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AACC 50th Anniversary Retrospective |
Wadsworth Center for Laboratories and Research, New York State Department of Health, and, State University of New York at Albany, School of Public Health, Albany, NY 12201-0509, E-mail rej{at}wadsworth.org
This year marks the 50th anniversary of the American Association for Clinical Chemistry. In tribute to this semicentenary, this journal will reflect on its published achievements over the past five decades.1 Our Editor has recently enumerated some of the publications that have had an impact on the field, as demonstrated by a solid history of citation (1). This editorial, the first in a projected series of four to appear this year, will reflect on those papers that have advanced the area of enzymes and protein markers–now a regular feature in these pages.
Of the papers that have achieved citation fame (1), approximately 20% deal with clinical enzymology (2)(3)(4)(5)(6)(7). Yet another 20% focus on the use of enzymes as analytical tools, e.g., those listed in references 8–10. In the first volume of this journal (1954), enzyme measurements as markers of human disease were the focal points of only two papers. The topics were amylase and arginase. None characterized the use of enzymes as analytical reagents, reflecting clinical laboratory practice of the day. Today, in most laboratories, of the two dozen "routine" chemistry analytes, nearly two-thirds are often determined by enzymatic analyses. This is largely the result of the explosion in the number of studies of enzymes as catalysts, markers of disease, and tools for the laboratorian over the 1960s and the subsequent two decades.
This growth phase in enzymology was concurrent with the growth of the practice of clinical chemistry and of the AACC. Without these advances, modern clinical laboratory analyses would not be possible. The detection of proteins in serum by their catalytic activity as a reporter of tissue damage is a cornerstone of medical laboratory analyses. The uses of a wide variety of enzymes from a still wider variety of sources are now firmly entrenched in the arsenal of the laboratorian. The breadth of analysis, from a humble but often critical glucose measurement to the large number of enzymes used in molecular biology, is astonishing. If I may be allowed a degree of nostalgia, this author, who (within acceptable round-off error) completes his 5th decade concurrently with the Association, recalls an analytical chemistry professor chiding him as an undergraduate for considering a career in clinical chemistry or biochemistry. "That's not real chemistry", he asserted, with an almost Nixonian emphasis on the word real, "they use enzymes for everything!". His disdain failed to dissuade me, but his words–unlike most else from that era, these were, after all, the 1960s–are often recalled with an appropriate sense of irony.
A paper that revolutionized the assay of what was, at that time, an
obscure enzyme, 
-glutamyltransferase (EC 2.3.2.2, Fig. 1
), is among the 10 most cited from these pages (810 citations).
It describes the use of -glutamyl-4-nitroanilide as a substrate that
is cleaved to form the easily measured 4-nitroaniline. Until this
publication, assay procedures were not only more cumbersome to perform,
they did not allow monitoring of the reaction rate. Szasz'
(2) method almost instantly was adopted by clinical
laboratories. It was simple, well-characterized, and for the first time
allowed facile measurement of a marker of enzyme induction and
cholestasis. It was widely used as a subsequent action to the finding
of an increased activity of alkaline phosphatase in serum. The method
is still in use some 30 years later, and the name of Szasz is indelibly
linked to the measurement of this enzyme. He and coworkers improved the
method by describing the use of more soluble, derivatized substrates
(11). However, this later method is firmly based on the
original work, and one of the more soluble substrates,
-glutamyl-3-carboxy-4-nitroanilide, was chosen so that reference
values would be comparable with those originally described
(2).
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Gabor Szasz was a European, but he had strong links to AACC, and he chose this journal for much of his work, foreshadowing a wave of manuscripts in subsequent years from outside the US. He is but one of two names that appear more than once in the list of highly cited papers. He alone appears as first author on two publications (2)(5). Seeing his name twice on this list gives us pause to reflect about contributions that might have come from his laboratory had the field not lost one of the pioneers of its growth phase. Upon Szasz' premature death early in 1979, Albert Dietz, then president of the AACC, reflected upon Szasz' collaboration with his American colleagues and recognized his "important contributions to enzymology and clinical chemistry".
I remember Gabor's kindness, wit, and insight. Once, on a visit to my laboratory, the conversation turned to publications and research. I asked if he had read the latest work of so-and-so on some topic of mutual interest. "No!" he replied immediately, in his unique Hungarian-German accent. "One only has time to read or write, not both. I write". I only recently came to know what he meant.
Late in his short life, Szasz turned his attention to creatine kinase
(CK, EC 2.7.3.2), which along with its isoenzyme forms, was at that
time the single most important laboratory marker for myocardial
infarction. His thorough investigation of the conditions for
measurement with Wolfgang Gruber and Erich Bernt (reference
5; Fig. 2
) established the foundation for today's measurement of this
enzyme. Five subsequent papers (12)(13)(14)(15)(16)–also appearing in
these pages–would round out these comprehensive efforts and form the
basis for standardization of measurement of this enzyme.
