McPherson A, Kuznetsov Y G, Malkin A J, Plomp M
University of California, Irvine Department of Molecular Biology and Biochemistry, 92697-3900, USA.
J Synchrotron Radiat. 2004 Jan 1;11(Pt 1):21-3. doi: 10.1107/s0909049503023914. Epub 2003 Nov 28.
Direct visualization of macromolecular crystal growth using atomic force microscopy (AFM) has provided a powerful tool in the delineation of mechanisms and the kinetics of the growth process. It has further allowed us to evaluate the wide variety of impurities that are incorporated into crystals of proteins, nucleic acids, and viruses. It is possible, using AFM, to image the defects and imperfections that afflict these crystals, the impurity layers that poison their surfaces, and the consequences of various factors on morphological development. All of these can be recorded under normal growth conditions, in native mother liquors, over time intervals ranging from minutes to days, and at the molecular level.
使用原子力显微镜(AFM)直接观察大分子晶体生长,为描述生长过程的机制和动力学提供了一个强大的工具。它还使我们能够评估掺入蛋白质、核酸和病毒晶体中的各种杂质。利用AFM可以对困扰这些晶体的缺陷和不完美之处、毒害其表面的杂质层以及各种因素对形态发育的影响进行成像。所有这些都可以在正常生长条件下、在天然母液中、在从几分钟到几天的时间间隔内以及在分子水平上进行记录。