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鸡V区和V区框架区对突变的多功能性。

The Versatility of Framework Regions of Chicken V and V to Mutations.

作者信息

Shin Jung Won, Kim Sang Il, Yoon Aerin, Jin Junyeong, Park Hyung Bae, Kim Hyori, Chung Junho

机构信息

Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul 03080, Korea.

Cancer Research Institute, Seoul National University College of Medicine, Seoul 03080, Korea.

出版信息

Immune Netw. 2018 Jan 31;18(2):e3. doi: 10.4110/in.2018.18.e3. eCollection 2018 Apr.

DOI:10.4110/in.2018.18.e3
PMID:29732232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5928418/
Abstract

To identify the interchangeability of V and V framework region (FR) residues, we artificially introduced random mutations at all residue positions in a chicken monoclonal antibody, which has only one functional V and V gene. When we classified the amino acids into 5 groups by their physicochemical properties, all FR residues could be replaced by another group except L23 (C), H36 (W), H86 (D), H104 (G), and H106 (G). Eighty-two (50.9%), 48 (29.8%), 17 (10.6%), and 9 FR residues (5.6%) could be replaced by 4, 3, 2, and 1 group(s), individually, without significant loss of reactivity. We also confirmed a similar level of versatility with 2 different chicken antibodies. This high level of versatility on FR residues has not been predicted because it has not been observed in the 150 chicken antibodies that we previously generated or in the 1,269 naïve chicken V sequences publically available. In conclusion, chicken antibody FR residues are highly interchangeable and this property can be applied for improving the physicochemical property of antibody including thermal stability, solubility and viscosity.

摘要

为了确定V区和V框架区(FR)残基的互换性,我们在一种鸡单克隆抗体的所有残基位置人工引入随机突变,该抗体只有一个功能性V基因和V基因。当我们根据氨基酸的物理化学性质将其分为5组时,除了L23(C)、H36(W)、H86(D)、H104(G)和H106(G)外,所有FR残基都可以被另一组取代。82个(50.9%)、48个(29.8%)、17个(10.6%)和9个FR残基(5.6%)可以分别被4、3、2和1组取代,而不会显著丧失反应活性。我们还用2种不同的鸡抗体证实了类似程度的通用性。FR残基的这种高度通用性此前并未被预测到,因为在我们之前产生的150种鸡抗体或公开可用的1269个天然鸡V序列中均未观察到。总之,鸡抗体的FR残基具有高度互换性,这一特性可用于改善抗体的物理化学性质,包括热稳定性、溶解性和粘度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/3bac8a4a3cfe/in-18-e3-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/f2de94a44c91/in-18-e3-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/89f84ef8733a/in-18-e3-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/d906278f58d7/in-18-e3-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/3bac8a4a3cfe/in-18-e3-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/f2de94a44c91/in-18-e3-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/89f84ef8733a/in-18-e3-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/d906278f58d7/in-18-e3-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7da7/5928418/3bac8a4a3cfe/in-18-e3-g004.jpg

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一种通用的抗体框架组合设计,用于移植不同的 CDR 序列:一种生物信息学方法。
Proteins. 2012 Mar;80(3):896-912. doi: 10.1002/prot.23246. Epub 2011 Dec 16.
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Fundamental characteristics of the immunoglobulin VH repertoire of chickens in comparison with those of humans, mice, and camelids.鸡的免疫球蛋白 VH 库与人类、小鼠和骆驼科动物的 VH 库的基本特征比较。
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