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2
Length Dependent Helix-Coil Transition Kinetics of Nine Alanine-Based Peptides.九种基于丙氨酸的肽的长度依赖性螺旋-卷曲转变动力学
J Phys Chem B. 2004 Sep 30;108(39). doi: 10.1021/jp037272j.
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Optimized molecular dynamics force fields applied to the helix-coil transition of polypeptides.应用于多肽螺旋-卷曲转变的优化分子动力学力场。
J Phys Chem B. 2009 Jul 2;113(26):9004-15. doi: 10.1021/jp901540t.
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Statistical prediction and molecular dynamics simulation.统计预测与分子动力学模拟。
Biophys J. 2008 Nov 15;95(10):4497-511. doi: 10.1529/biophysj.108.131623. Epub 2008 Aug 1.
5
The minimized dead-end elimination criterion and its application to protein redesign in a hybrid scoring and search algorithm for computing partition functions over molecular ensembles.最小化死端消除标准及其在用于计算分子系综配分函数的混合评分与搜索算法中对蛋白质重新设计的应用。
J Comput Chem. 2008 Jul 30;29(10):1527-42. doi: 10.1002/jcc.20909.
6
Statistical estimation of statistical mechanical models: helix-coil theory and peptide helicity prediction.统计力学模型的统计估计:螺旋-卷曲理论与肽螺旋度预测。
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7
Causal protein-signaling networks derived from multiparameter single-cell data.源自多参数单细胞数据的因果蛋白信号网络。
Science. 2005 Apr 22;308(5721):523-9. doi: 10.1126/science.1105809.
8
Helix induction in antimicrobial peptides by alginate in biofilms.生物膜中藻酸盐对抗菌肽的螺旋诱导作用。
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9
The structure of proteins; two hydrogen-bonded helical configurations of the polypeptide chain.蛋白质的结构;多肽链的两种氢键螺旋构型。
Proc Natl Acad Sci U S A. 1951 Apr;37(4):205-11. doi: 10.1073/pnas.37.4.205.
10
Osmolyte effects on helix formation in peptides and the stability of coiled-coils.渗透溶质对肽中螺旋形成及卷曲螺旋稳定性的影响。
Protein Sci. 2002 Aug;11(8):2048-51. doi: 10.1110/ps.0211702.

高效枚举和可视化的螺旋-卷曲集。

Efficient enumeration and visualization of helix-coil ensembles.

机构信息

Department of Biochemistry, Duke University, Durham, North Carolina.

Program in Computational Biology and Bioinformatics, Duke University, Durham, North Carolina.

出版信息

Biophys J. 2024 Feb 6;123(3):317-333. doi: 10.1016/j.bpj.2023.12.021. Epub 2023 Dec 29.

DOI:10.1016/j.bpj.2023.12.021
PMID:38158653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10870177/
Abstract

Helix-coil models are routinely used to interpret circular dichroism data of helical peptides or predict the helicity of naturally-occurring and designed polypeptides. However, a helix-coil model contains significantly more information than mean helicity alone, as it defines the entire ensemble-the equilibrium population of every possible helix-coil configuration-for a given sequence. Many desirable quantities of this ensemble are either not obtained as ensemble averages or are not available using standard helicity-averaging calculations. Enumeration of the entire ensemble can allow calculation of a wider set of ensemble properties, but the exponential size of the configuration space typically renders this intractable. We present an algorithm that efficiently approximates the helix-coil ensemble to arbitrary accuracy by sequentially generating a list of the M highest populated configurations in descending order of population. Truncating this list of (configuration, population) pairs at a desired accuracy provides an approximating sub-ensemble. We demonstrate several uses of this approach for providing insight into helix-coil ensembles and folding mechanisms, including landscape visualization.

摘要

螺旋-卷曲模型通常用于解释螺旋肽的圆二色性数据或预测天然存在和设计的多肽的螺旋性。然而,与平均螺旋度相比,螺旋-卷曲模型包含的信息量要大得多,因为它为给定的序列定义了整个集合——每个可能的螺旋-卷曲构象的平衡种群。该集合中的许多理想数量要么不能作为集合平均值获得,要么不能使用标准的螺旋平均值计算获得。对整个集合进行枚举可以允许计算更广泛的集合属性,但构象空间的指数大小通常使得这难以处理。我们提出了一种算法,通过顺序生成按种群递减顺序排列的 M 个最高种群的配置列表,以任意精度有效地逼近螺旋-卷曲集合。在所需精度处截断此(构象,种群)对列表提供了一个近似的子集合。我们展示了这种方法在提供对螺旋-卷曲集合和折叠机制的洞察力方面的几种用途,包括景观可视化。