Bauer Wolfgang R, Nadler Walter
Medizinische Universitätsklinik 1, Josef Schneider Strasse 2, D-97080 Würzburg, Germany.
Proc Natl Acad Sci U S A. 2006 Aug 1;103(31):11446-51. doi: 10.1073/pnas.0601769103. Epub 2006 Jul 21.
Facilitated translocation of molecules through channels and pores is of fundamental importance for transmembrane transport in biological systems. Several such systems have specific binding sites inside the channel, but a clear understanding of how the interaction between channel and molecules affects the flow is still missing. We present a generic analytical treatment of the problem that relates molecular flow to the first passage time across and the number of particles inside the channel. Both quantities depend in different ways on the channel properties. For the idealized case of noninteracting molecules, we find an increased flow whenever there is a binding site in the channel, despite an increased first passage time. In the more realistic case that molecules may block the channel, we find an increase of flow only up to a certain threshold value of the binding strength and a dependence on the sign of the concentration gradient, i.e., asymmetric transport. The optimal binding strength in that case is analyzed. In all cases the reason for transport facilitation is an increased occupation probability of a particle inside the channel that overcomes any increase in the first passage time because of binding.
分子通过通道和孔的易化转运对于生物系统中的跨膜运输至关重要。若干此类系统在通道内部具有特定结合位点,但对于通道与分子之间的相互作用如何影响流动仍缺乏清晰认识。我们给出了该问题的一种通用分析处理方法,它将分子流与穿过通道的首次通过时间以及通道内的粒子数联系起来。这两个量以不同方式依赖于通道特性。对于非相互作用分子的理想化情况,我们发现尽管首次通过时间增加,但只要通道中有一个结合位点,流动就会增加。在更现实的分子可能阻塞通道的情况下,我们发现只有当结合强度达到某个阈值时流动才会增加,并且依赖于浓度梯度的符号,即不对称运输。分析了该情况下的最佳结合强度。在所有情况下,运输易化的原因是通道内粒子的占据概率增加,这克服了由于结合导致的首次通过时间的任何增加。