ''filter'' (7-Angstrom diameter, 10 Angstrom long). If P(x) is described by just one parameter, independent of x (i.e., P(x) = P-0 = -4.2 M), the fits are satisfactory (RMS error/RMS current = 6.4/67), and the estimates of diffusion coefficients are reasonable D-K = 1.3 x -10(-6) cm(2)/s, D-Cl = 3.9 x 10(-6) cm(2)/s. The CRC seems to have a small selectivity filter with a very high density of permanent charge. This may be a design principle of channels specialized for large flux. The Appendix derives barrier models, and their prefactor, from diffusion theories (with variable fields) and argues that barrier models are poor descriptions of CRCs in particular and open channels in general.
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页码:1337 / 1354
页数:18
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