Homogeneous Immunosubtraction Integrated with Sample Preparation Enabled by a Microfluidic Format

被引:22
作者
Apori, Akwasi A. [1 ]
Herr, Amy E. [1 ]
机构
[1] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
CEREBROSPINAL-FLUID; CAPILLARY-ELECTROPHORESIS; POLYACRYLAMIDE-GELS; PROTEIN-LEVELS; S100; PROTEIN; SERUM; S-100; IMMUNOASSAYS; DISEASE; INJURY;
D O I
10.1021/ac103219x
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
Immunosubtraction is a powerful and resource-intensive laboratory medicine assay that reports both protein mobility and binding specificity. To expedite and automate this electrophoretic assay, we report on advances to the electrophoretic immunosubtraction assay by introducing a homogeneous, not heterogeneous, format with integrated sample preparation. To accomplish homogeneous immunosubtraction, a step-decrease in separation matrix pore-size at the head of a polyacrylamide gel electrophoresis (PAGE) separation channel enables "subtraction" of target analyte when capture antibody is present (as the large immune-complex is excluded from PAGE), but no subtraction when capture antibody is absent. Inclusion of sample preparation functionality via small pore size polyacrylamide membranes is also key to automated operation (i.e., sample enrichment, fluorescence sample labeling, and mixing of sample with free capture antibody). Homogeneous sample preparation and assay operation allows on-the-fly, integrated subtraction of one to multiple protein targets and reuse of each device. Optimization of the assay is detailed which allowed for similar to 95% subtraction of target with 20% non-specific extraction of large species at the optimal antibody antigen ratio, providing conditions needed for selective target identification. We demonstrate the assay on putative markers of injury and inflammation in cerebrospinal fluid (CSF), an emerging area of diagnostics research, by rapidly reporting protein mobility and binding specificity within the sample matrix. We simultaneously detect S100B and C-reactive protein, suspected biomarkers for traumatic brain injury (TBI), in similar to 2 min. Lastly, we demonstrate S100B detection (65 nM) in raw human CSF with an estimated lower limit of detection of 3.25 nM, within the clinically relevant concentration range for detecting TBI in CSF. Beyond the novel CSF assay introduced here, a fully automated immunosubtraction assay would impact a spectrum of routine but labor and time-intensive laboratory medicine assays.
引用
收藏
页码:2691 / 2698
页数:8
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