Sjöberg Ronald, Mattsson Cecilia, Andersson Eni, Hellström Cecilia, Uhlen Mathias, Schwenk Jochen M, Ayoglu Burcu, Nilsson Peter
Affinity Proteomics, SciLifeLab, School of Biotechnology, KTH - Royal Institute of Technology, Stockholm, Sweden.
Affinity Proteomics, SciLifeLab, School of Biotechnology, KTH - Royal Institute of Technology, Stockholm, Sweden.
N Biotechnol. 2016 Sep 25;33(5 Pt A):582-92. doi: 10.1016/j.nbt.2015.09.002. Epub 2015 Sep 28.
High-density protein microarrays of recombinant human protein fragments, representing 12,412 unique Ensembl Gene IDs, have here been produced and explored. These protein microarrays were used to analyse antibody off-target interactions, as well as for profiling the human autoantibody repertoire in plasma against the antigens represented by the protein fragments. Affinity-purified polyclonal antibodies produced within the Human Protein Atlas (HPA) were analysed on microarrays of three different sizes, ranging from 384 antigens to 21,120 antigens, for evaluation of the antibody validation criteria in the HPA. Plasma samples from secondary progressive multiple sclerosis patients were also screened in order to explore the feasibility of these arrays for broad-scale profiling of autoantibody reactivity. Furthermore, analysis on these near proteome-wide microarrays was complemented with analysis on HuProt™ Human Proteome protein microarrays. The HPA recombinant protein microarray with 21,120 antigens and the HuProt™ Human Proteome protein microarray are currently the largest protein microarray platforms available to date. The results on these arrays show that the Human Protein Atlas antibodies have few off-target interactions if the antibody validation criteria are kept stringent and demonstrate that the HPA-produced high-density recombinant protein fragment microarrays allow for a high-throughput analysis of plasma for identification of possible autoantibody targets in the context of various autoimmune conditions.
本文制备并探索了高密度蛋白质微阵列,其包含代表12412个独特Ensembl基因ID的重组人蛋白质片段。这些蛋白质微阵列用于分析抗体的脱靶相互作用,以及分析血浆中针对蛋白质片段所代表抗原的人类自身抗体库。对人类蛋白质图谱(HPA)中产生的亲和纯化多克隆抗体在三种不同大小的微阵列上进行分析,微阵列包含384种抗原到21120种抗原不等,以评估HPA中的抗体验证标准。还对继发进展型多发性硬化症患者的血浆样本进行了筛选,以探索这些阵列用于大规模分析自身抗体反应性的可行性。此外,对这些接近蛋白质组范围的微阵列的分析辅以对HuProt™人类蛋白质组蛋白质微阵列的分析。具有21120种抗原的HPA重组蛋白质微阵列和HuProt™人类蛋白质组蛋白质微阵列是目前可用的最大的蛋白质微阵列平台。这些阵列的结果表明,如果严格遵守抗体验证标准,人类蛋白质图谱抗体的脱靶相互作用很少,并表明HPA产生的高密度重组蛋白质片段微阵列允许对血浆进行高通量分析,以在各种自身免疫性疾病背景下鉴定可能的自身抗体靶点。