Polymer-antibody fragment conjugates for biomedical applications

结合 聚合物 化学 免疫原性 抗体 生物物理学 小分子 背景(考古学) 单克隆抗体 组合化学 药物输送 生物化学 有机化学 生物 古生物学 免疫学 数学分析 数学
作者
Akshay Srivastava,Iain B. O’Connor,Abhay Pandit,J. Gerard Wall
出处
期刊:Progress in Polymer Science [Elsevier]
卷期号:39 (2): 308-329 被引量:35
标识
DOI:10.1016/j.progpolymsci.2013.09.003
摘要

Many proteins benefit from improved solubility, immunocompatibility, pharmacokinetics or stability upon conjugation to polymers. For protein-conjugates used in delivery or imaging in vivo, this can mean increased efficacies due to longer circulatory half-lives or increased intracellular stability. In vitro, conjugation to polymers can increase stability, reduce aggregation, or mediate multimerization or phase separation of proteins to increase assay sensitivities or improve signal detection. The emergence of recombinant antibody technologies over the past two decades has allowed relatively simple isolation in vitro of (human) antibody fragments, such as Fabs and single chain variable fragments (scFvs), that retain the binding properties of their parent molecules and may exhibit additional properties such as reduced immunogenicity, improved tissue penetration or increased packing density on sensor surfaces due to their small sizes. In addition, protein engineering approaches that facilitate their chemical functionalization have seen antibody fragments linked to a broad spectrum of chemically and functionally diverse polymeric molecules. Of the varied strategies used in polymer–protein coupling, amine and cysteine conjugation are the most widely applied chemistries with antibody fragments. Simple conjugation to poly(ethyleneglycol) can increase half-life, decrease renal clearance, improve stability and reduce aggregation of antibody fragments without compromising their antigen binding. Meanwhile, engineering of antibody fragments can be used to control conjugation to polymers and coupling to responsive polymers can enable intracellular delivery or context responsive release of a drug payload from a polymer–antibody fragment complex. Recent years have seen polymer–antibody fragment conjugates increasingly encroach into areas traditionally associated with monoclonal antibody–polymers and we discuss the potential of such conjugates, in vivo and in vitro, in applications such as drug delivery, tissue engineering, diagnostics and bioseparation.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
lanyangyang完成签到,获得积分10
1秒前
YYY完成签到 ,获得积分10
1秒前
disjustar完成签到,获得积分10
2秒前
华仔应助科研通管家采纳,获得10
3秒前
prosperp应助科研通管家采纳,获得10
3秒前
小二郎应助科研通管家采纳,获得10
3秒前
3秒前
乐乐应助科研通管家采纳,获得10
4秒前
陈好人完成签到,获得积分10
4秒前
万能图书馆应助yyy采纳,获得10
5秒前
研友_汪老头完成签到,获得积分10
5秒前
一碗饭1982完成签到,获得积分10
6秒前
朝圣者完成签到,获得积分10
7秒前
鄂百川完成签到,获得积分10
7秒前
小陈发布了新的文献求助10
7秒前
8秒前
8秒前
Darkangel发布了新的文献求助10
9秒前
baizhi完成签到,获得积分10
9秒前
冷傲的芾发布了新的文献求助10
9秒前
10秒前
shawn发布了新的文献求助10
11秒前
复杂觅海完成签到 ,获得积分10
12秒前
miyano完成签到,获得积分10
12秒前
13秒前
科研副本发布了新的文献求助10
13秒前
稳赚赚完成签到,获得积分10
14秒前
豆腐青菜雨应助chujun采纳,获得10
14秒前
16秒前
柠檬小白完成签到,获得积分10
16秒前
17秒前
17秒前
龙抬头完成签到,获得积分10
17秒前
香蕉安双发布了新的文献求助10
18秒前
18秒前
和平使命应助陈好人采纳,获得10
19秒前
Lemon完成签到,获得积分10
19秒前
cocolu应助小羊哥采纳,获得10
20秒前
21秒前
高分求助中
Production Logging: Theoretical and Interpretive Elements 2000
Very-high-order BVD Schemes Using β-variable THINC Method 1200
BIOLOGY OF NON-CHORDATES 1000
进口的时尚——14世纪东方丝绸与意大利艺术 Imported Fashion:Oriental Silks and Italian Arts in the 14th Century 800
Autoregulatory progressive resistance exercise: linear versus a velocity-based flexible model 550
The Collected Works of Jeremy Bentham: Rights, Representation, and Reform: Nonsense upon Stilts and Other Writings on the French Revolution 320
Generative AI in Higher Education 300
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 细胞生物学 免疫学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3354530
求助须知:如何正确求助?哪些是违规求助? 2978841
关于积分的说明 8687964
捐赠科研通 2660478
什么是DOI,文献DOI怎么找? 1456652
科研通“疑难数据库(出版商)”最低求助积分说明 674435
邀请新用户注册赠送积分活动 665283