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CK isoenzyme measurements helped clinicians discriminate between
nonmyocardial and myocardial sources of the enzyme. Before the
development of polyclonal and monoclonal antibodies for isoenzyme
measurements, physical separation was the only option. Donald Mercer
(7) in his classic paper on chromatographic separation of CK
isoenzyme forms (Fig. 3
) provided the first rapid and quantitative technique for the
estimation of this critically important analyte.
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Mercer was frustrated that analysis by polyacrylamide gel electrophoresis and subsequent staining was not sufficiently quantitative for the measurement of CK-2 activity for clinical applications. Then fresh out of graduate school, he had previously used minicolumns for the purification of radiolabeled substrates and reasoned that such an approach would be useful in a clinical laboratory setting. This method served as the basis for many clinical studies (17) and provided the clinical insight that measurement of CK-2 was superior to that of total CK activity (18). The method was found by others to be reliable and highly reproducible, allowed a sufficiently large number of samples to be analyzed within a relatively short period of time, and was the standard for comparison of subsequent analytical techniques (19). The present and future assay of this isoenzyme now appears to be securely in the realm of immunoassay, but the "Mercer-column method" was the gold standard for all quantitative measurements for the decades when the diagnostic application of this test was secured.
Alkaline phosphatases have been nearly a lifelong labor for George
Bowers and Robert McComb. It would not be hyperbole to state that they
wrote the book on this topic (20). However, their
development of a continuous monitoring technique for measuring alkaline
phosphatase (reference 4, Fig. 4
) was their very first collaboration. Until that point, Bob
McComb's interest in the enzyme was as a basic researcher
investigating its activity in tumor cells. George Bowers' interest was
as clinician, but he is more of a chemist than many trained in that
discipline. One of the first lectures on clinical enzymology that I
heard was one presented by George Bowers. His incredible enthusiasm was
infectious.
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The synergistic cooperation of these two workers gave rise to many fruitful collaborations. Many readers will be familiar with papers dealing with enzyme measurements and their standardization from the Hartford team over three decades. It is, therefore, not surprising that their careful description of the conditions for measuring alkaline phosphatase formed the basis for the most popular technique for measuring its activity and the continued citation of this paper over the past 30 years.
As might be expected, the topics of the most highly cited papers (1) correspond well with the workload of most clinical laboratories. An exception is the description of an assay for dopamine-ß-hydroxylase (3), which ranks 12th on the list of citations. This method was developed for clinical applications and allowed investigation of the role of this enzyme in neurological dysfunction. As with the case of CK-2, immunoassay and immunolocalization of this enzyme have had an increased role in studies of neurochemical function.
A common thread of these papers is the thorough investigation of the
problem at hand, an attention to the details of measurement, and the
primary objective of developing techniques suitable for the clinical
application at hand. It is noteworthy that three of these papers
(2)(4)(5) have served to great
extent as the foundations of the International Federation of Clinical
Chemistry (IFCC) reference methods for the three enzymes studied:
-glutamyltransferase (21), creatine kinase
(22), and alkaline phosphatase (23). Those who
were active over the late 1960s through the early 1980s may recall the
plethora of techniques available for enzyme activity, each claiming
some degree of superiority over the others. That was the milieu when
these papers were written. Not unlike today's computer industry, the
benefits of some degree of standardization have allowed significant
progress and comparability of results. The basic work exemplified by
these three papers (2)(4)(5) has
measurably contributed to this accomplishment.
As we look towards the start of the new millennium and the 50th anniversary of this journal a few years later, it appears likely that we will continue to use enzymes for everything. These papers, and their new companions published each year in these pages, will continue to provide the useful tools in the field and exert an influence on still future work.
Footnotes
1 1 This journal followed the founding of the AACC by some six years (24). 
References
-glutamyl transpeptidase. Clin Chem 1969;15:124-136.
[Abstract]
-glutamyl transpeptidase activity. Z Klin Chem Klin Biochem 1974;12:228.[Web of Science][Medline]
[Order article via Infotrieve]
-glutamyltransferase [(-glutamyl)-peptide: amino acid -glutamyltransferase, EC 2.3.2.2]. J Clin Chem Clin Biochem 1983;21:633-646.
[Web of Science][Medline]
[Order article via Infotrieve]
The following articles in journals at HighWire Press have cited this article:
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  R. Rej Clinical Chemistry through Clinical Chemistry: A Journal Timeline Clin. Chem., December 1, 2004; 50(12): 2415 - 2458. [Abstract] [Full Text] [PDF]
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