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不同的视紫红质单克隆抗体在发育中和成年大鼠视网膜上显示出不同的结合模式。

Different rhodopsin monoclonal antibodies reveal different binding patterns on developing and adult rat retina.

作者信息

Hicks D, Barnstable C J

机构信息

Laboratory of Neurobiology, Rockefeller University, New York, New York 10021.

出版信息

J Histochem Cytochem. 1987 Nov;35(11):1317-28. doi: 10.1177/35.11.3655327.

Abstract

We used a battery of 10 monoclonal antibodies directed against different identified peptide sequences within the carboxyl, transmembrane loop, and amino terminal regions of rhodopsin to label retinas from early postnatal and adult rats. Intensity of label, age of initial appearance of staining, and distribution of label varied depending on the antibody. Most antibodies showed detectable labeling at postnatal day 1, and were eventually observed binding to the cell bodies and the inner and outer segments of the photoreceptors. One amino terminal and two carboxyl terminal antibodies, however, showed no detectable labeling until postnatal day 5 and were only transiently detectable in the cell body region. These patterns cannot be explained by accessibility of binding site, binding affinity, fixation artifact, or crossreactivity. The results indicate that physiological and experimental parameters can alter the apparent immunocytochemical localization of conformationally active molecules such as rhodopsin. The results also suggest that rhodopsin can undergo light-dependent conformational changes in several different compartments within rat retinal photoreceptors before the time of eye opening.

摘要

我们使用了一组10种单克隆抗体,这些抗体针对视紫红质羧基、跨膜环和氨基末端区域内不同的已确定肽序列,用于标记出生后早期和成年大鼠的视网膜。标记强度、染色最初出现的年龄以及标记分布因抗体而异。大多数抗体在出生后第1天显示出可检测到的标记,并最终观察到与光感受器的细胞体以及内、外节结合。然而,一种氨基末端抗体和两种羧基末端抗体直到出生后第5天才显示出可检测到的标记,并且仅在细胞体区域短暂可检测到。这些模式无法通过结合位点的可及性、结合亲和力、固定假象或交叉反应来解释。结果表明,生理和实验参数可以改变视紫红质等构象活性分子的表观免疫细胞化学定位。结果还表明,在睁眼之前,视紫红质可以在大鼠视网膜光感受器内的几个不同区室中经历光依赖性构象变化。

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