Dashevskaya Svetlana, Kopito Ronen Benjamine, Friedman Ran, Elbaum Michael, Epel Bernard L
Department of Plant Sciences, Tel Aviv University, Tel Aviv, Israel.
Protoplasma. 2008 Dec;234(1-4):13-23. doi: 10.1007/s00709-008-0014-7. Epub 2008 Sep 17.
Plasmodesmata (Pd) are trans-wall membrane channels that permit cell-to-cell transport of metabolites and other small molecules, proteins, RNAs, and signaling molecules. The transport of cytoplasmic soluble macromolecules is a function of the electrochemical gradient between adjacent cells, the number of Pd per interface between adjacent cells, Stokes radius (R(S)), area of the cytoplasmic annulus, and channel length. The size of the largest molecule that can pass through Pd defines the Pd size exclusion limit. However, since the shape and size of a molecule determines its capacity to diffuse through pores or tubes, R(S) is a better measure. Relatively small changes in R(S) can cause large differences in the mobility of molecular probes, particularly if the pore size is close to that of the probe. In addition, as the dimensions of a macromolecule approach that of the channel, membrane charge effects may become important. We employed quantitative tools and molecular modeling to measure the apparent coefficient of conductivity of Pd, C(Pd), for the non-targeted transport of macromolecules. This method allowed us to examine the influence of protein charge and R(S) on C(Pd) in Nicotiana benthamiana. The C(Pd) of modified green fluorescent proteins (GFPs) of different sizes but with the same charge as native GFP and of a more negatively charged derivative were determined. We found that the C(Pd) of cytoplasmic soluble GFP and cytoplasmic forms of modified GFP were the most strongly correlated with R(S) and that the apparent aberrant increase in C(Pd) of a negatively charged GFP derivative was, at least in part, the result of the charge effect on R(S).
胞间连丝(Pd)是贯穿细胞壁的膜通道,允许代谢物、其他小分子、蛋白质、RNA和信号分子在细胞间运输。细胞质可溶性大分子的运输取决于相邻细胞间的电化学梯度、相邻细胞间每个界面的Pd数量、斯托克斯半径(R(S))、细胞质环带面积以及通道长度。能够通过Pd的最大分子的大小定义了Pd的尺寸排阻极限。然而,由于分子的形状和大小决定了其通过孔隙或管道扩散的能力,R(S)是一个更好的衡量指标。R(S)相对较小的变化可能会导致分子探针迁移率的巨大差异,特别是当孔径接近探针大小时。此外,随着大分子尺寸接近通道尺寸,膜电荷效应可能变得重要。我们采用定量工具和分子建模来测量Pd的表观电导率系数C(Pd),用于大分子的非靶向运输。该方法使我们能够研究蛋白质电荷和R(S)对本氏烟草中C(Pd)的影响。我们测定了不同大小但与天然绿色荧光蛋白(GFP)电荷相同以及一种带更多负电荷衍生物的修饰绿色荧光蛋白(GFP)的C(Pd)。我们发现细胞质可溶性GFP和修饰GFP的细胞质形式的C(Pd)与R(S)的相关性最强,并且带负电荷的GFP衍生物的C(Pd)明显异常增加至少部分是电荷对R(S)影响的结果。