Chayen N E
Biophysics Section, Blackett Laboratory, Imperial College of Science, Technology and Medicine, London SW7 2BZ, England.
Acta Crystallogr D Biol Crystallogr. 1998 Jan 1;54(Pt 1):8-15. doi: 10.1107/s0907444997005374.
Numerous reports have been published in the literature which describe the crystallization of macromolecules by a variety of crystallization methods, including the vapour-diffusion and microbatch techniques. This topical review compares the results of examples of proteins which were crystallized by both vapour-diffusion and microbatch methods. The inherent features of the vapour-diffusion and microbatch methods are discussed and some specific conditions where one method appears more favourable than the other are reported. Guidelines for the conversion of crystallization conditions from vapour diffusion to microbatch (and vice versa) are also presented.
文献中已发表了大量报告,描述了通过多种结晶方法使大分子结晶的情况,包括气相扩散法和微量分批法。本专题综述比较了通过气相扩散法和微量分批法结晶的蛋白质实例的结果。讨论了气相扩散法和微量分批法的固有特征,并报告了在某些特定条件下一种方法比另一种方法更具优势的情况。还给出了将结晶条件从气相扩散法转换为微量分批法(反之亦然)的指导原则。