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Selective biochemical and synthetic biology approaches for improved delivery of recombinant proteins to the extracellular milieu

Selective biochemical and synthetic biology approaches for improved delivery of recombinant proteins to the extracellular milieu
用于改善重组蛋白向细胞外环境的递送的选择性生化和合成生物学方法
批准号:
BB/I020756/1
负责人:
Ian Henderson
金额:
$56.59万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2011
资助国家:
英国
项目状态:
已结题
起止时间:
2011 至 --

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中文摘要
翻译
生物技术产业每年产生的收入超过5000亿英镑。这个行业依靠蛋白质的生产来生产生物制药(新药和疫苗)、用于食品生产和食品中的生物制品(动物保健生物制剂、植物生长生物促进剂和杀虫剂、营养补充剂和食品添加剂),生物修复以净化环境(例如在石油泄漏后分解石油的酶),并可能为污染环境或消耗化石燃料的制造工艺提供替代品(例如从细菌生产氢气的方法;工业催化剂)。制造蛋白质的标准机制是在一种叫做E.杆菌然而,在E.杆菌由于这些蛋白质中的大多数不是来源于大肠杆菌。大肠杆菌中,并产生的水平远远高于E。大肠杆菌通常会产生任何天然蛋白质,E.大肠杆菌通常通过将蛋白质以非活性形式储存在称为包涵体的细胞隔室中来处理它们。蛋白质在包涵体中的积累导致商业生产的问题,包括以活性构象回收蛋白质的昂贵步骤。为了克服这些问题,一些蛋白质在细胞的另一个称为周质的隔室中产生。然而,如果在周质中产生太多的蛋白质,它会使细胞破裂,在此过程中杀死细胞,因此很少或没有蛋白质产生。即使是那些在周质中产生时稳定的,也需要昂贵的纯化,因为有许多其他的天然E。这部分细胞中的大肠杆菌蛋白。当表达非天然蛋白质时,E.大肠杆菌细菌将蛋白质放置在细胞外-这可以防止蛋白质在包涵体或周质中积累,这可能导致细胞死亡。此外,E.大肠杆菌在细胞外不产生或产生很少的天然蛋白质。因此,当蛋白质在细胞外产生时,它们相对清洁,并且需要更少的努力和投资来使它们达到纯度。然而,由于许多技术原因,已经证明在细菌细胞外生产蛋白质是非常困难的。在这里,我们将利用一个非常简单的系统,称为自动转运系统,该系统具有在细胞外产生非天然蛋白质的良好记录。我们已经用这个系统生产了一种与工业相关的蛋白质,证明了这个系统的有效性。我们现在将试图使该系统生产的蛋白质水平有利于工业。
英文摘要
The biotechnology industry produces revenues in excess of £500 billion per year. This industry relies on the production of proteins to produce biopharmaceuticals (novel drugs and vaccines), bioproducts for use in food production and in foods (animal health-care biologics, biological plant-growth promoters and pesticides, nutritional supplements, and food additives), bioremediation to clean up the environment (e.g. enzymes to break down oil after oil spillages) and may offer alternatives to environmentally polluting or fossil-fuel-consuming manufacturing processes (e.g. methods to produce hydrogen from bacteria; industrial catalysts). The standard mechanism for making proteins is to produce them in a non-pathogenic bacterium called E. coli. However, there are limits to the types of protein that can be produced in E. coli. As most of these proteins are not derived from E. coli and are produced at levels much greater than E. coli would normally produce any natural protein, the E. coli bacterium often deals with them by storing the proteins in an inactive form in a compartment of the cell called the inclusion body. The accumulation of proteins in inclusion bodies causes problems for commercial production, including expensive steps to recover the proteins in an active conformation. To overcome these problems some proteins are produced in another compartment of the cell called the periplasm. However, if too much protein is made in the periplasm it can burst the cell open, killing the cell in the process, and therefore little or no protein is produced. Even those that are stable when produced in the periplasm will need expensive purification as there are many other native E. coli proteins in this part of the cell. When expressing a non-native protein the best place for the E. coli bacterium to place the protein is outside of the cell - this prevents accumulation of the protein in inclusion bodies or in the periplasm which might lead to cell death. In addition, the laboratory strains of E. coli produce none, or very little, native proteins outside of the cell. Thus, when proteins are produce outside the cell they are relatively clean and need much less effort and investment to bring them to purity. However, for a number of technical reasons it has proved to be very difficult to produce proteins outside the bacterial cell. Here we will utilise a very simple system called the Autotransporter system which has a proven track record for producing non-native proteins outside of the cell. We have already used this system to produce a proteins relevant to industry proving the system works. We will now attempt to make the system produce proteins at levels which are beneficial to industry.
期刊论文(3)
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会议论文
DOI: 10.1371/journal.pone.0084512
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Browning DF, Matthews SA, Rossiter AE, Sevastsyanovich YR, Jeeves M, Mason JL, Wells TJ, Wardius CA, Knowles TJ, Cunningham AF, Bavro VN, Overduin M, Henderson IR]
通讯作者: Henderson IR
Validation of Early Warning Systems for Severe Maternal Morbidity and Individualised Prediction of Severe Maternal Morbidity within Ethnic Groups
  • 批准号:
    MR/X006115/1
  • 项目类别:
    Fellowship
  • 资助金额:
    $34.9万
  • 财政年份:
    2023
  • 负责人:
    Ian Henderson
  • 依托单位:
Assembling and recombining the Arabidopsis centromeres
  • 批准号:
    BB/V003984/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $81.15万
  • 财政年份:
    2021
  • 负责人:
    Ian Henderson
  • 依托单位:
AAFC IWYP Aligned Call; Circadian clock editing in wheat
  • 批准号:
    BB/T004282/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $25.28万
  • 财政年份:
    2019
  • 负责人:
    Ian Henderson
  • 依托单位:
18-BTT: High-throughput fluorescent crossover reporters to dissect control of tomato meiotic recombination
  • 批准号:
    BB/S020012/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $25.79万
  • 财政年份:
    2019
  • 负责人:
    Ian Henderson
  • 依托单位:
海外基金