Centro de Astrobiología (CAB), CSIC-INTA, 28850 Torrejón de Ardoz, Madrid, Spain.
PhD Program in Space Research and Astrobiology, University of Alcalá (UAH), 28805 Alcalá de Henares, Madrid, Spain.
Anal Chem. 2023 Mar 28;95(12):5323-5330. doi: 10.1021/acs.analchem.2c05386. Epub 2023 Mar 16.
Several mass spectrometry and spectroscopic techniques have been used in the search for molecular biomarkers on Mars. A major constraint is their capability to detect and identify large and complex compounds such as peptides or other biopolymers. Multiplex immunoassays can detect these compounds, but antibodies must be produced for a large number of sequence-dependent molecular targets. Ancestral Sequence Reconstruction (ASR) followed by protein "resurrection" in the lab can help to narrow the selection of targets. Herein, we propose an immunoanalytical method to identify ancient and universally conserved protein/peptide sequences as targets for identifying ancestral biomarkers in nature. We have developed, tested, and validated this approach by producing antibodies to eight previously described ancestral resurrected proteins (three β-lactamases, three thioredoxins, one Elongation Factor Tu, and one RuBisCO, all of them theoretically dated as Precambrian), and used them as a proxy to search for any potential feature of them that could be present in current natural environments. By fluorescent sandwich microarray immunoassays (FSMI), we have detected positive immunoreactions with antibodies to the oldest β-lactamase and thioredoxin proteins (ca. 4 Ga) in samples from a hydrothermal environment. Fine epitope mapping and inhibitory immunoassays allowed the identification of well-conserved epitope peptide sequences that resulted from ASR and were present in the sample. We corroborated these results by metagenomic sequencing and found several genes encoding analogue proteins with significant matches to the peptide epitopes identified with the antibodies. The results demonstrated that peptides inferred from ASR studies have true counterpart analogues in Nature, which validates and strengthens the well-known ASR/protein resurrection technique and our immunoanalytical approach for investigating ancient environments and metabolisms on Earth and elsewhere.
几种质谱和光谱技术已被用于在火星上寻找分子生物标志物。一个主要的限制是它们能够检测和识别大型复杂化合物的能力,如肽或其他生物聚合物。多重免疫分析可以检测到这些化合物,但必须为大量依赖序列的分子靶标生产抗体。祖先序列重建(ASR)后在实验室中进行蛋白质“复活”有助于缩小靶标的选择范围。在这里,我们提出了一种免疫分析方法,用于鉴定古老和普遍保守的蛋白质/肽序列作为识别自然界中祖先生物标志物的靶标。我们已经通过产生针对以前描述的八个祖先复活蛋白的抗体来开发、测试和验证了这种方法(三个β-内酰胺酶、三个硫氧还蛋白、一个延伸因子 Tu 和一个 RuBisCO,它们都被理论上追溯到前寒武纪),并将它们用作搜索任何可能存在于当前自然环境中的潜在特征的替代品。通过荧光夹心微阵列免疫分析(FSMI),我们在来自热液环境的样本中检测到针对最古老的β-内酰胺酶和硫氧还蛋白蛋白(约 4Ga)的抗体的阳性免疫反应。精细表位作图和抑制性免疫分析允许鉴定出由 ASR 产生并存在于样品中的保守表位肽序列。我们通过宏基因组测序证实了这些结果,并发现了几个编码与抗体识别的肽表位具有显著匹配的类似蛋白的基因。结果表明,从 ASR 研究推断出的肽在自然界中有真实的对应物模拟物,这验证并加强了众所周知的 ASR/蛋白质复活技术以及我们用于研究地球和其他地方古代环境和代谢物的免疫分析方法。