Maine Gabriel N, Gluck Nathan, Zaidi Iram W, Burstein Ezra
Department of Clinical Pathology, William Beaumont Hospital, Royal Oak, MI 48073, USA.
Cold Spring Harb Protoc. 2009 Nov;2009(11):pdb.prot5318. doi: 10.1101/pdb.prot5318.
The tandem affinity purification (TAP) procedure was pioneered in yeast for the purpose of purifying and characterizing protein complexes. While affinity purification is relatively easy to perform, nonspecific protein interactions can plague the identification of true interacting partners of the given bait utilized in the purification. To alleviate this problem, two sequential affinity purification steps are employed in the TAP procedure. Since its inception in yeast, TAP has gone through many adaptations and has been employed multiple times in diverse organisms, including mammalian systems. In all these approaches, two out of many possible affinity moieties are employed and are usually expressed as a fusion polypeptide in the amino or carboxyl-terminal region of the protein bait. In this protocol, we describe a variation on the TAP procedure in which the affinity moieties are placed on two different proteins of a molecular complex to isolate or detect components present in the complex. This variation, which we refer to as bimolecular affinity purification (BAP), is suited for the identification of specific molecular complexes marked by the presence of two known components.
串联亲和纯化(TAP)方法是在酵母中开创的,用于纯化和表征蛋白质复合物。虽然亲和纯化相对容易进行,但非特异性蛋白质相互作用可能会困扰纯化过程中所用特定诱饵真正相互作用伙伴的鉴定。为缓解这一问题,TAP方法采用了两个连续的亲和纯化步骤。自其在酵母中问世以来,TAP已历经多次改进,并多次应用于包括哺乳动物系统在内的多种生物体。在所有这些方法中,众多可能的亲和部分中有两个被采用,并且通常在蛋白质诱饵的氨基或羧基末端区域作为融合多肽表达。在本方案中,我们描述了TAP方法的一种变体,其中亲和部分置于分子复合物的两种不同蛋白质上,以分离或检测复合物中存在的组分。这种变体,我们称之为双分子亲和纯化(BAP),适用于鉴定由两种已知组分的存在所标记的特定分子复合物。