Guarente L
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1639-41. doi: 10.1073/pnas.90.5.1639.
Many problems in modern biology involve complex arrays of interacting protein and, in some cases, RNA molecules. The initial challenge facing investigators is to identify the important players that drive the process under study. This difficult task is ameliorated somewhat by the development of methods designed to keep pace with the magnitude of this challenge. I have outlined a few of these approaches at the cutting edge of cloning interacting proteins. A perhaps more daunting prospect is to dissect the important molecules once they are in hand, to identify key interactions, and, ultimately, to move to an understanding of function in cells. For this, of course, all of the tools of genetics, biochemistry, and molecular biology, extant and yet to be developed, will have to be tapped.
现代生物学中的许多问题涉及相互作用的蛋白质以及某些情况下的RNA分子的复杂阵列。研究人员面临的首要挑战是确定驱动所研究过程的重要参与者。旨在跟上这一挑战规模的方法的发展,在一定程度上缓解了这项艰巨的任务。我已经概述了一些处于克隆相互作用蛋白前沿的此类方法。一个可能更令人生畏的前景是,一旦掌握了重要分子,就要剖析它们,确定关键相互作用,并最终深入了解细胞中的功能。当然,为此必须利用遗传学、生物化学和分子生物学现有的以及尚未开发的所有工具。