Laufer Center for Physical and Quantitative Biology, Stony Brook University, Stony Brook, NY, USA; Department of Chemistry, Stony Brook University, Stony Brook, NY, USA.
Laufer Center for Physical and Quantitative Biology, Stony Brook University, Stony Brook, NY, USA.
J Mol Biol. 2021 Oct 1;433(20):167126. doi: 10.1016/j.jmb.2021.167126. Epub 2021 Jul 3.
The protein folding problem was first articulated as question of how order arose from disorder in proteins: How did the various native structures of proteins arise from interatomic driving forces encoded within their amino acid sequences, and how did they fold so fast? These matters have now been largely resolved by theory and statistical mechanics combined with experiments. There are general principles. Chain randomness is overcome by solvation-based codes. And in the needle-in-a-haystack metaphor, native states are found efficiently because protein haystacks (conformational ensembles) are funnel-shaped. Order-disorder theory has now grown to encompass a large swath of protein physical science across biology.
蛋白质的各种天然结构是如何从其氨基酸序列中编码的原子间驱动力中产生的,它们又是如何快速折叠的?这些问题现在已经通过理论和统计力学与实验的结合得到了很大程度的解决。有一些普遍的原则。链的随机性被基于溶剂的编码所克服。在“大海捞针”的比喻中,由于天然状态是有效的,所以可以有效地找到蛋白质针(构象集合)是漏斗形的。无序-有序理论现在已经发展到涵盖生物学中蛋白质物理科学的很大一部分。