Raeeszadeh-Sarmazdeh Maryam, Parthasarathy Ranganath, Boder Eric T
Dept. of Chemical and Biomolecular Engineering, University of Tennessee, Knoxville, TN, 37996.
Dept. of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19114.
Biotechnol Prog. 2017 May;33(3):824-831. doi: 10.1002/btpr.2449. Epub 2017 Mar 11.
Increasing interest in protein immobilization on surfaces has heightened the need for techniques enabling layer-by-layer protein attachment. Here, we report a technique for controlling enzyme-mediated immobilization of layers of protein on the surface using a genetically encoded protecting group. An enterokinase-cleavable peptide sequence was inserted at the N-terminus of bifunctional fluorescent proteins containing Sortase A substrate recognition tags at both ends to control Sortase A-mediated protein immobilization on the surface layer-by-layer. Efficient, sequential immobilization of a second layer of protein using Sortase A required removal of the N-terminal protecting group, suggesting the method enables multilayer synthesis using cyclic deprotection and coupling steps. © 2017 American Institute of Chemical Engineers Biotechnol. Prog., 33:824-831, 2017.
人们对蛋白质固定于表面的兴趣与日俱增,这使得对能够实现逐层蛋白质附着的技术需求更为迫切。在此,我们报告了一种利用基因编码保护基团来控制酶介导的蛋白质层在表面固定的技术。在两端均含有分选酶A底物识别标签的双功能荧光蛋白的N端插入了一个肠激酶可裂解的肽序列,以控制分选酶A介导的蛋白质在表面的逐层固定。使用分选酶A高效、顺序地固定第二层蛋白质需要去除N端保护基团,这表明该方法能够通过循环脱保护和偶联步骤实现多层合成。© 2017美国化学工程师学会 生物技术进展,33:824 - 831,2017年。