超分子化学
原子力显微镜
分子间力
结晶学
纳米技术
配体(生物化学)
材料科学
自组装
化学
突变体
超分子组装
格子(音乐)
化学物理
分子动力学
蛋白质结构
基因亚型
生物物理学
晶体结构
力谱学
光学(聚焦)
血浆蛋白结合
分子自组装
过程(计算)
显微镜
图像处理
作者
Yi‐Chih Lin,Shuangyu Luo,Arnav Patil,Nicholas Primanis-Erickson,Xiaoding Jiang,Bradley Webb,Ku‐Lung Hsu
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2026-05-12
标识
DOI:10.64898/2026.05.08.723867
摘要
Phosphofructokinase-1 (PFK-1) catalyzes the ATP-dependent conversion of fructose-6-phosphate (F6P) to fructose-1,6-bisphosphate (F1,6BP), the first committed step of glycolysis. Beyond classical allostery, the liver isoform PFKL forms higher-order assemblies, but how ligand binding redirects intermolecular interactions remains unclear. Here we use high-speed atomic force microscopy (HS-AFM), topology-based AFM image simulations, and molecular dynamics (MD) simulations to define ligand-dependent assembly switching of human PFKL. Wild-type PFKL (PFKL WT) forms lattice-like assemblies under APO and ATP conditions, whereas coordinated ATP and F6P loading redirects assembly toward filaments in a ligand-order-dependent manner. APO-PFKL WT also forms lattice-like assemblies on or near membrane-supported surfaces, suggesting that interfacial environments influence where assembly initiates. The filament-defective N702T mutant forms ordered double-layer lattices and preserves this geometry under APO, ATP, and ATP+F6P conditions. MD simulations suggest that lattice stabilization arises from distributed inter-tetramer contacts. These findings define a structural framework for ligand-dependent supramolecular regulation of glycolysis.
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