Hopper J E, Brahn E
J Immunol. 1977 Sep;119(3):847-9.
The N-terminal amino acid sequence of an unblocked human heavy chain of an IgGK paraprotein from patient Tho is reported. This unblocked VH sequence belongs to the VHI subgroup and has striking structural homology to an unblocked VHI sequence previously reported for the IgGK paraprotein isolated from the serum of patient Bro. Direct sequence comparison of the Tho and Bro proteins reveals complete structural identity in 25 of the N-terminal 27 residues, with unique amino acid substitutions shared at the N-terminus and positions 16, 18, and 24. This remarkable sequence homology suggests that the two VH sequences represent examples of an unblocked VHI sub-subgroup. The Tho and Bro sequences possess an ala-glu-val basic triplet at positions 9 to 11 in common with the other previously reported VHI proteins which help to further establish this sequence triplet as a recognizable VHI subgroup-specific region. Moreover, in this regard, the unblocked sequences of Tho and Bro emphasize the importance of extending an unblocked VHI sequence beyond positions 9 to 11 before a subgroup assignment can be determined.
报道了来自患者托(Tho)的IgGK副蛋白未封闭的人重链的N端氨基酸序列。这个未封闭的VH序列属于VHI亚组,并且与先前报道的从患者布罗(Bro)血清中分离出的IgGK副蛋白的未封闭VHI序列具有显著的结构同源性。对托和布罗蛋白的直接序列比较显示,在N端的27个残基中的25个残基上结构完全相同,在N端以及第16、18和24位有独特的氨基酸替换。这种显著的序列同源性表明,这两个VH序列代表了未封闭的VHI亚亚组的实例。托和布罗序列在第9至11位具有ala-glu-val碱性三联体,这与其他先前报道的VHI蛋白相同,这有助于进一步将这个序列三联体确立为可识别的VHI亚组特异性区域。此外,在这方面,托和布罗的未封闭序列强调了在确定亚组归属之前,将未封闭的VHI序列延伸到第9至11位之外的重要性。