Gastrointestinal Cell Biology Laboratory, Children's Hospital, and Harvard Medical School, Boston, Massachusetts 02115, USA.
J Biol Chem. 2010 Feb 26;285(9):6145-52. doi: 10.1074/jbc.M109.062067. Epub 2010 Jan 7.
Cholera toxin travels from the plasma membrane to the endoplasmic reticulum of host cells, where a portion of the toxin, the A1-chain, is unfolded and targeted to a protein-conducting channel for retrotranslocation to the cytosol. Unlike most retrotranslocation substrates, the A1-chain escapes degradation by the proteasome and refolds in the cytosol to induce disease. How this occurs remains poorly understood. Here, we show that an unstructured peptide appended to the N terminus of the A1-chain renders the toxin functionally inactive. Cleavage of the peptide extension prior to cell entry rescues toxin half-life and function. The loss of toxicity is explained by rapid degradation by the proteasome after retrotranslocation to the cytosol. Degradation of the mutant toxin does not follow the N-end rule but depends on the two Lys residues at positions 4 and 17 of the native A1-chain, consistent with polyubiquitination at these sites. Thus, retrotranslocation and refolding of the wild-type A1-chain must proceed in a way that protects these Lys residues from attack by E3 ligases.
霍乱毒素从质膜转运到宿主细胞的内质网,毒素的一部分,A1 链,展开并靶向蛋白传导通道进行逆行转运到细胞质。与大多数逆行转运底物不同,A1 链逃避蛋白酶体的降解,并在细胞质中重新折叠以诱导疾病。这是如何发生的仍然知之甚少。在这里,我们表明,A1 链 N 端附加的无结构肽使毒素失去功能。在细胞进入之前切割肽延伸可以挽救毒素的半衰期和功能。毒性丧失的原因是逆行转运到细胞质后被蛋白酶体迅速降解。突变毒素的降解不遵循 N 端规则,而是依赖于天然 A1 链第 4 位和第 17 位的两个赖氨酸残基,与这些位点的多泛素化一致。因此,野生型 A1 链的逆行转运和重折叠必须以一种保护这些赖氨酸残基免受 E3 连接酶攻击的方式进行。