Inoue Keiichi, Nomura Yurika, Kandori Hideki
From the Department of Frontier Materials and OptoBioTechnology Research Center, Nagoya Institute of Technology, Showa-ku, Nagoya 466-8555, Japan and PRESTO, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.
From the Department of Frontier Materials and.
J Biol Chem. 2016 May 6;291(19):9883-93. doi: 10.1074/jbc.M116.716498. Epub 2016 Feb 29.
In addition to the well-known light-driven outward proton pumps, novel ion-pumping rhodopsins functioning as outward Na(+) and inward Cl(-) pumps have been recently found in eubacteria. They convert light energy into transmembrane electrochemical potential difference, similar to the prototypical archaeal H(+) pump bacteriorhodopsin (BR) and Cl(-) pump halorhodopsin (HR). The H(+), Na(+), and Cl(-) pumps possess the conserved respective DTE, NDQ, and NTQ motifs in the helix C, which likely serve as their functional determinants. To verify this hypothesis, we attempted functional interconversion between selected pumps from each category by mutagenesis. Introduction of the proton-pumping motif resulted in successful Na(+) → H(+) functional conversion. Introduction of the respective characteristic motifs with several additional mutations leads to successful Na(+) → Cl(-) and Cl(-) → H(+) functional conversions, whereas remaining conversions (H(+) → Na(+), H(+) → Cl(-), Cl(-) → Na(+)) were unsuccessful when mutagenesis of 4-6 residues was used. Phylogenetic analysis suggests that a H(+) pump is the common ancestor of all of these rhodopsins, from which Cl(-) pumps emerged followed by Na(+) pumps. We propose that successful functional conversions of these ion pumps are achieved exclusively when mutagenesis reverses the evolutionary amino acid sequence changes. Dependence of the observed functional conversions on the direction of evolution strongly suggests that the essential structural mechanism of an ancestral function is retained even after the gain of a new function during natural evolution, which can be evoked by a few mutations. By contrast, the gain of a new function needs accumulation of multiple mutations, which may not be easily reproduced by limited mutagenesis in vitro.
除了众所周知的光驱动外向质子泵外,最近在真细菌中发现了新型离子泵视紫红质,其作为外向Na(+)泵和内向Cl(-)泵发挥作用。它们将光能转化为跨膜电化学势差,类似于典型的古菌H(+)泵细菌视紫红质(BR)和Cl(-)泵嗜盐视紫红质(HR)。H(+)、Na(+)和Cl(-)泵在螺旋C中具有保守的各自的DTE、NDQ和NTQ基序,这可能是它们的功能决定因素。为了验证这一假设,我们试图通过诱变在每一类选定的泵之间进行功能互变。引入质子泵基序导致成功的Na(+)→H(+)功能转换。引入各自的特征基序并进行一些额外的突变导致成功的Na(+)→Cl(-)和Cl(-)→H(+)功能转换,而当使用4-6个残基的诱变时,其余的转换(H(+)→Na(+)、H(+)→Cl(-)、Cl(-)→Na(+))未成功。系统发育分析表明,H(+)泵是所有这些视紫红质的共同祖先,Cl(-)泵从其中出现,随后是Na(+)泵。我们提出,只有当诱变逆转进化氨基酸序列变化时,这些离子泵才能成功进行功能转换。观察到的功能转换对进化方向的依赖性强烈表明,即使在自然进化过程中获得新功能后,祖先功能的基本结构机制仍然保留,这可以由少数突变引发。相比之下,新功能的获得需要多个突变的积累,这在体外有限的诱变中可能不容易重现。