Departments of Chemical and Biological Engineering and ‡Molecular Biology, Princeton University , Princeton, New Jersey 08544, United States.
J Am Chem Soc. 2016 Nov 2;138(43):14214-14217. doi: 10.1021/jacs.6b09454. Epub 2016 Oct 21.
Lasso peptides exist naturally in a threaded state as [1]rotaxanes, and we reasoned that lasso peptides cleaved in their loop region could serve as building blocks for catenanes. Mutagenesis of the lasso peptide microcin J25 (MccJ25) with two cysteine residues followed by cleavage of the peptide with trypsin led to a [2]rotaxane structure that self-assembled into a [3]catenane and [4]catenanes at room temperature in aqueous solution. The [3]catenane represents the smallest ring size of a catenane composed solely of polypeptide segments. The NMR structure of the [3]catenane was determined, suggesting that burial of hydrophobic residues may be a driving force for assembly of the catenane structure.
套索肽以[1]轮烷的形式自然存在于螺旋状态,我们推断,在环区切割的套索肽可以作为[3]轮烷的构建块。用两个半胱氨酸残基对微菌素 J25(MccJ25)进行突变,然后用胰蛋白酶切割肽,得到[2]轮烷结构,该结构在室温下在水溶液中自组装成[3]轮烷和[4]轮烷。[3]轮烷代表仅由多肽片段组成的轮烷的最小环尺寸。[3]轮烷的 NMR 结构已确定,表明疏水性残基的埋藏可能是组装轮烷结构的驱动力。