Thiel G, Blatt M R, Fricker M D, White I R, Millner P
Department of Biological Sciences, University of London, Wye College, Kent, England.
Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11493-7. doi: 10.1073/pnas.90.24.11493.
Transduction of the auxin stimulus in plants is thought to entail binding of the hormone to a soluble auxin-binding protein (ABP) outside the cell and subsequent interaction between this auxin-protein complex and an integral membrane receptor ("docking") protein that couples the signal across the plasma membrane. To explore the structural requirements for ABP function, synthetic peptides were prepared to the amino acid sequences of the predicted surface domains of ABPzm1, the dominant ABP from Zea. Biological function was assayed under voltage clamp, monitoring the ability of the peptides to evoke auxin-related modulations in inward- (IK,in) and outward-rectifying (IK,out) K+ channel activities of Vicia guard cells in the absence of added auxin. Only the peptide corresponding to the C-terminal domain of ABPzm1 was active. The dominant response was an inactivation of IK,in, although the peptide also evoked an activation of IK,out. Inactivation of IK,in was complete within 20-30 s and was fully reversible, was marked by a slowing of voltage-dependent activation and deactivation, and was dependent on peptide concentration (K1/2, 16 +/- 6 microM). Buffering cytoplasmic-free [Ca2+] with EGTA had no effect on IK,in response to the peptide. However, virtually complete and reversible block of the response was achieved when cytoplasmic pH (pHi) was brought under experimental control using the weak acid butyrate. Parallel measurements of pHi using the fluorescent dye 2',7'-bis(2-carboxyethyl-5(6)-carboxyfluorescein (BCECF) and dual-wavelength laser-scanning confocal microscopy demonstrated that the C-terminal peptide evoked rapid and reversible cytoplasmic alkalinizations of 0.4 +/- 0.1 pHi unit and confirmed the antagonism of the pHi response in the presence of butyrate. These, and comparable results with the auxins indole acetic acid and 1-naphthyleneacetic acid, implicate the C-terminal domain of ABPzm1 in auxin-ABP coupling to pHi and an associated intracellular signaling cascade.
植物中生长素刺激的转导被认为需要激素与细胞外可溶性生长素结合蛋白(ABP)结合,随后该生长素 - 蛋白复合物与整合膜受体(“对接”)蛋白相互作用,该受体蛋白将信号跨质膜传递。为了探索ABP功能的结构要求,根据玉米中主要的ABP即ABPzm1预测表面结构域的氨基酸序列制备了合成肽。在电压钳制下测定生物学功能,监测肽在不添加生长素的情况下诱发蚕豆保卫细胞内向(IK,in)和外向整流(IK,out)钾通道活性中生长素相关调节的能力。只有对应于ABPzm1 C末端结构域的肽具有活性。主要反应是IK,in失活,尽管该肽也诱发了IK,out的激活。IK,in的失活在20 - 30秒内完成且完全可逆,其特征是电压依赖性激活和失活减慢,并依赖于肽浓度(K1/2,16±6 microM)。用EGTA缓冲细胞质游离[Ca2+]对肽引起的IK,in反应没有影响。然而,当使用弱酸丁酸盐使细胞质pH(pHi)处于实验控制之下时,几乎完全且可逆地阻断了该反应。使用荧光染料2',7'-双(2 - 羧乙基 - 5(6)-羧基荧光素(BCECF)和双波长激光扫描共聚焦显微镜对pHi进行的平行测量表明,C末端肽诱发了0.4±0.1个pHi单位的快速且可逆的细胞质碱化,并证实了在丁酸盐存在下pHi反应的拮抗作用。这些以及与生长素吲哚乙酸和1 - 萘乙酸的可比结果表明,ABPzm1的C末端结构域参与了生长素 - ABP与pHi的偶联以及相关的细胞内信号级联反应。