验证点印迹免疫测定法测量纳米粒子的补体溶血作用

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Yue Li , Andrew Monte , Layne Dylla , S. Moein Moghimi , Dmitri Simberg
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引用次数: 0

摘要

补体在对纳米材料的免疫反应中起着至关重要的作用。补体对异物表面的攻击会导致 C3 沉积、C3 转化酶组装、释放出抗苊毒素 C3a 和 C5a,最后形成膜攻击复合物 C5b-9。有多种技术可以测量液相中的补体活化标记物,但测量表面 C3 沉积的技术却不常见。此前,我们开发了一种基于超速离心的点印迹免疫测定(DBI),用于测量纳米颗粒上 C3 和其他蛋白电晕成分的沉积。在此,我们验证了 DBI 的可重复性及其与通路特异性和常见液相标记物的相关性。此外,我们还讨论了 DBI 的优势,如成本效益和多功能性,同时探讨了其潜在的局限性。这项研究为纳米表面的补体激活提供了见解,为该领域的纳米医学研究人员提供了宝贵的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Validation of dot blot immunoassay for measurement of complement opsonization of nanoparticles

Validation of dot blot immunoassay for measurement of complement opsonization of nanoparticles

Complement plays a critical role in the immune response toward nanomaterials. The complement attack on a foreign surface results in the deposition of C3, assembly of C3 convertases, the release of anaphylatoxins C3a and C5a, and finally, the formation of membrane attack complex C5b-9. Various technologies can measure complement activation markers in the fluid phase, but measurements of surface C3 deposition are less common. Previously, we developed an ultracentrifugation-based dot blot immunoassay (DBI) to measure the deposition of C3 and other protein corona components on nanoparticles. Here, we validate the repeatability of the DBI and its correlation with pathway-specific and common fluid phase markers. Moreover, we discuss the advantages of DBI, such as cost-effectiveness and versatility, while addressing potential limitations. This study provides insights into complement activation at the nanosurface level, offering a valuable tool for nanomedicine researchers in the field.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
120
审稿时长
3 months
期刊介绍: The Journal of Immunological Methods is devoted to covering techniques for: (1) Quantitating and detecting antibodies and/or antigens. (2) Purifying immunoglobulins, lymphokines and other molecules of the immune system. (3) Isolating antigens and other substances important in immunological processes. (4) Labelling antigens and antibodies. (5) Localizing antigens and/or antibodies in tissues and cells. (6) Detecting, and fractionating immunocompetent cells. (7) Assaying for cellular immunity. (8) Documenting cell-cell interactions. (9) Initiating immunity and unresponsiveness. (10) Transplanting tissues. (11) Studying items closely related to immunity such as complement, reticuloendothelial system and others. (12) Molecular techniques for studying immune cells and their receptors. (13) Imaging of the immune system. (14) Methods for production or their fragments in eukaryotic and prokaryotic cells. In addition the journal will publish articles on novel methods for analysing the organization, structure and expression of genes for immunologically important molecules such as immunoglobulins, T cell receptors and accessory molecules involved in antigen recognition, processing and presentation. Submitted full length manuscripts should describe new methods of broad applicability to immunology and not simply the application of an established method to a particular substance - although papers describing such applications may be considered for publication as a short Technical Note. Review articles will also be published by the Journal of Immunological Methods. In general these manuscripts are by solicitation however anyone interested in submitting a review can contact the Reviews Editor and provide an outline of the proposed review.
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