Truhlar Stephanie M E, Cervantes Carla F, Torpey Justin W, Kjaergaard Magnus, Komives Elizabeth A
Department of Chemistry and Biochemistry, University of California San Diego, La Jolla 92093-0378, California, USA.
Protein Sci. 2008 Sep;17(9):1636-9. doi: 10.1110/ps.036418.108. Epub 2008 Jun 20.
Advances in NMR spectroscopy have enabled the study of larger proteins that typically have significant overlap in their spectra. Specific (15)N-amino acid incorporation is a powerful tool for reducing spectral overlap and attaining reliable sequential assignments. However, scrambling of the label during protein expression is a common problem. We describe a rapid method to evaluate the fidelity of specific (15)N-amino acid incorporation. The selectively labeled protein is proteolyzed, and the resulting peptides are analyzed using MALDI mass spectrometry. The (15)N incorporation is determined by analyzing the isotopic abundance of the peptides in the mass spectra using the program DEX. This analysis determined that expression with a 10-fold excess of unlabeled amino acids relative to the (15)N-amino acid prevents the scrambling of the (15)N label that is observed when equimolar amounts are used. MALDI TOF-TOF MS/MS data provide additional information that shows where the "extra" (15)N labels are incorporated, which can be useful in confirming ambiguous assignments. The described procedure provides a rapid technique to monitor the fidelity of selective labeling that does not require a lot of protein. These advantages make it an ideal way of determining optimal expression conditions for selectively labeled NMR samples.
核磁共振波谱技术的进步使得对更大的蛋白质进行研究成为可能,这些蛋白质的光谱通常存在显著重叠。特定的(15)N-氨基酸掺入是减少光谱重叠并获得可靠序列归属的有力工具。然而,蛋白质表达过程中标记的混乱是一个常见问题。我们描述了一种快速方法来评估特定(15)N-氨基酸掺入的保真度。将选择性标记的蛋白质进行蛋白酶解,然后使用基质辅助激光解吸电离质谱法(MALDI-MS)分析所得的肽段。通过使用DEX程序分析质谱图中肽段的同位素丰度来确定(15)N的掺入情况。该分析确定,相对于(15)N-氨基酸,使用过量10倍的未标记氨基酸进行表达可防止在使用等摩尔量时观察到的(15)N标记混乱。基质辅助激光解吸电离飞行时间串联质谱(MALDI TOF-TOF MS/MS)数据提供了额外信息,显示了“额外”(15)N标记的掺入位置,这有助于确认模糊的归属。所描述的程序提供了一种快速技术来监测选择性标记的保真度,且不需要大量蛋白质。这些优点使其成为确定选择性标记核磁共振样品最佳表达条件的理想方法。